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 Contents

Chemistry
Allied Health Chemistry������������������������������������������ 2
Analytical Chemistry��������������������������������������������� 36
Biochemistry��������������������������������������������������������� 38
General Chemistry����������������������������������������������� 42
Inorganic Chemistry��������������������������������������������� 87
Introductory / Preparatory Chemistry������������������� 88
Liberal Arts Chemistry���������������������������������������� 104
Organic Chemistry��������������������������������������������� 106
Physical Chemistry��������������������������������������������� 139
Spectroscopy����������������������������������������������������� 140
Combined Author/Title Index����������������������������� 142

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Special price requests for class adoption are subject to approval. Please contact your
Cengage Learning Representative for details.

Information contained in this catalog is correct at the time of printing.

Prices are subject to change without prior notice.

 CHEMISTRY
ALLIED HEALTH CHEMISTRY
GENERAL, ORGANIC, AND
BIOLOGICAL CHEMISTRY, 7E
H. Stephen Stoker, Weber State University
Emphasizing the applications of chemistry and
minimizing complicated mathematics, GENERAL,
ORGANIC, AND BIOLOGICAL CHEMISTRY, 7E
is written throughout to help students succeed in
the course and master the biochemistry content so
important to their future careers. The Six Edition’s
clear explanations, visual support, and effective
pedagogy combine to make the text ideal for allied
health majors. Early chapters focus on fundamental
chemical principles while later chapters build on
the foundations of these principles. Mathematics
is introduced at point-of-use and only as needed.
NEW TO THIS EDITION
• The most powerful online learning solution for
chemistry is better than ever. OWLv2 now has
more flexible student and instructor functionality,
new personalized study tools, enhanced
integration with learning management systems,
and improved analytics. For this course, OWLv2
also includes Quick Prep, an online short course to
review key chemistry concepts and essential skills,
new iPad-compatible visualizations, tutorials, and
simulations, and new Adaptive Study Plans. In
addition, Tutors, Visualizations and Simulations
have been converted from Flash to HTML,
allowing for easier navigation and streamlined
2 www.cengageasia.com
grading.
• Section Quizzes--new section quizzes at the end
of each of section test student understanding of the
section. The quizzes test student understanding at
the micro-level and reinforce key concepts. There
are 356 section quizzes; total of 1, 252 questions.
• Learning Focus--new feature called “Learning
Focus”. Learning focuses are placed at the
beginning of each section and provide students
with insight into what each section is going to
focus on and the associated learning outcomes
for those sections.
FEATURES
• OWLv2 is the most trusted online learning solution
for chemistry. Featuring chemist-developed
content, OWLv2 is the only system designed
to elevate thinking through Mastery Learning,
allowing students to work at their own pace until
they understand each concept and skill. Each
time a student tries a problem, OWLv2 changes
the, chemistry, values, and sometimes even
the wording of the question to ensure students
are learning the concepts and not cheating the
system. With detailed, instant feedback and
interactive learning resources, students get the
help they need when they need it. Now with
improved student and instructor tools and greater
functionality, OWLv2 is more robust than ever.
Discover the power of OWLv2 and take learning
to a higher level.
• Chemistry at-a-Glance features provide brief
visual summaries of core chapter concepts to help
students visualize difficult material.
• Chemical Connection Boxes show chemistry as it
relates to everyday life, highlighting its relevance
to students’ future careers in the health and
environmental fields.
• A wide range of examples throughout the book
help students improve their problem-solving skills.
• Early chapters focus on fundamental chemical
principles; later chapters build on the foundation
of these principles.
• The book is fully integrated with the OWL online
learning system, which saves instructors time
and helps students master concepts and improve
their grades.
 CONTENTS
PART I: GENERAL CHEMISTRY.1. Basic Concepts
About Matter.2. Measurements in Chemistry.3.
Atomic Structure and the Periodic Table.4. Chemical
Bonding: The Ionic Bond Model.5. Chemical Bonding:
The Covalent Bond Model.6. Chemical Calculations:
Formula Masses, Moles, and Chemical Equations.7.
Gases, Liquids, and Solids.8. Solutions.9. Chemical
Reactions.10. Acids, Bases, and Salts.11. Nuclear
Chemistry.PART II: ORGANIC CHEMISTRY.12.
Saturated Hydrocarbons.13. Unsaturated
Hydrocarbons.14. Alcohols, Phenols, and Ethers.15.
Aldehydes and Ketones.16. Carboxylic Acids,
Esters, and Other Acid Derivatives.17. Amines and
Amides.PART III: BIOLOGICAL CHEMISTRY.18.
Carbohydrates.19. Lipids.20. Proteins.21. Enzymes
and Vitamins.22. Nucleic Acids.23. Biochemical
Energy Production.24. Carbohydrate Metabolism.25.
Lipid Metabolism.26. Protein Metabolism.Answers
to Selected ExercisesIndex Glossary
© 2016, 1232pp, Hardback, 9781285853918
www.cengageasia.com
GENERAL, ORGANIC, AND
BIOLOGICAL CHEMISTRY, HYBRID
(WITH OWLV2 QUICK PREP FOR
GENERAL CHEMISTRY PRINTED
ACCESS CARD), 7E
H. Stephen Stoker, Weber State University
Emphasizing the applications of chemistry and
minimizing complicated mathematics, GENERAL,
ORGANIC, AND BIOLOGICAL CHEMISTRY is
written throughout to help students succeed in
the course and master the biochemistry content
so important to their future careers. This Edition’s
clear explanations, visual support, and effective
pedagogy combine to make the text ideal for allied
health majors. Early chapters focus on fundamental
chemical principles while later chapters build on
the foundations of these principles. Mathematics
is introduced at point-of-use and only as needed.
NEW TO THIS EDITION
• The most powerful online learning solution for
chemistry is better than ever. OWLv2 now has
more flexible student and instructor functionality,
new personalized study tools, enhanced
integration with learning management systems,
and improved analytics. For this course, OWLv2
also includes Quick Prep, an online short course to
review key chemistry concepts and essential skills,
new iPad-compatible visualizations, tutorials, and
simulations, and new Adaptive Study Plans. In
addition, Tutors, Visualizations and Simulations
have been converted from Flash to HTML,
allowing for easier navigation and streamlined
grading.
3
 • Section Quizzes--new quick quizzes at the end of About Matter. 2. Measurements in Chemistry.
each of section test student understanding at the 3. Atomic Structure and the Periodic Table. 4.
section level, and reinforce key concepts. There Chemical Bonding: The Ionic Bond Model. 5.
are 356 section quizzes; total of 1, 252 questions. Chemical Bonding: The Covalent Bond Model. 6.
• Learning Focus--new feature called “Learning Chemical Calculations: Formula Masses, Moles,
Focus”. Learning focuses are placed at the and Chemical Equations. 7. Gases, Liquids, and
beginning of each section and provide students Solids. 8. Solutions. 9. Chemical Reactions. 10.
with insight into what each section is going to Acids, Bases, and Salts. 11. Nuclear Chemistry.
focus on and the associated learning outcomes PART II: ORGANIC CHEMISTRY.12. Saturated
for those sections. Hydrocarbons. 13. Unsaturated Hydrocarbons. 14.
FEATURES Alcohols, Phenols, and Ethers. 15. Aldehydes and
Ketones. 16. Carboxylic Acids, Esters, and Other
• OWLv2 is the most trusted online learning solution Acid Derivatives. 17. Amines and Amides. PART III:
for chemistry. Featuring chemist-developed BIOLOGICAL CHEMISTRY.18. Carbohydrates. 19.
content, OWLv2 is the only system designed Lipids. 20. Proteins. 21. Enzymes and Vitamins. 22.
to elevate thinking through Mastery Learning, Nucleic Acids. 23. Biochemical Energy Production.
allowing students to work at their own pace until 24. Carbohydrate Metabolism. 25. Lipid Metabolism.
they understand each concept and skill. Each 26. Protein Metabolism. Answers to Selected
time a student tries a problem, OWLv2 changes Exercises.Index Glossary.
the, chemistry, values, and sometimes even
the wording of the question to ensure students © 2016, 1040pp, Paperback, 9781305253070
are learning the concepts and not cheating the
system. With detailed, instant feedback and
interactive learning resources, students get the
help they need when they need it. Now with
improved student and instructor tools and greater
functionality, OWLv2 is more robust than ever.
Discover the power of OWLv2 and take learning
to a higher level.
• Chemistry at-a-Glance features provide brief
visual summaries of core chapter concepts to help
students visualize difficult material.
• Chemical Connection Boxes show chemistry as it
relates to everyday life, highlighting its relevance
to students’ future careers in the health and
environmental fields.
• A wide range of examples throughout the book
help students improve their problem-solving skills.
• Early chapters focus on fundamental chemical
principles; later chapters build on the foundation
of these principles.
• The book is fully integrated with the OWL online
learning system, which saves instructors time
and helps students master concepts and improve
their grades.
CONTENTS
PART I: GENERAL CHEMISTRY.1. Basic Concepts

4 www.cengageasia.com

INTRODUCTION TO GENERAL,
ORGANIC AND BIOCHEMISTRY, 11E
Frederick A. Bettelheim, Adelphi University; William H. Brown,
Beloit College; Mary K. Campbell, Mount Holyoke College;
Shawn O. Farrell, Olympic Training Center
This bestselling text continues to lead the way with
a strong focus on current issues, pedagogically rich
framework, wide variety of medical and biological
applications, visually dynamic art program, and
exceptionally strong and varied end-of-chapter
problems. Revised and updated throughout, the
tenth edition now includes new biochemistry
content, new Chemical Connections essays, new
and revised problems, and more. Most end of
chapter problems are now available in the OWL
online learning system.
NEW TO THIS EDITION
• The most powerful online learning solution for
chemistry is better than ever. OWLv2 now has
more flexible student and instructor functionality,
new personalized study tools, enhanced
integration with learning management systems,
and improved analytics. For this course, OWLv2
also includes Quick Prep, an online short course
to review key chemistry concepts and essential
skills, hundreds of new interactive end-of-chapter
questions from the text, and new Adaptive Study
Plans. In addition, Tutors, Visualizations and
Simulations have been converted from Flash
to HTML, allowing for easier navigation and
streamlined grading.
• Features to highlight: Updated and new Chemical
Connection boxes featuring the latest hot topics
www.cengageasia.com
in general, organic and biochemistry.
• New Challenge Problems--these problems test
understanding of important concepts by building
on material presented in earlier chapters. For
example in chapter 4 the challenge problems draw
of material introduced in chapters 1-4.
• General Chemistry: Chapter 1--Emphasis
on solving healthcare application conversion
problems related to a clinical setting. Chapter
4, Chemical Reactions, introduces the various
intricacies in writing and balancing chemical
reactions before stoichiometry is introduced. This
chapter includes the How To box, How to Balance
a Chemical Equation, which illustrates a step-by-
step method for balancing an equation. Twenty-
three new challenge problems were added.
• Expanded the list of common organic functional
groups to include amides and presented a
schematic of a tripeptide to show the importance
of amide bonds in the structure of polypeptides
and proteins. Expanded the discussion of the
reactions of phenols to include the oxidation
of phenols to quinones and the use of the
hydroquinone to quinone interconversion in black-
and-white photography and continuing with role of
Coenzyme Q (ubiquinone) in the respiratory chain
as a carrier of electrons and concluding with the
structure of vitamin K and its role in blood clotting.
• Biochemistry--this edition introduces three of the
newest RNA types to be discovered and there is
a new section on epigenetics.
FEATURES
• OWLv2 is the most trusted online learning solution
for chemistry. Featuring chemist-developed
content, OWLv2 is the only system designed
to elevate thinking through Mastery Learning,
allowing students to work at their own pace until
they understand each concept and skill. Each
time a student tries a problem, OWLv2 changes
the, chemistry, values, and sometimes even
the wording of the question to ensure students
are learning the concepts and not cheating the
system. With detailed, instant feedback and
interactive learning resources, students get the
help they need when they need it. Now with
improved student and instructor tools and greater
functionality, OWLv2 is more robust than ever.
5
 Discover the power of OWLv2 and take learning
to a higher level.
• Problem-Solving Strategies: To help students
organize the information to solve a problem, each
chapter example includes a description of the
strategy used to arrive at the solution.
• Visual Impact: Many illustrations have heightened
pedagogical impact. Figures such as Figures 6.4
(Henry’s Law) and 6.11 (electrolytic conductance)
show the microscopic and macroscopic aspects
of a topic under discussion.
• Chemical Connections: More than 150 essays with
photos describe applications of chemical concepts
presented in the text, linking the chemistry to their LAB MANUAL FOR STOKER’S
real uses. In addition, application boxes cover GENERAL, ORGANIC, AND
diverse topics such as diseases, drugs, and BIOLOGICAL CHEMISTRY, 7TH, 7E
biochemical pathways. H. Stephen Stoker, Weber State University
CONTENTS
Each experiment in this manual was selected
1. Matter, Energy, and Measurement.2. Atoms.3. to match topics in your textbook and includes
Chemical Bonds.4. Chemical Reactions.5. Gases, an introduction, a procedure, a page of pre-lab
Liquids, and Solids.6. Solutions and Colloids.7. exercises about the concepts the lab illustrates, and
Reaction Rates and Chemical Equilibrium.8. a report form. Some have a scenario that places
Acids and Bases.9. Nuclear Chemistry.10. the experiment in a real-world context. In addition,
Organic Chemistry.11. Alkanes.12. Alkenes and each experiment has a link to a set of references
Alkynes.13. Benzene and Its Derivatives.14. and helpful online resources.
Alcohols, Ethers, and Thiols.15. Chirality: The
© 2016, 448pp, Paperback, 9781305081093
Handedness of Molecules.16. Amines.17.
Aldehydes and Ketones.18. Carboxylic Acids.19.
Carboxylic Anhydrides, Esters, and Amides.20.
Carbohydrates.21. Lipids.22. Proteins.23.
Enzymes.24. Chemical Communications:
Neurotransmitters and Hormones.25. Nucleotides,
Nucleic Acids, and Heredity.26. Gene Expression
and Protein Synthesis.27. Bioenergetics: How
the Body Converts Food to Energy.28. Specific
Catabolic Pathways: Carbohydrate, Lipid, and
Protein Metabolism.29. Biosynthetic Pathways.30.
Nutrition.31. Immunochemistry32. Body Fluids.
Appendix 1. Exponential Notation.Appendix
2. Significant Figures.Answers to In-Text and
Odd-Numbered End-of-Chapter Problems.
GlossaryCreditsIndex.
© 2016, 1056pp, Hardback, 9781285869759

6 www.cengageasia.com
 a wide range of possibilities to suit their lab.
CONTENTS
Preface.Acknowledgements.Practice Safe
Laboratory.1. Laboratory Measurements.2. Density
Determination.3. Classes of Chemical Reactions.4.
Physical Properties of Chemicals: Melting Point,
Sublimation, and Boiling Point.5. Factors Affecting
Rate of Reactions.6. The Law of Chemical
Equilibrium and the Le Chatelier Principle.7.
pH and Buffer Solutions.8. Structure in Organic
Compounds: Use of Molecular Models.9. Aspirin:
Preparation and Properties (Acetylsalicylic Acid).10.
BASIC LABORATORY EXPERIMENTS Carbohydrates.11. Fats and Oils: Preparation
FOR GENERAL, ORGANIC, AND and Properties of Soap.12. Separation of Amino
BIOCHEMISTRY, 2E Acids by Paper Chromotography.13. Isolation and
Joseph M. Landesberg, Adelphi University Identification of Casein.14. Enzymes.Appendix 1:
Use of the Laboratory Gas Burner.Appendix 2: List
Focused, streamlined, and designed throughout of Apparatus and Equipment in Student’s Locker.
to meet the needs of the one-term GOB Lab Appendix 3: List of Common Equipment and Material
course, this manual features 14 easy-to-follow in the Laboratory.Appendix 4: Special Equipment
experiments (6 general chemistry, 4 organic and Chemical Preparations for Each Experiment.
chemistry, and 4 biochemistry) that illustrate the
© 2015, 240pp, Paperback, 9781285459653
key concepts that every allied health student must
know. Clear directions help students complete labs
successfully, while pre- and post-lab questions for
every experiment test their ability to apply concepts.
NEW TO THIS EDITION
• Labs have been updated with the most recent
data and values in order to accurately reflect the
changes in lab courses. Experiments 2 and 12
have been heavily revised, and includes new art.
FEATURES
• DESIGNED FOR NURSING AND HEALTH
SCIENCE MAJORS. Focusing on the key
concepts most important to allied health majors,
this streamlined lab manual is ideal for the
one-term General, Organic, and Biochemistry
laboratory course.
• CLEAR AND STRAIGHTFORWARD. Clear
directions help students complete labs successfully.
• A FOCUS ON APPLICATION. Pre- and post-lab
questions for every experiment test the student’s
ability to understand and apply concepts.
• OPTIONS. Many labs include multiple equipment
and technique options to provide instructors with

www.cengageasia.com
7

GENERAL, ORGANIC, AND
BIOCHEMISTRY, 2E
An Applied Approach
James Armstrong, City College of San Francisco
Focusing on the needs of allied health and nursing
majors, this engaging book is ideal for students
who have had no prior exposure to chemistry. The
author takes the time to explain how to do tasks
that students find difficult, rather than just providing
terse descriptions. Emphasizing problem-solving
techniques without skipping steps and using terms
students can grasp, the book takes the most direct
path to biomolecules and metabolic processes,
provides a wealth of worked examples to help
students understand key chemical concepts,
includes novel and relevant “Health Notes” in
the margins, and weaves biological and medical
applications throughout.
NEW TO THIS EDITION
• The #1 online homework and learning system
for chemistry, OWLv2, is available for this text-
now with new instructor features and enhanced
functionality: a Dashboard that consolidates
all course materials; easy, intuitive assignment
creation and management; ability to preview and
select activities/questions for each assignment;
new assignment settings and options; improved
gradebook; Personalized Study tools to help
students focus their time on the key concepts and
skills; and MindTap Reader™, a new eBook with
apps and embedded video, audio, annotations,
and activities. OWLv2 courses for Gen Chem,
GOB, and Liberal Arts now include Quick Prep
8 www.cengageasia.com
essential skills assignments that can be taken
before the semester begins or during the first few
weeks, to help students succeed in the course. For
this course, OWLv2 also includes new interactive
versions of the end-of-chapter questions from
the text and new iPad-compatible visualizations,
tutorials, and simulations.
• The chapter on nuclear chemistry (formerly
Chapter 16) has been moved to the end of the
material on general chemistry, becoming Chapter
8 in the second edition.
• To streamline the text, the following peripheral
topics have been eliminated: heating and cooling
curves, the ideal gas law, precipitation reactions,
Le Châtelier’s principle, mass-energy conversion
calculations, bombardment reactions and the
production of radioisotopes, Markovnikov’s rule,
the solubility of organic compounds in organic
solvents, the structures and functions of steroids,
and anabolic pathways.
• The sections on biologically important amines and
on radioisotopes in medicine have been replaced
by new end-of-chapter “Connections” essays
covering much of the same material.
• Coverage of the moles and molar masses has
been moved from Chapter 5 to the end of Chapter
2, allowing early exposure to this often-difficult
concept.
• The topic sequence in Chapter 2 has been revised
extensively, giving a more logical flow of subject
matter. The electronic structure of atoms is now
covered immediately after the introduction to
atoms, allowing uninterrupted coverage of atomic
structure. The separate sections on the periodic
table have been combined into a single section,
which appears after the material on electronic
structure. The material on chemical similarities
has been compressed and moved to Chapter 3.
• The material on gas law computations, which
was formerly placed in the appendices, has been
streamlined and moved into Chapter 4. At the
same time, the two sections on solubility have
been moved from Chapter 4 to Chapter 5. The
remaining sections of Chapter 4 have been edited
to improve the flow of this chapter. These changes
give a better topic balance between Chapters 2,
4 and 5.
• Condensed structures for unbranched hydrocarbon
chains are introduced in Chapter 5, simplifying the
molecular structures required in the discussion of
amphipathic compounds.
• A discussion of the carbon cycle has been
added to Chapter 6, following the introduction of
combustion reactions.
• The coverage of the properties of acids and
bases in Chapter 7 has been simplified, with the
elimination of subsections on the relationship
between the pH of a solution and the molarity and
strength of the acid or base in the solution.
CONTENTS
1. MEASUREMENTS IN SCIENCE AND
MEDICINE.1.1 Measuring size: distance, mass,
and volume. 1.2 Measurements in science:
precision and accuracy. 1.3 Metric units and
their relationships. 1.4 Unit conversions and
conversion factors. 1.5 Using multiple conversion
factors. 1.6 Density, dosage, and other compound
units1.7 Temperature. Connections: Why Do We
Struggle Against the Metric System?2. ATOMS,
ELEMENTS, AND COMPOUNDS.2.1 Classifying
matter: mixtures, compounds, and elements. 2.2
Atoms and atomic structure.2.3 Electron shells and
valence electrons. 2.4 An introduction to the periodic
table. 2.5 Isotopes and atomic weight. 2.6 Moles.
2.7 Compounds, chemical formulas, and moles.
Connections: The Elements of Life.3. CHEMICAL
BONDS.3.1 Covalent bonds and the octet rule. 3.2
Double and triple bonds. 3.3 Electronegativity and
polar bonds. 3.4 Naming covalent compounds. 3.5
Ions and ionic compounds. 3.6 Writing formula for
ionic compounds. 3.7 Naming ionic compounds. 3.8
Polyatomic ions. 3.9 Recognizing ionic and molecular
compounds. Connections: Nitrogen and Oxygen:
A Remarkable Partnership.4. ENERGY AND
PHYSICAL PROPERTIES.4.1 Heat and energy.
4.2 The three states of matter. 4.3 The properties of
gases. 4.4 Gas law calculations. 4.5 Attractive forces
and the physical properties of matter. 4.6 Solutions
and the dissolving process. 4.7 Electrolytes
and dissociation. Connections: Temperature,
Pressure, and Volume in Everyday Life.5.
SOLUTION CONCENTRATION.5.1 Concentration.
5.2 Solubility. 5.3 The relationship between
solubility and molecular structure. 5.4 Molarity. 5.5
www.cengageasia.com
Osmosis, dialysis, and tonicity. 5.6 Equivalents. 5.7
Dilution. Connections: Physiological Dehydration.6.
CHEMICAL REACTIONS.6.1 Physical changes
and chemical reactions. 6.2 Chemical equations.
6.3 Mass relationships in a chemical reaction. 6.4
Heats of reaction. 6.5 Combustion reactions and
the carbon cycle. 6.6 Reaction rate and activation
energy. 6.7 Chemical equilibrium. Connections:
Energy from Food.7. ACIDS AND BASES.7.1
The self-ionization of water. 7.2 The pH scale. 7.3
Properties of acids. 7.4 Properties of bases. 7.5
Acid-base reactions. 7.6 Amphiprotic molecules
and ions. 7.7 Buffers. 7.8 The role of buffers in
human physiology. Connections: Consequences of
Blood pH Changes.8. NUCLEAR CHEMISTRY.8.1
Nuclear symbols. 8.2 Writing nuclear equations.
8.3 Energy and nuclear reactions.8.4 Measuring
radiation. 8.5 Radiation sources and shielding. 8.6
Nuclear decay and half-life. 8.7 Nuclear fission
and fusion. Connections: Diagnostic Imaging.9.
HYDROCARBONS: AN INTRODUCTION TO
ORGANIC MOLECULES.9.1 The special properties
of carbon. 9.2 Linear alkanes: the foundation
of organic chemistry.9.3 Branched alkanes,
cycloalkanes, and isomers. 9.4 Naming branched
alkanes: the IUPAC system. 9.5 Functional groups.
9.6 Alkenes and alkynes. 9.7 Cis and trans isomers
of alkenes.9.8 Benzene and aromatic compounds.
9.9 Properties of hydrocarbons. Connections:
High-Octane Hydrocarbons.10. HYDRATION,
DEHYDRATION, AND ALCOHOLS.10.1 The
hydration reaction. 10.2 Controlling the product: an
introduction to enzymes. 10.3 Naming alcohols. 10.4
The physical properties of alcohols. 10.5 Chirality in
organic molecules. 10.6 The dehydration reaction.
10.7 Phenols and thiols. Connections: Alcohols for
Drinking – Or Not.11. CARBONYL COMPOUNDS
AND REDOX REACTIONS.11.1 Hydrogenation
and dehydrogenation. 11.2 Oxidation and reduction
reactions and the carbonyl group. 11.3 The naming
and properties of aldehydes and ketones. 11.4 Other
oxidation and reduction reactions. 11.5 Carboxylic
acids. 11.6 Biological oxidations and reductions: the
redox coenzymes. 11.7 Introduction to metabolic
pathways. Connections: Fragrances and Flavors.12.
ORGANIC ACIDS AND BASES.12.1 Reactions of
organic acids. 12.2 Decarboxylation reactions. 12.3
9
 Amines. 12.4 Acid-base reactions of amines. 12.5
The physiological behavior of organic acids and
bases. Connections: Messing With Your Mind: The
Power of Tryptamines.13. CONDENSATION AND
HYDROLYSIS REACTIONS.13.1 An introduction to
condensation reactions: ethers. 13.2 Esterification,
amidation, and phosphorylation. 13.3 Condensation
polymers. 13.4 Hydrolysis. 13.5 The effect of
pH on the products of hydrolysis. 13.6 The ATP
cycle. Connections: Common Pain Relievers.14.
PROTEINS.14.1 Amino acids. 14.2 Peptide bonds
and the secondary structure of a protein. 14.3
Side chain interactions and tertiary structure. 14.4
Protein denaturation. 14.5 Enzyme structure and
function. 14.6 Sources and metabolism of amino
acids. Connections: Enzyme Assays in Medicine.15.
CARBOHYDRATES.15.1 Monosaccharides. 15.2
Isomeric forms of monosaccharides: anomers
and enantiomers.15.3 Disaccharides and the
glycosidic linkage. 15.4 Common disaccharides
and polysaccharides. 15.5 Carbohydrate
catabolism. Connections: The Importance of Blood
Glucose.16. LIPIDS AND MEMBRANES.16.1
Fatty acids and triglycerides. 16.2 Chemical
reactions of triglycerides. 16.3 Catabolism of
fatty acids. 16.4 Glycerophospholipids and cell
membranes. 16.5 Concentration gradients and ATP
formation. Connections: Brown Adipose Tissue
and Uncouplers.17. NUCLEIC ACIDS, PROTEIN
SYNTHESIS, AND HEREDITY.17.1 Nucleotides.
17.2 Structures of nucleic acid. 17.3 DNA replication.
17.4 Transcription and RNA processing. 17.5
Translation and the genetic code. 17.6 The
mechanism of protein synthesis. 17.7 Mutations
and genetic disorders. Connections: The Human
Genome Project and Genetic Screening.Appendix
A Mathematics Supplement.Appendix B Summary
of Organic Functional Groups.Appendix C Answers
to Selected Problems.
© 2015, 736pp, Hardback, 9781285430232
10 www.cengageasia.com
GENERAL, ORGANIC, AND
BIOCHEMISTRY, HYBRID EDITION
(WITH OWLV2 24-MONTHS PRINTED
ACCESS CARD), 2E
James Armstrong, City College of San Francisco
Reflecting Cengage Learning’s commitment to
offering flexible teaching solutions and value for
students and instructors, this new hybrid version
features the instructional presentation found in the
printed text while delivering all the end-of chapter
exercises online in OWLv2, the leading online
learning system for chemistry. The result—a briefer
printed text that engages students online! Help your
students improve their grades and understanding of
concepts with this value-packed Hybrid Edition. An
access code to OWLV2 WITH MINDTAP READER,
is included with the text, providing students with
powerful online resources that include tutorials,
simulations, randomized homework questions,
videos, a complete interactive electronic version of
the textbook, and more! Focusing on the needs of
allied health and nursing majors, this engaging book
is ideal for students who have had no prior exposure
to chemistry. The author takes the time to explain
how to do tasks that students find difficult, rather
than just providing terse descriptions. Emphasizing
problem-solving techniques without skipping steps
and using terms students can grasp, the book takes
the most direct path to biomolecules and metabolic
processes, provides a wealth of worked examples
to help students understand key chemical concepts,
includes novel and relevant “Health Notes” in
the margins, and weaves biological and medical
applications throughout.
 NEW TO THIS EDITION
• The #1 online homework and learning system
for chemistry, OWLv2, is available for this text-
now with new instructor features and enhanced
functionality: a Dashboard that consolidates
all course materials; easy, intuitive assignment
creation and management; ability to preview and
select activities/questions for each assignment;
new assignment settings and options; improved
gradebook; Personalized Study tools to help
students focus their time on the key concepts and
skills; and MindTap Reader™, a new eBook with
apps and embedded video, audio, annotations,
and activities. OWLv2 courses for Gen Chem,
GOB, and Liberal Arts now include Quick Prep
essential skills assignments that can be taken
before the semester begins or during the first few
weeks, to help students succeed in the course. For
this course, OWLv2 also includes new interactive
versions of the end-of-chapter questions from
the text and new iPad-compatible visualizations,
tutorials, and simulations.
• The chapter on nuclear chemistry (formerly
Chapter 16) has been moved to the end of the
material on general chemistry, becoming Chapter
8 in the second edition.
• To streamline the text, the following peripheral
topics have been eliminated: heating and cooling
curves, the ideal gas law, precipitation reactions,
Le Châtelier’s principle, mass-energy conversion
calculations, bombardment reactions and the
production of radioisotopes, Markovnikov’s rule,
the solubility of organic compounds in organic
solvents, the structures and functions of steroids,
and anabolic pathways.
• The sections on biologically important amines and
on radioisotopes in medicine have been replaced
by new end-of-chapter “Connections” essays
covering much of the same material.
• Coverage of the moles and molar masses has
been moved from Chapter 5 to the end of Chapter
2, allowing early exposure to this often-difficult
concept.
• The topic sequence in Chapter 2 has been revised
extensively, giving a more logical flow of subject
matter. The electronic structure of atoms is now
covered immediately after the introduction to
www.cengageasia.com
atoms, allowing uninterrupted coverage of atomic
structure. The separate sections on the periodic
table have been combined into a single section,
which appears after the material on electronic
structure. The material on chemical similarities
has been compressed and moved to Chapter 3.
• The material on gas law computations, which
was formerly placed in the appendices, has been
streamlined and moved into Chapter 4. At the
same time, the two sections on solubility have
been moved from Chapter 4 to Chapter 5. The
remaining sections of Chapter 4 have been edited
to improve the flow of this chapter. These changes
give a better topic balance between Chapters 2,
4 and 5.
• Condensed structures for unbranched hydrocarbon
chains are introduced in Chapter 5, simplifying the
molecular structures required in the discussion of
amphipathic compounds.
• A discussion of the carbon cycle has been
added to Chapter 6, following the introduction of
combustion reactions.
• The coverage of the properties of acids and
bases in Chapter 7 has been simplified, with the
elimination of subsections on the relationship
between the pH of a solution and the molarity and
strength of the acid or base in the solution.
CONTENTS
1. MEASUREMENTS IN SCIENCE AND MEDICINE.
Measuring size: distance, mass, and volume.
Measurements in science: precision and accuracy.
Metric units and their relationships. Unit conversions
and conversion factors. Using multiple conversion
factors. Density, dosage, and other compound
unitsTemperature. Connections: Why Do We
Struggle Against the Metric System?2. ATOMS,
ELEMENTS, AND COMPOUNDS.Classifying
matter: mixtures, compounds, and elements. Atoms
and atomic structureElectron shells and valence
electrons. An introduction to the periodic table.
Isotopes and atomic weight. Moles. Compounds,
chemical formulas, and moles. Connections: The
Elements of Life.3. CHEMICAL BONDS.Covalent
bonds and the octet rule. Double and triple
bonds. Electronegativity and polar bonds. Naming
covalent compounds. Ions and ionic compounds.
Writing formula for ionic compounds. Naming ionic
11
 compounds. Polyatomic ions. Recognizing ionic and
molecular compounds. Connections: Nitrogen and
Oxygen: A Remarkable Partnership.4. ENERGY
AND PHYSICAL PROPERTIES.Heat and energy.
The three states of matter. The properties of gases.
Gas law calculations. Attractive forces and the
physical properties of matter. Solutions and the
dissolving process. Electrolytes and dissociation.
Connections: Temperature, Pressure, and Volume
in Everyday Life.5. SOLUTION CONCENTRATION.
Concentration. Solubility. The relationship between
solubility and molecular structure. Molarity.
Osmosis, dialysis, and tonicity. Equivalents.
Dilution. Connections: Physiological Dehydration.6.
CHEMICAL REACTIONS.Physical changes and
chemical reactions. Chemical equations. Mass
relationships in a chemical reaction. Heats of
reaction. Combustion reactions and the carbon
cycle.Reaction rate and activation energy. Chemical
equilibrium. Connections: Energy from Food.7.
ACIDS AND BASES.The self-ionization of water.
The pH scale. Properties of acids. Properties of
bases. Acid-base reactions. Amphiprotic molecules
and ions. Buffers. The role of buffers in human
physiology. Connections: Consequences of Blood
pH Changes.8. NUCLEAR CHEMISTRY.Nuclear
symbols. Writing nuclear equations. Energy and
nuclear reactions. Measuring radiation. Radiation
sources and shielding. Nuclear decay and half-life.
Nuclear fission and fusion. Connections: Diagnostic
Imaging.9. HYDROCARBONS: AN INTRODUCTION
TO ORGANIC MOLECULES.The special properties
of carbon. Linear alkanes: the foundation of organic
chemistry.Branched alkanes, cycloalkanes, and
isomers. Naming branched alkanes: the IUPAC
system. Functional groups. Alkenes and alkynes.
Cis and trans isomers of alkenes. Benzene and
aromatic compounds. Properties of hydrocarbons.
Connections: High-Octane Hydrocarbons.10.
HYDRATION, DEHYDRATION, AND ALCOHOLS.
The hydration reaction. Controlling the product: an
introduction to enzymes. Naming alcohols. The
physical properties of alcohols. Chirality in organic
molecules.The dehydration reaction. Phenols and
thiols. Connections: Alcohols for Drinking – Or
Not.11. CARBONYL COMPOUNDS AND REDOX
REACTIONS.Hydrogenation and dehydrogenation.
12 www.cengageasia.com
Oxidation and reduction reactions and the carbonyl
group. The naming and properties of aldehydes
and ketones. Other oxidation and reduction
reactions. Carboxylic acids. Biological oxidations
and reductions: the redox coenzymes. Introduction
to metabolic pathways. Connections: Fragrances
and Flavors.12. ORGANIC ACIDS AND BASES.
Reactions of organic acids. Decarboxylation
reactions. Amines. Acid-base reactions of amines.
The physiological behavior of organic acids and
bases. Connections: Messing With Your Mind:
The Power of Tryptamines.13. CONDENSATION
AND HYDROLYSIS REACTIONS.An introduction
to condensation reactions: ethers. Esterification,
amidation, and phosphorylation. Condensation
polymers. Hydrolysis. The effect of pH on the
products of hydrolysis. The ATP cycle. Connections:
Common Pain Relievers.14. PROTEINS.Amino
acids. Peptide bonds and the secondary structure
of a protein. Side chain interactions and tertiary
structure. Protein denaturation. Enzyme structure
and function. Sources and metabolism of amino
acids. Connections: Enzyme Assays in Medicine.15.
CARBOHYDRATES.Monosaccharides. Isomeric
forms of monosaccharides: anomers and enantiomers.
Disaccharides and the glycosidic linkage. Common
disaccharides and polysaccharides. Carbohydrate
catabolism. Connections: The Importance of Blood
Glucose.16. LIPIDS AND MEMBRANES.Fatty acids
and triglycerides. Chemical reactions of triglycerides.
Catabolism of fatty acids. Glycerophospholipids and
cell membranes. Concentration gradients and ATP
formation. Connections: Brown Adipose Tissue
and Uncouplers.17. NUCLEIC ACIDS, PROTEIN
SYNTHESIS, AND HEREDITY.Nucleotides.
Structures of nucleic acids. DNA replication.
Transcription and RNA processing. Translation
and the genetic code. The mechanism of protein
synthesis. Mutations and genetic disorders.
Connections: The Human Genome Project and
Genetic Screening.Appendix A: Mathematics
Supplement.Appendix B: Summary of Organic
Functional Groups.Appendix C: Answers to
Selected Problems.
© 2015, 688pp, Paperback, 9781285461434

CHEMISTRY FOR TODAY, 8E
General, Organic and Biochemistry, International
Edition
Spencer L. Seager, Weber State University; Michael R.
Slabaugh, Weber State University
Distinguished by its superior allied health focus and
integration of technology, Seager and Slabaugh’s
CHEMISTRY FOR TODAY: GENERAL, ORGANIC,
and BIOCHEMISTRY, 8E, International Edition
meets students’ needs through diverse applications,
examples, boxes, interactive technology tools,
and, new to this edition, real life case studies.
CHEMISTRY FOR TODAY: GENERAL, ORGANIC,
and BIOCHEMISTRY, 8E, International Edition
dispels students’ inherent fear of chemistry and
instills an appreciation for the role chemistry
plays in our daily lives through a rich pedagogical
structure and an accessible writing style with lucid
explanations. In addition, the book provides greater
support in both problem-solving and critical-thinking
skills--the skills necessary for student success.
By demonstrating the importance of chemistry
concepts to students’ future careers, the authors
not only help students set goals, but also help them
focus on achieving them.
NEW TO THIS EDITION
• CASE STUDIES/CASE STUDY FOLLOW UPS:
New Case Studies open each chapter with real
life scenarios that students may encounter at
home and at work. Each case study incorporates
critical chemistry concepts from the chapter in an
exciting real life scenario in which the reader feels
as if they are a part of the experience. The case
studies require the student to make a decision
www.cengageasia.com
about what they would do if they were in that
situation. A follow up to each Case Study appears
at the end of each chapter.
• ASK THE EXPERT: Featured on both the book
cover and woven throughout the text the “Ask
the Expert” boxes begin with important questions
about nutrition and fitness as related to chemistry-
-questions that students need to ask and need
to know the answers to. The “Ask the Expert”
questions and answers are written by CNN Doctor
Melina D. Jampolis--one of the leading Nutrition
and Fitness experts in the country.
• NEW END-OF-CHAPTER EXERCISES: A
significant number of the end-of-chapter questions
are new.
• ENHANCED OWL (ONLINE WEB LEARNING)
INTEGRATION: For CHEMISTRY FOR TODAY:
GENERAL, ORGANIC, and BIOCHEMISTRY,
8E, International Edition, OWL now includes
more parameterized end-of-chapter questions,
encouraging students to practice multiple
questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts.
OWL also includes Student Self-Assessments,
Interactive Examples from the text, the interactive
customizable Cengage YouBook, a customizable
iPad-compatible multimedia eBook, and an
optional Solutions Manual eBook.
FEATURES
• A UNIQUE AND INSTRUCTIVE ART PROGRAM:
“Talking Labels” in the art itself walk students
through each figure, pointing out what they need
to see. Explanations of figures are incorporated
into the art, rather than appearing in the caption,
to help students follow processes and understand
exactly what is happening within each figure
without having to go back and forth between figure
and caption.
• STUDENT-FOCUSED BOXED FEATURES: New
“Ask the Expert” boxes written by CNN Nutrition
and Fitness Expert Melina D. Jampolis, M.D.
discuss important questions and answers about
nutrition and fitness as related to chemistry; “At
the Counter” boxes focus on drugs and products
found on drugstore shelves and at the pharmacy;
“Chemistry Around Us” boxes present everyday
13
 applications of chemistry; and updated “Chemistry
and Your Health” boxes relate to students’ health
and the health of the patients that they may care
for in their future roles as a part of the allied health
work force.
• A WEALTH OF END-OF-CHAPTER EXERCISES:
The book’s wide range of end-of-chapter exercises
include “Additional Exercises” that are not tied to
a specific section and often consist of problems
that integrate several concepts and “Chemistry for
Thought” exercises that focus on conceptual and
cumulative questions and ask students to apply
what they have learned to a particular cumulative
question.
• ALLIED HEALTH CONNECTION: An “Allied-
Health Exam Connection” section follows
each chapter’s end-of-chapter exercises and
includes chemistry questions found on entrance
examinations used to screen applicants applying
to Allied-Health professional programs.
• INTEGRATED LEARNING OBJECTIVES:
The book’s Learning Objectives are integrated
throughout each chapter and within the summary
to help students focus on the chapter’s key skills
and concepts.
• LEARNING CHECKS: These short, self-check
exercises follow the book’s worked-out examples
and discussions of key or difficult concepts to help
students assess their understanding.
CONTENTS
1. Matter, Measurements, and Calculations.2. Atoms
and Molecules.3. Electronic Structure and the Periodic
Law.4. Forces Between Particles.5. Chemical
Reactions.6. The States of Matter.7. Solutions
and Colloids.8. Reaction Rates and Equilibrium.9.
Acids, Bases, and Salts.10. Radioactivity and
Nuclear Processes.11. Organic Compounds:
Alkanes.12. Unsaturated Hydrocarbons.13.
Alcohols, Phenols, and Ethers.14. Aldehydes
and Ketones.15. Carboxylic Acids and Esters.16.
Amines and Amides.17. Carbohydrates.18.
Lipids.19. Proteins.20. Enzymes.21. Nucleic Acids
and Protein Synthesis.22. Nutrition and Energy for
Life.23. Carbohydrate Metabolism.24. Lipid and
Amino Acid Metabolism.25. Body Fluids.Appendix
A: The International System of Measurements.
Appendix B: Answers to Even-Numbered End-
14 www.cengageasia.com
of-Chapter Exercises.Appendix C: Solutions to
Learning Checks.Glossary.Index.
© 2014, 960pp, Paperback, 9781133604334
CHEMISTRY FOR TODAY, 8E
General Organic and Biochemistry, Hybrid Edition (with
OWLv2 with MindTap Reader 24-Month Printed Access
Card)
Spencer L. Seager, Weber State University; Michael R.
Slabaugh, Weber State University
Reflecting Cengage Learning’s commitment to
offering flexible teaching solutions and value for
students and instructors, this new hybrid version
features the instructional presentation found in
the printed text while delivering all the end-of
chapter exercises online in OWL, the leading
online learning system for chemistry. The result—a
briefer printed text that engages students online!
Distinguished by its superior allied health focus
and integration of technology, The Hybrid Edition
with MindTap Reader of Seager and Slabaugh’s
CHEMISTRY FOR TODAY: GENERAL, ORGANIC,
and BIOCHEMISTRY 8e meets students’ needs
through diverse applications, examples, boxes,
interactive technology tools, and, new to this
edition, real life case studies. CHEMISTRY FOR
TODAY dispels students’ inherent fear of chemistry
and instills an appreciation for the role chemistry
plays in our daily lives through a rich pedagogical
structure and an accessible writing style with lucid
explanations. In addition, the book provides greater
support in both problem-solving and critical-thinking
skills—the skills necessary for student success.
By demonstrating the importance of chemistry
concepts to students’ future careers, the authors
not only help students set goals, but also help them
focus on achieving them.
NEW TO THIS EDITION
• CASE STUDIES/CASE STUDY FOLLOW UPS:
New Case Studies open each chapter with real
life scenarios that students may encounter at
home and at work. Each case study incorporates
critical chemistry concepts from the chapter in an
exciting real life scenario in which the reader feels
as if they are a part of the experience. The case
studies require the student to make a decision
about what they would do if they were in that
situation. A follow up to each Case Study appears
at the end of each chapter.
• ASK AN EXPERT: Featured on both the book
cover and woven throughout the text the “Ask
An Expert” boxes begin with important questions
about nutrition and fitness as related to chemistry—
questions that students need to ask and need
to know the answers to. The “Ask an Expert”
questions and answers are written by CNN Doctor
Melina B. Jampolis—one of the leading Nutrition
and Fitness experts in the country.
• NEW END-OF-CHAPTER EXERCISES: A
significant number of the end-of-chapter questions
are new.
• ENHANCED OWL (ONLINE WEB LEARNING)
INTEGRATION: For the Eighth Edition, OWL
now includes more parameterized end-of-chapter
questions, encouraging students to practice
multiple questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts.
OWL also includes Student Self-Assessments,
Interactive Examples from the text, and more. It
also includes MindTap Reader. MindTap Reader
is a free upgrade to existing readers in Cengage’
s existing digital platforms offering significant new
functionality while also preparing the platforms to
take advantage of future MindTap services.
FEATURES
• A UNIQUE AND INSTRUCTIVE ART PROGRAM:
“Talking Labels” in the art itself walk students
through each figure, pointing out what they need
to see. Explanations of figures are incorporated
www.cengageasia.com
into the art, rather than appearing in the caption,
to help students follow processes and understand
exactly what is happening within each figure
without having to go back and forth between figure
and caption.
• STUDENT-FOCUSED BOXED FEATURES: New
“Ask An Expert” boxes written by CNN Nutrition
and Fitness Expert Melina B. Jampolis, M.D.
discuss important questions and answers about
nutrition and fitness as related to chemistry; “At
the Counter” boxes focus on drugs and products
found on drugstore shelves and at the pharmacy;
“Chemistry Around Us” boxes present everyday
applications of chemistry; and updated “Chemistry
and Your Health” boxes relate to students’ health
and the health of the patients that they may care
for in their future roles as a part of the allied health
work force.
• A WEALTH OF END-OF-CHAPTER EXERCISES:
The book’s wide range of end-of-chapter exercises
include “Additional Exercises” that are not tied to
a specific section and often consist of problems
that integrate several concepts and “Chemistry for
Thought” exercises that focus on conceptual and
cumulative questions and ask students to apply
what they have learned to a particular cumulative
question.
• ALLIED HEALTH CONNECTION: An “Allied-
Health Exam Connection” section follows
each chapter’s end-of-chapter exercises and
includes chemistry questions found on entrance
examinations used to screen applicants applying
to Allied-Health professional programs.
• INTEGRATED LEARNING OBJECTIVES:
The book’s Learning Objectives are integrated
throughout each chapter and within the summary
to help students focus on the chapter’s key skills
and concepts.
• LEARNING CHECKS: These short, self-check
exercises follow the book’s worked-out examples
and discussions of key or difficult concepts to help
students assess their understanding.
CONTENTS
1. Matter, Measurements, and Calculations.2. Atoms
and Molecules.3. Electronic Structure and the Periodic
Law.4. Forces Between Particles.5. Chemical
Reactions.6. The States of Matter.7. Solutions
15
 and Colloids.8. Reaction Rates and Equilibrium.9.
Acids, Bases, and Salts.10. Radioactivity and
Nuclear Processes.11. Organic Compounds:
Alkanes.12. Unsaturated Hydrocarbons.13.
Alcohols, Phenols, and Ethers.14. Aldehydes
and Ketones.15. Carboxylic Acids and Esters.16.
Amines and Amides.17. Carbohydrates.18.
Lipids.19. Proteins.20. Enzymes.21. Nucleic Acids
and Protein Synthesis.22. Nutrition and Energy for
Life.23. Carbohydrate Metabolism.24. Lipid and
Amino Acid Metabolism.25. Body Fluids.Appendix
A: The International System of Measurements.
Appendix B: Answers to Even-Numbered End-
of-Chapter Exercises.Appendix C: Solutions to
Learning Checks.Glossary.Index.
© 2014, 784pp, Paperback, 9781285185972
INTRODUCTORY CHEMISTRY FOR
TODAY, INTERNATIONAL EDITION, 8E
Spencer L. Seager, Weber State University; Michael R.
Slabaugh, Weber State University
Distinguished by its superior allied health focus and
integration of technology, Seager and Slabaugh’s
INTRODUCTORY CHEMISTRY FOR TODAY, 8E,
International Edition meets students’ needs through
diverse applications, examples, boxes, interactive
technology tools, and -- new to this edition -- real
life case studies. The Eighth Edition dispels
students’ inherent fear of chemistry and instills an
appreciation for the role chemistry plays in our daily
lives through a rich pedagogical structure and an
accessible writing style with lucid explanations. In
addition, the book provides greater support in both
16
problem-solving and critical-thinking skills--the skills
necessary for student success. By demonstrating
the importance of chemistry concepts to students’
future careers, the authors not only help students
set goals, but also help them focus on achieving
them.
NEW TO THIS EDITION
• CASE STUDIES/CASE STUDY FOLLOW UPS:
New Case Studies open each chapter with real
life scenarios that students may encounter at
home and at work. Each case study incorporates
critical chemistry concepts from the chapter in an
exciting real life scenario in which the reader feels
as if they are a part of the experience. The case
studies require the student to make a decision
about what they would do if they were in that
situation. A follow up to each Case Study appears
at the end of each chapter.
• ASK THE EXPERT: Featured on both the book
cover and woven throughout the text the “Ask
the Expert” boxes begin with important questions
about nutrition and fitness as related to chemistry-
-questions that students need to ask and need
to know the answers to. The “Ask the Expert”
questions and answers are written by CNN Doctor
Melina D. Jampolis--one of the leading Nutrition
and Fitness experts in the country.
• NEW END-OF-CHAPTER EXERCISES: A
significant number of the end-of-chapter questions
are new.
• ENHANCED OWL (ONLINE WEB LEARNING)
INTEGRATION: For the Eighth Edition, OWL
now includes more parameterized end-of-chapter
questions, encouraging students to practice
multiple questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts.
OWL also includes Student Self-Assessments,
Interactive Examples from the text, the interactive
customizable Cengage YouBook, a customizable
iPad-compatible multimedia eBook, and an
optional Solutions Manual eBook.
FEATURES
• A UNIQUE AND INSTRUCTIVE ART PROGRAM:
“Talking Labels” in the art itself walk students
through each figure, pointing out what they need
www.cengageasia.com
 to see. Explanations of figures are incorporated
into the art, rather than appearing in the caption,
to help students follow processes and understand
exactly what is happening within each figure
without having to go back and forth between figure
and caption.
• STUDENT-FOCUSED BOXED FEATURES: New
“Ask the Expert” boxes written by CNN Nutrition
and Fitness Expert Melina D. Jampolis, M.D.
discuss important questions and answers about
nutrition and fitness as related to chemistry; “At
the Counter” boxes focus on drugs and products
found on drugstore shelves and at the pharmacy;
“Chemistry Around Us” boxes present everyday
applications of chemistry; and updated “Chemistry
and Your Health” boxes relate to students’ health
and the health of the patients that they may care
for in their future roles as a part of the allied health
work force.
• A WEALTH OF END-OF-CHAPTER EXERCISES:
The book’s wide range of end-of-chapter exercises
include “Additional Exercises” that are not tied to
a specific section and often consist of problems
that integrate several concepts and “Chemistry for
Thought” exercises that focus on conceptual and
cumulative questions and ask students to apply
what they have learned to a particular cumulative
question.
• ALLIED HEALTH CONNECTION: An “Allied-
Health Exam Connection” section follows
each chapter’s end-of-chapter exercises and
includes chemistry questions found on entrance
examinations used to screen applicants applying
to Allied-Health professional programs.
• INTEGRATED LEARNING OBJECTIVES:
The book’s Learning Objectives are integrated
throughout each chapter and within the summary
to help students focus on the chapter’s key skills
and concepts.
• LEARNING CHECKS: These short, self-check
exercises follow the book’s worked-out examples
and discussions of key or difficult concepts to help
students assess their understanding.
CONTENTS
1. Matter, Measurements, and Calculations.2. Atoms
and Molecules.3. Electronic Structure and the Periodic
Law.4. Forces Between Particles.5. Chemical
www.cengageasia.com
Reactions.6. The States of Matter.7. Solutions
and Colloids.8. Reaction Rates and Equilibrium.9.
Acids, Bases, and Salts.10. Radioactivity and
Nuclear Processes.11. Organic Compounds:
Alkanes.12. Unsaturated Hydrocarbons.13.
Alcohols, Phenols, and Ethers.14. Aldehydes
and Ketones.15. Carboxylic Acids and Esters.16.
Amines and Amides.17. Carbohydrates.18.
Lipids.19. Proteins.20. Enzymes.21. Nucleic Acids
and Protein Synthesis.22. Nutrition and Energy for
Life.23. Carbohydrate Metabolism.24. Lipid and
Amino Acid Metabolism.25. Body Fluids.Appendix
A: The International System of Measurements.
Appendix B: Answers to Even-Numbered End-
of-Chapter Exercises.Appendix C: Solutions to
Learning Checks.Glossary.Index.
© 2014, 528pp, Paperback, 9781133605119
ORGANIC AND BIOCHEMISTRY FOR
TODAY, INTERNATIONAL EDITION, 8E
Spencer L. Seager, Weber State University; Michael R.
Slabaugh, Weber State University
Distinguished by its superior allied health focus and
integration of technology, Seager and Slabaugh’s
ORGANIC AND BIOCHEMISTRY FOR TODAY,
8E, International Edition meets students’ needs
through diverse applications, examples, boxes,
interactive technology tools, and -- new to this
edition -- real life case studies. The Eighth Edition
dispels students’ inherent fear of chemistry and
instills an appreciation for the role chemistry
plays in our daily lives through a rich pedagogical
structure and an accessible writing style with lucid
17
 explanations. In addition, the book provides greater
support in both problem-solving and critical-thinking
skills--the skills necessary for student success.
By demonstrating the importance of chemistry
concepts to students’ future careers, the authors
not only help students set goals, but also help them
focus on achieving them.
NEW TO THIS EDITION
• CASE STUDIES AND CASE STUDY FOLLOW
UPS: New Case Studies open each chapter with
real life scenarios that students may encounter at
home and at work. Each case study incorporates
critical chemistry concepts from the chapter in an
exciting real life scenario in which readers feel
as if they are a part of the experience. The case
studies require students to make a decision about
what they would do if they were in that situation. A
follow up to each Case Study appears at the end
of each chapter.
• “ASK THE EXPERT” BOXES: Featured on both
the book cover and woven throughout the text
the “Ask the Expert” boxes begin with important
questions about nutrition and fitness as related
to chemistry--questions that students need to ask
and need to know the answers to. The “Ask the
Expert” questions and answers are written by CNN
Doctor Melina D. Jampolis--one of the leading
Nutrition and Fitness experts in the country.
• NEW END-OF-CHAPTER EXERCISES: A
significant number of the end-of-chapter questions
are new.
• ENHANCED OWL (ONLINE WEB LEARNING)
INTEGRATION: For the Eighth Edition, OWL
now includes more parameterized end-of-chapter
questions, encouraging students to practice
multiple questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts.
OWL also includes Student Self-Assessments,
Interactive Examples from the text, the interactive
customizable Cengage YouBook, a customizable
iPad-compatible multimedia eBook, and an
optional Solutions Manual eBook.
FEATURES
• A UNIQUE AND INSTRUCTIVE ART PROGRAM:
“Talking Labels” in the art itself walk students
18 www.cengageasia.com
through each figure, pointing out what they need
to see. Explanations of figures are incorporated
into the art, rather than appearing in the caption,
to help students follow processes and understand
exactly what is happening within each figure
without having to go back and forth between figure
and caption.
• STUDENT-FOCUSED BOXED FEATURES: New
“Ask the Expert” boxes written by CNN Nutrition
and Fitness Expert Melina D. Jampolis, M.D.
discuss important questions and answers about
nutrition and fitness as related to chemistry; “At
the Counter” boxes focus on drugs and products
found on drugstore shelves and at the pharmacy;
“Chemistry Around Us” boxes present everyday
applications of chemistry; and updated “Chemistry
and Your Health” boxes relate to students’ health
and the health of the patients that they may care
for in their future roles as a part of the allied health
work force.
• A WEALTH OF END-OF-CHAPTER EXERCISES:
The book’s wide range of end-of-chapter exercises
include “Additional Exercises” that are not tied to
a specific section and often consist of problems
that integrate several concepts and “Chemistry for
Thought” exercises that focus on conceptual and
cumulative questions and ask students to apply
what they have learned to a particular cumulative
question.
• ALLIED HEALTH CONNECTION: An “Allied-
Health Exam Connection” section follows
each chapter’s end-of-chapter exercises and
includes chemistry questions found on entrance
examinations used to screen applicants applying
to Allied-Health professional programs.
• INTEGRATED LEARNING OBJECTIVES:
The book’s Learning Objectives are integrated
throughout each chapter and within the summary
to help students focus on the chapter’s key skills
and concepts.
• LEARNING CHECKS: These short, self-check
exercises follow the book’s worked-out examples
and discussions of key or difficult concepts to help
students assess their understanding.
CONTENTS
1. Organic Compounds: Alkanes.2. Unsaturated
Hydrocarbons.3. Alcohols, Phenols, and Ethers.4.
Aldehydes and Ketones.5. Carboxylic Acids and
Esters.6. Amines and Amides.7. Carbohydrates.8.
Lipids.9. Proteins.10. Enzymes.11. Nucleic Acids
and Protein Synthesis.12. Nutrition and Energy for
Life.13. Carbohydrate Metabolism.14. Lipid and
Amino Acid Metabolism.15. Body Fluids.Appendix
A: The International System of Measurements.
Appendix B: Answers to Even-Numbered End-
of-Chapter Exercises.Appendix C: Solutions to
Learning Checks.Glossary.Index.
© 2014, 544pp, Paperback, 9781133607496
SAFETY-SCALE LABORATORY
EXPERIMENTS FOR CHEMISTRY FOR
TODAY, 8E
Spencer L. Seager, Weber State University; Michael R.
Slabaugh, Weber State University
This proven lab manual offers a unique blend of
laboratory skills and exercises that effectively
illustrate concepts from the main text, CHEMISTRY
FOR TODAY: GENERAL, ORGANIC, AND
BIOCHEMISTRY, 8e. The book’s 15 general
chemistry and 20 organic/biochemistry safety-
scale laboratory experiments use small quantities
of chemicals and emphasize safety and proper
disposal of materials. “Safety-scale’ is the authors’
own term for describing the amount of chemicals
each lab experiment requires--less than macroscale
quantities, which are expensive and hazardous, and
more than microscale quantities, which are difficult
to work with and require special equipment.
www.cengageasia.com
NEW TO THIS EDITION
• Updated and thoroughly reviewed labs.
FEATURES
• ACCURATE AND CLASS-TESTED. The Eighth
Edition includes 15 general chemistry and 20
organic/biochemistry safety-scale laboratory
experiments--all thoroughly class-tested--that
effectively illustrate the main text’s key concepts.
• A KEY CONCEPT FOCUS: The manual’s blend
of laboratory skills and exercises illustrate key
concepts from the main textbook.
• BUILT-IN PEDAGOGY: Pre-lab questions prepare
students for each lab and end-of-experiment
questions assess student understanding.
• FLEXIBLE AND CONVENIENT. The manual
is three-hole punched and features perforated
pages, which make it easy for student to hand
in lab reports and answers to pre- and post-lab
questions and exercises upon instructor request.
CONTENTS
1. Matter, Measurements, and Calculations.2. Atoms
and Molecules.3. Electronic Structure and the Periodic
Law.4. Forces Between Particles.5. Chemical
Reactions.6. The States of Matter.7. Solutions
and Colloids.8. Reaction Rates and Equilibrium.9.
Acids, Bases, and Salts.10. Radioactivity and
Nuclear Processes.11. Organic Compounds:
Alkanes.12. Unsaturated Hydrocarbons.13.
Alcohols, Phenols, and Ethers.14. Aldehydes
and Ketones.15. Carboxylic Acids and Esters.16.
Amines and Amides.17. Carbohydrates.18.
Lipids.19. Proteins.20. Enzymes.21. Nucleic Acids
and Protein Synthesis.22. Nutrition and Energy for
Life.23. Carbohydrate Metabolism.24. Lipid and
Amino Acid Metabolism.25. Body Fluids.Appendix
A: The International System of Measurements.
Appendix B: Answers to Even-Numbered End-
of-Chapter Exercises.Appendix C: Solutions to
Learning Checks.Glossary.Index.
© 2014, 544pp, Paperback, 9781133604259
19

GENERAL, ORGANIC, AND
BIOLOGICAL CHEMISTRY,
INTERNATIONAL EDITION, 6E
H. Stephen Stoker, Weber State University
Emphasizing the applications of chemistry and
minimizing complicated mathematics, GENERAL,
ORGANIC, AND BIOLOGICAL CHEMISTRY, 6E,
International Edition is written throughout to help
students succeed in the course and master the
biochemistry content so important to their future
careers. The Sixth Edition’s clear explanations,
visual support, and effective pedagogy combine to
make the text ideal for allied health majors. Early
chapters focus on fundamental chemical principles
while later chapters build on the foundations of
these principles. Mathematics is introduced at point-
of-use and only as needed.
NEW TO THIS EDITION
• Several new Chemistry—At-A-Glance boxes
covering critical chemistry concepts have been
added to this edition.
• New Chemical Connection Boxes covering a
variety of topics that relate chemistry to our
everyday lives!.
• Heavily revised art and photography program.
Talking labels have been added to many of
the illustrations—these labels help students
understand the concepts being discussed in the
figure.
• New questions and problems have been added to
the end of chapter question/problem sets including
a new type of problem that is related to the
Chemical Connection boxes—the new questions
20 www.cengageasia.com
are identified with an icon.
• Up to date coverage throughout the text, but
especially the biochemistry chapters. Biochemistry
is an ever changing field and the new edition has
been updated with the latest information in that
field.
• OWL and Youbook: OWL now includes more
parameterized end-of-chapter questions,
encouraging students to practice multiple
questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts. Also
includes Student Self Assessments, the interactive
customizable Cengage YouBook, and an optional
Solutions Manual eBook.
FEATURES
• Chemistry at-a-Glance features provide brief
visual summaries of core chapter concepts to help
students visualize difficult material.
• Chemical Connection Boxes show chemistry as it
relates to everyday life, highlighting its relevance
to students’ future careers in the health and
environmental fields.
• Chemical Connection Boxes show chemistry as it
relates to everyday life, highlighting its relevance
to students’ future careers in the health and
environmental fields.
• Chemical Connection Boxes show chemistry as it
relates to everyday life, highlighting its relevance
to students’ future careers in the health and
environmental fields.
CONTENTS
PART I: GENERAL CHEMISTRY.1. Basic Concepts
About Matter. Chemistry: The Study of Matter.
Physical States of Matter. Properties of Matter.
Changes in Matter. CHEMISTRY AT A GLANCE:
Use of the Terms Physical and Chemical. Pure
Substances and Mixtures. Elements and
Compounds. CHEMISTRY AT A GLANCE: Classes
of Matter. Discovery and Abundance of the
Elements. Names and Chemical Symbols of the
Elements. Atoms and Molecules. Chemical
Formulas. CHEMICAL CONNECTIONS: “Good”
Versus “Bad” Properties for a Chemical Substance
Elemental Composition of the Human Body. 2.
Measurements in Chemistry. Measurement
Systems. Metric System Units. Exact and Inexact
Numbers. Uncertainty in Measurement and
Significant Figures. CHEMISTRY AT A GLANCE:
Significant Figures. Significant Figures and
Mathematical Operations. Scientific Notation.
Conversion Factors. Dimensional Analysis.
CHEMISTRY AT A GLANCE: Conversion Factors.
Density. Temperature Scales. Heat Energy and
Specific Heat. CHEMICAL CONNECTIONS: Body
Density and Percent Body Fat; Normal Human Body
Temperature. 3. Atomic Structure and the Periodic
Table. Internal Structure of an Atom. Atomic Number
and Mass Number. Isotopes and Atomic Masses.
CHEMISTRY AT A GLANCE: Atomic Structure. The
Periodic Law and the Periodic Table. Metals and
Nonmetals. Electron Arrangements Within Atoms.
CHEMISTRY AT A GLANCE: Shell–Subshell–
Orbital Interrelationships. Electron Configurations
and Orbital Diagrams. The Electronic Basis for the
Periodic Law and the Periodic Table. Classification
of the Elements. CHEMISTRY AT A GLANCE:
Element Classification Schemes and the Periodic
Table. CHEMICAL CONNECTIONS: Protium,
Deuterium, and Tritium: The Three Isotopes of
Hydrogen; Metallic Elements and the Human Body;
Iron: The Most Abundant Transition Element in the
Human Body. 4. Chemical Bonding: The Ionic Bond
Model. Chemical Bonds. Valence Electrons and
Lewis Symbols. The Octet Rule. The Ionic Bond
Model. The Sign and Magnitude of Ionic Charge.
Lewis Structures for Ionic Compounds. Chemical
Formulas for Ionic Compounds. The Structure of
Ionic Compounds. Recognizing and Naming Binary
Ionic Compounds. CHEMISTRY AT A GLANCE:
Ionic Bonds and Ionic Compounds. Polyatomic Ions
Chemical Formulas and Names for Ionic Compounds
Containing Polyatomic Ions. CHEMISTRY AT A
GLANCE: Nomenclature of Ionic Compounds.
CHEMICAL CONNECTIONS: Fresh Water,
Seawater, Hard Water, and Soft Water: A Matter of
Ions; Tooth Enamel: A Combination of Monatomic
and Polyatomic Ions. 5. Chemical Bonding: The
Covalent Bond Model. The Covalent Bond Model.
Lewis Structures for Molecular Compounds. Single,
Double, and Triple Covalent Bonds. Valence
Electrons and Number of Covalent Bonds Formed.
Coordinate Covalent Bonds. Systematic Procedures
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for Drawing Lewis Structures. Bonding in Compounds
with Polyatomic Ions Present. Molecular Geometry.
CHEMISTRY AT A GLANCE: The Geometry of
Molecules. Electronegativity. Bond Polarity.
Molecular Polarity. CHEMISTRY AT A GLANCE:
Covalent Bonds and Molecular Compounds.
Naming Binary Molecular Compounds. CHEMICAL
CONNECTIONS: Nitric Oxide: A Molecule Whose
Bonding Does Not Follow “The Rules”; The
Chemical Senses of Smell and Taste. 6. Chemical
Calculations: Formula Masses, Moles, and Chemical
Equations. Formula Masses. The Mole: A Counting
Unit for Chemists. The Mass of a Mole. Chemical
Formulas and the Mole Concept. The Mole and
Chemical Calculations. Writing and Balancing
Chemical Equations. Chemical Equations and the
Mole Concept. CHEMISTRY AT A GLANCE:
Relationships Involving the Mole Concept. Chemical
Calculations Using Chemical Equations. CHEMICAL
CONNECTIONS: Carbon Monoxide Air Pollution: A
Case of Combining Ratios Chemical Reactions on
an Industrial Scale: Sulfuric Acid. 7. Gases, Liquids,
and Solids. The Kinetic Molecular Theory of Matter.
Kinetic Molecular Theory and Physical States. Gas
Law Variables. Boyle’s Law: A Pressure-Volume
Relationship. Charles’s Law: A Temperature-
Volume Relationship. The Combined Gas Law. The
Ideal Gas Law. Dalton’s Law of Partial Pressures.
CHEMISTRY AT A GLANCE: The Gas Laws.
Changes of State. Evaporation of Liquids. Vapor
Pressure of Liquids. Boiling and Boiling Point.
Intermolecular Forces in Liquids. CHEMISTRY AT
A GLANCE: Intermolecular Forces. CHEMICAL
CONNECTIONS: The Importance of Gas Densities;
Blood Pressure and the Sodium Ion/Potassium Ion
Ratio; Hydrogen Bonding and the Density of Water.
8. Solutions. Characteristics of Solutions. Solubility.
Solution Formation. Solubility Rules. Solution
Concentration Units. Dilution. CHEMISTRY AT A
GLANCE: Solutions. Colloidal Dispersions and
Suspensions. Colligative Properties of Solutions.
Osmosis and Osmotic Pressure. CHEMISTRY AT
A GLANCE: Summary of Colligative Property
Terminology. Dialysis. CHEMICAL CONNECTIONS:
Factors Affecting Gas Solubility; Solubility of
Vitamins; Controlled-Release Drugs: Regulating
Concentration, Rate, and Location of Release; The
21
 Artificial Kidney: A Hemodialysis Machine. 9.
Chemical Reactions. Types of Chemical Reactions.
Redox and Nonredox Chemical Reactions.
CHEMISTRY AT A GLANCE: Types of Chemical
Reactions. Terminology Associated with Redox
Processes. Collision Theory and Chemical
Reactions. Exothermic and Endothermic Chemical
Reactions. Factors That Influence Chemical
Reaction Rates. Chemical Equilibrium. CHEMISTRY
AT A GLANCE: Factors That Increase Reaction
Rates. Equilibrium Constants. Altering Equilibrium
Conditions: Le Châtelier’s Principle. CHEMICAL
CONNECTIONS: Combustion Reactions, Carbon
Dioxide, and Global Warming; “Undesirable”
Oxidation–Reduction Processes: Metallic Corrosion;
Stratospheric Ozone: An Equilibrium Situation. 10.
Acids, Bases, and Salts. Arrhenius Acid–Base
Theory. Brønsted–Lowry Acid–Base Theory. Mono-
, Di-, and Triprotic Acids. CHEMISTRY AT A
GLANCE: Acid–Base Definitions. Strengths of Acids
and Bases. Ionization Constants for Acids and
Bases. Salts. Acid–Base Neutralization Chemical
Reactions. Self-Ionization of Water. The pH
Concept. The pKa Method for Expressing Acid
Strength. The pH of Aqueous Salt Solutions.
CHEMISTRY AT A GLANCE: Acids and Acidic
Solutions. Buffers. The Henderson–Hasselbalch
Equation. CHEMISTRY AT A GLANCE: Buffer
Systems. Electrolytes. Equivalents and
Milliequivalents of Electrolytes. Acid–Base Titrations.
CHEMICAL CONNECTIONS: Excessive Acidity
Within the Stomach: Antacids and Acid Inhibitors;
Acid Rain: Excess Acidity; Blood Plasma pH and
Hydrolysis; Buffering Action in Human Blood;
Electrolytes and Body Fluids. 11. Nuclear Chemistry.
Stable and Unstable Nuclides. The Nature of
Radioactive Emissions. Equations for Radioactive
Decay. Rate of Radioactive Decay. CHEMISTRY
AT A GLANCE: Radioactive Decay. Transmutation
and Bombardment Reactions. Radioactive Decay
Series. Chemical Effects of Radiation. Biochemical
Effects of Radiation. Detection of Radiation. Sources
of Radiation Exposure. Nuclear Medicine. Nuclear
Fission and Nuclear Fusion. CHEMISTRY AT A
GLANCE: Characteristics of Nuclear Reactions.
Nuclear and Chemical Reactions Compared.
CHEMICAL CONNECTIONS: Tobacco Radioactivity
22 www.cengageasia.com
and the Uranium-238 Decay Series; Preserving
Food Through Food Irradiation; The Indoor
Radon-222 Problem.PART II: ORGANIC
CHEMISTRY.12. Saturated Hydrocarbons. Organic
and Inorganic Compounds. Bonding Characteristics
of the Carbon Atom. Hydrocarbons and Hydrocarbon
Derivatives. Alkanes: Acyclic Saturated
Hydrocarbons. Structural Formulas. Alkane
Isomerism. Conformations of Alkanes. IUPAC
Nomenclature for Alkanes. Line-Angle Structural
Formulas for Alkanes. CHEMISTRY AT A GLANCE:
Structural Representations for Alkane Molecules.
Classification of Carbon Atoms. Branched-Chain
Alkyl Groups. Cycloalkanes. IUPAC Nomenclature
for Cycloalkanes. Isomerism in Cycloalkanes.
Sources of Alkanes and Cycloalkanes. Physical
Properties of Alkanes and Cycloalkanes. Chemical
Properties of Alkanes and Cycloalkanes.
CHEMISTRY AT A GLANCE: Properties of Alkanes
and Cycloalkanes. Nomenclature and Properties of
Halogenated Alkanes. CHEMICAL CONNECTIONS:
The Occurrence of Methane; The Physiological
Effects of Alkanes; Chlorofluorocarbons and the
Ozone Layer. 13. Unsaturated Hydrocarbons.
Unsaturated Hydrocarbons. Characteristics of
Alkenes and Cycloalkenes. IUPAC Nomenclature
for Alkenes and Cycloalkenes. Line-Angle Structural
Formulas for Alkenes. Constitutional Isomerism in
Alkenes. Cis–Trans Isomerism in Alkenes. Naturally
Occurring Alkenes. Physical Properties of Alkenes
and Cycloalkenes. Chemical Reactions of Alkenes.
Polymerization of Alkenes: Addition Polymers.
Alkynes. CHEMISTRY AT A GLANCE: Chemical
Reactions of Alkenes 383. CHEMISTRY AT A
GLANCE: IUPAC Nomenclature for Alkanes,
Alkenes, and Alkynes. Aromatic Hydrocarbons.
Names for Aromatic Hydrocarbons. Aromatic
Hydrocarbons: Physical Properties and Sources.
Chemical Reactions of Aromatic Hydrocarbons.
Fused-Ring Aromatic Hydrocarbons. CHEMICAL
CONNECTIONS: Ethene: A Plant Hormone and
High-Volume Industrial Chemical; Cis–Trans
Isomerism and Vision; Carotenoids: A Source of
Color; Fused-Ring Aromatic Hydrocarbons and
Cancer. 14. Alcohols, Phenols, and Ethers. Bonding
Characteristics of Oxygen Atoms in Organic
Compounds. Structural Characteristics of Alcohols.
Nomenclature for Alcohols. Isomerism for Alcohols.
Important Commonly Encountered Alcohols.
Physical Properties of Alcohols. Preparation of
Alcohols. Classification of Alcohols. Chemical
Reactions of Alcohols. CHEMISTRY AT A GLANCE:
Summary of Chemical Reactions Involving Alcohols.
Polymeric Alcohols. Structural Characteristics of
Phenols. Nomenclature for Phenols. Physical and
Chemical Properties of Phenols. Occurrence of and
Uses for Phenols. Structural Characteristics of
Ethers. Nomenclature for Ethers. Isomerism for
Ethers. Physical and Chemical Properties of Ethers.
Cyclic Ethers. Sulfur Analogs of Alcohols. Sulfur
Analogs of Ethers. CHEMICAL CONNECTIONS:
Menthol: A Useful Naturally Occurring Terpene
Alcohol; Ethers as General Anesthetics; Marijuana:
The Most Commonly Used Illicit Drug; Garlic and
Onions: Odiferous Medicinal Plants. CHEMISTRY
AT A GLANCE: Alcohols, Thiols, Ethers, and
Thioethers. 15. Aldehydes and Ketones. The
Carbonyl Group. Compounds Containing a Carbonyl
Group. The Aldehyde and Ketone Functional
Groups. Nomenclature for Aldehydes. Nomenclature
for Ketones. Isomerism for Aldehydes and Ketones.
Selected Common Aldehydes and Ketones.
Physical Properties of Aldehydes and Ketones.
Preparation of Aldehydes and Ketones. Oxidation
and Reduction of Aldehydes and Ketones. Reaction
of Aldehydes and Ketones with Alcohols.
CHEMISTRY AT A GLANCE: Summary of Chemical
Reactions Involving Aldehydes and Ketones.
Formaldehyde-Based Polymers. Sulfur-Containing
Carbonyl Groups. CHEMICAL CONNECTIONS:
Lachrymatory Aldehydes and Ketones; Melanin: A
Hair and Skin Pigment; Diabetes, Aldehyde
Oxidation, and Glucose Testing.16. Carboxylic
Acids, Esters, and Other Acid Derivatives. Structure
of Carboxylic Acids and Their Derivatives. IUPAC
Nomenclature for Carboxylic Acids. Common
Names for Carboxylic Acids. Polyfunctional
Carboxylic Acids. Metabolic Acids. Physical
Properties of Carboxylic Acids. Preparation of
Carboxylic Acids. Acidity of Carboxylic Acids.
Carboxylic Acid Salts. Structure of Esters.
Preparation of Esters. CHEMISTRY AT A GLANCE:
Summary of the “H Versus R” Relationship for Pairs
of Hydrocarbon Derivatives. Nomenclature for
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Esters. Selected Common Esters. Isomerism for
Carboxylic Acids and Esters. Physical Properties of
Esters. Chemical Reactions of Esters. Sulfur
Analogs of Esters. CHEMISTRY AT A GLANCE:
Summary of Chemical Reactions Involving
Carboxylic Acids and Esters. Polyesters. Acid
Chlorides and Acid Anhydrides. Esters and
Anhydrides of Inorganic Acids. CHEMICAL
CONNECTIONS: Nonprescription Pain Relievers
Derived from Propanoic Acid Carboxylic Acids and
Skin Care; Aspirin; Nitroglycerin: An Inorganic
Triester. 17. Amines and Amides. Bonding
Characteristics of Nitrogen Atoms in Organic
Compounds. Structure and Classification of Amines.
Nomenclature for Amines. Isomerism for Amines.
Physical Properties of Amines. Basicity of Amines.
Amine Salts. Preparation of Amines and Quaternary
Ammonium Salts. Heterocyclic Amines. Selected
Biochemically Important Amines. Alkaloids.
Structure and Classification of Amides. Nomenclature
for Amides. Selected Amides and Their Uses.
Physical Properties of Amides. Preparation of
Amides. Hydrolysis of Amides.Polyamides and
Polyurethanes. CHEMISTRY AT A GLANCE:
Summary of Chemical Reactions Involving Amines
and Amides. CHEMICAL CONNECTIONS: Caffeine:
The Most Widely Used Central Nervous System
Stimulant; Nicotine Addiction: A Widespread
Example of Drug Dependence; Alkaloids Present in
Chocolate; Acetaminophen: A Substituted Amide.
PART III: BIOLOGICAL CHEMISTRY.18.
Carbohydrates. Biochemistry—An Overview.
Occurrence and Functions of Carbohydrates.
Classification of Carbohydrates. Chirality:
Handedness in Molecules. Stereoisomerism:
Enantiomers and Diastereomers. Designating
Handedness Using Fischer Projection Formulas.
CHEMISTRY AT A GLANCE: Constitutional Isomers
and Stereoisomers. Properties of Enantiomers.
Classification of Monosaccharides. Biochemically
Important Monosaccharides. Cyclic Forms of
Monosaccharides. Haworth Projection Formulas.
Reactions of Monosaccharides. Disaccharides.
CHEMISTRY AT A GLANCE: “Sugar Terminology”
Associated with Monosaccharides and Their
Derivatives. General Characteristics of
Polysaccharides. Storage Polysaccharides.
23
 Structural Polysaccharides. CHEMISTRY AT A
GLANCE: Types of Glycosidic Linkages for Common
Glucose-Containing Diand Polysaccharides. Acidic
Polysaccharides. Glycolipids and Glycoproteins:
Cell Recognition. Dietary Considerations and
Carbohydrates. CHEMICAL CONNECTIONS: Blood
Types and Monosaccharides; Lactose Intolerance
and Galactosemia; Changing Sugar Patterns:
Decreased Sucrose, Increased Fructose; Artificial
Sweeteners; “Good and Bad Carbs”: The Glycemic
Index. 19. Lipids. Structure and Classification of
Lipids. Types of Fatty Acids. Physical Properties of
Fatty Acids. Energy-Storage Lipids: Triacylglycerols.
Dietary Considerations and Triacylglycerols.
Chemical Reactions of Triacylglycerols. CHEMISTRY
AT A GLANCE: Classification Schemes for Fatty
Acid Residues Present in Triacylglycerols.
Membrane Lipids: Phospholipids. Membrane Lipids:
Sphingoglycolipids. CHEMISTRY AT A GLANCE:
Terminology for and Structural Relationships Among
Various Types of Fatty-Acid-Containing Lipids.
Membrane Lipids: Cholesterol. Cell Membranes.
Emulsification Lipids: Bile Acids. Messenger Lipids:
Steroid Hormones. Messenger Lipids: Eicosanoids.
Protective-Coating Lipids: Biological Waxes.
CHEMISTRY AT A GLANCE: Types of Lipids in
Terms of How They Function. CHEMICAL
CONNECTIONS: The Fat Content of Tree Nuts and
Peanuts; Artificial Fat Substitutes; The Cleansing
Action of Soap; Trans Fatty Acids and Blood
Cholesterol Levels; Steroid Drugs in Sports; The
Mode of Action for Anti-Inflammatory Drugs. 20.
Proteins. Characteristics of Proteins. Amino Acids:
The Building Blocks for Proteins. Chirality and Amino
Acids. Acid–Base Properties of Amino Acids.
Cysteine: A Chemically Unique Amino Acid.
Peptides. Biochemically Important Small Peptides.
General Structural Characteristics of Proteins.
Primary Structure of Proteins. Secondary Structure
of Proteins. Tertiary Structure of Proteins. Quaternary
Structure of Proteins. Protein Classification Based
on Shape. Protein Classification Based on Function.
CHEMISTRY AT A GLANCE: Protein Structure.
Protein Hydrolysis. Protein Denaturation.
Glycoproteins. Lipoproteins. CHEMICAL
CONNECTIONS: The Essential Amino Acids;
Substitutes for Human Insulin Protein Structure and
24 www.cengageasia.com
the Color of Meat; Denaturation and Human Hair;
Cyclosporine: An Antirejection Drug; Lipoproteins
and Heart Disease Risk. 21. Enzymes and Vitamins.
General Characteristics of Enzymes. Enzyme
Structure. Nomenclature and Classifi cation of
Enzymes. Models of Enzyme Action. Enzyme
Specificity. Factors That Affect Enzyme Activity.
CHEMISTRY AT A GLANCE: Enzyme Activity.
Enzyme Inhibition. CHEMISTRY AT A GLANCE:
Enzyme Inhibition. Regulation of Enzyme Activity.
Antibiotics That Inhibit Enzyme Activity. Medical
Uses of Enzymes. General Characteristics of
Vitamins. Water-Soluble Vitamins. Fat-Soluble
Vitamins. CHEMICAL CONNECTIONS: H. pylori
and Stomach Ulcers; Enzymatic Browning:
Discoloration of Fruits and Vegetables; Heart
Attacks and Enzyme Analysis. 22. Nucleic Acids.
Types of Nucleic Acids. Nucleotides: Building Blocks
of Nucleic Acids. Primary Nucleic Acid Structure.
CHEMISTRY AT A GLANCE: Nucleic Acid
Structure. The DNA Double Helix. Replication of
DNA Molecules. Overview of Protein Synthesis.
Ribonucleic Acids. CHEMISTRY AT A GLANCE:
DNA Replication. Transcription: RNA Synthesis. The
Genetic Code. Anticodons and tRNA Molecules.
Translation: Protein Synthesis. Mutations. Nucleic
Acids and Viruses. CHEMISTRY AT A GLANCE:
Protein Synthesis: Transcription and Translation.
Recombinant DNA and Genetic Engineering. The
Polymerase Chain Reaction. DNA Sequencing.
CHEMICAL CONNECTIONS: Use of Synthetic
Nucleic Acid Bases in Medicine; Antibiotics That
Inhibit Bacterial Protein Synthesis. 23. Biochemical
Energy Production. Metabolism. Metabolism and
Cell Structure. Important Intermediate Compounds
in Metabolic Pathways. High-Energy Phosphate
Compounds. An Overview of Biochemical Energy
Production. The Citric Acid Cycle. CHEMISTRY AT
A GLANCE: Simplified Summary of the Four Stages
of Biochemical Energy Production. CHEMISTRY AT
A GLANCE: Summary of the Reactions of the Citric
Acid Cycle. The Electron Transport Chain.
CHEMISTRY AT A GLANCE: Summary of the Flow
of Electrons Through the Four Complexes of the
Electron Transport Chain. Oxidative Phosphorylation.
CHEMISTRY AT A GLANCE: Summary of the
Common Metabolic Pathway. ATP Production for
the Common Metabolic Pathway. The Importance
of ATP. Non-ETC Oxygen-Consuming Reactions.
CHEMICAL CONNECTIONS: Cyanide Poisoning;
Brown Fat, Newborn Babies, and Hibernating
Animals; Flavonoids: An Important Class of Dietary
Antioxidants. 24. Carbohydrate Metabolism.
Digestion and Absorption of Carbohydrates.
Glycolysis. Fates of Pyruvate. ATP Production for
the Complete Oxidation of Glucose. Glycogen
Synthesis and Degradation. Gluconeogenesis.
Terminology for Glucose Metabolic Pathways. The
Pentose Phosphate Pathway. CHEMISTRY AT A
GLANCE: Glucose Metabolism. Hormonal Control
of Carbohydrate Metabolism. CHEMICAL
CONNECTIONS: Lactate Accumulation; Diabetes
Mellitus. 25. Lipid Metabolism. Digestion and
Absorption of Lipids. Triacylglycerol Storage and
Mobilization. Glycerol Metabolism. Oxidation of
Fatty Acids. ATP Production from Fatty Acid
Oxidation. Ketone Bodies. Biosynthesis of Fatty
Acids: Lipogenesis. Relationships Between
Lipogenesis and Citric Acid Cycle Intermediates.
Biosynthesis of Cholesterol. CHEMISTRY AT A
GLANCE: Interrelationships Between Carbohydrate
and Lipid Metabolism. Relationships Between Lipid
and Carbohydrate Metabolism. CHEMICAL
CONNECTIONS: High-Intensity Versus Low-
Intensity Workouts; Statins: Drugs That Lower
Plasma Levels of Cholesterol. 26. Protein
Metabolism. Protein Digestion and Absorption.
Amino Acid Utilization. Transamination and
Oxidative Deamination. The Urea Cycle. Amino Acid
Carbon Skeletons. Amino Acid Biosynthesis.
Hemoglobin Catabolism. CHEMISTRY AT A
GLANCE: Interrelationships Among Carbohydrate,
Lipid, and Protein Metabolism. Interrelationships
Among Metabolic Pathways. CHEMICAL
CONNECTIONS: The Chemical Composition of
Urine Arginine, Citrulline, and the Chemical
Messenger Nitric Oxide. Answers to Selected
Exercises A-1.
© 2013, 1056pp, Paperback, 9781133106869
www.cengageasia.com
INTRODUCTION TO GENERAL,
ORGANIC AND BIOCHEMISTRY,
INTERNATIONAL EDITION, 10E
Frederick A. Bettelheim, Adelphi University; William H. Brown,
Beloit College; Mary K. Campbell, Mount Holyoke College;
Shawn O. Farrell, Olympic Training Center
This bestselling text continues to lead the way with
a strong focus on current issues, pedagogically rich
framework, wide variety of medical and biological
applications, visually dynamic art program, and
exceptionally strong and varied end-of-chapter
problems. Revised and updated throughout, the
tenth edition now includes new biochemistry
content, new Chemical Connections essays, new
and revised problems, and more. Every problem
from the tenth edition is now available in the OWL
online learning system.
NEW TO THIS EDITION
• Ten percent of the book’s problems are new or
revised. In addition, all problems in the tenth
edition are now available in the OWL online
learning system.
• New “Chemical Connections” boxes such as,
“DDT, A Boon and a Curse,” “From Moldy Clover
to a Blood Thinner,” and “Is There a Connection
Between Carbohydrates and Obesity?” have
been added to the text’s more than 150 Chemical
Connections essays. End-of-chapter problems
associated with “Chemical Connections” are
now keyed to provide students with immediate
reinforcement.
• New up-to-date biochemistry coverage includes
material on Membrane Cholesterol Function
(Chapter 21), Transition Metals and Their Effect
on the Structure of Proteins (Chapter 22), Enzyme
25
 Inhibitors in Medicine (Chapter 23), Obesity and
Type-II Diabetes (Chapter 24), Synthetic Genome
(Chapter 26), Nutrient Deficiencies Linked to
Depression (Chapter 30), and Immunization
(Chapter 31).
• Coverage of balancing chemical equations now
appears earlier in Chapter 4, Chemical Reactions,
and the more difficult calculations involving mass
relationships have been moved to the end of the
chapter.
• Allotropes of carbon are now included in an
expanded Section 5.9, What Are the Characteristics
of the Various Types of Solids?
• Chapter 8, Acids and Bases, now covers the
Activity Series.
• A new “How To” box in Chapter 11 emphasizes
the skills students need to master “How to Draw
Alternative Chair Conformations of Cyclohexane.”
• Organic mechanisms are now simplified into easy-
to-remember steps: add a proton, take a proton
away, break a bond, and make a bond in Chapter
12, Alkenes and Alkynes.
• An enhanced version of the OWL online learning
system now includes Interactive Examples from
the text and more parameterized end-of-chapter
questions that encourage students to practice
multiple questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts. In
addition, OWL now includes a multimedia eBook,
the interactive customizable Cengage YouBook,
as well as an optional Solutions Manual eBook.
CONTENTS
1. Matter, Energy, and Measurement. 2. Atoms. 3.
Chemical Bonds. 4. Chemical Reactions. 5. Gases,
Liquids, and Solids. 6. Solutions and Colloids.
7. Reaction Rates and Chemical Equilibrium. 8.
Acids and Bases.9. Nuclear Chemistry. 10. Organic
Chemistry. 11. Alkanes. 12. Alkenes and Alkynes.
13. Benzene and Its Derivatives. 14. Alcohols,
Ethers, and Thiols. 15. Chirality: The Handedness of
Molecules. 16. Amines. 17. Aldehydes and Ketones.
18. Carboxylic Acids. 19. Carboxylic Anhydrides,
Esters, and Amides. 20. Carbohydrates. 21.
Lipids. 22. Proteins. 23. Enzymes. 24 Chemical
Communications: Neurotransmitters and Hormones.
25. Nucleotides, Nucleic Acids, and Heredity.
26 www.cengageasia.com
26. Gene Expression and Protein Synthesis. 27.
Bioenergetics: How the Body Converts Food
to Energy. 28. Specific Catabolic Pathways:
Carbohydrate, Lipid, and Protein Metabolism.
29. Biosynthetic Pathways. 30. Nutrition. 31.
Immunochemistry.32. Body Fluids.(Chapter 32
can be found on this book’s companion website,
which is accessible from http://www.cengage.com/
chemistry/bettelheim)Appendix 1. Exponential
Notation. Appendix 2. Significant Figures. Answers
to In-Text and Odd-Numbered End-of-Chapter
Problems. Glossary.Credits.Index.
© 2013, 1008pp, Paperback, 9781133109112
LABORATORY EXPERIMENTS FOR
INTRODUCTION TO GENERAL,
ORGANIC AND BIOCHEMISTRY,
INTERNATIONAL EDITION, 8E
Frederick A. Bettelheim, Adelphi University; Joseph M.
Landesberg, Adelphi University
The 48 experiments in this well-conceived manual
illustrate important concepts and principles in
general, organic, and biochemistry. As in previous
editions, three basic goals guided the development
of all the experiments: (1) the experiments
illustrate the concepts learned in the classroom;
(2) the experiments are clearly and concisely
written so that students will easily understand the
task at hand, will work with minimal supervision
because the manual provides enough information
on experimental procedures, and will be able to
perform the experiments in a 2-1/2 hour laboratory
period; and (3) the experiments are not only
simple demonstrations, but also contain a sense
of discovery. This edition includes many revised
experiments and two new experiments.
NEW TO THIS EDITION
• Many of the experiments have been updated.
• Two new experiments Beer’s Law and Standard
Curves, and Tyrosinase Enzyme Kinetics have
been added.
• Many of the pre- and post-lab questions have
been revised.
FEATURES
• The 48 experiments in this manual illustrate
important concepts and principles in general,
organic, and biochemistry.
• The experiments illustrate the concepts learned
in the classroom, and are clearly and concisely
written.
• T h e e x p e r i m e n t s a r e n o t o n l y s i m p l e
demonstrations, but also contain a sense of
discovery.
CONTENTS
Experiment 1: Laboratory Techniques:
Using the Laboratory Gas Burner; Making
LaboratoryMeasurementsExperiment 2: Density
DeterminationExperiment 3: Separation of the
Components of a MixtureExperiment 4: Resolution of
a Mixture by DistillationExperimnet 5: The Empirical
Formula of a Compound: The Law of Constant
CompositionExperiment 6: Determination of the
Formula of a Metal OxideExperiment 7: Classes
of Chemical ReactionsExperiment 8: Chemical
Properties of Consumer ProductsExperiment 9:
Calorimetry: The Determination of the Specific
Heat of a MetalExperimment 10: Boyle’s
Law: The Pressure–Volume Relationship of a
GasExperiment 11: Charles’s Law: The Volume–
Temperature Relationship of a GasExperiment
12: Properties of Gases: Determination of the
Molar Mass of a Volatile LiquidExperiment 13:
Physical Properties of Chemicals: Melting Point,
Sublimation, and Boiling PointExperiment 14:
Solubility and SolutionsExperiment 15: Water
of HydrationExperiment 16: Factors Affecting
Reaction RatesExperiment 17: The Law of Chemical
Equilibrium and Le Chatelier’s PrincipleExperiment
18: pH and Buffer SolutionsExperiment 19:
www.cengageasia.com
Analysis of Vinegar by TitrationExperiment
20: Analysis of Antacid TabletsExperiment 21:
Structure in Organic Compounds: Use of Molecular
Models. IExperiment 22: Stereochemistry: Use
of Molecular Models. IIExperiment 23: Column
and Paper Chromatography: Separation of
Plant PigmentsExperiment 24: Classification
and Identification of HydrocarbonsExperiment
25: Classification and Identification of Alcohols
and PhenolsExperiment 26: Classification and
Identification of Aldehydes and KetonesExperiment 27:
Properties of Carboxylic Acids and EstersExperiment
28: Properties of Amines and AmidesExperiment
29: Polymerization ReactionsExperiment 30:
Preparation of Acetylsalicylic Acid (Aspirin)
Experiment 31: Isolation of Caffeine from Tea
LeavesExperiment 32: CarbohydratesExperiment
33: Fermentation of a Carbohydrate:Ethanol from
SucroseExperiment 34: Preparation and Properties
of a SoapExperiment 35: Preparation of a Hand
CreamExperiment 36: Extraction and Identification
of Fatty Acids from Corn OilExperiment 37: Analysis
of LipidsExperimnet 38: Separation of Amino Acids
by Paper ChromatographyExperiment 39: Acid–
Base Properties of Amino AcidsExperiment 40:
Isolation and Identification of CaseinExperiment
41: Properties of EnzymesExperiment 42:
Neurotransmission: An Example of Enzyme
SpecificityExperiment 43: Isolation and Identification
of DNA from OnionExperiment 44: Viscosity
and Secondary Structure of DNAExperiment 45:
Beer’s Law and Standard CurvesExperiment
46: Tyrosinase Enzyme KineticsExperiment 47:
Quantitative Analysis of Vitamin C Contained in
FoodsExperiment 48: Analysis of Vitamin A in
Margarine
© 2013, 656pp, Paperback, 9781133113102
27

BASIC LABORATORY EXPERIMENTS
FOR GENERAL, ORGANIC, AND
BIOCHEMISTRY
Joseph M. Landesberg, Adelphi University
Succeed in your GOB Lab course with the easy-
to-follow experiments in this streamlined and
focused manual. Fourteen experiments (6 general
chemistry, 4 organic chemistry, and 4 biochemistry)
illustrate the concepts you must know for your
future allied health career, while pre- and post-lab
questions test your ability to apply concepts.
FEATURES
• DESIGNED FOR NURSING AND HEALTH
SCIENCE MAJORS. Focusing on the key
concepts most important to allied health majors,
this streamlined lab manual is ideal for the
one-term General, Organic, and Biochemistry
laboratory course.
• CLEAR AND STRAIGHTFORWARD. Clear
directions help students complete labs successfully.
• A FOCUS ON APPLICATION. Pre- and post-lab
questions for every experiment test the student’s
ability to understand and apply concepts.
CONTENTS
1. Laboratory Measurements.2. Density
Determination.3. Classes of Chemical Reactions.4.
Separation of Components of a Mixture.5. Factors
Affecting Rate of Reactions.6. The Law of Chemical
Equilibrium and the Le Chatelier Principle.7. pH and
Buffer Solutions.8. Structure and Stereochemistry
in Organic Compounds, the Use of Molecular
Models.9. Aspirin: Preparation and Properties
(Acetylsalicylic Acid).10. Carbohydrates.11. Fats
and Oils: Preparation and Properties of Soap.12.
28 www.cengageasia.com
Acid-Base Properties of Amino Acids.13. Isolation
and Identification of Casein.14. Enzymes.
© 2012, 256pp, Paperback, 9781111426613
GENERAL, ORGANIC, AND
BIOCHEMISTRY
An Applied Approach, International Edition
James Armstrong, City College of San Francisco
Focusing on the needs of allied health and nursing
majors, this engaging book is ideal for students
who have had no prior exposure to chemistry. The
author takes the time to explain how to do tasks
that students find difficult, rather than just providing
terse descriptions. Emphasizing problem-solving
techniques without skipping steps and using terms
students can grasp, the book takes the most direct
path to biomolecules and metabolic processes,
provides a wealth of worked examples to help
students understand key chemical concepts,
includes novel and relevant “Health Notes” in
the margins, and weaves biological and medical
applications throughout.
FEATURES
• DESIGNED FOR NURSING AND HEALTH
SCIENCES MAJORS. This allied health-focused
book takes the most direct path to biomolecules
and metabolic processes, includes novel and
relevant “Health Notes” in the margins, and
weaves biological and medical applications
throughout to prepare students for their future
careers.
• E M P H A S I S O N P R O B L E M S O L V I N G
STRATEGIES. Each Sample Problem is paired
with a closely related “Try It Yourself” question.
 Most sample problems list additional Core
Problems that students can do to practice new
skills. Steps for solving the conversion problems
appear in the margins to guide students through
the problem-solving process.
• FOCUSED ON STUDENT LEARNING. Each
chapter begins with a short health-related,
‘story type’ introduction, followed by numbered
sections with learning objectives. Section-
ending Core Problems immediately reinforce the
section objectives and help students’ gauge their
knowledge of the content. Key Terms appear in
boldface type the first time they are used and are
collected at the back of the chapter to facilitate
student review.
• BUILT-IN STUDY GUIDE. End-of-chapter material
(keyed to each section) helps students master
chapter concepts and problem-solving skills and
review for quizzes and tests. Concept Questions
encourage students to describe how the ideas
in the chapter apply to specific examples, while
Summary and Challenge Problems cover all
sections and give instructors the opportunity
to assign questions at a wide range of levels.
Challenge problems are marked with an asterisk
and require a greater depth of understanding;
many involve concepts from earlier chapters.
• OWL INTEGRATION. Improve student learning
outcomes with OWL, the #1 online homework
and learning system for chemistry. Developed
by chemistry instructors for teaching chemistry,
OWL includes course management tools that
make homework management a breeze, as well
as advanced reporting and grade book features
that save time in grading homework and tracking
student progress. OWL enables you to address
students’ different learning styles through
tutorials, simulations, visualization exercises, and
algorithmically-generated homework questions
with answer-specific feedback. With OWL’s
mastery learning approach, students work at their
own pace until they understand each concept/
skill. OWL includes an eBook, enhanced with
multimedia learning tools.
• EXPERT REVIEW: The entire text was reviewed
by Nursing Professor Kellee Hollyman, RN,BSN,
MN-Nurse Educator to ensure the relevance and
www.cengageasia.com
accuracy of the health material.
CONTENTS
1. MEASUREMENTS IN SCIENCE AND
MEDICINE.Measuring Size: Distance, Mass, and
Volume. Metric Units and Their Relationships.
Rounding and Precision In Measurements. Unit
Conversions and Conversion Factors. Rounding
and Significant Figures. Temperature. Density,
Dosage, and Other Compound Units.2. ATOMS,
ELEMENTS, AND COMPOUNDS.Classifying
Matter: Mixtures, Compounds, and Elements.
The Chemical Elements: An Introduction to the
Periodic Table. Atoms. Subatomic Particles and
Atomic Structure.Isotopes And Atomic Weight.
Chemical Formulas. Electron Shells. Chemical
Behavior, Valence Electrons, and the Periodic
Law. The Organization of the Periodic Table.3.
CHEMICAL BONDS.Covalent Bonds and the Octet
Rule. Double And Triple Bonds. Drawing Lewis
Structures for Complex Molecules. Electronegativity
and Polar Bonds. Naming Covalent Compounds.
Ions and Ionic Compounds. Writing Formulas for
Ionic Compounds. Naming Ionic Compounds.
Polyatomic Ions. Recognizing Ionic and Molecular
Compounds.4. ENERGY AND THE PHYSICAL
BEHAVIOR OF CHEMICAL SUBSTANCES.Heat
and Energy. The Three States of Matter. The
Properties of Gases. Changes of State. Attractive
Forces and the Physical Properties of Matter.5.
SOLUTIONS AND CONCENTRATION.Solutions
and the Dissolving Process. Electrolytes and
Dissociation. Solubility. The Relationship Between
Solubility and Molecular Structure. Concentration.
Moles and Formula Weights. Molarity. Osmosis,
Dialysis, And Tonicity. Equivalents. Dilution.6.
CHEMICAL REACTIONS.Physical Changes
and Chemical Reactions. Chemical Equations.
Mass Relationships in a Chemical Reaction.
Heats of Reaction. Combustion and Precipitation
Reactions. Reaction Rate and Activation Energy.
Chemical Equilibrium.7. ACIDS AND BASES.
The Self-Ionization of Water. The Ph Scale. The
Properties of Acids. The Properties of Bases. Acid-
Base Reactions. Amphiprotic Molecules and Ions.
Buffers.The Role of Buffers in Human Physiology.8.
HYDROCARBONS – AN INTRODUCTION TO
ORGANIC MOLECULES.The Special Properties of
29
 Carbon. Linear Alkanes: The Foundation of Organic Glycolysis. The Citric Acid Cycle. Beta Oxidation –
Chemistry. Branched Alkanes, Cycloalkanes, and Obtaining Energy from Fatty Acids. Catabolism of
Isomers. Naming Branched Alkanes: The IUPAC Amino Acids. Anabolic Pathways and the Control
System. Functional Groups. Alkenes and Alkynes. of Metabolism.16. NUCLEIC ACIDS, PROTEIN
Geometric Isomers. Benzene and Aromatic SYNTHESIS, AND HEREDITY.Nucleotides. The
Compounds. The Properties of Hydrocarbons.9. Structure of Nucleic Acids. DNA Replication.
HYDRATION, DEHYDRATION AND ALCOHOLS. Transcription and RNA Processing. Translation
The Hydration Reaction. Controlling the Product – and The Genetic Code. The Mechanism of
An Introduction to Enzymes. Naming Alcohols. The Protein Synthesis.Regulation of Protein Synthesis.
Physical Properties of Alcohols. The Dehydration Mutations and Genetic Disorders.17. NUCLEAR
Reaction. Phenols and Thiols.10. CARBONYL CHEMISTRY.Symbols for Nuclei And Subatomic
COMPOUNDS AND REDOX REACTIONS. Particles. Writing Nuclear Equations. Energy and
Hydrogenation and Dehydrogenation. Oxidation Nuclear Reactions. Physiological Effects of Ionizing
and Reductions. Reactions and the Carbonyl Radiation. Measuring Radiation. Nuclear Decay
Group. The Naming and Properties of Aldehydes and Half-Life. Medical Applications of Nuclear
and Ketones. Other Oxidation and Reduction Radiation. Nuclear Fission and Fusion.APPENDIX
Reactions. Carboxylic Acids. Biological Oxidations A: ESSENTIAL MATHEMATICS FOR CHEMISTRY.
and Reductions – The Redox Coenzymes. Decimal Notation. Place Value, Fractions, and
Introduction to Metabolic Pathways.11. ORGANIC Division. Order of Operations. Exponents. Scientific
ACIDS AND BASES.Reactions of Organic Acids. Notation. Calculator Use.APPENDIX B: THE
Decarboxylation Reactions. Amines. The Acid- QUANTITATIVE BEHAVIOR OF GASES.(Kelvin
Base Reactions of Amines. Amines in Biology and temperature, combined gas law, Avogadro’s law,
Medicine. The Relationship Between Structure ideal gas law).
and Ph.12. BUILDING LARGE MOLECULES
© 2012, 832pp, Paperback, 9780840068286
– CONDENSATION AND HYDROLYSIS
REACTIONS.Introduction to Condensation
Reactions – Ethers. Esterification, Amidation,
and Phosphorylation. Condensation Polymers.
Hydrolysis. The Effect of Ph on the Products of
Hydrolysis. The Equilibrium Between Condensation
and Hydrolysis.13. PROTEINS.Amino acids. Peptide
bonds and the secondary structure of a protein. Side
chain interactions and tertiary structure. Protein
denaturation. Enzyme structure and function.
Cofactors. Antibodies and the immune response.
Sources of amino acids.14: CARBOHYDRATES
AND LIPIDS.Monosaccharides. Isomeric Forms
Of Monosaccharides – Anomers and Enantiomers.
Disaccharides and the Glycosidic Linkage. Common
Disaccharides and Polysaccharides.Fatty Acids
and Triglycerides. The Chemical Reactions of
Triglycerides. Glycerophospholipids and Cell
Membranes. Steroids and Lipoproteins. Sources
of Carbohydrates and Fats.15. METABOLISM
– THE CHEMICAL WEB OF LIFE.Catabolism,
Anabolism, and the ATP Cycle. An Overview of
Catabolism. ATP Production and the Mitochondria.

30 www.cengageasia.com

INTRODUCTORY CHEMISTRY FOR
TODAY, INTERNATIONAL EDITION, 7E
Spencer L. Seager, Weber State University; Michael R.
Slabaugh, Weber State University
Distinguished by its superior allied health focus and
integration of technology, Seager and Slabaugh’s
INTRODUCTORY CHEMISTRY FOR TODAY, 7e,
International Edition continues to meet students’
needs through diverse applications, examples,
boxes, and outstanding technology tools. Prompts
throughout the new edition lead students to
OWL (web-based learning system)—two unique
online programs that extend the lessons of the
text and help students study smarter. In addition
to the many resources found in OWL, the book
and website contain questions modeled after the
Nursing School and Allied Health Entrance Exams.
INTRODUCTORY CHEMISTRY FOR TODAY, 7e,
International Edition dispels students’ inherent fear
of chemistry and instills an appreciation for the role
chemistry plays in our daily lives through a rich
pedagogical structure and an accessible writing
style with lucid explanations. In addition, the book
provides greater support in both problem-solving
and critical-thinking skills—the skills necessary for
student success. By demonstrating the importance
of chemistry concepts to students’ future careers
and by providing important career information
online, the authors not only help students set goals
but also help them focus on achieving them.
NEW TO THIS EDITION
• ALLIED HEALTH CONNECTION. An expanded
“Allied-Health Exam Connection” section follows
the exercises of each chapter and includes
examples of chemistry questions found on typical
www.cengageasia.com
entrance examinations used to screen applicants
to Allied-Health professional programs.
• U P D A T E D A R T A N D P H O T O G R A P H Y
PROGRAM. In addition to adding many new
photos to illustrate key concepts, explanations of
figures are now incorporated into the art, rather
than appearing in the caption, to help students
follow processes and understand exactly what is
happening within each figure without having to go
back and forth between figure and caption.
• OWL ONLINE LEARNING INTEGRATION.
The new edition now contains algorithmically
generated versions of most of the end-of-chapters
question from the text.
• NEW AND UPDATED BOXED FEATURES.
New “At the Counter” boxes focus on drugs and
products found on drugstore shelves and at the
pharmacy; “Chemistry Around Us” boxes present
everyday applications of chemistry; and updated
“Chemistry and Your Health” boxes relate to
students’ health and the health of the patients that
they may care for in their future roles as a part of
the allied health work force.
• NEW END-OF-CHAPTER EXERCISES. A
significant number of the end-of-chapter questions
are new.
FEATURES
• A WEALTH OF END-OF-CHAPTER EXERCISES.
The book’s wide range of end-of-chapter exercises
include “Additional Exercises” that are not tied to
a specific section and often consist of problems
that integrate several concepts and “Chemistry for
Thought” exercises that focus on conceptual and
cumulative questions and ask students to apply
what they have learned to a particular cumulative
question.
• INTEGRATED LEARNING OBJECTIVES.
The book’s Learning Objectives are integrated
throughout each chapter and within the summary
to help students focus on the chapter’s key skills
and concepts.
• LEARNING CHECKS. These short, self-check
exercises follow the book’s worked-out examples
and discussions of key or difficult concepts to help
students assess their understanding.
• CONCEPT SUMMARY SECTIONS. These end-
of-chapter sections summarize each chapter’s key
31
 concepts and include one or two appropriate end-
of-chapter exercises per concept. By solving these
exercises, students will have an approximate but
quick assessment of how well they understand
the Learning Objective related to that concept.
• HOW REACTIONS OCCUR SECTIONS. These
sections present the mechanisms of representative
organic reactions to help dispel the mystery of how
these reactions take place.
CONTENTS
1. Matter, Measurements, and Calculations. 2.
Atoms and Molecules. 3. Electronic Structure and
the Periodic Law. 4. Forces Between Particles.
5. Chemical Reactions. 6. The States of Matter.
7. Solutions and Colloids. 8. Reaction Rates
and Equilibrium. 9. Acids, Bases, and Salts.
10. Radioactivity and Nuclear Processes. 11.
Organic Compounds: Alkanes. 12. Unsaturated
Hydrocarbons. Appendix A: The International
System of Measurements. Appendix B: Answers
to Even-Numbered End-of-Chapter Exercises.
Appendix C: Solutions to Learning Checks.
Glossary. Index.
© 2011, 496pp, Paperback, 9780538734868
32 www.cengageasia.com
ORGANIC AND BIOCHEMISTRY FOR
TODAY, INTERNATIONAL EDITION, 7E
Spencer L. Seager, Weber State University; Michael R.
Slabaugh, Weber State University
Distinguished by its superior allied health focus and
integration of technology, Seager and Slabaugh’s
ORGANIC AND BIOCHEMISTRY FOR TODAY, 7e,
International Edition continues to meet students’
needs through diverse applications, examples,
boxes, and outstanding technology tools and now
offers an updated and improved art program.
Prompts throughout the new edition lead students
to OWL (web-based learning system)—two unique
online programs that extend the lessons of the
text and help students study smarter. In addition
to the many resources found in CengageNOW
and OWL, the book and website contain questions
modeled after the Nursing School and Allied Health
Entrance Exams. ORGANIC AND BIOCHEMISTRY
FOR TODAY, 7e, International Edition dispels
students’ inherent fear of chemistry and instills
an appreciation for the role chemistry plays in our
daily lives through a rich pedagogical structure and
an accessible writing style with lucid explanations.
In addition, the book provides greater support
in both problem-solving and critical-thinking
skills—the skills necessary for student success.
By demonstrating the importance of chemistry
concepts to students’ future careers and by
providing important career information online, the
authors not only help students set goals but also
help them focus on achieving them.
NEW TO THIS EDITION
• ALLIED HEALTH CONNECTION. An expanded
“Allied-Health Exam Connection” section follows
 the exercises of each chapter and includes • CONCEPT SUMMARY SECTIONS. These end-
examples of chemistry questions found on typical of-chapter sections summarize each chapter’s key
entrance examinations used to screen applicants concepts and include one or two appropriate end-
to Allied-Health professional programs. of-chapter exercises per concept. By solving these
• U P D A T E D A R T A N D P H O T O G R A P H Y exercises, students will have an approximate but
PROGRAM. In addition to adding many new quick assessment of how well they understand
photos to illustrate key concepts, explanations of the Learning Objective related to that concept.
figures are now incorporated into the art, rather • HOW REACTIONS OCCUR SECTIONS. These
than appearing in the caption, to help students sections present the mechanisms of representative
follow processes and understand exactly what is organic reactions to help dispel the mystery of how
happening within each figure without having to go these reactions take place.
back and forth between figure and caption. CONTENTS
• OWL ONLINE LEARNING INTEGRATION.
The new edition now contains algorithmically 1. Organic Compounds: Alkanes. 2. Unsaturated
generated versions of most of the end-of-chapters Hydrocarbons. 3. Alcohols, Phenols, and Ethers.
question from the text. 4. Aldehydes and Ketones. 5. Carboxylic Acids and
• NEW AND UPDATED BOXED FEATURES. Esters. 6. Amines and Amides. 7. Carbohydrates. 8.
New “At the Counter” boxes focus on drugs and Lipids. 9. Proteins. 10. Enzymes. 11. Nucleic Acids
products found on drugstore shelves and at the and Protein Synthesis. 12. Nutrition and Energy for
pharmacy; “Chemistry Around Us” boxes present Life. 13. Carbohydrate Metabolism. 14. Lipid and
everyday applications of chemistry; and updated Amino Acid Metabolism. 15. Body Fluids. Appendix
“Chemistry and Your Health” boxes relate to A: The International System of Measurements.
students’ health and the health of the patients that Appendix B: Answers to Even-Numbered End-
they may care for in their future roles as a part of of-Chapter Exercises. Appendix C: Solutions to
the allied health work force. Learning Checks. Glossary. Index.
• NEW END-OF-CHAPTER EXERCISES. A © 2011, 512pp, Paperback, 9780538734851
significant number of the end-of-chapter questions
are new.
FEATURES
• A WEALTH OF END-OF-CHAPTER EXERCISES.
The book’s wide range of end-of-chapter exercises
include “Additional Exercises” that are not tied to
a specific section and often consist of problems
that integrate several concepts and “Chemistry for
Thought” exercises that focus on conceptual and
cumulative questions and ask students to apply
what they have learned to a particular cumulative
question.
• INTEGRATED LEARNING OBJECTIVES.
The book’s Learning Objectives are integrated
throughout each chapter and within the summary
to help students focus on the chapter’s key skills
and concepts.
• LEARNING CHECKS. These short, self-check
exercises follow the book’s worked-out examples
and discussions of key or difficult concepts to help
students assess their understanding.

www.cengageasia.com
33

SAFETY-SCALE LABORATORY
EXPERIMENTS FOR CHEMISTRY FOR
TODAY, 7E
Spencer L. Seager, Weber State University; Michael R.
Slabaugh, Weber State University
Providing a unique blend of laboratory skills
and exercises that illustrate concepts from the
authors’ main text, CHEMISTRY FOR TODAY:
GENERAL, ORGANIC, AND BIOCHEMISTRY,
7e, this accurate and well-tested lab manual
contains 15 general chemistry and 20 organic/
biochemistry safety-scale laboratory experiments.
The experiments are designed to use small
quantities of chemicals and emphasize safety and
proper disposal of materials. “Safety-scale” is the
authors’ own term for describing the amount of
chemicals each lab experiment requires--less than
macroscale quantities, which are expensive and
hazardous--and more than microscale quantities,
which are difficult to work with and require special
equipment.
NEW TO THIS EDITION
• ACCURATE AND CLASS-TESTED. The Seventh
Edition includes 15 general chemistry and 20
organic/biochemistry safety-scale laboratory
experiments--all thoroughly class-tested--that
effectively illustrate the main text’s key concepts.
FEATURES
• A KEY CONCEPT FOCUS: The manual’s blend
of laboratory skills and exercises illustrate key
concepts from the main textbook.
• BUILT-IN PEDAGOGY: Pre-lab questions prepare
students for each lab and end-of-experiment
questions assess student understanding.
34
• FLEXIBLE AND CONVENIENT. The manual
is three-hole punched and features perforated
pages, which make it easy for student to hand
in lab reports and answers to pre- and post-lab
questions and exercises upon instructor request.
CONTENTS
Introduction.Experiment 1: Measurements and
Significant Figures.Experiment 2: The Use of
Chemical Balances.Experiment 3: The Use of
Volumetric Ware and the Determination of Density.
Experiment 4: Physical and Chemical Changes.
Experiment 5: Separations and Analysis.
Experiment 6: Classification of Chemical Reactions.
Experiment 7: Analysis Using Decomposition
Reactions.Experiment 8: Gas Laws.Experiment
9: Solution Formation and Characteristics.
Experiment 10: Colligative Properties of Solutions.
Experiment 11: Reactions Rates and Equilibrium.
Experiment 12: Acids, Bases, Salts, and Buffers.
Experiment 13: Analysis of Vinegar.Experiment 14:
Determination of Ka for Weak Acids.Experiment
15: The Acidic Hydrogens of Acids.Experiment 16:
The Use of Melting Points in the Identification of
Organic Compounds.Experiment 17: Isolation and
Purification of an Organic Compound.Experiment 18:
Hydrocarbons.Experiment 19: Reactions of Alcohols
and Phenols.Experiment 20: Reactions of Aldehydes
and Ketones.Experiment 21: Reactions of Carboxylic
Acids, Amines, and Amides.Experiment 22: The
Synthesis of Aspirin and Other Esters.Experiment
23: Identifying Functional Groups in Unknowns.
Experiment 24: Synthetic Polymers.Experiment
25: Dyes, Inks, and Food Colorings.Experiment
26: A Study of Carbohydrates.Experiment 27:
Preparations of Soap by Lipid Saponification.
Experiment 28: Isolation of Natural Products:
Trimyristin and Cholesterol.Experiment 29: Amino
Acids and Proteins.Experiment 30: Enzymes:
Nature’s Catalysts.Experiment 31: Factors That
Influence Enzyme Activity.Experiment 32: Vitamin
C Content of Foods Part I: Assigned Samples.
Experiment 33: Vitamin C Content of Foods Part II:
Samples from Home.Experiment 34: Extraction of
DNA from Wheat Germ.Experiment 35: Detection
www.cengageasia.com
of Minerals in Breakfast Cereals.APPENDIX A: • Sample Exercises: Providing step-by-step
Graphs and Graphing.APPENDIX B: Equipment, instruction, Sample Exercises provide detailed
Chemicals, Reagents, and Supplies.APPENDIX C: explanations to help students gain a solid
Table of Atomic Weights and Numbers. understanding of GOB concepts and principles.
• Avoiding Pitfalls: Included throughout the text,
© 2011, 544pp, Paperback, 9780538734547 Caution icons alert students to common mistakes
and help them understand how to avoid such
missteps.
• Tips and Tools: Problem Solving Tips give
students additional insight for successfully working
through exercises.
• Flexibility: The modular organization makes this
resource an excellent companion for any GOB
textbook.
CONTENTS
Module 1: GENERAL CHEMISTRY.1. Metric System,
Dimensional Analysis, Significant Figures, Density,
and Heat.2. Atomic Theory, Periodicity, Chemical
SURVIVAL GUIDE FOR GENERAL, Bonding, and Nomenclature.3. Nuclear Chemistry.4.
ORGANIC AND BIOCHEMISTRY Chemical Reactions and Stoichiometry.5. States
Richard Morrison, University of Georgia; Charles H. Atwood, of Matter, Solutions, and Colligative Properties.6.
University of Georgia; Joel Caughran, University of Georgia Chemical Kinetics.7. Acids and Bases.Module 2:
ORGANIC CHEMISTRY.8. Functional Groups and
Available free in a package with any Cengage
Nomenclature.9. Stereoisomerism.10. Substitution
Learning chemistry text or available for separate
Reactions.11. Addition Reactions.12. Elimination
purchase at www.cengagebrain.com, this
Reactions.13. Oxidation-Reduction Reactions.
straightforward, thorough SURVIVAL GUIDE FOR
Module 3: BIOCHEMISTRY.14. Carbohydrates.15.
GENERAL, ORGANIC AND BIOCHEMISTRY
Lipids.16. Proteins, Protein Synthesis and
provides everything students need to survive and
Enzymes.17. Nucleotides and Gene Expression.
thrive in the GOB course. Modeled after Atwood’s
widely popular GENERAL CHEMISTRY SURVIVAL © 2008, 350pp, Paperback, 9780495554691
GUIDE, this guide helps students master concepts,
improve essential problem-solving skills, and make
the most of their study time, for optimal exam
results. Designed as a reader’s guide to a GOB
textbook, this extremely reader friendly guide offers
detailed step-by-step problem-solving sequences,
giving students the competency--and confidence--
they need. This brief but powerful resource covers
the most fundamental aspects of GOB in a succinct,
straightforward series of essential modules.
NEW TO THIS EDITION
• Student-Friendly Content: Key Terms, Concepts,
and Equations highlight key GOB issues for
students, helping them focus on essential
concepts and maximize their study time.

www.cengageasia.com
35

ANALYTICAL CHEMISTRY
APPLICATIONS OF MICROSOFT®
EXCEL IN ANALYTICAL CHEMISTRY,
2E
F. James Holler, University of Kentucky; Stanley R. Crouch,
Michigan State University
This supplement can be used in any analytical
chemistry course. The exercises teach students how
to use Microsoft® Excel® using applications from
statistics, data analysis equilibrium calculations,
curve fitting, and more. Operations include
everything from basic arithmetic and cell formatting
to Solver, Goal Seek, and the Data Analysis
Toolpak. The authors show students how to use
a spreadsheet to construct log diagrams and to
plot the results. Statistical data treatment includes
descriptive statistics, linear regression, hypothesis
testing, and analysis of variance. Tutorial exercises
include nonlinear regression such as fitting the Van
Deemter equation, fitting kinetics data, determining
error coefficients in spectrophotometry, and
calculating titration curves. Additional features
include solving complex systems of equilibrium
equations and advanced graphical methods: error
bars, charts with insets, matrices and determinants,
and much more.
NEW TO THIS EDITION
• The description and instructions were completely
changed from those of Excel 2003 to Excel 2010
(2007).
• There is now a better coordination with Skoog,
Fundamentals of Analytical Chemistry, 9e in terms
36
of worked examples. The Spreadsheet examples,
formerly in the Skoog book were off-loaded to the
new Excel book so that the burden for teaching
about Excel is now on the Excel book.
• Precipitation titrations were included in Chapter 9.
• Descriptions and instructions written so that they
can be used with either the Office 2007 or 2010
versions of Excel.
• Cross references to Skoog Fundamentals of
Analytical Chemistry, 9e and Skoog, Analytical
Chemistry: An Introduction are included.
FEATURES
• Exercises teach students how to use Microsoft®
Excel® with applications from statistics, data
analysis equilibrium calculations, curve fitting,
and more.
• Operations include everything from basic
arithmetic and cell formatting to Solver, Goal
Seek, and the Data Analysis Toolpak.
• The authors show students how to use a
spreadsheet to construct log diagrams and to
plot the results.
• Statistical data treatment includes descriptive
statistics, linear regression, hypothesis testing,
and analysis of variance.
• Tutorial exercises include nonlinear regression
such as fitting the Van Deemter equation, fitting
kinetics data, determining error coefficients in
spectrophotometry, and calculating titration
curves.
CONTENTS
1. Excel Basics.2. Basic Statistical Analysis with
Excel.3. Statistical Tests with Excel.4. Least-Squares
and Calibration Methods.5. Equilibrium, Activity and
Solving Equations.6. The Systematic Approach to
Equilibria: Solving Many Equations.7. Neutralization
Titrations and Graphical Representations.8.
Polyfunctional Acids and Bases.9. Complexometric
and Precipitation Titrations.10. Potentiometry and
Redox Titrations.11. Dynamic Electrochemistry.12.
Spectrochemical Methods.13. Kinetic Methods.14.
Chromatography.15. Electrophoresis and Other
Separation Methods.16. Data Processing with
Excel.
© 2014, 480pp, Paperback, 9781285087955
www.cengageasia.com

CTE FUNDAMENTALS OF ANALYTICAL
CHEMISTRY WITH CB COURSESMART
EBOOK, 9E
Douglas A. Skoog, Stanford University; Donald M. West,
San Jose State University; F. James Holler, University of
Kentucky; Stanley R. Crouch, Michigan State University
Please note that the digital access code that comes
with the print book is valid for use in a specific
Asia territory only.CB CourseSmart eBook – The
ultimate eBook experience has arrived! Easily
access our eBooks with features that will improve
your reading experience, and tools to help you
take notes and organize your studies.Known for its
readability and systematic, rigorous approach, this
fully updated Ninth Edition of FUNDAMENTALS
OF ANALYTICAL CHEMISTRY offers extensive
coverage of the principles and practices of analytic
chemistry and consistently shows students its
applied nature. The book’s award-winning authors
begin each chapter with a story and photo of how
analytic chemistry is applied in industry, medicine,
and all the sciences. To further reinforce student
learning, a wealth of dynamic photographs by
renowned chemistry photographer Charlie Winters
appear as chapter-openers and throughout the text.
NEW TO THIS EDITION
• OWL (Online Web Learning) is available for the
first time with this Ninth Edition. OWL includes
parameterized Mastery homework assignments
correlated to sections in the text and parameterized
end-of-chapter questions. OWL encourages
students to practice multiple questions of the
same type with different chemicals, wording, and
www.cengageasia.com
numbers to ensure their mastery of the underlying
chemical concepts. OWL also includes the
interactive customizable Cengage YouBook and
an optional Solutions Manual eBook.
• All chapters have been rewritten for Excel 2010
(or 2007).
• A new Chapter 29 on Mass Spectrometry
incorporates atomic mass spectrometry (formerly
in Chapter 28) with new material on molecular
mass spectrometry.
• New end-of-chapter problems have been added.
• All examples are now titled for easy reference.
• New Feature Boxes appear throughout, such as
Feature 14-4 on the Master Equation. Approach.
• Chapter 17 has a new section on Precipitation
Titrations.
• In Chapter 25, the discussion on thermal IR
detectors now puts more emphasis on the DTGS
pyroelectric detector.
• Part VII on Practical Aspects of Chemical Analysis
is now online to make it easier for students to
access the material on preparing and analyzing
real samples.
CONTENTS
1. The Nature of Analytical ChemistryPART
I: TOOLS OF ANALYTICAL CHEMISTRY2.
Chemicals, Apparatus, and Unit Operations
of Analytical Chemistry3. Using Spreadsheets
in Analytical Chemistry 4. Calculations Used
in Analytical Chemistry 5. Errors in Chemical
Analyses 6. Random Errors in Chemical Analysis7.
Statistical Data Treatment and Evaluation 8.
Sampling, Standardization, and Calibration PART
II: CHEMICAL EQUILIBRIA9. Aqueous Solutions
and Chemical Equilibria 10. Effect of Electrolytes on
Chemical Equilibria 11. Solving Equilibrium Problems
for Complex Systems PART III: CLASSICAL
METHODS OF ANALYSIS12. Gravimetric Methods
of Analysis13. Titrimetric Methods; Precipitation
Titrimetry 14. Principles of Neutralization
Titrations15. Titration Curves for Complex Acid/
Bases Systems16. Applications of Neutralization
Titrations 17. Complexation Reactions and Titrations
PART IV: ELECTROCHEMICAL METHODS 18.
Introduction to Electrochemistry19. Applications of
Standard Electrode Potentials20. Applications of
Oxidation/Reduction Titrations 21. Potentiometry22.
37
 Bulk Electrolysis: Electrogravimetry and Coulometry
23. Voltammetry PART V: SPECTROCHEMICAL
ANALYSIS 24. Introduction to Spectrochemical
Methods 25. Instruments for Optical Spectroscopy26.
Molecular Absorption Spectroscopy27.
Molecular Fluorescence Spectroscopy28. Atomic
Spectroscopy29. Mass SpectrometryPART VI:
KINETICS AND SEPARATIONS 30. Kinetic
Methods of Analysis31. Introduction to Analytical
Separations 32. Gas Chromatography 33.
High-Performance Liquid Chromatography 34.
Miscellaneous Separation MethodsPART VII:
PRACTICAL ASPECTS OF CHEMICAL ANALYSIS
To access the following online-only chapters, enter
ISBN 978-0-495-55828-6 at www.cengagebrain.
com and visit this book’s companion website.35.
Analysis of Real Samples 36. Preparing Samples
for Analysis 37. Decomposing and Dissolving the
Sample 38. Selected Methods of Analysis
© 2014, 744pp, Paperback, 9789814591447
38 www.cengageasia.com
BIOCHEMISTRY
BIOCHEMISTRY, INTERNATIONAL
EDITION, 5E
Reginald H. Garrett, University of Virginia; Charles M.
Grisham, University of Virginia
Continuing Garrett and Grisham’s innovative
conceptual and organizing “Essential Questions”
framework, BIOCHEMISTRY, 5E, International
Edition guides students through course concepts
in a way that reveals the beauty and usefulness
of biochemistry in the everyday world. Offering a
balanced and streamlined presentation, this edition
has been updated throughout with new material and
revised presentations. For the first time, this book
is integrated with OWL, a powerful online learning
system for chemistry that engages students and
improves learning outcomes.
NEW TO THIS EDITION
• Revised Art and Graphics: To increase the
pedagogical effectiveness of the art program
and to help students better visualize chemical
processes, the book’s molecular art has been
revised to allow for greater consistency in use of
atomic color code and now includes more current
PyMOL-based molecular graphics.
• New End-of-Chapter Material: A new “Things You
Should Know” study section has been added to the
end-of-chapter material. In addition, new topical
headers in the problem sets make it easier to
assign problems that pertain to a particular topic.
• New Coverage: New material has been added on
the Ventor Institute’s creation of synthetic life; new
discussions of protein sectors and metamorphic
proteins have been added to Chapter 6; and
 various free online protein databases have been
incorporated throughout the book’s narrative.
• Revised and Updated Coverage: This edition
features thoroughly updated coverage of human
gene therapy in Chapter 12 and heavily revised
coverage of DNA metabolism in Chapter 28.
• Reorganized Material: Material on reduction
potentials and free energy changes in redox
reactions has been placed earlier in the book
(moved from Chapter 20 to Chapter 3); the
discussion of protein techniques was moved
from an appendix to Chapter 5 into the chapter
proper as an “A Deeper Look” box; and the DNA
Sequencing boxed essay is now expanded and
incorporated into the Chapter 11 text narrative.
• Full Integration with OWL (Online Web Learning):
For the first time, this book is fully integrated
with OWL, a powerful online learning system
for chemistry that engages students, assesses
performance, and improves learning outcomes.
OWL includes parameterized mastery homework
assignments correlated to text sections that
encourage students to practice multiple questions
of the same type with different chemicals, wording,
and numbers to ensure their mastery of the
underlying chemical concepts. OWL also includes
an interactive customizable Cengage YouBook
(OWL’s multimedia e-book).
FEATURES
• Each chapter in this book is framed around an
Essential Question that engages students in
the material and encourages curiosity about the
subject matter.
• Human Biochemistry essays emphasize the
central role of basic biochemistry in medicine and
the health sciences with information on clinically
important issues such as diet, diabetes, and
cardiovascular health.
• Critical Developments in Biochemistry essays
emphasize recent and historical advances in the
field, while A Deeper Look essays expand on the
text, highlighting selected topics or experimental
observations.
• End-of-chapter summaries review and briefly
answer the key questions posed in each section.
www.cengageasia.com
CONTENTS
Part I: MOLECULAR COMPONENTS OF
CELLS.1. Chemistry is the Logic of Biological
Phenomena.2. Water—The Medium of Life.3.
Thermodynamics of Biological Systems.4. Amino
Acids.5. Proteins: Their Primary Structure and
Biological Functions.6. Proteins: Secondary,
Tertiary, and Quaternary Structure.7. Carbohydrates
and Glyco-Conjugates of the Cell Surface.8. Lipids.
9. Membranes and Membrane Transport.10.
Nucleotides and Nucleic Acids.11. Structure of
Nucleic Acids.12. Recombinant DNA: Cloning and
Creation of Chimeric Genes.Part II: PROTEIN
DYNAMICS.13. Enzyme Kinetics.14. Mechanisms
of Enzyme Action.15. Enzyme Regulation.16.
Molecular Motors.Part III: METABOLISM
AND ITS REGULATION.17. Nutrition and the
Organization of Metabolism.18. Glycolysis.19. The
Tricarboxylic Acid Cycle.20. Electron Transport and
Oxidative Phosphorylation.21. Photosynthesis.22.
Gluconeogenesis, Glycogen Metabolism, and
the Pentose Phosphate Pathway.23. Fatty Acid
Catabolism.24. Lipid Biosynthesis.25. Nitrogen
Acquisition and Amino Acid Metabolism.26. The
Synthesis and Degradation of Nucleotides.27.
Metabolic Integration and Organ Specialization.
Part IV: INFORMATION TRANSFER.28. DNA
Metabolism.29. Transcription and the Regulation
of Gene Expression.30. Protein Synthesis.31. Post-
Translational Processing of Proteins and Protein
Degradation.32. The Reception and Transmission
of Extracellular Information.
© 2013, 1280pp, Paperback, 9781133108795
39
 in Biochemistry” now reflect the latest advances in
the field. Count on BIOCHEMISTRY, 8th Edition,
to lead the way in currency, clarity, and innovation
for your one-semester biochemistry course
NEW TO THIS EDITION
• The #1 online homework and learning system
for chemistry, OWLv2, is available for this text-
now with new instructor features and enhanced
functionality: a Dashboard that consolidates
all course materials; easy, intuitive assignment
creation and management; ability to preview and
CTE BIOCHEMISTRY WITH CB select activities/questions for each assignment;
COURSESMART EBOOK, 8E new assignment settings and options; improved
Mary K. Campbell, Mount Holyoke College; Shawn O. Farrell, gradebook; Personalized Study tools to help
Olympic Training Center students focus their time on the key concepts and
skills; and MindTap Reader™, a new eBook with
Please note that the digital access code that comes
apps and embedded video, audio, annotations,
with the print book is valid for use in a specific Asia
and activities. OWLv2 courses for Gen Chem,
territory only.CB CourseSmart eBook – The ultimate
GOB, and Liberal Arts now include Quick Prep
eBook experience has arrived! Easily access our
essential skills assignments that can be taken
eBooks with features that will improve your reading
before the semester begins or during the first few
experience, and tools to help you take notes and
weeks, to help students succeed in the course. For
organize your studies.Introduce your students to the
this course, OWLv2 also includes new interactive
latest developments in biotechnology and genomics
versions of the end-of-chapter questions from
with this new edition of Campbell and Farrell’s best-
the text and new iPad-compatible visualizations,
selling text for the one-term course. Known for its
tutorials, and simulations.
logical organization, appropriate depth of coverage,
• New Hot Topics articles featured in Biochemistry
and vibrant illustrations, BIOCHEMISTRY, 8th
Magazine Insert: The Hop Topics in Biochemistry
Edition, helps your students synthesize the flood
Magazine which is bound inside the printed
of information that has inundated the field since
book and available online in the MindTap
the decoding of the human genome, while showing
Reader features 15 articles that are hot topics
them how biochemistry principles connect to their
in the biochemistry field right now. 8 articles are
everyday lives. The book incorporates up-to-date
available in the printed book, and 7 extra articles
developments in stem cell research, cloning, and
are available in MindTap. The Hot Topics are
immunology and offers revised coverage of major
great for in class discussions, or can be assigned
topics, such as Molecular Biology. Balancing
as student presentations. The hot topics show
scientific detail with readability, the book is ideal
how biochemistry is relevant and important to our
for students studying biochemistry for the first time.
lives-after all biochemistry is the chemistry of the
For example, in-text questions and problem sets
human body.
categorized by problem type help students master
• Hot Topics in Biochemistry Magazine: Green
chemistry and prepare for exams, and “Biochemical
Fluorescent Protein: Jellyfish and Green Monkeys,
Connections” demonstrate how biochemistry
DNA and Family Trees: Who is a Relative,
applies to other fields such as health and sports
Diabetes: An epidemic for Modern Times, Just
medicine. In addition, the book’s revised state-of-
One Word: Nanotechnology, Small, Smaller,
the-art visual program improves learning outcomes
Smallest: Beyond the Electron Microscope to
and its innovative magazine articles, “Hot Topics
Single Molecules, HPV Vaccines: Waging the War

40 www.cengageasia.com
 on Cervical Cancer, Stem Cells: Hype or Hope?, 22. Photosynthesis. 23. The Metabolism of Nitrogen.
Doping in Sports: Good Science Gone Bad, 24. Integration of Metabolism: Cellular Signaling.
Aging – Looking for the Biochemical Fountain of Answers. Glossary. Index.
Youth, The Science of Happiness and Depression,
© 2015, Paperback, 9789814624244
Humans vs. Flu, Malaria, G-Protein-Coupled
Receptors, The Genetics of Breast Cancer,
and Proteins and Magnets: Nuclear Magnetic
Resonance in Biochemistry.
• NEW BIOCHEMICAL CONNECTIONS. Several
new Biochemical Connections demonstrate how
biochemistry topics relate to the real world in
high-interest areas such as allied health, sports
medicine, and biotechnology. Biochemical
Connections are now flowed in with the text where
they are relevant to the conversation. These are
meant to be read with the narrative, but they have
a special design and magazine style voice to liven
up the narrative! These are like crescendos in the
narrative that keep student interest at a high level,
and show them how biochemistry is a part of them
and their daily lives.
• New Marginal Glossary! Per student and faculty
requests we added a marginal glossary to each
page making it easier for students to learn key
terms and understand concepts while reading
the narrative.
CONTENTS
1. Biochemistry and the Organization of Cells. 2.
Water: The Solvent for Biochemical Reactions. 3.
Amino Acids and Peptides. 4. The Three-Dimensional
Structure of Proteins. 5. Protein Purification and
Characterization Techniques. 6. The Behavior of
Proteins: Enzymes. 7. The Behavior of Proteins:
Enzymes, Mechanisms, and Control. 8. Lipids and
Proteins Are Associated in Biological Membranes. 9.
Nucleic Acids: How Structure Conveys Information.
10. Biosynthesis of Nucleic Acids: Replication. 11.
Transcription of the Genetic Code: The Biosynthesis
of RNA. 12. Protein Synthesis: Translation of the
Genetic Message. 13. Nucleic Acid Biotechnology
Techniques. 14. Viruses, Cancer and Immunology.
15. The Importance of Energy Changes and
Electron Transfer in Metabolism. 16. Carbohydrates.
17. Glycolysis. 18. Storage Mechanisms and
Control in Carbohydrate Metabolism. 19. The
Citric Acid Cycle. 20. Electron Transport and
Oxidative Phosphorylation. 21. Lipid Metabolism.

www.cengageasia.com
41

GENERAL CHEMISTRY
CTE CHEMISTRY FOR ENGINEERING
STUDENTS WITH CB COURSESMART
EBOOK, 3E
Larry Brown, Texas A&M University; Tom Holme, Iowa State
University
Please note that the digital access code that comes
with the print book is valid for use in a specific Asia
territory only.CB CourseSmart eBook – The ultimate
eBook experience has arrived! Easily access our
eBooks with features that will improve your reading
experience, and tools to help you take notes and
organize your studies.Enhanced with a remarkable
number of new problems and applications, the
Third Edition of CHEMISTRY FOR ENGINEERING
STUDENTS provides a concise, thorough, and
relevant introduction to chemistry that prepares
learners for further study in any engineering field.
Updated with even more questions and applications
specifically geared toward engineering, the book
emphasizes the connection between molecular
properties and observable physical properties
and the connections between chemistry and other
subjects such as mathematics and physics. This
new edition is now fully supported by OWL, the most
widely-used online learning system for chemistry.
42 www.cengageasia.com
NEW TO THIS EDITION
• Access to the #1 online homework and learning
system for chemistry, OWLv2, is packaged with
this hybrid edition and now with new instructor
features and enhanced functionality: a Dashboard
that consolidates all course materials; easy,
intuitive assignment creation and management;
ability to preview and select activities/questions
for each assignment; new assignment settings
and options; improved gradebook; Personalized
Study tools to help students focus their time on the
key concepts and skills; and MindTap Reader™, a
new eBook with apps and embedded video, audio,
annotations, and activities. OWLv2 courses for
Gen Chem, GOB, and Liberal Arts now include
Quick Prep essential skills assignments that can
be taken before the semester begins or during
the first few weeks, to help students succeed in
the course. For this course, OWLv2 also includes
new interactive versions of the end-of-chapter
questions from the text and new iPad-compatible
visualizations, tutorials, and simulations.
• NEW EOC Problems: Replaced several end-
of-chapter problems and added several end-of-
chapter problems.
• Updated art and design program!
• Content Changes to based on chemistry in the
news and technological advances that are of
special important in the engineering field as
related to chemistry.
• In chapter 3 the authors changed the context for
the entire chapter from explosions to biofuels.
• In chapter 4 the authors replaced “Focus on
Problem Solving” with a new style of problem for
this feature that includes graphical reasoning.
• In chapter 6 the authors changed the context for
the entire chapter from light bulbs to trace analysis.
• Added a discussion in Section 14.6 about the
Fukushima reactor accident and the release of
radioactivity from it.
 CONTENTS
1. Introduction to Chemistry.2. Atoms and
Molecules.3. Molecules, Moles, & Chemical
Equations.4. Stoichiometry.5. Gases.6. The Periodic
Table and Atomic Structure.7. Chemical Bonding and
Molecular Structure.8. Molecules and Materials.9.
Energy and Chemistry.10. Entropy and the Second
Law of Thermodynamics.11. Chemical Kinetics.12.
Chemical Equilibrium.13. Electrochemistry.14.
Nuclear Chemistry.Appendices.
© 2015, 416pp, Paperback, 9789814624862

CTE CHEMISTRY WITH CB

COURSESMART EBOOK, 9E
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Susan A. Zumdahl, University of Illinois, Urbana-Champaign

Please note that the digital access code that comes

with the print book is valid for use in a specific
Asia territory only.CB CourseSmart eBook – The
ultimate eBook experience has arrived! Easily
access our eBooks with features that will improve
your reading experience, and tools to help you take
notes and organize your studies.This fully updated
Ninth Edition of Steven and Susan Zumdahl’s
CHEMISTRY brings together the solid pedagogy,
easy-to-use media, and interactive exercises that
today’s instructors need for their general chemistry
course. Rather than focusing on rote memorization,
CHEMISTRY uses a thoughtful approach built on
problem-solving. For the Ninth Edition, the authors
have added a new emphasis on critical systematic
problem solving, new critical thinking questions,
and new computer-based interactive examples
to help students learn how to approach and solve
chemical problems--to learn to think like chemists-
-so that they can apply the process of problem
solving to all aspects of their lives. Students are
provided with the tools to become critical thinkers:
to ask questions, to apply rules and develop models,
and to evaluate the outcome. In addition, Steven
and Susan Zumdahl crafted ChemWork, an online
program included in OWL Online Web Learning to
support their approach, much as an instructor would
offer support during office hours. ChemWork is just
one of many study aids available with CHEMISTRY
that supports the hallmarks of the textbook--a strong
emphasis on models, real world applications, visual

www.cengageasia.com
43
 learning, and independent problem solving. are taught how to select a limiting reactant both by
NEW TO THIS EDITION comparing the amounts of reactants present and
by calculating the amounts of products that can be
• A NEW EMPHASIS ON SYSTEMATIC PROBLEM
formed by complete consumption of each reactant.
SOLVING now appears in the applications of
• A NEW SECTION ON PHOTOELECTRON
dimensional analysis.
SPECTROSCOPY was added to Chapter 9
• NEW CRITICAL THINKING QUESTIONS have
(Section 9.6).
been added throughout the text to emphasize the
• ENHANCED OWL (ONLINE WEB LEARNING)
importance of conceptual learning.
INTEGRATION: For the Ninth Edition, OWL now
• NEW COMPUTER-BASED INTERACTIVE
includes more parameterized end-of-chapter
EXAMPLES force students to think through the
questions, encouraging students to practice
example step-by-step rather than simply scan the
multiple questions of the same type with different
written example in the text as many students do.
chemicals, wording, and numbers to ensure their
New Interactive Examples are available in OWL
mastery of the underlying chemical concepts.
Online Web Learning. In addition, key examples
OWL also includes Student Self- Assessments,
from the text have been made into Interactive
ChemWork problems, Interactive Examples from
Tutorial problems and are available to assign in
the text, the interactive customizable Cengage
the OWL program.
YouBook, a customizable iPad-compatible
• NEW CHEMWORK PROBLEMS have been
multimedia eBook, and an optional Solutions
added to the end-of-chapter problems throughout
Manual eBook.
the text to test students’ understanding of core
• PROBLEM-SOLVING STRATEGY BOXES focus
concepts. They can be worked as pencil-and-
the student’s attention on the very important
paper problems or in interactive form in OWL,
process of problem solving, helping them learn
where students who solve a problem with no
to think like chemists.
assistance can proceed directly to the answer
and students who need help can get assistance
through a series of hints. The hints in OWL--
usually in the form of interactive questions that
guide students through the problem-solving
process--are modeled after the way an instructor
would assist a student with homework problems
during office hours. Students cannot derive the
answer in OWL through pattern recognition;
rather, they are encouraged to continue working
though the hints to arrive at the answer.
• NEW END-OF–CHAPTER QUESTIONS AND
PROBLEMS have been added throughout the text.
• THE REVISED AND UPDATED ART PROGRAM
has been modified as needed, and new macro/
micro illustrations have been added.
• A NEW SECTION ON LIMITING REACTANTS
in Chapter 3, the treatment of stoichiometry,
emphasizes calculating the amounts of products
that can be obtained from each reactant. Students

44 www.cengageasia.com
 CONTENTS
1. Chemical Foundations.2. Atoms, Molecules,
and Ions.3. Stoichiometry.4. Types of Chemical
Reactions and Solution Stoichiometry.5. Gases6.
Thermochemistry.7. Atomic Structure and
Periodicity.8. Bonding: General Concepts.9.
Covalent Bonding: Orbitals.10. Liquids and
Solids.11. Properties of Solutions.12. Chemical
Kinetics.13. Chemical Equilibrium.14. Acids and
Bases.15. Acid-Base Equilibria.16. Solubility and
Complex Ion Equilibria.17. Spontaneity, Entropy,
and Free Energy.18. Electrochemistry.19. The
Nucleus: A Chemist’s View.20. The Representative
Elements.21. Transition Metals and Coordination
Chemistry.22. Organic and Biological Molecules.
Appendix 1. Mathematical Procedures.A1.1
Exponential Notation.A1.2 Logarithms.A1.3
Graphing Functions.A1.4 Solving Quadratic
Equations.A1.5 Uncertainties in Measurements.
Appendix 2. The Quantitative Kinetic Molecular
Model.Appendix 3. Spectral Analysis.Appendix
4. Selected Thermodynamic Data.Appendix 5.
Equilibrium Constants and Reduction Potentials.
A5.1 Values of Ka for Some Common Monoprotic
Acids.A5.2 Stepwise Dissociation Constants for
Several Common Polyprotic Acids.A5.3 Values
of Kb for Some Common Weak Bases.A5.4 Ksp
Values at 25_C for Common Ionic Solids.A5.5
Standard Reduction Potentials at 25_C (298K)
for Many Common Half-Reactions.Appendix 6. SI
Units and Conversion Factors.Glossary.Answers to
Selected Exercises.
© 2014, 752pp, Paperback, 9789814568715

www.cengageasia.com
45

CTE GENERAL CHEMISTRY WITH CB
COURSESMART EBOOK, 10E
Darrell D. Ebbing, Wayne State University; Steven D.
Gammon, Western Washington University
Please note that the digital access code that comes
with the print book is valid for use in a specific Asia
territory only.CB CourseSmart eBook – The ultimate
eBook experience has arrived! Easily access our
eBooks with features that will improve your reading
experience, and tools to help you take notes and
organize your studies.The tenth edition of this
market-leading text has been substantially revised
to meet the rapidly changing instructional demands
of GENERAL CHEMISTRY professors. Known for
its carefully developed, thoroughly integrated, step-
by-step approach to problem solving, GENERAL
CHEMISTRY helps students master quantitative
skills and build a lasting conceptual understanding
of key chemical concepts. The tenth edition
retains this hallmark approach and builds upon
the conceptual focus through key new features
and revisions.
46
NEW TO THIS EDITION
• Beautiful new book design that is user friendly, but
also conveys the sense of excitement surrounding
chemistry that the author team wants students
to see!
• Heavily revised art and photography program that
helps highlight the excitement of chemistry while
explaining key concepts. New talking labels have
been added to the art and photos. These talk
students through the figure and explain what they
are seeing--what they need to know.
• A new pedagogical feature has been added to
all of the examples that are woven throughout
the book. The new feature in the examples is
called the “Gaining Mastery Toolbox.” Every tool
box contains “Critical Concepts” and “Solution
Essentials.” Critical Concepts are concepts from
the relevant chapter that the student needs to
know in order to work through the example.
The Solution Essential segment features a list
of information needed to solve the problem
presented--for example, a student may need the
periodic table, Avogadro’s number, etc.
• Many new and revised end-of-chapter problems
and questions including a new type of strategy
problem.
• TWO TIER questions are ones that ask a student
a question and then they must choose the answer.
The second tier question is where they choose why
they chose that answer. Students often choose the
correct answer but not the correct reason they
answered it correctly, which reveals that they do
not under the concept being demonstrated
• New end of chapter “Check List for Review”
feature--this new feature is presented in an easy-
to-follow tabular format that includes a summary of
facts and concepts, learning objectives, important
terms, and key equations. This innovative
presentation is organized by section.
• Up-to-date coverage in every chapter of the latest
changes in chemistry.
www.cengageasia.com
 CONTENTS
Part I: BASICS OF CHEMISTRY.1. Chemistry
and Measurement.2. Atoms, Molecules, and
Ions.3. Calculations with Chemical Formulas and
Equations.4. Chemical Reactions.5. The Gaseous
State.6. Thermochemistry.Part II: ATOMIC AND
MOLECULAR STRUCTURE.7. Quantum Theory of
the Atom.8. Electron Configurations and Periodicity.9.
Ionic and Covalent Bonding.10. Molecular Geometry
and Chemical Bonding Theory.Part III: STATES OF
MATTER AND SOLUTIONS.11. States of Matter;
Liquids and Solids.12. Solutions.Part IV: CHEMICAL
REACTIONS AND EQUILIBRIUM.13. Rates of
Reaction.14. Chemical Equilibrium.15. Acids
and Bases.16. Acid-Base Equilibria.17. Solubility
and Complex-Ion Equilibria.18. Thermodynamics
and Equilibrium.19. Electrochemistry.Part V:
NUCLEAR CHEMISTRY AND CHEMISTRY OF THE
ELEMENTS.20. Nuclear Chemistry.21. Chemistry
of the Main-Group Elements.22. The Transition
Elements and Coordination Compounds.23. Organic
Chemistry.24. Polymer Materials: Synthetic and
Biological.APPENDIXES.Answers to Exercises.
Answers to Concept Checks. Answers to Self-
Assessment Questions.Answers to Selected Odd-
Numbered Problems.
© 2013, 792pp, Paperback, 9789814601146

www.cengageasia.com
47

CTE CHEMISTRY WITH CB
COURSESMART EBOOK, 10E
Kenneth W. Whitten, University of Georgia; Raymond E.
Davis, University of Texas, Austin; Larry Peck, Texas A&M
University; George G. Stanley, Louisiana State University
Please note that the digital access code that comes
with the print book is valid for use in a specific
Asia territory only.CB CourseSmart eBook – The
ultimate eBook experience has arrived! Easily
access our eBooks with features that will improve
your reading experience, and tools to help you
take notes and organize your studies.This new
edition of CHEMISTRY continues to incorporate
a strong molecular reasoning focus, amplified
problem-solving exercises, a wide range of real-
life examples and applications, and innovative
technological resources. With this text’s focus on
molecular reasoning, readers will learn to think at
the molecular level and make connections between
molecular structure and macroscopic properties.
The Tenth Edition has been revised throughout and
now includes a reorganization of the descriptive
chemistry chapters to improve the flow of topics,
a new basic math skills Appendix, an updated art
program with new “talking labels” that fully explain
what is going on in the figure, and much more.
48
NEW TO THIS EDITION
• R E O R G A N I Z A T I O N O F D E S C R I P T I V E
CHEMISTRY CHAPTERS (22-28): To facilitate
an improved flow of the descriptive chemistry
topics optionally covered in many courses and
to provide more convenient options for custom
versions of the textbook, Chapters 22 through 28
have been reorganized as follows: Chapter 22
is now Nuclear Chemistry; Chapter 23, Organic
Chemistry I: Formulas, Names and Properties;
Chapter 24, Organic Chemistry II: Shapes,
Selected Reactions, and Biopolymers; Chapter 25,
Coordination Compounds; Chapter 26, Metals I:
Metallurgy; Chapter 27, Metals II: Properties and
Reactions; and Chapter 28, Some Nonmetals
and Metalloids.
• NEW BASIC MATH SKILLS APPENDIX: To aid
the flow of introductory chemistry material in
Chapter 1, a review of topics in basic mathematics
skills, including scientific notation and use of
significant figures, with numerous Examples, now
appears in Appendix A. Related Exercises remain
in the Measurements and Calculations area at the
end of Chapter 1.
• MORE COMPREHENSIVE COVERAGE OF
CENTRAL ATOM LONE PAIRS: In Chapter 8,
a more comprehensive tabular summary of the
influence of central atom lone pairs on molecular
geometry has been added to enhance student
understanding.
• A REVISED AND UPDATED ART PROGRAM:
The Tenth Edition’s art program has been revised
to include “talking labels” placed strategically
within figures to explain what is going on in the
illustration, so students can focus on learning
instead of trying to figure out what is going on by
going back and forth between a caption and the
art. To exemplify the beauty and excitement of
chemistry, the individual layouts of many figures
have been revised to be more visually pleasing,
balanced, and organized. The art program now
includes more molecular models generated by the
latest software to enhance the molecular reasoning
theme. All electrostatic charge potential (ECP) art
includes a more thorough explanation of its use.
www.cengageasia.com
• ENHANCED OWL ONLINE WEB LEARNING:
For the Tenth Edition, OWL now includes
more parameterized end-of-chapter questions,
encouraging students to practice multiple
questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts.
OWL also includes the Cengage YouBook, a
customizable iPad-compatible multimedia eBook,
Quick Prep assignments that help students learn
skills essential for success in General Chemistry,
and an optional solutions manual eBook.
FEATURES
• REORGANIZED INTRODUCTION TO AQUEOUS
SOLUTIONS: Section 6-1 has been reorganized
to improve the descriptive introduction to aspects
of aqueous solutions, including ionization
and dissociation, acids, bases, and solubility
guidelines. These basic ideas are then elaborated
in the classification of reactions in the remainder
of Chapter 6 and serve as a foundation throughout
the textbook for further discussion of physical and
chemical properties of solutions.
Chemistry I: Formulas, Names and Properties.24.
Organic Chemistry II: Shapes, selected Reactions,
and Biopolymers.25. Coordination Compounds.26.
Metals I: Metallurgy.27. Metals II: Properties and
Reactions.28. Some Nonmetals and Metalloids.
Appendix A: Basic Math Skills (includes new
significant figure section).Appendix B: Electron
Configurations of the Atoms of the Elements.
Appendix C: Common Units, Equivalences,
and Conversion Factors.Appendix D: Physical
Constants.Appendix E: Some Physical Constants
for a Few Common Substances.Appendix F:
Ionization Constants for Weak Acids at 25°C.
Appendix G: Ionization Constants for Weak Bases
at 25°C.Appendix H: Solubility Product Constants
for Some Inorganic Compounds at 25°C.Appendix
I: Dissociation Constants for Some Complex Ions.
Appendix J: Standard Reduction Potentials in
Aqueous Solution at 25°C.Appendix K: Selected
Thermodynamic Values at 298.15 K.Appendix L:
Answers to Selected Even-Numbered Numerical
Exercises.Index of Equations.Glossary/Index.
© 2014, 792pp, Paperback, 9789814601368

• MOLECULAR REASONING AND VISUALIZATION

EMPHASIS: Molecular reasoning is woven
throughout the text in chapter objectives, chapter
essays, examples, and end-of-chapter problems
and highlighted by a molecular reasoning icon.
CONTENTS
1. The Foundations of Chemistry.2. Chemical
Formulas and Composition Stoichiometry.3.
Chemical Equations and Reaction Stoichiometry.4.
The Structure of Atoms.5. Chemical Periodicity.6.
Some Types of Chemical Reactions.7. Chemical
Bonding.8. Molecular Structure and Covalent
Bonding Theories.9. Molecular Orbitals in Chemical
Bonding.10. Reactions in Aqueous Solutions I:
Acids, Bases, and Salts.11. Reactions in Aqueous
Solutions II: Calculations.12. Gases and the
Kinetic-Molecular Theory.13. Liquids and Solids.14.
Solutions.15. Chemical Thermodynamics.16.
Chemical Kinetics.17. Chemical Equilibrium.18.
Ionic Equilibria I: Acids and Bases.19. Ionic
Equilibria II: Buffers and Titration Curves.20. Ionic
Equilibria III: The Solubility Product Principle.21.
Electrochemistry.22. Nuclear Chemistry.23. Organic

www.cengageasia.com
49

CTE CHEMISTRY AND CHEMICAL
REACTIVITY WITH CB COURSESMART
EBOOK, 9E
John C. Kotz, State University of New York, Oneonta; Paul M.
Treichel, University of Wisconsin, Madison; John Townsend,
West Chester University of Pennsylvania; David Treichel,
Nebraska Wesleyan University
Please note that the digital access code that comes
with the print book is valid for use in a specific Asia
territory only.CB CourseSmart eBook – The ultimate
eBook experience has arrived! Easily access our
eBooks with features that will improve your reading
experience, and tools to help you take notes and
organize your studies. Succeed in chemistry with
the clear explanations, problem-solving strategies,
and dynamic study tools of CHEMISTRY &
CHEMICAL REACTIVITY, 9e. Combining thorough
instruction with the powerful multimedia tools
you need to develop a deeper understanding of
general chemistry concepts, the text emphasizes
the visual nature of chemistry, illustrating the close
interrelationship of the macroscopic, symbolic, and
particulate levels of chemistry. The art program
illustrates each of these levels in engaging detail--
and is fully integrated with key media components.
In addition access to OWLv2 may be purchased
separately or at a special price if packaged with
this text. OWLv2 is an online homework and tutorial
system that helps you maximize your study time
and improve your success in the course. OWLv2
includes an interactive eBook, as well as hundreds
of guided simulations, animations, and video clips.
NEW TO THIS EDITION
• The five topical interchapters in previous editions
50 www.cengageasia.com
have been integrated into standard chapters:
Milestones in the Development of Chemistry and
the Modern World View of Atoms and Molecules
have been folded into Chapter 2. The Chemistry of
Fuels and Energy Resources and The Chemistry
of the Environment have been incorporated into
an expanded new chapter on Environmental
Chemistry (Chapter 20). The Chemistry of Life:
Biochemistry has been expanded into a full
chapter (Chapter 24). The Chemistry of Modern
Materials has been incorporated into the chapter
on solids (Chapter 12).
• Chapter Goals (and Chapter Goals Revisited)
have been recast into three categories that most
express what students should get out of the course:
1. Understand: chapter concepts. 2. Do: Be able to
carry out calculations, draw molecular structures,
and make chemical decisions. 3. Remember:
important facts and chemical concepts.
• All answers are now combined into a single
comprehensive appendix organized by chapter.
• Over 100 new end of chapter Study Questions
have been added.
• The #1 online homework and learning system
for chemistry, OWLv2, is available for this text--
now with new instructor features and enhanced
functionality: a Dashboard that consolidates
all course materials; easy, intuitive assignment
creation and management; ability to preview and
select activities/questions for each assignment;
new assignment settings and options; improved
gradebook; Personalized Study tools to help
students focus their time on the key concepts and
skills; and MindTap Reader™, a new eBook with
apps and embedded video, audio, annotations,
and activities. OWLv2 courses for Gen Chem,
GOB, and Liberal Arts now include Quick Prep
essential skills assignments that can be taken
before the semester begins or during the first few
weeks, to help students succeed in the course. For
this course, OWLv2 also includes new interactive
versions of the end-of-chapter questions from
the text and new iPad-compatible visualizations,
tutorials, and simulations.
CONTENTS
PART I: CONCEPTS OF CHEMISTRY.1. Basic
Concepts of Chemistry.Let’s Review: The Tools
of Quantitative Chemistry.2. Atoms, Molecules,
and Ions.3. Chemical Reactions.4. Stoichiometry:
Quantitative Information from Chemical Reactions.5.
Principles of Chemical Reactivity: Energy and
Chemical Reactions.PART II: ATOMS AND
MOLECULES.6. The Structure of Atoms.7. The
Structure of Atoms and Periodic Trends.8. Covalent
Bonding and Molecular Structure.9. Bonding and
Molecular Structure - Valence Bond and Molecular
Orbital Theory.Part 3: States of Matter.10. Gases
and Their Properties.11. Intermolecular Forces and
Liquids.12. Ionic Bonding, Metals, and the Solid
State.13. Solutions and Their Behavior.PART IV:
THE CONTROL OF CHEMICAL REACTIONS.14.
Chemical Kinetics - The Rates of Chemical
Reactions.15. Principles of Reactivity: Chemical
Equilibria.16. Equlibria and Acids and Bases.17.
Principles of Reactivity: Other Aspects of Aqueous
Equilibria.18. Thermodynamics - Entropy and
Free Energy.19. Principles of Reactivity: Electron
Transfer Reactions.PART V: THE CHEMISTRY
OF THE ELEMENTS.20. Environmental Chemistry:
Earth’s Environment, Energy, and Sustainability.21.
The Chemistry of the Main Group Elements.22. The
Chemistry of the Transition Elements.23. Carbon: Not
Just Another Element.24. Biochemistry.25. Nuclear
Chemistry.Appendix A: Using Logarithms and the
Quadratic Equation.Appendix B: Some Important
Physical Concepts.Appendix C: Abbreviations
and Useful Conversion Factors.Appendix D:
Physical Constants.Appendix E: Naming Organic
Compounds.Appendix F: Values for the Ionization
Energies and Electron Affinities of the Elements.
Appendix G: Vapor Pressure of Water at Various
Temperatures.Appendix H: Ionization Constants
for Weak Acids at 25ºC.Appendix I: Ionization
Constants for Weak Bases at 25ºC.Appendix J:
Solubility Product Constants for Some Inorganic
Compounds at 25ºC.Appendix K: Formation
Constants for Some Complex Ions in Aqueous
Solution.Appendix L: Selected Thermodynamic
Values.Appendix M: Standard Reduction Potentials
in Aqueous Solution at 25ºC.Appendix N: Answers
to Chapter Opening and Case Study Questions,
Check Your Understanding Questions, Review and
Check Questions, and Selected Study Questions.
© 2015, 928pp, Paperback, 9789814617796
www.cengageasia.com
GENERAL CHEMISTRY (WITH
MINDTAP CHEMISTRY 24-MONTHS
PRINTED ACCESS CARD)
William Vining, State University of New York at Oneonta;
Susan Young, Assistant Professor of Chemistry, University
of Colorado at Boulder; Roberta Day, Professor Emeritus,
University of Massachusetts; Beatrice Botch, University of
Massachusetts, Amherst
MindTap General Chemistry is a personalized
teaching and learning experience that allows
instructors to control what students see and focus
on relevant assignments that guide them to analyze,
apply, and improve thinking. Seamlessly integrating
interactive simulations, videos and diagnostic
quizzes, it helps students achieve course learning
outcomes by bringing chemistry concepts to life.
Measure skills and outcomes with ease using
powerful analytics that provide a visual dashboard
with at-a-glance performance and engagement data
that is used to provide direction regarding class
and student needs. This version is accompanied
by a print text that includes the narrative from the
MindTap General Chemistry course.
FEATURES
• Easily Set Your Own Course: Manage, administer
and customize to meet your course needs. Do it
yourself or let us help.
• Elevate Thinking: Use relevant activities that take
students from basic knowledge and understanding
to higher level learning.
• Promote Better Outcomes: Track progress and
know where students stand in class at all times.
• Seamlessly deliver appropriate content and
technology assets from a number of providers to
students, as they need them.
51
 • Break course content down into movable objects and CompoundsStoichiometryChemical
to promote personalization, encourage interactivity Reactions and Solution Stoichiometry
and ensure student engagement. ThermochemistryElectromagnetic Radiation and
• Customize the course – from tools to text – and the Electronic Structure of the AtomElectron
make adjustments ‘on the fly,’ making it possible Configurations and the Properties of AtomsCovalent
to intertwine breaking news into their lessons and
Bonding and Molecular StructureTheories of Chemical
incorporate today’s teachable moments.
BondingGasesIntermolecular Forces and the Liquid
• Bring interactivity into learning through the
integration of multimedia assets (apps from StateThe Solid StateChemical Mixtures: Solutions
Cengage Learning and other providers), and and Other MixturesChemical KineticsChemical
numerous in-context exercises and supplements. EquilibriumAcids and BasesAdvanced Acid-Base
Student engagement will increase, leading to EquilibriaPrecipitation and Lewis Acid-Base
better student outcomes. EquilibriaThermodynamics: Entropy and Free
• Track students’ use, activities and comprehension EnergyElectrochemistryHydrocarbonsApplying
in real-time, which provides opportunities for early Chemical Principles to the Main Group ElementsThe
intervention to influence progress and outcomes. Transition ElementsNuclear Chemistry
Grades are visible and archived so students
and instructors always have access to current © 2015, 880pp, Paperback, 978130527515
standings in the class.
• Assess knowledge throughout each section: after
readings, in activities, homework, and quizzes.
• Automatically grade all homework and quizzes.
CONTENTS
The Learning Path guides students through the
course. Instructors are provided a fully loaded
version that consists of interactive content and
exercises that can be reassembled and rearranged
by the instructor. Instructors may also add their
own content and assignments anywhere within
the Learning Path and its readings.Instructional
DesignMindTap for General Chemistry is designed
to be used in the first year general chemistry
course, and is comprised of twenty-two units. The
Learning Path for each unit guides the students
through the course. Each unit contains interactive
narrative with assignable conceptual and problem
solving activities, mastery questions, and challenge
problems that will help students achieve conceptual
understanding as well as master problem-solving
skills. A study center tracks individual student
and overall class progress on course learning
objectives and identifies where they need to focus
their study time. Instructors can also add their
own content anywhere in the Learning Path.Unit
ListChemistry: Matter on the Atomic ScaleElements

52 www.cengageasia.com

THE GUIDE TO SURVIVING GENERAL
CHEMISTRY, 2E
Michael Rosen
Available packaged with any CENGAGE textbook,
this helpful guide is a frontline resource for students
who need extra help or want to improve their
General Chemistry grade. Written by a student with
extensive tutoring experience who understands
where students struggle most and using terms
that they most relate to and understand, this guide
helps students see that they can actually master
chemistry concepts. GUIDE TO SURVIVING
GENERAL CHEMISTRY includes study tips and
example problems with worked out solutions for
all topics in general chemistry, and is endorsed by
Professor Mark Oram, Ph.D, for accuracy and topic
coverage. This book is also available for students to
purchase separately at www.CENGAGEbrain.com.
NEW TO THIS EDITION
• The second edition has been edited by college
chemistry professor, Dr Mark Oram. The book
combines the legitimacy of a conventional
textbook with the one-of-a-kind perspective of a
student who understands the pitfalls of learning
general chemistry. Bridging the gap between
a professor’s level of understanding and that of
a student is the hallmark of this unique survival
guide.
www.cengageasia.com
FEATURES
• Saves instructors time by offering students a
resource that they can use first to help answer
questions before coming to see instructors for
help.
• Provides a front line resource for students who
need extra help or want to improve their General
Chemistry grade.
• Written by a student for students, general
chemistry topics are presented at a level that
students can relate to and understand which
gives students the confidence that they can learn
general chemistry.
• Offers effective study tips for learning general
chemistry concepts.
• Provides example problems and worked out
solutions so that students can strengthen their
problem-solving skills.
CONTENTS
1. Acids and Bases.2. Colligative Properties.3.
Concentration Unites and Conversions for
Solutions.4. Dimensional Analysis and Significant
Figures.5. Electrochemistry and Redox.6.
Electrons.7. Equilibrium Calculations.8. Gas Laws.9.
Kinetics.10. Lewis Structures and VSEPR Theory.11.
Nomenclature.12. Organic chemistry.13. Periodic
Table.14. Phase Diagrams and Crystalline Solids.15.
Quantitative Calculations.16. Solubility and Net Ionic
Equations.17. Statistics.18. Thermodynamics.
© 2015, 192pp, Paperback, 9781305391383
53

CTE CHEMICAL PRINCIPLES WITH CB
COURSESMART EBOOK, 7E
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Donald J. DeCoste, University of Illinois, Urbana-Champaign
Please note that the digital access code that comes
with the print book is valid for use in a specific
Asia territory only.CB CourseSmart eBook – The
ultimate eBook experience has arrived! Easily
access our eBooks with features that will improve
your reading experience, and tools to help you
take notes and organize your studies.Develop the
qualitative, conceptual foundation you need to
think like a chemist with CHEMICAL PRINCIPLES,
7e. Designed for students with solid mathematical
preparation, this best-seller offers a unique
organization that emphasizes models, everyday
applications of chemistry, and a thoughtful, step-
by-step problem-solving approach.
NEW TO THIS EDITION
• New Co-author: Don DeCoste, brings his wealth
of teaching experience to this exceptional Seventh
Edition
• New “Learning to Solve Problems” Section: A
new Section 3.4 emphasizes the importance of
conceptual problem solving by showing students
how to think their way through a problem. This
section discusses how to solve problems in a
flexible, creative way based on understanding
the fundamental ideas of chemistry and asking
and answering key questions. Students will learn
that this “big picture approach” produces more
long term, meaningful learning rather than simply
memorizing specific steps that are easily forgotten.
• New Chemical Insights Boxes: Many new and
revised Chemical Insights boxes cover such up-
54 www.cengageasia.com
to-date topics as geoengineering, laser cooling,
graphene, and nanogenerators.
• New and Revised Problems: Many of the book’s
end-of-chapter questions and problems have been
revised and more than 50 new visual problems
have been added.
• New In-text Learning Aids. A list of Key Terms has
been added at the end of each chapter along with
an Outline that reviews each chapter. In addition,
many of the book’s figures have been revised to
better serve visual learners.
FEATURES
• Unique Organization: The authors cover equilibria
and acid-base chemistry early and delay coverage
of atomic theory and bonding until the second half
of the text. The text includes sections on Exact
Treatment of Buffered Solutions (Chapter 8),
Adiabatic Processes (Chapter 10), and Molecular,
Rotational, Vibrational, Electronic, and Nuclear
Magnetic Spectroscopy (Chapter 14). These
sections provide more depth at a slightly more
rigorous level, consistent with the book’s overall
focus.
CONTENTS
1. Chemists and Chemistry.2. Atoms, Molecules,
and Ions.3. Stoichiometry.4. Types of Chemical
Reactions and Solution Stoichiometry.5. Gases.6.
Chemical Equilibrium.7. Acids and Bases.8.
Applications of Aqueous Equilibria.9. Energy,
Enthalpy, and Thermochemistry.10. Spontaneity,
Entropy, and Free Energy.11. Electrochemistry.12.
Quantum Mechanics and Atomic Theory.13.
Bonding: General Concepts.14. Covalent Bonding:
Orbitals.15. Chemical Kinetics.16. Liquids
and Solids.17. Properties of Solutions.18. The
Representative Elements.19. Transition Metals
and Coordination Chemistry.20. The Nucleus:
A Chemist’s View.21. Organic and Biochemical
Molecules.Appendix 1. Mathematical Procedures.
Appendix 2. Units of Measurement and Conversions
Among Units.Appendix 3. Spectral Analysis.
Appendix 4. Selected Thermodynamic Data.
Appendix 5. Equilibrium Constants and Reduction
Potentials.Glossary.Answers to Selected Exercises.
© 2013, 832pp, Paperback, 9789814605083

CTE CHEMISTRY AND CHEMICAL
REACTIVITY WITH CB COURSESMART
EBOOK, 9E
John C. Kotz, State University of New York, Oneonta; Paul M.
Treichel, University of Wisconsin, Madison; John Townsend,
West Chester University of Pennsylvania; David Treichel,
Nebraska Wesleyan University
Please note that the digital access code that comes
with the print book is valid for use in a specific Asia
territory only.CB CourseSmart eBook – The ultimate
eBook experience has arrived! Easily access our
eBooks with features that will improve your reading
experience, and tools to help you take notes and
organize your studies. Succeed in chemistry with
the clear explanations, problem-solving strategies,
and dynamic study tools of CHEMISTRY &
CHEMICAL REACTIVITY, 9e. Combining thorough
instruction with the powerful multimedia tools
you need to develop a deeper understanding of
general chemistry concepts, the text emphasizes
the visual nature of chemistry, illustrating the close
interrelationship of the macroscopic, symbolic, and
particulate levels of chemistry. The art program
illustrates each of these levels in engaging detail--
and is fully integrated with key media components.
In addition access to OWLv2 may be purchased
separately or at a special price if packaged with
this text. OWLv2 is an online homework and tutorial
system that helps you maximize your study time
and improve your success in the course. OWLv2
includes an interactive eBook, as well as hundreds
of guided simulations, animations, and video clips.
www.cengageasia.com
NEW TO THIS EDITION
• The five topical interchapters in previous editions
have been integrated into standard chapters:
Milestones in the Development of Chemistry and
the Modern World View of Atoms and Molecules
have been folded into Chapter 2. The Chemistry of
Fuels and Energy Resources and The Chemistry
of the Environment have been incorporated into
an expanded new chapter on Environmental
Chemistry (Chapter 20). The Chemistry of Life:
Biochemistry has been expanded into a full
chapter (Chapter 24). The Chemistry of Modern
Materials has been incorporated into the chapter
on solids (Chapter 12).
• Chapter Goals (and Chapter Goals Revisited)
have been recast into three categories that most
express what students should get out of the course:
1. Understand: chapter concepts. 2. Do: Be able to
carry out calculations, draw molecular structures,
and make chemical decisions. 3. Remember:
important facts and chemical concepts.
• All answers are now combined into a single
comprehensive appendix organized by chapter.
• Over 100 new end of chapter Study Questions
have been added.
• The #1 online homework and learning system
for chemistry, OWLv2, is available for this text--
now with new instructor features and enhanced
functionality: a Dashboard that consolidates
all course materials; easy, intuitive assignment
creation and management; ability to preview and
select activities/questions for each assignment;
new assignment settings and options; improved
gradebook; Personalized Study tools to help
students focus their time on the key concepts and
skills; and MindTap Reader™, a new eBook with
apps and embedded video, audio, annotations,
and activities. OWLv2 courses for Gen Chem,
GOB, and Liberal Arts now include Quick Prep
essential skills assignments that can be taken
before the semester begins or during the first few
weeks, to help students succeed in the course. For
this course, OWLv2 also includes new interactive
versions of the end-of-chapter questions from
the text and new iPad-compatible visualizations,
tutorials, and simulations.
55
 CONTENTS Check Your Understanding Questions, Review and
PART I: CONCEPTS OF CHEMISTRY.1. Basic Check Questions, and Selected Study Questions.
Concepts of Chemistry.Let’s Review: The Tools
of Quantitative Chemistry.2. Atoms, Molecules, © 2015, 928pp, Paperback, 9789814617796
and Ions.3. Chemical Reactions.4. Stoichiometry:
Quantitative Information from Chemical Reactions.5.
Principles of Chemical Reactivity: Energy and
Chemical Reactions.PART II: ATOMS AND
MOLECULES.6. The Structure of Atoms.7. The
Structure of Atoms and Periodic Trends.8. Covalent
Bonding and Molecular Structure.9. Bonding and
Molecular Structure - Valence Bond and Molecular
Orbital Theory.Part 3: States of Matter.10. Gases
and Their Properties.11. Intermolecular Forces and
Liquids.12. Ionic Bonding, Metals, and the Solid
State.13. Solutions and Their Behavior.PART IV:
THE CONTROL OF CHEMICAL REACTIONS.14.
Chemical Kinetics - The Rates of Chemical
Reactions.15. Principles of Reactivity: Chemical CHEMISTRY, 2E
Equilibria.16. Equlibria and Acids and Bases.17. An Atoms First Approach
Principles of Reactivity: Other Aspects of Aqueous Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Equilibria.18. Thermodynamics - Entropy and Susan A. Zumdahl, University of Illinois, Urbana-Champaign
Free Energy.19. Principles of Reactivity: Electron
Steve and Susan Zumdahl’s texts focus on helping
Transfer Reactions.PART V: THE CHEMISTRY
students build critical thinking skills through the
OF THE ELEMENTS.20. Environmental Chemistry:
process of becoming independent problem-solvers.
Earth’s Environment, Energy, and Sustainability.21.
They help students learn to “think like chemists”
The Chemistry of the Main Group Elements.22. The
Chemistry of the Transition Elements.23. Carbon: Not so they can apply the problem-solving process to
Just Another Element.24. Biochemistry.25. Nuclear all aspects of their lives. In this Second Edition of
Chemistry.Appendix A: Using Logarithms and the CHEMISTRY: AN ATOMS FIRST APPROACH, the
Quadratic Equation.Appendix B: Some Important Zumdahls use a meaningful approach that begins
Physical Concepts.Appendix C: Abbreviations with the atom and proceeds through the concept
and Useful Conversion Factors.Appendix D: of molecules, structure, and bonding to more
Physical Constants.Appendix E: Naming Organic complex materials and their properties. Because
Compounds.Appendix F: Values for the Ionization this approach differs from what most students have
Energies and Electron Affinities of the Elements. experienced in high school courses, it encourages
Appendix G: Vapor Pressure of Water at Various them to focus on conceptual learning early in the
Temperatures.Appendix H: Ionization Constants course, rather than relying on memorization and
for Weak Acids at 25ºC.Appendix I: Ionization a “plug and chug” method of problem solving that
Constants for Weak Bases at 25ºC.Appendix J: even the best students can fall back on when
Solubility Product Constants for Some Inorganic confronted with familiar material. The atoms first
Compounds at 25ºC.Appendix K: Formation organization provides an opportunity for students to
Constants for Some Complex Ions in Aqueous use the tools of critical thinkers: to ask questions, to
Solution.Appendix L: Selected Thermodynamic apply rules and models, and to evaluate outcomes.
Values.Appendix M: Standard Reduction Potentials
in Aqueous Solution at 25ºC.Appendix N: Answers NEW TO THIS EDITION
to Chapter Opening and Case Study Questions, • R E O R G A N I Z E D FOR ENHANCED

56 www.cengageasia.com
 UNDERSTANDING: A reorganization of key
chapters (3, 4, 5, and 6) allows for stoichiometry
to be taught earlier (Chapter 5), which coincides
with labs being done at that time. In addition, the
organization of various sections has been fine-
tuned (for example, the Gas Stoichiometry section
moved to the Gases chapter and the Calorimetry
section moved to the Chemical Energy chapter).
The combined chapter and section reorganization
improves the flow of the text to better meet the
needs of those teaching and learning from an
atoms first approach.
• NEW “CRITICAL THINKING” QUESTIONS
provide a greater emphasis on the importance of
conceptual learning.
• NEW CHEMWORK EXERCISES, which can be
worked using the online system or as pencil-and-
paper problems, test students’ understanding of
core chapter concepts.
• NEW ATOMS FIRST MARGIN NOTES throughout
the text enhance teaching and learning using an
atoms first approach.
• NEW ATOMS FIRST BOXED FEATURES
“CONNECTING TO ATOMS” help students
understand how varying chapter content works
together under an atoms first approach through
a summary of key concepts at point-of-use, which
provides both a review of atoms first concepts and
a glimpse of what is ahead.
• ENHANCED ONLINE LEARNING: The #1 online
homework and learning system for chemistry,
OWLv2, is available for this text--and now
features more flexible student and instructor
functionality, new personalized study tools,
enhanced integration with learning management
systems, and improved analytics. OWLv2 for this
text also includes Quick Prep, an online short
course that reviews key chemistry concepts
and essential skills, new Adaptive Study Plans,
hundreds of new interactive versions of the
text’s end-of-chapter questions, and new tutors,
visualizations, and simulations that have been
converted from Flash to HTML, allowing for easier
navigation and streamlined grading.
FEATURES
• AN ATOMS FIRST APPROACH: By taking
an atoms first approach, the authors provide
www.cengageasia.com
students with a unified story built around an
organizing principle--start the course with the
smallest element, the atom, and build from there.
Building their explanations around this structure,
the authors consistently show the importance and
relevance of studying chemistry.
• A FOCUS ON CONCEPTUAL UNDERSTANDING:
Rather than focusing on memorizing, the book
gives students the tools they need to become
critical thinkers: to ask questions, to apply rules
and develop models, and to evaluate the outcome.
• A STRONG PROBLEM-SOLVING ORIENTATION:
Throughout the text, problem-solving strategies
help students learn to solve problems by thinking
them through rather than brute-force memorizing.
Section 5.3 “Learning to Solve Problems”
emphasizes the importance of thoughtful, creative
problem solving, demonstrating that thinking
through a problem produces more long-term,
meaningful learning that can be applied to “real
life” than memorizing steps that apply only to a
particular type of problem. The problem-solving
process is organized in terms of “Where are we
going?”; “How do we get there?”; and “Reality
Check,” which prompts students to check whether
their answer makes sense.
• STUDENT-ORIENTED LEARNING AIDS:
Problem-solving strategy boxes help students
focus on particular aspects of problem-solving;
concept summary boxes help students organize
their thinking about crucial concepts; critical-
thinking questions help students to contemplate
various atoms first concepts; chemical connections
boxes present applications of chemistry in various
fields and in daily life; and atoms first boxes
provide an overall summary at critical junctures
that ties together concepts to enhance student
understanding.
CONTENTS
Review: Measurement and Calculations in
Chemistry.1. Chemical Foundations.2. Atomic
Structure and Periodicity.3. Bonding: General
Concepts.4. Molecular Structure and Orbitals.5.
Stoichiometry.6. Types of Chemical Reactions
and Solution Stoichiometry.7. Chemical Energy.8.
Gases.9. Liquids and Solids.10. Properties of
Solutions.11. Chemical Kinetics.12. Chemical
57
 Equilibrium.13. Acids and Bases.14. Acid-Base
Equilibria15. Solubility and Complex Ion Equilibria.16.
Spontaneity, Entropy, and Free Energy.17.
Electrochemistry.18. The Nucleus: A Chemist’s
View.19. The Representative Elements.20.
Transition Metals and Coordination Chemistry.21.
Organic and Biological Molecules.
© 2016, 1216pp, Hardback, 9781305079243
CHEMISTRY, 8E
Principles and Reactions
William L. Masterton, University of Connecticut, Emeritus;
Cecile N. Hurley, University of Connecticut
This latest edition of CHEMISTRY: PRINCIPLES
AND REACTIONS takes students directly to the
crux of chemistry’s fundamental concepts and
allows you to efficiently cover all topics found in
a typical general chemistry book. Based on the
authors’ extensive teaching experience, the book
includes rigorous graded and concept-driven
examples, as well as examples that focus on
molecular reasoning and understanding. The Eighth
Edition features a new and innovative example
format, new “talking labels” within artwork, 25%
new or revised problems, “Chemistry: Beyond the
Classroom” essays that highlight some of the most
up-to-date uses of chemistry, and end-of-chapter
questions and Key Concepts that correlate to
OWLv2, the #1 online homework and tutorial system
for chemistry.
NEW TO THIS EDITION
• NEW AND INNOVATIVE EXAMPLE FORMAT:
Clear, consistent, and easy to follow, the new
58
Example format includes analysis, strategy, and
solution sections after each individual part of the
Example. Each example ends with an End Point,
which provides additional insight into the problem.
• NEW “TALKING LABELS”: This edition moves
relevant text from captions to talking labels within
the art for a clearer presentation of visual images.
Contemporary photographs, modern molecular
models, and new concept flowcharts help further
clarify key concepts.
• MORE FLOWCHARTS: Owing to the enthusiastic
response to them in the last edition, more
flowcharts have been added and existing ones
revised to help students visualize a pathway to
follow for various topics.
• BALANCING REDOX EQUATIONS MOVED
TO CHAPTER 17: In response to instructor and
reviewer feedback, the discussion of balancing
redox equations has been moved from Chapter 4
to Chapter 17 and redox reactions are treated in
Chapter 4 only as far as stoichiometric calculations
are involved (balanced equations are provided for
these reactions).
• 25% NEW AND REVISED PROBLEMS: To keep
the end-of-chapter questions fresh, approximately
25% of the problems are either new or revised.
• NEW AND REVISED SUMMARY PROBLEMS:
Almost all of the summary problems have either
been revised or are completely new to this edition.
• NEW CHAPTER-OPENING ARTWORK: Almost
all of the fine art used in the chapter-opening
images to illustrate chemical principles and
applications is new.
• ENHANCED ONLINE LEARNING: The most
powerful online learning solution for chemistry
is better than ever. OWLv2 now has more
flexible student and instructor functionality, new
personalized study tools, enhanced integration
with learning management systems, and improved
analytics. For this course, OWLv2 also includes
Quick Prep, an online short course to review
key chemistry concepts and essential skills, new
Adaptive Study Plans, and new iPad-compatible
visualizations, tutorials, and simulations that have
been converted from Flash to HTML, allowing for
easier navigation and streamlined grading.
www.cengageasia.com
 FEATURES
• CONNECTION TO FINE ARTS: The text connects
the hard science of chemistry to the humanities
and fine arts through chapter openers and literary
quotations that enhance each chapter’s content.
• LATEST WORK FROM SPECIALISTS: Guest
authors and leaders in specialized fields profile
the latest research in “Chemistry: Beyond the
Classroom” boxes. Students see the relevance
of concepts in some of the most current work
in chemistry, including coloration of biological
organisms, molecular structure of rubbery
materials, and fuel cells. LAB MANUAL FOR ZUMDAHL/
CONTENTS ZUMDAHL’S CHEMISTRY: AN ATOMS
1. Matter and Measurements.2. Atoms, Molecules, FIRST APPROACH, 2ND, 2E
and Ions.3. Mass Relations in Chemistry; Charles H. Atwood, University of Georgia
Stoichiometry.4. Reactions in Aqueous Solution.5. Build skill and confidence in the lab with the
Gases.6. Electronic Structure and the Periodic experiments included in this manual. Safety is
Table.7. Covalent Bonding.8. Thermochemistry.9. strongly emphasized.
Liquids and Solids.10. Solutions.11. Rate of
Reaction.12. Gaseous Chemical Equilibrium.13. © 2016, 624pp, Paperback, 9781305398313
Acids and Bases.14. Equilibria in Acid-Base
Solutions.15. Complex ion and Precipitation
Equilibria.16. Spontaneity of Reaction.17.
Electrochemistry.18. Nuclear Reactions.19.
Complex Ions and Coordination Compounds.20.
Chemistry of the Metals.21. Chemistry of the
Nonmetals.22. Organic Chemistry.23. Organic
Polymers, Natural and Synthetic.Appendix 1.
Units, Constants, and Reference Data.Appendix 2.
Properties of the Elements.Appendix 3. Exponents
and Logarithms.Appendix 4. Molecular Orbitals.
Appendix 5. Answers to Even-Numbered and
Challenge Questions and Problems.Index/Glossary
© 2016, 800pp, Hardback, 9781305079373

www.cengageasia.com
59

PRINCIPLES OF MODERN
CHEMISTRY, 8E
David W. Oxtoby, Pomona College; H. Pat Gillis, University
of California - Los Angeles; Laurie J. Butler, The University of
Chicago
Long considered the standard for honors and
high-level mainstream general chemistry courses,
PRINCIPLES OF MODERN CHEMISTRY
continues to set the standard as the most modern,
rigorous, and chemically and mathematically
accurate text on the market. This authoritative text
features an “atoms first” approach and thoroughly
revised chapters on Quantum Mechanics and
Molecular Structure (Chapter 6), Electrochemistry
(Chapter 17), and Molecular Spectroscopy and
Photochemistry (Chapter 20). In addition, the text
utilizes mathematically accurate and artistic atomic
and molecular orbital art, and is student friendly
without compromising its rigor. End-of-chapter
study aids focus on only the most important key
objectives, equations and concepts, making it
easier for students to locate chapter content, while
applications to a wide range of disciplines, such
as biology, chemical engineering, biochemistry,
and medicine deepen students’ understanding of
the relevance of chemistry beyond the classroom.
NEW TO THIS EDITION
• The most powerful online learning solution for
chemistry is better than ever. OWLv2 now has
more flexible student and instructor functionality,
new personalized study tools, enhanced
integration with learning management systems,
and improved analytics. For this course, OWLv2
also includes Quick Prep, an online short course to
60
review key chemistry concepts and essential skills,
new iPad-compatible visualizations, tutorials, and
simulations, and new Adaptive Study Plans. In
addition, Tutors, Visualizations and Simulations
have been converted from Flash to HTML,
allowing for easier navigation and streamlined
grading.
• The most powerful online learning solution for
chemistry is better than ever. OWLv2 now has
more flexible student and instructor functionality,
new personalized study tools, enhanced
integration with learning management systems,
and improved analytics. For this course, OWLv2
also includes Quick Prep, an online short course to
review key chemistry concepts and essential skills,
new iPad-compatible visualizations, tutorials, and
simulations, and new Adaptive Study Plans. In
addition, Tutors, Visualizations and Simulations
have been converted from Flash to HTML,
allowing for easier navigation and streamlined
grading.
• Recognizing that in the top colleges and
universities that use this text over 90 percent
of students taking introductory chemistry have
taken a single variable calculus course in high
school, or are taking calculus as a co-requisite
for the course, we have improved several portions
of the text. These revisions include a more
quantitative treatment of the forces and potential
energy in molecules, dipole moments, molecular
collisions, and the Maxwell-Boltzmann distribution
of molecular speeds. The concepts of slope and
area are introduced in the physical and chemical
contexts in which they arise, and differential and
integral notation is used in parallel with these
concepts. Thus, students with a single-variable
calculus background are engaged fully, while
students without that background will not be at
a disadvantage. Simple vectors are introduced
to aid in discussing force and velocity, with a
new section in Appendix C covering vectors in
Cartesian coordinates.
FEATURES
• OWLv2 is the most trusted online learning solution
for chemistry. Featuring chemist-developed
content, OWLv2 is the only system designed
to elevate thinking through Mastery Learning,
www.cengageasia.com
 allowing students to work at their own pace until
they understand each concept and skill. Each
time a student tries a problem, OWLv2 changes
the chemicals, values, and sometimes even
the wording of the question to ensure students
are learning the concepts and not cheating the
system. With detailed, instant feedback and
interactive learning resources, students get the
help they need when they need it. Now with
improved student and instructor tools and greater
functionality, OWLv2 is more robust than ever.
Discover the power of OWLv2 and take learning
to a higher level.
• AN “ATOMS FIRST” APPROACH places coverage
of structure and bonding early in the text (Chapter
4-6), taking students right into the core topics
of the course and helping them build a strong
conceptual understanding of chemistry.
• A U N I Q U E A P P R O A C H T O L E A R N I N G
CHEMICAL PRINCIPLES emphasizes the
scientific process from observation to application,
placing general chemistry into perspective for
serious-minded science and engineering students.
• MATHEMATICALLY ACCURATE MOLECULAR
ORBITAL ART helps students visualize how
orbital equations translate into the shapes of the
orbitals.
• A FOCUS ON PROBLEM SOLVING. Problems
are grouped into three categories: 1) Paired
problems in the first set are grouped by section,
with answers to the odd-numbered paired
problems collected in Appendix G so students can
check their answer to the first problem in a pair
before undertaking the second parallel problem.
2) Additional Problems (unpaired) provide
further applications of the principles developed
in the chapter. 3) Cumulative Problems integrate
material from the chapter with topics presented
earlier in the book. More challenging problems
are integrated throughout the problem sets and
are indicated with asterisks.
• PEDAGOGICALLY IMPORTANT APPENDICES.
Appendix A discusses experimental error and
scientific notation; Appendix B introduces the
SI system of units used throughout the book,
describes the methods used for converting units,
and provides a brief review of some fundamental
www.cengageasia.com
principles in physics. Appendix C provides a
review of mathematics for general chemistry,
including a new section on vectors in Cartesian
coordinates. Appendices D, E, and F are
compilations of thermodynamic, electrochemical,
and physical data, respectively.
CONTENTS
Unit I. Introduction to the Study of Modern
Chemistry.1. The Atom in Modern Chemistry.2.
Chemical Formulas, Equations, and Reaction
Yields.Unit II. Chemical Bonding and Molecular
Structure.3. Atomic Shells and Classical Models
of Chemical Bonding.4. Introduction to Quantum
Mechanics.5. Quantum Mechanics and Atomic
Structure.6. Quantum Mechanics and Molecular
Structure.7. Bonding in Organic Molecules.8.
Bonding in Transition Metal Compounds and
Coordination Complexes.Unit III. Kinetic Molecular
Description of the States of Matter.9. The Gaseous
State.10. Solids, Liquids, and Phase Transitions.11.
Solutions.Unit IV. Equilibrium in Chemical
Reactions.12. Thermodynamic Processes and
Thermochemistry.13. Spontaneous Processes
and Thermodynamic Equilibrium.14. Chemical
Equilibrium.15. Acid–Base Equilibria.16. Solubility
and Precipitation Equilibria.17. Electrochemistry.Unit
V. Rates of Chemical and Physical Processes.18.
Chemical Kinetics.19. Nuclear Chemistry.20.
Molecular Spectroscopy and Photochemistry.
Unit VI. Materials.21. Structure and Bonding
in Solids.22. Inorganic Materials.23. Polymeric
Materials and Soft Condensed Matter.Appendix A.
Scientific Notation and Experimental Error.Appendix
B. SI Units, Unit Conversions, and Physics for
General Chemistry.Appendix C. Mathematics for
General Chemistry.Appendix D. Standard Chemical
Thermodynamic Properties.Appendix E. Standard
Reaction Potentials at 25°C.Appendix F. Physical
Properties of the Elements.Appendix G. Solutions
to the Odd-Numbered Problems.Index/Glossary.
© 2016, 1280pp, Hardback, 9781305079113
61

PRINCIPLES OF MODERN
CHEMISTRY, HYBRID EDITION (WITH
OWLV2 PRINTED ACCESS CARD), 8E
David W. Oxtoby, Pomona College; H. Pat Gillis, University
of California - Los Angeles; Laurie J. Butler, The University of
Chicago
Long considered the standard for honors and
high-level mainstream general chemistry courses,
PRINCIPLES OF MODERN CHEMISTRY
continues to set the standard as the most modern,
rigorous, and chemically and mathematically
accurate text on the market. This authoritative text
features an “atoms first” approach and thoroughly
revised chapters on Quantum Mechanics and
Molecular Structure (Chapter 6), Electrochemistry
(Chapter 17), and Molecular Spectroscopy and
Photochemistry (Chapter 20). In addition, the text
utilizes mathematically accurate and artistic atomic
and molecular orbital art, and is student friendly
without compromising its rigor. End-of-chapter
study aids focus on only the most important key
objectives, equations and concepts, making it
easier for students to locate chapter content, while
applications to a wide range of disciplines, such
as biology, chemical engineering, biochemistry,
and medicine deepen students’ understanding of
the relevance of chemistry beyond the classroom.
NEW TO THIS EDITION
• The most powerful online learning solution for
chemistry is better than ever. OWLv2 now has
more flexible student and instructor functionality,
new personalized study tools, enhanced
integration with learning management systems,
and improved analytics. For this course, OWLv2
62
also includes Quick Prep, an online short course to
review key chemistry concepts and essential skills,
new iPad-compatible visualizations, tutorials, and
simulations, and new Adaptive Study Plans. In
addition, Tutors, Visualizations and Simulations
have been converted from Flash to HTML,
allowing for easier navigation and streamlined
grading.
• The most powerful online learning solution for
chemistry is better than ever. OWLv2 now has
more flexible student and instructor functionality,
new personalized study tools, enhanced
integration with learning management systems,
and improved analytics. For this course, OWLv2
also includes Quick Prep, an online short course to
review key chemistry concepts and essential skills,
new iPad-compatible visualizations, tutorials, and
simulations, and new Adaptive Study Plans. In
addition, Tutors, Visualizations and Simulations
have been converted from Flash to HTML,
allowing for easier navigation and streamlined
grading.
• Recognizing that in the top colleges and
universities that use this text over 90 percent
of students taking introductory chemistry have
taken a single variable calculus course in high
school, or are taking calculus as a co-requisite
for the course, we have improved several portions
of the text. These revisions include a more
quantitative treatment of the forces and potential
energy in molecules, dipole moments, molecular
collisions, and the Maxwell-Boltzmann distribution
of molecular speeds. The concepts of slope and
area are introduced in the physical and chemical
contexts in which they arise, and differential and
integral notation is used in parallel with these
concepts. Thus, students with a single-variable
calculus background are engaged fully, while
students without that background will not be at
a disadvantage. Simple vectors are introduced
to aid in discussing force and velocity, with a
new section in Appendix C covering vectors in
Cartesian coordinates.
FEATURES
• OWLv2 is the most trusted online learning solution
for chemistry. Featuring chemist-developed
content, OWLv2 is the only system designed
www.cengageasia.com
 to elevate thinking through Mastery Learning,
allowing students to work at their own pace until
they understand each concept and skill. Each
time a student tries a problem, OWLv2 changes
the, chemistry, values, and sometimes even
the wording of the question to ensure students
are learning the concepts and not cheating the
system. With detailed, instant feedback and
interactive learning resources, students get the
help they need when they need it. Now with
improved student and instructor tools and greater
functionality, OWLv2 is more robust than ever.
Discover the power of OWLv2 and take learning
to a higher level.
• AN “ATOMS FIRST” APPROACH places coverage
of structure and bonding early in the text (Chapter
4-6), taking students right into the core topics
of the course and helping them build a strong
conceptual understanding of chemistry.
• A U N I Q U E A P P R O A C H T O L E A R N I N G
CHEMICAL PRINCIPLES emphasizes the
scientific process from observation to application,
placing general chemistry into perspective for
serious-minded science and engineering students.
• MATHEMATICALLY ACCURATE MOLECULAR
ORBITAL ART helps students visualize how
orbital equations translate into the shapes of the
orbitals.
• A FOCUS ON PROBLEM SOLVING. Problems
are grouped into three categories: 1) Paired
problems in the first set are grouped by section,
with answers to the odd-numbered paired
problems collected in Appendix G so students can
check their answer to the first problem in a pair
before undertaking the second parallel problem.
2) Additional Problems (unpaired) provide
further applications of the principles developed
in the chapter. 3) Cumulative Problems integrate
material from the chapter with topics presented
earlier in the book. More challenging problems
are integrated throughout the problem sets and
are indicated with asterisks.
• PEDAGOGICALLY IMPORTANT APPENDICES.
Appendix A discusses experimental error and
scientific notation; Appendix B introduces the
SI system of units used throughout the book,
describes the methods used for converting units,
www.cengageasia.com
and provides a brief review of some fundamental
principles in physics. Appendix C provides a
review of mathematics for general chemistry,
including a new section on vectors in Cartesian
coordinates. Appendices D, E, and F are
compilations of thermodynamic, electrochemical,
and physical data, respectively.
CONTENTS
Unit I. Introduction to the Study of Modern
Chemistry.1. The Atom in Modern Chemistry.2.
Chemical Formulas, Equations, and Reaction
Yields.Unit II. Chemical Bonding and Molecular
Structure.3. Atomic Shells and Classical Models
of Chemical Bonding.4. Introduction to Quantum
Mechanics.5. Quantum Mechanics and Atomic
Structure.6. Quantum Mechanics and Molecular
Structure.7. Bonding in Organic Molecules.8.
Bonding in Transition Metal Compounds and
Coordination Complexes.Unit III. Kinetic Molecular
Description of the States of Matter.9. The Gaseous
State.10. Solids, Liquids, and Phase Transitions.11.
Solutions.Unit IV. Equilibrium in Chemical
Reactions.12. Thermodynamic Processes and
Thermochemistry.13. Spontaneous Processes
and Thermodynamic Equilibrium.14. Chemical
Equilibrium.15. Acid–Base Equilibria.16. Solubility
and Precipitation Equilibria.17. Electrochemistry.Unit
V. Rates of Chemical and Physical Processes.18.
Chemical Kinetics.19. Nuclear Chemistry.20.
Molecular Spectroscopy and Photochemistry.
Unit VI. Materials.21. Structure and Bonding
in Solids.22. Inorganic Materials.23. Polymeric
Materials and Soft Condensed Matter.Appendix A.
Scientific Notation and Experimental Error.Appendix
B. SI Units, Unit Conversions, and Physics for
General Chemistry.Appendix C. Mathematics for
General Chemistry.Appendix D. Standard Chemical
Thermodynamic Properties.Appendix E. Standard
Reaction Potentials at 25°C.Appendix F. Physical
Properties of the Elements.Appendix G. Solutions
to the Odd-Numbered Problems.Index/Glossary.
© 2016, 1136pp, Paperback, 9781305395893
63

CHEMISTRY, 5E
The Molecular Science
John W. Moore, University of Wisconsin, Madison; Conrad L.
Stanitski, Franklin and Marshall College
Authors Moore and Stanitski, both winners of the
ACS Pimentel Award in Chemical Education, infuse
CHEMISTRY: THE MOLECULAR SCIENCE, Fifth
Edition, with timely everyday applications that
reveal chemistry as a lively and relevant subject that
is fundamental to a broad range of disciplines such
as engineering, biology, and environmental science.
A revised, annotated art program emphasizes the
three concept levels in a pedagogically sound
approach to understanding molecules, concepts,
and mathematical equations. Many of the book’s
end-of-chapter questions are accompanied by
interactive, assignable, online lessons in OWL—the
#1 online learning system for chemistry. Engage
your students in active study of chemistry with this
text.
NEW TO THIS EDITION
• The first five chapters of the previous edition have
been condensed into three chapters. The new
Chapter 1 includes material on the metric system,
and significant figures (previously in Chapter 2)
along with the periodic table coverage previously
in Chapters 2 and 3. Chapter 2 now includes
the material previously in Chapters 2 and 3. The
approach to reactions in aqueous solution has
been completely revised and content previous
in Chapters 4 and 5 is consolidate into a new
Chapter 3. Balancing chemical equations and
three reaction types (precipitation; acid-base,
and redox) are now discussed before quantitative
64 www.cengageasia.com
treatments (reaction stoichiometry, solution
concentrations and solution stoichiometry/
titrations) in Chapter 3.
• Partly due to consolidating changes cited above,
the book has been reduced to 20 chapters instead
of 22 previously.
• Revised all Problem-Solving Examples (PSEs)
to a four-step Analyze, Plan, Execute, and
Check Result format. Problem-solving strategy
is clearly delineated in Chapter 1 where students
are provided a study strategy for problem solving
examples.
• Each CO photo has an associated caption that
raises chemistry-based questions that are then
answered within the chapter. Specific chapter
sections are noted with the questions.
• Made much greater use of annotations (“balloons”)
that are incorporated into award-winning
illustrations; this pedagogically sound practice
reduces the need for running text, helps shorten
the book, and helps students learn better.
• The variety, comprehensiveness, and conceptual
level of chapter-end Questions for Review and
Thought (QRTs) have been expanded.
• There are many new chapter-end Questions for
Review and Thought (QRTs).
• Aligned QRTs for each chapter with the end-of-
chapter summary Having Studied… objectives
based on Bloom’s Taxonomy of Learning
Objectives.
• Assessed each QRT based on Bloom’s Taxonomy
to insure adequate numbers of questions for each
taxonomic category. New QRTs written to insure
meeting this number.
• Summary Problems at the end of each chapter
help students learn and integrate chapter concepts
and provide good study aids for exams. Many
Summary Problems are entirely new and all have
been edited and improved.
CONTENTS
1. The Nature of Chemistry.2. Chemical
Compounds.3. Chemical Reactions.4. Energy
and Reactions.5. Electron Configurations and
the Periodic Table.6. Covalent Bonding.7.
Molecular Structures.8. Properties of Gases.9.
Liquids, Solids, and Materials.10. Fuels, Organic
Chemicals, and Polymers.11. Chemical Kinetics:
Rates of Reactions12. Chemical Equilibrium.13.
The Chemistry of Solutes and Solutions.14.
Acids and Bases.15. Additional Aqueous
Equilibria.16. Thermodynamics: Directionality
of Chemical Reactions.17. Electrochemistry
and Its Applications.18. Nuclear Chemistry.19.
The Chemistry of the Main Group Elements.20.
Chemistry of Selected Transition Elements and
Coordination Compounds.Appendix A: Problem
Solving and Mathematical Operations.Appendix
B: Units, Equivalences, and Conversion Factors.
Appendix C: Physical Constants and Sources
of Data.Appendix D: Ground-State Electron
Configurations of Atoms.Appendix E: Naming
Simple Organic Compounds.Appendix F: Ionization
Constants for Weak Acids at 25°C.Appendix G:
Ionization Constants for Weak Bases at 25°C.
Appendix H: Solubility Product Constants for Some
Inorganic Compounds at 25°C.Appendix I: Standard
Reduction. Potentials in Aqueous Solution at 25
°C.Appendix J: Selected Thermodynamic Values.
Appendix K: Answers to Problem-Solving Practice
Problems.Appendix L: Answers to Exercises.
Appendix M: Answers to Selected Questions for
Review and Thought.
© 2015, 1264pp, Hardback, 9781285199047
www.cengageasia.com
CHEMISTRY, 5E
The Molecular Science, Hybrid Edition (with OWLv2
24-Months Printed Access Card)
John W. Moore, University of Wisconsin, Madison; Conrad L.
Stanitski, Franklin and Marshall College
Reflecting Cengage Learning’s commitment to
offering flexible teaching solutions and value for
students and instructors, this new hybrid version
features the instructional presentation found in the
printed text while delivering all the end-of chapter
exercises online in OWLv2, the leading online
learning system for chemistry. The result--a briefer
printed text that engages students online! Help your
students improve their grades and understanding
of concepts with this value-packed Hybrid Edition.
An access code to OWLv2 with MindTap Reader,
is included with the text, providing students with
powerful online resources that include tutorials,
simulations, randomized homework questions,
videos, a complete interactive electronic version
of the textbook, and more! Your students will be
engaged in the active study of chemistry with
CHEMISTRY: THE MOLECULAR SCIENCE,
Fifth Edition. Authors Moore and Stanitski, both
winners of the ACS Pimentel Award in Chemical
Education, infuse their text with timely everyday
applications that reveal chemistry as a lively and
relevant subject that is fundamental to a broad
range of disciplines such as engineering, biology,
and environmental science. A revised, annotated
art program emphasizes the three concept levels in
a pedagogically sound approach to understanding
molecules, concepts, and mathematical equations.
Many of the book’s end-of-chapter questions are
accompanied by interactive, assignable, online
65
 lessons in OWLv2--the #1 online learning system
for chemistry.
NEW TO THIS EDITION
• The first five chapters of the previous edition have
been condensed into three chapters. The new
Chapter 1 includes material on the metric system,
and significant figures (previously in Chapter 2)
along with the periodic table coverage previously
in Chapters 2 and 3. Chapter 2 now includes
the material previously in Chapters 2 and 3. The
approach to reactions in aqueous solution has
been completely revised and content previous
in Chapters 4 and 5 is consolidate into a new
Chapter 3. Balancing chemical equations and
three reaction types (precipitation; acid-base,
and redox) are now discussed before quantitative
treatments (reaction stoichiometry, solution
concentrations and solution stoichiometry/
titrations) in Chapter 3.
• Partly due to consolidating changes cited above,
the book has been reduced to 20 chapters instead
of 22 previously.
• Revised all Problem-Solving Examples (PSEs)
to a four-step Analyze, Plan, Execute, and
Check Result format. Problem-solving strategy
is clearly delineated in Chapter 1 where students
are provided a study strategy for problem solving
examples.
• Each CO photo has an associated caption that
raises chemistry-based questions that are then
answered within the chapter. Specific chapter
sections are noted with the questions.
• Made much greater use of annotations (“balloons”)
that are incorporated into award-winning
illustrations; this pedagogically sound practice
reduces the need for running text, helps shorten
the book, and helps students learn better.
• The variety, comprehensiveness, and conceptual
level of chapter-end Questions for Review and
Thought (QRTs) have been expanded.
• There are many new chapter-end Questions For
Review and Thought (QRTs).
• Aligned QRTs for each chapter with the end-of-
chapter summary Having Studied… objectives
based on Bloom’s Taxonomy of Learning
Objectives.
• Assessed each QRT based on Bloom’s Taxonomy
66 www.cengageasia.com
to insure adequate numbers of questions for each
taxonomic category. New QRTs written to insure
meeting this number.
• Summary Problems at the end of each chapter
help students learn and integrate chapter concepts
and provide good study aids for exams. Many
Summary Problems are entirely new and all have
been edited and improved.
CONTENTS
1. The Nature of Chemistry.2. Chemical
Compounds.3. Chemical Reactions.4. Energy
and Reactions.5. Electron Configurations and
the Periodic Table.6. Covalent Bonding.7.
Molecular Structures.8. Properties of Gases.9.
Liquids, Solids, and Materials.10. Fuels, Organic
Chemicals, and Polymers.11. Chemical Kinetics:
Rates of Reactions12. Chemical Equilibrium.13.
The Chemistry of Solutes and Solutions.14.
Acids and Bases.15. Additional Aqueous
Equilibria.16. Thermodynamics: Directionality of
Chemical Reactions.17. Electrochemistry and
Its Applications.18. Nuclear Chemistry.19. The
Chemistry of the Main Group Elements.20. Chemistry
of Selected Transition Elements and Coordination
Compounds.Appendix A: Problem Solving and
Mathematical Operations.Appendix B: Units,
Equivalences, and Conversion Factors.Appendix C:
Physical Constants and Sources of Data.Appendix
D: Ground-State Electron Configurations of Atoms.
Appendix E: Naming Simple Organic Compounds.
Appendix F: Ionization Constants for Weak Acids
at 25 °C,Appendix G: Ionization Constants for
Weak Bases at 25°CAppendix H: Solubility Product
Constants for Some Inorganic Compounds at 25°C.
Appendix I : Standard Reduction. Potentials in
Aqueous Solution at 25°C.Appendix J: Selected
Thermodynamic Values.Appendix K: Answers to
Problem-Solving Practice Problems.Appendix L:
Answers to Exercises.Appendix M: Answers to
Selected Questions for Review and Thought.
© 2015, 1056pp, Paperback, 9781285461847

CHEMISTRY & CHEMICAL
REACTIVITY, HYBRID EDITION
(WITH OWLV2 24-MONTHS PRINTED
ACCESS CARD), 9E
John C. Kotz, State University of New York, Oneonta; Paul M.
Treichel, University of Wisconsin, Madison; John Townsend,
West Chester University of Pennsylvania; David Treichel,
Nebraska Wesleyan University
Reflecting Cengage Learning’s commitment to
offering flexible teaching solutions and value for
students and instructors, this new hybrid version
features the instructional presentation found in the
printed text while delivering all the end-of chapter
exercises online in OWLv2, the leading online
learning system for chemistry. The result--a briefer
printed text that engages students online! Help your
students improve their grades and understanding
of concepts with this value-packed Hybrid Edition.
An access code to OWLv2 with MindTap Reader,
is included with the text, providing students with
powerful online resources that include tutorials,
simulations, randomized homework questions,
videos, a complete interactive electronic version
of the textbook, and more! Help your students
succeed in chemistry with the clear explanations,
problem-solving strategies, and dynamic study
tools of CHEMISTRY & CHEMICAL REACTIVITY,
9th edition. Combining thorough instruction with
the powerful multimedia tools you need to develop
a deeper understanding of general chemistry
concepts, the text emphasizes the visual nature of
chemistry, illustrating the close interrelationship of
the macroscopic, symbolic, and particulate levels of
chemistry. The art program illustrates each of these
levels in engaging detail--and is fully integrated with
www.cengageasia.com
key media components.
NEW TO THIS EDITION
• The five topical interchapters in previous editions
have been integrated into standard chapters:
Milestones in the Development of Chemistry and
the Modern World View of Atoms and Molecules
has been folded into Chapter 2. The Chemistry of
Fuels and Energy Resources and The Chemistry
of the Environment have been incorporated into
an expanded new chapter on Environmental
Chemistry (Chapter 20). The Chemistry of Life:
Biochemistry has been expanded into a full
chapter (Chapter 24). The Chemistry of Modern
Materials has been incorporated into the chapter
on solids (Chapter 12).
• Chapter Goals (and Chapter Goals Revisited)
have been recast into three categories that
most express what students should get out of
the course: 1. Understand: chapter concepts.
2. Do: Be able to carry out calculations, draw
molecular structures, make chemical decisions.
3. Remember: important facts and chemical
concepts.
• Access to the #1 online homework and learning
system for chemistry, OWLv2, is packaged
with this text. Now with new instructor features
and enhanced functionality: a Dashboard that
consolidates all course materials; easy, intuitive
assignment creation and management; ability
to preview and select activities/questions for
each assignment; new assignment settings and
options; improved gradebook; Personalized Study
tools to help students focus their time on the key
concepts and skills; and MindTap Reader™, a
new eBook with apps and embedded video, audio,
annotations, and activities. OWLv2 courses for
Gen Chem, GOB, and Liberal Arts now include
Quick Prep essential skills assignments that can
be taken before the semester begins or during
the first few weeks, to help students succeed in
the course. For this course, OWLv2 also includes
new interactive versions of the end-of-chapter
questions from the text and new iPad-compatible
visualizations, tutorials, and simulations.
FEATURES
• WORKED EXAMPLES. Through the text’s six-part
67
 worked example structure, students learn how
to approach a problem rather than to memorize
problem types and solution approaches. Worked
example headers use the following structure:
1) A Problem statement; 2) A “What Do You
Know?” section that asks students to outline what
information they have and begin to think about a
solution; 3) A Strategy section that combines the
information available with the objective to devise a
path to the solution; 4) A fully worked Solution; 5)
A “Think About Your Answer” section that prompts
students to ask if the answer is reasonable; 6) A
“Check Your Understanding” problem similar to
the example to confirm students understand.
• PROBLEM STRATEGY MAPS. Selected worked
examples have Strategy Maps that give students
a visual view of the complete problem-solving
strategy. Video Strategy Solutions based on these
maps are integrated into the MindTap eBook.
• REVIEW & CHECK PROBLEMS. These section-
ending problems help students hone their skill in
assessing whether they understand the concepts
in the section.
• VISUAL TOOLS. With the text’s extensive use
of molecular representations, your students can
move beyond plugging numbers into an equation
to a true understanding of what’s going on at the
molecular level. The authors consistently depict
molecules in chemical equations and use unique
space-filling molecular art that more completely
ties the text’s molecular art to problem solving
and media.
• CASE STUDY BOXES. Cases show students
where chemistry has been used to solve a problem
or where chemistry is important in everyday
matters. Examples include the use of isotopes
to catch athletes who cheat using illegal drugs,
a washing machine that injects silver into the
wash, acrylamide in French fries, a comparison
of ethanol and gasoline, and the amount of salt in
seawater. Questions posed in each Case Study
are answered in an appendix.
• “IN THE LABORATORY” QUESTIONS. These
questions in OWLv2 address techniques used
and work performed in the general chemistry
laboratory to help students make the connection
between lecture topics and lab work.
68 www.cengageasia.com
• BEYOND THE EXAM. The text correlates Chapter
Goals with Study Questions to help students
develop a conceptual understanding of chemistry
and a skill in problem-solving that will serve them
long after their final exams.
CONTENTS
PART I: CONCEPTS OF CHEMISTRY.1. Basic
Concepts of Chemistry.Let’s Review: The Tools
of Quantitative Chemistry.2. Atoms, Molecules,
and Ions.3. Chemical Reactions.4. Stoichiometry:
Quantitative Information from Chemical Reactions.5.
Principles of Chemical Reactivity: Energy and
Chemical Reactions.PART II: ATOMS AND
MOLECULES.6. The Structure of Atoms.7. The
Structure of Atoms and Periodic Trends.8. Covalent
Bonding and Molecular Structure.9. Bonding and
Molecular Structure - Valence Bond and Molecular
Orbital Theory.Part 3: States of Matter.10. Gases
and Their Properties.11. Intermolecular Forces and
Liquids.12. Ionic Bonding, Metals, and the Solid
State.13. Solutions and Their Behavior.PART IV:
THE CONTROL OF CHEMICAL REACTIONS.14.
Chemical Kinetics - The Rates of Chemical
Reactions.15. Principles of Reactivity: Chemical
Equilibria.16. Equlibria and Acids and Bases.17.
Principles of Reactivity: Other Aspects of Aqueous
Equilibria.18. Thermodynamics - Entropy and
Free Energy.19. Principles of Reactivity: Electron
Transfer Reactions.PART V: THE CHEMISTRY
OF THE ELEMENTS.20. Environmental Chemistry:
Earth’s Environment, Energy, and Sustainability.21.
The Chemistry of the Main Group Elements.22. The
Chemistry of the Transition Elements.23. Carbon: Not
Just Another Element.24. Biochemistry.25. Nuclear
Chemistry.Appendix A: Using Logarithms and the
Quadratic Equation.Appendix B: Some Important
Physical Concepts.Appendix C: Abbreviations
and Useful Conversion Factors.Appendix D:
Physical Constants.Appendix E: Naming Organic
Compounds.Appendix F: Values for the Ionization
Energies and Electron Affinities of the Elements.
Appendix G: Vapor Pressure of Water at Various
Temperatures.Appendix H: Ionization Constants
for Weak Acids at 25ºC.Appendix I: Ionization
Constants for Weak Bases at 25ºC.Appendix J:
Solubility Product Constants for Some Inorganic
Compounds at 25ºC.Appendix K: Formation
Constants for Some Complex Ions in Aqueous
Solution.Appendix L: Selected Thermodynamic
Values.Appendix M: Standard Reduction Potentials
in Aqueous Solution at 25ºC.Appendix N: Answers
to Chapter Opening and Case Study Questions,
Check Your Understanding Questions, Review and
Check Questions
© 2015, 1152pp, Paperback, 9781285462530
EXPERIMENTS IN GENERAL
CHEMISTRY, 6E
Steven L. Murov, Modesto Junior College
EXPERIMENTS IN GENERAL CHEMISTRY, Sixth
Edition, has been designed to stimulate curiosity
and insight, and to clearly connect lecture and
laboratory concepts and techniques. To accomplish
this goal, an extensive effort has been made to
develop experiments that maximize a discovery-
oriented approach and minimize personal hazards
and ecological impact. Like earlier editions, the use
of chromates, barium, lead, mercury, and nickel
salts has been avoided. The absence of these
hazardous substances should minimize disposal
problems and costs. This lab manual focuses not
only on what happens during chemical reactions,
but also helps students understand why chemical
reactions occur. The sequence of experiments
has been refined to follow topics covered in most
general chemistry textbooks. In addition, Murov
has included a correlation chart that links the
experiments in the manual to the corresponding
chapter topics in several Cengage Learning general
chemistry titles. Each experiment--framed by pre-
www.cengageasia.com
and post-laboratory exercises and concluding
thought-provoking questions--helps to enhance
students’ conceptual understanding.
NEW TO THIS EDITION
• Labs have been updated with the most recent
data and values in order to accurately reflect the
changes in lab courses.
• The new Activity 35 adds additional challenges
and experiments, and Activity 36 provides
exercises that develop graphing skills.
FEATURES
• Murov focuses not only on what happens during
chemical reactions but also helps students
understand “why” chemical reactions occur.
• Each experiment includes pre-laboratory exercises
and thought-provoking questions (with answers to
selected questions).
• Review Exercises, found at the end of the manual,
help students test their understanding of key
concepts and synthesize the material they have
learned.
• A number of experiments include post-laboratory
exercises and conclude with a set of review
exercises.
• A procedure for following the visual clock reaction
spectroscopically, instead of visually, is included in
the kinetics experiment. This also provides a link
between the equilibrium and kinetics experiments.
• As with the previous editions, the use of chromates,
barium, lead, mercury, and nickel salts has been
avoided, effectively minimizing disposal problems
and decreasing costs.
• A correlation chart links the experiments to
corresponding chapter topics in several Cengage
Learning general chemistry titles, including Kotz,
Masterton, Moore, and Whitten.
• An Online Instructor’s Manual contains resources
designed to streamline and maximize the
effectiveness of course preparation. It includes a
list of chemicals and quantities required for each
experiment per student and solutions to Pre-Lab
problems.
CONTENTS
Preface, Correlation table and Chemistry
Resources SAFETY FIRST1. Early Explorations
69
 and Terminology.2. Separation of Mixtures.3.
Measurements and Identification Techniques.4.
Density, Accuracy, Precision and Graphing.5.
Empirical Formulas.6. Classification of Chemical
Reactions.7. Quantitative Precipitation.8. Electrical
Conductivity and Electrolytes.9. Ionic Reactions.10.
Activities of Metals.11. Quantitative Solution
Chemistry.12. Thermochemistry.13. Properties of
Elements and Compounds: An Internet Study.14.
Spectroscopy of Cobalt (II) Ion.15. Lewis Structures
and Molecular Models.16. Molecular Polarity and
Chromatography.17. Gas Law Studies.18. Cooling
Curves and Crystal Structures.19. Water Purification
and Analysis.20. Organic Models and Isomerism.21.
Acids and Bases: Reactions and Standardization.22.
Acids and Bases: Analysis.23. Acids and Bases:
pH, pKa Measurements.24. Equilibrium - Solubility
Product.25. Equilibrium - Determination of
Keq.26. Complexes.27. Rates and Mechanisms
of Reactions - Visual and/or Spectroscopic
Monitoring.28. Synthesis of Copper (II) Glycinate.29.
Standardization of Thiosulfate.30. Analysis of Bleach
and Copper (II) Glycinate.31. Redox Reactions.32.
Electrochemistry.33. Spectroscopic Analysis of
Aspirin.34. Polymer Properties and Selections35.
Additional Challenges and Experiments36.
Graphing Quantitative RelationshipsAppendix 1:
Properties of SubstancesAppendix 2: Common
Ions by ChargeAppendix 3: Solubilities of Ionic
CompoundsAppendix 4: Solutions to Starred
Prelaboratory Problems
© 2015, 464pp, Paperback, 9781285458540
70 www.cengageasia.com
CHEMISTRY, 9E
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Susan A. Zumdahl, University of Illinois, Urbana-Champaign
This fully updated Ninth Edition of Steven and
Susan Zumdahl’s CHEMISTRY brings together
the solid pedagogy, easy-to-use media, and
interactive exercises that today’s instructors need
for their general chemistry course. Rather than
focusing on rote memorization, CHEMISTRY uses
a thoughtful approach built on problem-solving. For
the Ninth Edition, the authors have added a new
emphasis on critical systematic problem solving,
new critical thinking questions, and new computer-
based interactive examples to help students learn
how to approach and solve chemical problems--to
learn to think like chemists--so that they can apply
the process of problem solving to all aspects of
their lives. Students are provided with the tools to
become critical thinkers: to ask questions, to apply
rules and develop models, and to evaluate the
outcome. In addition, Steven and Susan Zumdahl
crafted ChemWork, an online program included
in OWL Online Web Learning to support their
approach, much as an instructor would offer support
during office hours. ChemWork is just one of many
study aids available with CHEMISTRY that supports
the hallmarks of the textbook--a strong emphasis
on models, real world applications, visual learning,
and independent problem solving. Available with
InfoTrac® Student Collections http://gocengage.
com/infotrac.
NEW TO THIS EDITION
• A NEW EMPHASIS ON SYSTEMATIC PROBLEM
SOLVING now appears in the applications of
 dimensional analysis.
• NEW CRITICAL THINKING QUESTIONS have
been added throughout the text to emphasize the
importance of conceptual learning.
• NEW COMPUTER-BASED INTERACTIVE
EXAMPLES force students to think through the
example step-by-step rather than simply scan the
written example in the text as many students do.
New Interactive Examples are available in OWL
Online Web Learning. In addition, key examples
from the text have been made into Interactive
Tutorial problems and are available to assign in
the OWL program.
• NEW CHEMWORK PROBLEMS have been
added to the end-of-chapter problems throughout
the text to test students’ understanding of core
concepts. They can be worked as pencil-and-
paper problems or in interactive form in OWL,
where students who solve a problem with no
assistance can proceed directly to the answer
and students who need help can get assistance
through a series of hints. The hints in OWL--
usually in the form of interactive questions that
guide students through the problem-solving
process--are modeled after the way an instructor
would assist a student with homework problems
during office hours. Students cannot derive the
answer in OWL through pattern recognition;
rather, they are encouraged to continue working
though the hints to arrive at the answer.
• NEW END-OF–CHAPTER QUESTIONS AND
PROBLEMS have been added throughout the text.
• THE REVISED AND UPDATED ART PROGRAM
has been modified as needed, and new macro/
micro illustrations have been added.
• A NEW SECTION ON LIMITING REACTANTS
in Chapter 3, the treatment of stoichiometry,
emphasizes calculating the amounts of products
that can be obtained from each reactant. Students
are taught how to select a limiting reactant both by
comparing the amounts of reactants present and
by calculating the amounts of products that can be
formed by complete consumption of each reactant.
• A NEW SECTION ON PHOTOELECTRON
SPECTROSCOPY was added to Chapter 9
(Section 9.6).
• ENHANCED OWL (ONLINE WEB LEARNING)
www.cengageasia.com
INTEGRATION: For the Ninth Edition, OWL now
includes more parameterized end-of-chapter
questions, encouraging students to practice
multiple questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts.
OWL also includes Student Self- Assessments,
ChemWork problems, Interactive Examples from
the text, the interactive customizable Cengage
YouBook, a customizable iPad-compatible
multimedia eBook, and an optional Solutions
Manual eBook.
FEATURES
• PROBLEM-SOLVING STRATEGY BOXES focus
the student’s attention on the very important
process of problem solving, helping them learn
to think like chemists.
CONTENTS
1. Chemical Foundations.2. Atoms, Molecules,
and Ions.3. Stoichiometry.4. Types of Chemical
Reactions and Solution Stoichiometry.5. Gases6.
Thermochemistry.7. Atomic Structure and
Periodicity.8. Bonding: General Concepts.9.
Covalent Bonding: Orbitals.10. Liquids and
Solids.11. Properties of Solutions.12. Chemical
Kinetics.13. Chemical Equilibrium.14. Acids and
Bases.15. Acid-Base Equilibria.16. Solubility and
Complex Ion Equilibria.17. Spontaneity, Entropy,
and Free Energy.18. Electrochemistry.19. The
Nucleus: A Chemist’s View.20. The Representative
Elements.21. Transition Metals and Coordination
Chemistry.22. Organic and Biological Molecules.
Appendix 1. Mathematical Procedures.A1.1
Exponential Notation.A1.2 Logarithms.A1.3
Graphing Functions.A1.4 Solving Quadratic
Equations.A1.5 Uncertainties in Measurements.
Appendix 2. The Quantitative Kinetic Molecular
Model.Appendix 3. Spectral Analysis.Appendix
4. Selected Thermodynamic Data.Appendix 5.
Equilibrium Constants and Reduction Potentials.
A5.1 Values of Ka for Some Common Monoprotic
Acids.A5.2 Stepwise Dissociation Constants for
Several Common Polyprotic Acids.A5.3 Values
of Kb for Some Common Weak Bases.A5.4 Ksp
Values at 25_C for Common Ionic Solids.A5.5
Standard Reduction Potentials at 25_C (298K)
71
 for Many Common Half-Reactions.Appendix 6. SI
Units and Conversion Factors.Glossary.Answers to
Selected Exercises.
© 2014, 1200pp, Hardback, 9781133611097
CHEMISTRY, HYBRID EDITION
(WITH OWLV2 24-MONTHS PRINTED
ACCESS CARD), 10E
Kenneth W. Whitten, University of Georgia; Raymond E.
Davis, University of Texas, Austin; Larry Peck, Texas A&M
University; George G. Stanley, Louisiana State University
Reflecting Cengage Learning’s commitment to
offering flexible teaching solutions and value for
students and instructors, this new hybrid version
features the instructional presentation found in the
printed text while delivering all the end-of chapter
exercises online in OWL, the leading online learning
system for chemistry. The result—a briefer printed
text that engages students online! This new Hybrid
edition of CHEMISTRY continues to incorporate
a strong molecular reasoning focus, amplified
problem-solving exercises, a wide range of real-
life examples and applications, and innovative
technological resources. With this text’s focus on
molecular reasoning, your students will learn to
think at the molecular level and make connections
between molecular structure and macroscopic
properties. The Tenth Edition has been revised
throughout and now includes a reorganization of
the descriptive chemistry chapters to improve the
flow of topics, a new basic math skills Appendix,
an updated art program with new “talking labels”
that fully explain what is going on in the figure, and
72
much more.
NEW TO THIS EDITION
• R E O R G A N I Z A T I O N O F D E S C R I P T I V E
CHEMISTRY CHAPTERS (22-28): To facilitate
an improved flow of the descriptive chemistry
topics optionally covered in many courses and
to provide more convenient options for custom
versions of the textbook, Chapters 22 through 28
have been reorganized as follows: Chapter 22
is now Nuclear Chemistry; Chapter 23, Organic
Chemistry I: Formulas, Names and Properties;
Chapter 24, Organic Chemistry II: Shapes,
Selected Reactions, and Biopolymers; Chapter 25,
Coordination Compounds; Chapter 26, Metals I:
Metallurgy; Chapter 27, Metals II: Properties and
Reactions; and Chapter 28, Some Nonmetals
and Metalloids.
• NEW BASIC MATH SKILLS APPENDIX: To aid
the flow of introductory chemistry material in
Chapter 1, a review of topics in basic mathematics
skills, including scientific notation and use of
significant figures, with numerous Examples, now
appears in Appendix A. Related Exercises remain
in the Measurements and Calculations area at the
end of Chapter 1.
• REORGANIZED INTRODUCTION TO AQUEOUS
SOLUTIONS: Section 6-1 has been reorganized
to improve the descriptive introduction to aspects
of aqueous solutions, including ionization
and dissociation, acids, bases, and solubility
guidelines. These basic ideas are then elaborated
in the classification of reactions in the remainder
of Chapter 6 and serve as a foundation throughout
the textbook for further discussion of physical and
chemical properties of solutions.
• MORE COMPREHENSIVE COVERAGE OF
CENTRAL ATOM LONE PAIRS: In Chapter 8,
a more comprehensive tabular summary of the
influence of central atom lone pairs on molecular
geometry has been added to enhance student
understanding.
• A REVISED AND UPDATED ART PROGRAM:
The Tenth Edition’s art program has been revised
to include “talking labels” placed strategically
within figures to explain what is going on in the
illustration, so students can focus on learning
instead of trying to figure out what is going on by
www.cengageasia.com
 going back and forth between a caption and the
art. To exemplify the beauty and excitement of
chemistry, the individual layouts of many figures
have been revised to be more visually pleasing,
balanced, and organized. The art program now
includes more molecular models generated by
the latest software to enhance the molecular
reasoning theme. All electrostatic charge potential
(ECP) art includes a more thorough explanation
of its use.
• ENHANCED OWL ONLINE WEB LEARNING:
For the Tenth Edition, OWL now includes
more parameterized end-of-chapter questions,
encouraging students to practice multiple
questions of the same type with different chemicals,
wording, and numbers to ensure their mastery of
the underlying chemical concepts. OWL also
includes MindTap Reader. MindTap Reader is
a free upgrade to existing readers in Cengage’s
existing digital platforms offering significant new
functionality while also preparing the platforms to
take advantage of future MindTap services.
FEATURES
• MOLECULAR REASONING AND VISUALIZATION
EMPHASIS: Molecular reasoning is woven
throughout the text in chapter objectives, chapter
essays, examples, and end-of-chapter problems
and highlighted by a molecular reasoning icon.
• CHAPTER-OPENING APPLICATIONS AND
“CHEMISTRY IN USE” BOXES: These built-in
learning aids illustrate the practical applications of
chemistry in such areas as the environment, the
development of science, research and technology,
and our daily lives.
• “BEYOND THE TEXTBOOK” QUESTIONS:
These end-of-chapter questions ask students to
solve problems through the use of online exercises
in OWL, as well as other materials.
• “STOP & THINK” BOXES: Throughout the text,
these boxes alert students to common mistakes
and points of emphasis in problem solving.
CONTENTS
1. The Foundations of Chemistry.2. Chemical
Formulas and Composition Stoichiometry.3.
Chemical Equations and Reaction Stoichiometry.4.
The Structure of Atoms.5. Chemical Periodicity.6.
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Some Types of Chemical Reactions.7. Chemical
Bonding.8. Molecular Structure and Covalent
Bonding Theories.9. Molecular Orbitals in Chemical
Bonding.10. Reactions in Aqueous Solutions I:
Acids, Bases, and Salts.11. Reactions in Aqueous
Solutions II: Calculations.12. Gases and the
Kinetic-Molecular Theory.13. Liquids and Solids.14.
Solutions.15. Chemical Thermodynamics.16.
Chemical Kinetics.17. Chemical Equilibrium.18.
Ionic Equilibria I: Acids and Bases.19. Ionic
Equilibria II: Buffers and Titration Curves.20. Ionic
Equilibria III: The Solubility Product Principle.21.
Electrochemistry.22. Nuclear Chemistry.23. Organic
Chemistry I: Formulas, Names and Properties.24.
Organic Chemistry II: Shapes, selected Reactions,
and Biopolymers.25. Coordination Compounds.26.
Metals I: Metallurgy.27. Metals II: Properties and
Reactions.28. Some Nonmetals and Metalloids.
Appendix A: Basic Math Skills (includes new
significant figure section).Appendix B: Electron
Configurations of the Atoms of the Elements.
Appendix C: Common Units, Equivalences,
and Conversion Factors.Appendix D: Physical
Constants.Appendix E: Some Physical Constants
for a Few Common Substances.Appendix F:
Ionization Constants for Weak Acids at 25°C.
Appendix G: Ionization Constants for Weak Bases
at 25°C.Appendix H: Solubility Product Constants
for Some Inorganic Compounds at 25°C.Appendix
I: Dissociation Constants for Some Complex Ions.
Appendix J: Standard Reduction Potentials in
Aqueous Solution at 25°C.Appendix K: Selected
Thermodynamic Values at 298.15 K.Appendix L:
Answers to Selected Even-Numbered Numerical
Exercises.Index of Equations.Glossary/Index.
© 2014, 1008pp, Paperback, 9781285186054
73

CHEMISTRY, HYBRID EDITION
(WITH OWLV2 24-MONTHS PRINTED
ACCESS CARD), 9E
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Susan A. Zumdahl, University of Illinois, Urbana-Champaign
Reflecting Cengage Learning’s commitment to
offering flexible teaching solutions and value for
students and instructors, this new hybrid version
features the instructional presentation found in the
printed text while delivering all the end-of chapter
exercises online in OWL, the leading online learning
system for chemistry. The result—a briefer printed
text that engages students online! This fully updated
Hybrid Edition of Steven and Susan Zumdahl’s
CHEMISTRY 9e brings together the solid pedagogy,
easy-to-use media, and interactive exercises that
today’s instructors need for their general chemistry
course. Rather than focusing on rote memorization,
CHEMISTRY uses a thoughtful approach built on
problem-solving. For the Ninth Edition, the authors
have added a new emphasis on critical systematic
problem solving, new critical thinking questions, and
new computer-based interactive examples to help
students learn how to approach and solve chemical
problems—to learn to think like chemists—so that
they can apply the process of problem solving to all
aspects of their lives. Students are provided with the
tools to become critical thinkers: to ask questions, to
apply rules and develop models, and to evaluate the
outcome. In addition, Steven and Susan Zumdahl
crafted ChemWork, an online program included
in OWL Online Web Learning to support their
approach, much as an instructor would offer support
during office hours. ChemWork is just one of many
74 www.cengageasia.com
study aids available with CHEMISTRY that supports
the hallmarks of the textbook—a strong emphasis
on models, real world applications, visual learning,
and independent problem solving.
NEW TO THIS EDITION
• A NEW EMPHASIS ON SYSTEMATIC PROBLEM
SOLVING now appears in the applications of
dimensional analysis.
• NEW CRITICAL THINKING QUESTIONS have
been added throughout the text to emphasize the
importance of conceptual learning.
• NEW COMPUTER-BASED INTERACTIVE
EXAMPLES force students to think through the
example step-by-step rather than simply scan the
written example in the text as many students do.
New Interactive Examples are available in OWL
Online Web Learning. In addition, key examples
from the text have been made into Interactive
Tutorial problems and are available to assign in
the OWL program.
• NEW CHEMWORK PROBLEMS have been
added to the end-of-chapter problems throughout
the text to test students’ understanding of core
concepts. They can be worked as pencil-and-
paper problems or in interactive form in OWL,
where students who solve a problem with no
assistance can proceed directly to the answer
and students who need help can get assistance
through a series of hints. The hints in OWL--
usually in the form of interactive questions that
guide students through the problem-solving
process--are modeled after the way an instructor
would assist a student with homework problems
during office hours. Students cannot derive the
answer in OWL through pattern recognition;
rather, they are encouraged to continue working
though the hints to arrive at the answer.
• NEW END-OF–CHAPTER QUESTIONS AND
PROBLEMS have been added throughout the text.
• THE REVISED AND UPDATED ART PROGRAM
has been modified as needed, and new macro/
micro illustrations have been added.
• A NEW SECTION ON LIMITING REACTANTS
in Chapter 3, the treatment of stoichiometry,
emphasizes calculating the amounts of products
that can be obtained from each reactant. Students
are taught how to select a limiting reactant both by
 comparing the amounts of reactants present and
by calculating the amounts of products that can be
formed by complete consumption of each reactant.
• A NEW SECTION ON PHOTOELECTRON
SPECTROSCOPY was added to Chapter 9
(Section 9.6).
• ENHANCED OWL (ONLINE WEB LEARNING)
INTEGRATION: For the Ninth Edition, OWL now
includes more parameterized end-of-chapter
questions, encouraging students to practice
multiple questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts.
OWL also includes Student Self- Assessments,
ChemWork problems, and Interactive Examples
from the text. OWL also includes MindTap Reader.
MindTap Reader is a free upgrade to existing
readers in Cengage’s existing digital platforms
offering significant new functionality while also
preparing the platforms to take advantage of future
MindTap services.
FEATURES
• PROBLEM-SOLVING STRATEGY BOXES focus
the student’s attention on the very important
process of problem solving, helping them learn
to think like chemists.
CONTENTS
1. Chemical Foundations.2. Atoms, Molecules,
and Ions.3. Stoichiometry.4. Types of Chemical
Reactions and Solution Stoichiometry.5. Gases6.
Thermochemistry.7. Atomic Structure and
Periodicity.8. Bonding: General Concepts.9.
Covalent Bonding: Orbitals.10. Liquids and
Solids.11. Properties of Solutions.12. Chemical
Kinetics.13. Chemical Equilibrium.14. Acids and
Bases.15. Acid-Base Equilibria.16. Solubility and
Complex Ion Equilibria.17. Spontaneity, Entropy,
and Free Energy.18. Electrochemistry.19. The
Nucleus: A Chemist’s View.20. The Representative
Elements.21. Transition Metals and Coordination
Chemistry.22. Organic and Biological Molecules.
Appendix 1. Mathematical Procedures.A1.1
Exponential Notation.A1.2 Logarithms.A1.3
Graphing Functions.A1.4 Solving Quadratic
Equations.A1.5 Uncertainties in Measurements.
Appendix 2. The Quantitative Kinetic Molecular
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Model.Appendix 3. Spectral Analysis.Appendix
4. Selected Thermodynamic Data.Appendix 5.
Equilibrium Constants and Reduction Potentials.
A5.1 Values of Ka for Some Common Monoprotic
Acids.A5.2 Stepwise Dissociation Constants for
Several Common Polyprotic Acids.A5.3 Values
of Kb for Some Common Weak Bases.A5.4 Ksp
Values at 25_C for Common Ionic Solids.A5.5
Standard Reduction Potentials at 25_C (298K)
for Many Common Half-Reactions.Appendix 6. SI
Units and Conversion Factors.Glossary.Answers to
Selected Exercises.
© 2014, 944pp, Paperback, 9781285188492
EXPERIMENTS IN GENERAL
CHEMISTRY: INQUIRY AND SKILL
BUILDING, 2E
Vickie Williamson, Texas A&M University; Larry Peck, Texas
A&M University
With many years of teaching experience in the
classroom and laboratory, Vickie Williamson and
Larry Peck have created EXPERIMENTS IN
GENERAL CHEMISTRY: INQUIRY AND SKILL
BUILDING, 2nd edition with carefully crafted and
tested experiments designed to complement any
general chemistry curriculum. The authors have
selected three types of lab experiments to meet
all of the needs of students and instructors looking
for a selection of laboratory pedagogy. There are
Skill Building experiments to develop techniques
and demonstrate previously developed concepts,
Guided Inquiry experiments to direct the students to
collect data on variables without previously studying
75
 the concepts and guide them to look for patterns in 14 (was 12) - Alka-Seltzer®: An Application of Gas
the data, and Open Inquiry experiments to allow the Laws(A Guided Inquiry Experiment).EXPERIMENT
students to apply concepts or relationships in a new 15 (was 13) - Freezing Points of Solutions(A
setting. Twenty-eight experiments feature Pre-Lab Guided Inquiry Experiment).EXPERIMENT 16
questions and Post-Lab questions on perforated (was 14) - Spectrochemical Analysis(A Guided
pages for easy removal of worksheets, and there Inquiry Experiment).EXPERIMENT 17 (was
is a Common Procedures and Concepts section as 15) - Heat of Crystallization(A Skill Building
an appendix for easy retrieval of basic information Experiment).EXPERIMENT 18 (was 16) - Enthalpy
for students. of Reaction (A Guided Inquiry Experiment).
NEW TO THIS EDITION EXPERIMENT 19 (was 17) - The Kinetics of the
Decomposition of Hydrogen Peroxide(A Guided
• Updated experiments throughout with 2 brand new Inquiry Experiment).EXPERIMENT 20 (was
experiments added to this edition. 18) - Kinetics of Decoloration of Crystal Violet(A
FEATURES Guided Inquiry Experiment).EXPERIMENT 21
(was 19) - Factors Affecting Reactions(A Guided
• Two-semester safety agreements.
Inquiry Experiment).EXPERIMENT 22 (was
• Perforated pages allow for easy removal of
20) - Formation of a Complex(A Skill Building
worksheets.
Experiment).EXPERIMENT 23 (was 21) - Acids and
• Thirty total experiments (2 completely new)
pH(A Guided Inquiry Experiment).EXPERIMENT 24
featuring Skill Building experiments, Guided Inquiry
(was 22) - Reactions of Acids And Bases(A Guided
experiments and Open Inquiry experiments, meet
Inquiry Experiment).EXPERIMENT 25 (was 23)
all of the needs of students and instructors looking
- Acids and Bases(An Open Inquiry Experiment).
for a selection of laboratory pedagogy.
EXPERIMENT 26 (was 24) - Electrochemistry(A
• Common Procedures and Concepts section allows
Guided Inquiry Experiment).EXPERIMENT 27
for easy retrieval of basic information for students.
(was 25) - Small-Scale Redox Titration(A Skill
CONTENTS Building Experiment).EXPERIMENT 28 (was 26)
EXPERIMENT 1 - Are Labels Accurate or Precise? - The Copper Cycle(A Open Inquiry Experiment).
(An Open Inquiry Experiment).EXPERIMENT 2 - EXPERIMENT 29 (was 27) - Organic Molecules(A
Density Measurements (A Skill Building Experiment). Guided Inquiry Experiment).EXPERIMENT 30 (was
EXPERIMENT 3 - Cost of a Chemical Product(A 28) - Reactions of Organic Compounds(A Guided
Guided Inquiry Experiment).EXPERIMENT 4 - Soap Inquiry Experiment).Common Procedures and
Making (A Skill Building Experiment).EXPERIMENT Concepts.
5 - Reactions of Calcium(A Guided Inquiry © 2014, 412pp, Paperback, 9781285433172
Experiment).EXPERIMENT 6 - Aluminum and
Copper (II) Chloride(A Guided Inquiry Experiment).
EXPERIMENT 7 (was 6) - Recycling Aluminum
Cans (A Skill Building Experiment).EXPERIMENT
8 - Patterns(A Guided Inquiry Experiment).
EXPERIMENT 9 (was 7) - Solutions and Crystals of
Alum (A Guided Inquiry Experiment).EXPERIMENT
10 (was 8) - Analysis of a Carbonated Beverage(A
Guided Inquiry Experiment).EXPERIMENT 11 (was
9) - Mass Relationships in Reactions(An Open Inquiry
Experiment).EXPERIMENT 12 (was 10) - Shapes of
Molecules and Ions(A Guided Inquiry Experiment).
EXPERIMENT 13 (was 11) - The Fuel in a Bic®
Lighter(A Guided Inquiry Experiment).EXPERIMENT

76 www.cengageasia.com

LAB MANUAL FOR ZUMDAHL/
ZUMDAHL’S CHEMISTRY, 9TH, 9E
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Susan A. Zumdahl, University of Illinois, Urbana-Champaign
Build skill and confidence in the lab with the 61
experiments included in this manual. Safety is
strongly emphasized throughout the lab manual.
© 2014, 624pp, Paperback, 9781133611486
www.cengageasia.com
EXPERIMENTS IN GENERAL
CHEMISTRY, LAB MANUAL, 10E
Rupert Wentworth, Indiana University; Barbara H. Munk
Each experiment in this manual was selected
to match topics in the textbook and includes
an introduction, a procedure, a page of pre-lab
exercises about the concepts the lab illustrates, and
a report form. Some have a scenario that places
the experiment in a real-world context. In addition,
each experiment has a link to a set of references
and helpful online resources.
© 2013, 512pp, Paperback, 9781111989422
77

A BEGINNER’S GUIDE TO SCIENTIFIC
METHOD, INTERNATIONAL EDITION,
4E
Stephen S. Carey, Portland Community College
This concise yet comprehensive guide provides an
introduction to the scientific method of inquiry as well
as detailed coverage of the many misapplications
of scientific method that define pseudoscience.
Compact enough to be used as a supplementary
book in a science class, yet thorough enough in
its coverage to be used as a core text in a class
on scientific method, this text assists students in
using the scientific method to design and assess
experiments.
NEW TO THIS EDITION
• The explanations have been thoroughly to ensure
clarity and readability for the student audience.
• The discussion of causation in Chapter 3 has been
greatly expanded.
• In Chapter 4, the basic framework for discussing
experimental design has been revised to center
on false confirmation and rejection.
• In Chapter 5, the discussion of probability and
statistical inference is greatly simplified. Each
section now begins with and explains all points
in terms of recent causal studies.
• Two new pseudoscientific fallacies have been
added and the text now contains many new and
recent illustrations of all the fallacies.
• Dozens of new exercises and examples have
been added to every chapter.
• End of chapter concept quizzes have been added.
FEATURES
• An introduction to the scientific method which
78 www.cengageasia.com
acknowledges that good science must remain
utterly open to revision.
• Over one hundred practical, relevant exercises
and examples address common conceptual issues
and pitfalls confronted in students’ own practices
of scientific learning.
• Real-life examples from scientific literature provide
immediate practical applications of the concepts
encountered in the book.
CONTENTS
Preface.1. SCIENCE. Just What is Science? Asking
Why. Scientific Method. The Consequences of
Science. Scientific Method in Daily Life. Things
to Come. Exercises2. OBSERVATION. Making
Accurate Observations. Anomalous Phenomena.
Observing Anomalies. The Burden of Proof. Concept
Quiz. Exercises3. EXPLANATION. Explanation,
Theory and Hypothesis. Causation. Correlation.
Causal Mechanisms. Underlying Processes. Laws.
Function. The Interdependence of Explanatory
Methods. Rival Explanations and Ockham’s Razor.
Explanation and Description. Ultimate Explanations.
Concept Quiz. Exercises.4. EXPERIMENTATION.
The Basic Method. Confirmation and Rejection.
Designing a Good Test. Real World Experiments.
How Not to Design a Test. Conceptual Vagueness.
Testing Extraordinary Claims. Predictive Clarity.
Bias and Expectation. Concept Quiz. Exercises.5.
ESTABLISHING CAUSAL LINKS. Causal Studies.
Ruling Out Chance. Multiple Causal Factors.
Randomized, Prospective and Retrospective
Studies. Reading Between the Lines. Concept
Quiz. Exercises.6. FALLACIES IN THE NAME OF
SCIENCE. What is a Fallacy? False Anomalies.
Questionable Arguments by Elimination. Illicit Causal
Inferences. Unsupported Analogies and Similarities.
Untestable Explanations and Predictions. Empty
Jargon. Ad Hoc Rescues. Exploiting Uncertainty.
Science and Pseudoscience. Concept Quiz.
Exercises.FURTHER READINGINDEX
© 2012, 160pp, Paperback, 9781111726010

CHEMISTRY
An Atoms First Approach, International Edition
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Susan A. Zumdahl, University of Illinois, Urbana-Champaign
Steve and Susan Zumdahl’s texts focus on helping
students build critical thinking skills through the
process of becoming independent problem-solvers.
They help students learn to “think like a chemists”
so they can apply the problem solving process to all
aspects of their lives. In CHEMISTRY: AN ATOMS
FIRST APPROACH, 1e, International Edition the
Zumdahls use a meaningful approach that begins
with the atom and proceeds through the concept
of molecules, structure, and bonding, to more
complex materials and their properties. Because
this approach differs from what most students have
experienced in high school courses, it encourages
them to focus on conceptual learning early in the
course, rather than relying on memorization and
a “plug and chug” method of problem solving that
even the best students can fall back on when
confronted with familiar material. The atoms first
organization provides an opportunity for students
to use the tools of critical thinkers: to ask questions,
to apply rules and models and to
FEATURES
• AN ATOMS FIRST APPROACH. By taking an
atoms first approach, the authors are able to
provide students with a unified story built around
an organizing principle – start the course with
smallest element, the atom, and build from there.
Building their explanations around this structure,
the authors consistently show the importance and
relevance of studying chemistry.
• A FOCUS ON CONCEPTUAL UNDERSTANDING.
www.cengageasia.com
Rather than focusing on memorizing, the book
gives students the tools they need to become
critical thinkers: to ask questions, to apply rules
and develop models, and to evaluate the outcome.
• A LOGICAL ORGANIZATION. Chapter 1 provides
an introduction to the key components of the
story—the atom, atomic structure, energy, and
the mole. Chapter 2 initiates the plan of going
from the simple to the complex. Chapter 3 covers
counting by weighing, atomic masses, the mole,
and introduces chemical equations. Chapter
4 covers the fundamental ideas of bonding to
explain how atoms are tied together. Chapter 5
covers detailed models of bonding and structure:
Chapter 6 covers chemical energy; Chapters
7 and 8 cover gases, liquids, and solids, and
Chapter 9 covers stoichiometry.
• A STRONG PROBLEM-SOLVING ORIENTATION.
Throughout the text, problem-solving strategies
help students learn to solve problems by thinking
them through rather than brute-force memorizing.
Section 6.2 “Learning to Solve Problems”
emphasizes the importance of thoughtful, creative
problem solving, demonstrating that thinking
through a problem produces more long-term,
meaningful learning that can be applied to “real
life” than memorizing steps that apply only to a
particular type of problem. The problem-solving
process is organized in terms of “Where are we
going?’; “How do we get there?” and “Reality
Check,” which prompts students to check whether
their answer makes sense.
• STUDENT-ORIENTED LEARNING AIDS.
Problem-solving strategy boxes help students
focus on particular aspects of problem-solving;
concept summary boxes help students organize
their thinking about crucial concepts; and chemical
connections boxes present applications of
chemistry in various fields and in daily life.
• INTERACTIVE EXAMPLES encourage students
to think their way through the example instead of
passively reading through the solution. Electronic
versions of select examples are assignable
in OWL. Students can work these Interactive
Examples multiple times to help them master
the problem-solving process, receiving slightly
different examples each time they attempt an
79
 Interactive Example. Appendix 4: Spectral Analysis. Appendix 5: Selected
• END-OF-CHAPTER VISUAL EXERCISES, Thermodynamic Data. Appendix 6: Equilibrium
called out with an icon, provide students with Constants and Reduction Potentials.
opportunities to demonstrate a conceptual
© 2012, 1152pp, Paperback, 9780840065865
understanding of fundamental chemical principles.
Many take an “atomic view” of matter to help
students appreciate the usefulness of the atomic
model in understanding macroscopic properties.
Other problems ask students to interpret graphs
or to explain figures.
• A FOCUS ON THE FUNDAMENTAL IDEAS
OF CHEMISTRY. Numerous discussions,
illustrations, and exercises are designed to help
students overcome misconceptions by providing a
more accurate picture of the fundamental ideas of
chemistry. The book emphasizes the importance
of developing a qualitative understanding
of concepts before approaching quantitative
CHEMISTRY, 7E
problems. Principles and Reactions
• AN OUTSTANDING ART PROGRAM. The book William L. Masterton, University of Connecticut, Emeritus;
represents the microscopic world of chemistry Cecile N. Hurley, University of Connecticut; Edward Neth,
to give students a picture in their minds of “what University of Connecticut
the atoms and molecules are doing” through an
Masterton/Hurley/Neth’s CHEMISTRY:
excellent art program and animations.
PRINCIPLES AND REACTIONS, 7e, takes
• END-OF-CHAPTER ACTIVE LEARNING
students directly to the crux of chemistry’s
QUESTIONS. Because students often learn the
fundamental concepts and allows you to efficiently
most when they teach each other, these questions
cover all topics found in the typical general
are intended for group discussion.
chemistry book. Based on the authors’ extensive
CONTENTS teaching experience, this updated edition includes
Review Chapter: Measurement and Calculations new concept-driven, rigorous examples, updated
in Chemistry.1. Chemical Foundations. 2. Atomic examples that focus on molecular reasoning
Structure and Periodicity.3. Atoms to Molecules.4. and understanding, and “Chemistry: Beyond the
Bonding: General Concepts.5. Molecular Structure Classroom” essays that demonstrate the relevance
and Orbitals.6. Chemical Energy.7. Gases.8. of the concepts and highlight some of the most up-
Liquids and Solids.9. Stoichiometry.10. Types of to-date uses of chemistry. A strong, enhanced art
Chemical Reactions and Solution Stoichiometry.11. program assists students in visualizing chemical
Properties of Solutions.12. Chemical Kinetics.13. concepts. Integrated end-of-chapter questions and
Chemical Equilibrium.14. Acids and Bases.15. Key Concepts correlate to OWL Online Learning,
Acid-Base Equilibria.16. Solubility and Complex the #1 online homework and tutorial system for
Ion Equilibria.17. Spontaneity, Entropy, and Free chemistry. OWL also includes an interactive eBook
Energy.18. Electrochemistry.19. The Nucleus: for the 7th edition of the textbook and an optional
A Chemist’s View.20. The Representative ebook for the Student Study Guide.
Elements.21. Transition Metals and coordination NEW TO THIS EDITION
Chemistry.22. Organic and Biological Molecules.
• R E O R G A N I Z A T I O N : T h e a u t h o r s h a v e
Appendix 1: SI Units and Conversion Factors.
reorganized Chapters 13, 15, and 19 to create
Appendix 2: Mathematical Procedures. Appendix
a better flow from single to multiple equilibria. In
3: The Quantitative Kinetic Molecular Model.

80 www.cengageasia.com
 addition, Chapters 2-5 have been reorganized to
enhance student understanding and mirror the
way this material is presented in the classroom.
• NEW CHAPTER 15: This new chapter covers
complex ion and precipitation equilibria to enhance
the book’s coverage.
• N E W E N D - O F - C H A P T E R P R O B L E M S /
QUESTIONS: Approximately 25% of the book’s
end- of-chapter problems and questions are new.
• REVISED VISUALS FOR BETTER CLARITY:
Ensure your students’ understanding of concepts
as this edition moves relevant text from captions
to talking labels within the art for a clearer
presentation of visual images. Contemporary
photographs, modern molecular models, and
new concept flow charts help further clarify key
concepts.
• NEW AND INNOVATIVE EXAMPLE FORMAT--
ONE/TWO COLUMN COMBO: Revised examples
provide rigorous practice and opportunities to
apply concepts. Each Example begins with a
problem statement followed by three problem-
solving steps: 1) Analysis (two columns), 2)
Strategy (one column), and 3) Solution (two
column). This innovative new worked Example
format presentation is clear, consistent, and easy
to follow. Each example concludes with an End
Point, which provides additional insight into the
problem.
• REVISED GRADED AND CONCEPTUAL
EXAMPLES: Revised in-text Graded Examples
now show the gradual increase in difficulty as
problems progress from Step “a” to Step “c.”
The Graded Examples simulate the presentation
of problems on a test. Additional Conceptual
Examples lead students through conceptualizing
the chemistry principles just discussed and
demonstrate how to refine thinking skills at critical
points in the chapter.
FEATURES
• CONNECTION TO FINE ARTS: This edition
connects the hard science of chemistry to the
humanities and fine arts through chapter openers
and literary quotations that enhance each
chapter’s content.
• LATEST WORK FROM SPECIALISTS: Guest
authors and leaders in specialized fields profile
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the latest research in “Chemistry: Beyond the
Classroom” boxes. Students see the relevance
of concepts in some of the most current work
in chemistry, including photochromic and
thermochromic materials, coloration biological
organisms, molecular structure of rubbery
materials, and fuel cells.
• S T R O N G C O V E R A G E O F O R G A N I C
CHEMISTRY: Students leave your course well
equipped with organic chemistry skills through
coverage of nomenclature and a greater number
of functional groups, as well as coverage of types
of organic reactions and material on proteins and
carbohydrates.
• MOLECULAR MODEL ART PROGRAM: Effective
models visually reinforce students’ conceptual
understanding. Revised nanoscale views of
atoms, molecules, and ions use molecular
modeling software and an exacting three-
dimensional style to offer effective visual learning
tools throughout the text.
CONTENTS
1. Matter and Measurements.2. Atoms, Molecules,
and Ions.3. Mass Relations in Chemistry;
Stoichiometry.4. Reactions in Aqueous Solution.5.
Gases.6. Electronic Structure and the Periodic
Table.7. Covalent Bonding.8. Thermochemistry.9.
Liquids and Solids.10. Solutions.11. Rate of
Reaction.12. Gaseous Chemical Equilibrium.13.
Acids and Bases.14. Equilibria in Acid-Base
Solutions.15. Complex ion and Precipitation
Equilibria16. Spontaneity of Reaction17.
Electrochemistry.18. Nuclear Reactions.19.
Complex Ions and Coordination compounds20.
Chemistry of the Metals.21. Chemistry of the
Nonmetals.22. Organic Chemistry.23. Organic
Polymers, Natural and Synthetic.
© 2012, 800pp, Hardback, 9781111427108
81

CHEMISTRY, 3E
Principles and Practice, International Edition
Daniel L. Reger, University of South Carolina; Scott R. Goode,
University of South Carolina; David W. Ball, Cleveland State
University
A text that truly embodies its name, CHEMISTRY:
PRINCIPLES AND PRACTICE, 3rd, International
Edition connects the chemistry students learn in
the classroom (principles) with real-world uses of
chemistry (practice). The authors accomplish this
by starting each chapter with an application drawn
from a chemical field of interest and revisiting that
application throughout the chapter. The Case
Studies, Practice of Chemistry essays, and Ethics
in Chemistry questions reinforce the connection of
chemistry topics to areas such as forensics, organic
chemistry, biochemistry, and industry.
NEW TO THIS EDITION
• Each chapter begins with an opening application
drawn from a chemical field of interest, which is
revisited throughout the chapter.
• Worked Examples include problem flow diagrams
that map out the problem-solving process in a
graphical manner, aiding students in developing
problem-solving thought processes and strategies.
Many examples use color to aid students in
showing how the initial data in the problem is
transformed through the various steps of the
problem to the answer.
• Case Studies are multi-pronged, multi-step
problems that examine real world uses of
chemistry. Summary Problems focus on a problem
of chemical interest and draw on material from the
entire chapter for their solutions.
• Ethics in Chemistry questions, located at the
82
end of each chapter before the problem sets,
emphasize the human side of chemistry and
remind students that chemistry is not just a set of
facts. These questions discuss the ethical issues
and dilemmas scientists face in practicing their
profession. They also are good exercises for
schools that have a writing-across-the-curriculum
requirement.
• This edition fully integrates OWL (Online Web-
based Learning), the homework management
system trusted by tens of thousands of students.
• Integrated end-of-chapter questions correlate to
OWL. An optional e-book of this edition is also
available in OWL. In addition, Go Chemistry™
learning modules developed by award-winning
chemists offer mini-lectures and learning tools
that play on video iPods, personal video players,
QuickTime, Windows Media Player, and iTunes.
(iPods, iTunes, iPhone are products of Apple, Inc.)
FEATURES
• This book presents chemistry concepts in an
experimental context by demonstrating how the
facts and theories have come from many years
of experimentation. This is emphasized in the text
with margin icons.
• Each section begins with a set of Learning
Objectives and ends with an Objectives Review.
The exercises also are grouped by objectives.
• Principles of Chemistry essays expand and/or
reinforce important topics discussed in the book.
Practice of Chemistry essays are real-world
applications of chemistry; i.e., why and how
chemists and other professionals use chemistry
in their jobs and daily lives.
• The text includes approximately 2000 Questions
and Exercises. Questions are qualitative in nature,
often conceptual, and include problem-solving
skills. Questions that are suitable for a brief writing
exercise are designated with the symbol of a
pencil. The more-challenging items are designated
with a triangle. The text also has end-of-chapter
exercises available for use in OWL, Brooks/
Cole’s online homework and assessment system.
Exercises are paired, with the odd-numbered ones
having answers in the appendix and a similar even-
numbered problem immediately following. While
most exercises appear in the order in which they
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 are discussed, there are also Chapter Exercises
that are uncategorized, and Cumulative Exercises
that integrate concepts and methods introduced
in earlier chapters. Cumulative Exercises often
contain multiple parts and/or multiple steps.
CONTENTS
1. Introduction to Chemistry.2. Atoms, Molecules,
and Ions.3. Equations, the Mole, and Chemical
Formulas.5. Chemical Reactions in Solution
Thermochemistry.6. The Gaseous State.7. Electronic
Structure.8. The Periodic Table: Structure and
Trends.9. Chemical Bonds.10. Molecular Structure
and Bonding Theories.11. Liquids and Solids.12.
Solutions.13. Chemical Kinetics.14. Chemical
Equilibrium.15. Solutions of Acids and Bases.16.
Reactions Between Acids and Bases.17. Chemical
Thermodynamics.18. Electrochemistry.19. Metals,
Coordination Chemistry, and Metallurgy.20. The
Chemistry of Hydrogen, Elements in Groups 3A
through 6A, and the Noble Gases.21. Nuclear
Chemistry.22. Organic Chemistry and Biochemistry.
Appendix A: Math Procedures.Appendix B: Selected
Physical Constants.Appendix C: Unit Conversion
Factors.Appendix D: Names of Ions.Appendix E:
Properties of Water.Appendix F: Solubility Products,
Acids, and Bases.Appendix G: Thermodynamic
Constants for Selected Compounds.Appendix H:
Standard Reduction Potentials at 25.Appendix
I: Glossary.Appendix J: Answers to Selected
Exercises.
© 2010, 1120pp, Paperback, 9780495559832
www.cengageasia.com
EXPERIMENTS IN GENERAL
CHEMISTRY, 2E
Featuring MeasureNet
Bobby Stanton, University of Georgia; Lin Zhu, University of
Georgia; Charles “Butch” Atwood, University of Georgia
Innovative and self-directed, EXPERIMENTS
IN GENERAL CHEMISTRYFEATURING
MEASURENET, 2nd Edition prepares students
for the laboratory setting by asking them multi-
component questions, building their knowledge
from previous experiments, and incorporating the
innovative MeasureNet network data collection
system into the manual. MeasureNet improves the
laboratory experience by requiring smaller amounts
of chemicals for experiments—making the lab safer
and more environmentally friendly—and greatly
increasing precision through its electronic data
collection, analysis, and reduction features.
NEW TO THIS EDITION
• Convey the most relevant ideas with the most
current experiments. All 28 experiments in the
manual have been revised for this edition.
• Help students develop their own experiments with
6 new experiments in the more challenging self-
directed format. Students use their knowledge,
skills, and techniques from prior concept/
technique-oriented experiments to solve an
assigned problem.
• Encourage strong laboratory fundamentals with 22
guided inquiry experiments, which lead students
through an experiment by asking a series of
questions.
• Heighten interest in chemistry and its real-world
applications with four all-new, self-directed
experiments: “Quality Control for GlassEx Window
83
 Cleaner,” “Determining the Iron Content in Cereal,”
“Analyzing the Chemical Content of Chromite,”
and “Determining the Time Interval Between
Doses of a Cardiac Drug.”
• Reinforce important concepts with new pre- and
post-lab questions for all self-guided experiments.
Students will also appreciate the new easier-to-
use format and lab reports for these experiments.
FEATURES
• Focus students’ efforts with experiments that
require less time collecting data and encourage
more time analyzing and manipulating it for a
better, more useful grasp of chemistry.
• Stimulate learning on a deeper level. Students
will express their ideas and conclusions in formal
writings that help them better comprehend the
concepts, techniques, and theories in the manual.
• Run an environmentally friendly lab! With
MeasureNet, experiments are more precise and
require smaller quantities of chemicals, making
the lab safer for students and better for the planet.
CONTENTS
Safety Rules.Common Laboratory Glassware
and Equipment.1. Densities of Some Liquids
and Solids.2. Specific Heat of Substances.3.
Chromatography.4. Determination of the Percent by
Mass of the Components in a Mixture by Thermal
Gravimetric Analysis.5. Self Directed—Thermal
Insulating Materials.6. Reaction Stoichiometry.7.
Types of Chemical Reactions.8. Identifying Metal
Ions and Inorganic Compounds by their Chemical
Interactions.9. Gravimetric Analysis of a Chloride,
Sulfate, or Carbonate Compound.10. Emission
Analysis of Aqueous Solutions of Group IA and IIA
Metal Salts.11. Determination of Chromium (VI)
Concentrations via Absorption Spectroscopy.12.
Determination of the Concentration of Acetic Acid
in Vinegar.13. Solubility, Polarity, Electrolytes, and
Nonelectrolytes.14. Self-Directed—Determination
of the Cause of a Fish-Kill in the Clark Fork of the
Columbia River.15. Self-Directed—Quality Control
for the Athenium Baking Soda Company.16. Gas
Laws.17. Colligative Properties.18. Soaps and
Detergents.19. Heats of Chemical and Physical
Processes.20. Hess’s Law.21. Determination of the
Heat of Neutralization of a Variety of Strong Acids
84 www.cengageasia.com
and Bases.22. Dystan Medical Supply Company—
Cold Packs and Hot Packs.23. Kinetics—Reaction
Orders.24. Chemical Equilibria.25. Determining the
Equilibrium Constant for a Reaction.26. Determining
Ka of an Acid by Titration and from pH.27. pH and
Buffer Solutions.28. Self-Directed—Identifying an
Unknown Weak Acid.29. Quality Control for GlassEx
Window Cleaner.30. Determining the Iron Content
in Cereal.31. Analyzing the Chemical Content
of Chromite.32. Determining the Time Interval
Between Doses of a Cardiac Drug.33. What is in
This Container?
© 2010, 448pp, Paperback, 9780495561798
LABORATORY INQUIRY IN
CHEMISTRY, 3E
Richard Bauer, Arizona State University; James Birk, Arizona
State University; Doug Sawyer, Scottsdale Community
College
LABORATORY INQUIRY IN CHEMISTRY, Thrid
Edition provides a unique set of guided-inquiry
investigations that focus on constructing knowledge
about the conceptual basis of laboratory techniques,
instead of simply learning techniques. By focusing
on developing skills for designing experiments,
solving problems, thinking critically, and selecting
and applying appropriate techniques, the authors
expose students to a realistic laboratory experience,
typical of the practicing chemist. This new edition
continues the proven three-phase learning cycle:
exploration of chemical behaviors within the context
of the problems posed; concept invention--the use
of data and observations to construct accepted
scientific knowledge about the concepts explored
in the laboratory investigation; and, concept
application--where students apply their conceptual Coin?22. Which Iron Compound Is It?23. Should
understanding of the investigation at hand by We Mine This Ore?24. Why Do Liquids Evaporate
modifying or extending the experiments, and write at Different Rates?25. What Are the Structures of
a report that emphasizes conceptual relevance. Some Alloys?26. How Is LED Light Color Related
These college and honors level inquiry-based to Composition?27. What Is the Molar Mass of
experiments correlate well with the recommended Mars Ice Gas?28. How Much Gas Is Produced?29.
experiments outlined by the Advanced Placement Which Alcohols Are in the Barrels?30. How Is Heat
Chemistry Development Committee. of Combustion Measured Indirectly?31. What Is
NEW TO THIS EDITION the Rate Law?32. How Fast Does the Crystal
Violet Decolorize?33. Why Is the Vinegar Factory
• The following new experiments have been Rusting?34. What Factors Affect the Solubility
added to this editon:5. What Relationships Exist of Kidney Stones?35. How Many Chemicals Are
Among Elements?11. How Much Acetic Acid in the Vial?36. What Factors Affect Chemical
Is in Vinegar?24. Why Do Liquids Evaporate at Equilibrium?37. What Is the Formation Constant?38.
Different Rates?In addition, new photos have Are Household Items Acidic, Basic, or Neutral?39.
been added throughout to better demonstrate lab What Is the pH of Soil?40. What Is the Acid
instruments, procedures and techniques. Dissociation Constant?41. What Is the Solubility
FEATURES Product?42. What Are Some Chemical Properties
of Cream of Tartar?43. What Are the Metals?44.
• Proven three-phase learning cycle: exploration
How Can a Battery Be Made from Coins?45. What
of chemical behaviors within the context of the
Is the Complex Ion?46. What Formulation Makes
problems posed; concept invention--the use of
the Best Toy?47. How Are Anions Identified?48.
data and observations to construct accepted
How Are Cations Identified?49. How Are More
scientific knowledge about the concepts explored
Cations Identified?50. How Are Ionic Solids
in the laboratory investigation; and concept
Identified?Appendix A: Automated Data Collection.
application--where students apply their conceptual
Appendix B: Transmittance and Absorbance Data
understanding of the investigation at hand by
Collection.Appendix C: Measuring pH.Appendix
modifying or extending the experiments, and write
D: Temperature Data Collection.Appendix E:
a report that emphasizes conceptual relevance.
Pressure Data Collection.Appendix F: Voltage
CONTENTS Data Collection.Appendix G: Selected Laboratory
The Investigations.1. What Are the Safety Concerns Techniques.Appendix H: Laboratory Equipment.
in the Laboratory?2. Whats in the Flask?3. How Appendix I: Sample Material Safety Data Sheet.
Should Data Trends Be Presented?4. How Is Lab Appendix J: Tables
Equipment Used?5. What Relationships Exist © 2009, 288pp, Paperback, 9780495113454
Among Elements?6. What’s in the Bottles?7. How
Can the Waste Be Made Useful?8. Is the Water
Hard or Soft?9. How Hot Is the Water?10. Which
Metal Will Burn the Skin?11. How Much Acetic Acid
Is in Vinegar?12. Are All Neutralization Reactions
the Same?13. How Many Waters of Hydration Are
in the Formula?14. How Much Sodium Bicarbonate
Is in the Mixture?15. Is It Economical to Recycle
Aluminum?16. What Is a Copper Cycle?17. Who
Wrote the Ransom Note?18. How Can UV Sensitive
Beads Be Used to Test Sunscreens?19. What
Factors Affect the Intensity of Color?20. How Much
Cobalt Is in the Soil?21. How Much Copper Is in the

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85

SURVIVAL GUIDE FOR GENERAL
CHEMISTRY WITH MATH REVIEW, 2E
Charles H. Atwood, University of Georgia
Available for packaging with any CENGAGE
textbook, this survival guide focuses on helping
students practice for exams by showing them how
to solve difficult problems by dissecting them into
manageable chunks. The guide includes three
levels of proficiency questions – A, B, and minimal
– to quickly build student confidence as they master
the knowledge needed to succeed in the course.
This book is also available for students to purchase
separately at www.CENGAGEbrain.com.
CONTENTS
Module 1: Metric System, Dimensional Analysis,
Significant Figures, and Density.Module 2:
Understanding Chemical Formulas.Module 3:
Chemical Nomenclature.Module 4: The Mole
Concept.Module 5: Chemical Reaction Stoichiometry.
Module 6: Types of Chemical Reactions.Module 7:
Electronic Structure of Atoms.Module 8: Chemical
Periodicity.Module 9: Chemical Bonding.Module
10: Molecular Shapes.Module 11: Hybridization
and Polarity of Molecules.Module 12: Acids and
Bases.Module 13: States of Matter.Module 14:
Solutions.Module 15: Heat Transfer, Calorimetry,
and Thermodynamics.Module 16: Chemical
Kinetics.Module 17: Gas Phase Equilibria.Module
18: Aqueous Equilibria.Module 19: Electrochemistry.
Module 20: Nuclear Chemistry.Math Review.
© 2008, 216pp, Paperback, 9780495387510
86 www.cengageasia.com
INORGANIC CHEMISTRY
DESCRIPTIVE INORGANIC,
COORDINATION, AND SOLID STATE
CHEMISTRY, 3E
Glen E. Rodgers, Allegheny College
This proven, sophomore-level text introduces the
basics of coordination, solid-state, and descriptive
main-group chemistry in a uniquely accessible
manner, featuring a “less is more” approach. This
approach allows you to present concepts and
applications that you find particularly important
and fascinating. Consistent with the “less is more”
philosophy, the book does not review topics covered
in introductory courses, but rather moves directly
into topics central to inorganic chemistry. Written in
a conversational prose style that is enjoyable and
easy to understand, this book presents not only the
basic theories and methods of inorganic chemistry
(in three self-standing sections), but also a great
deal of the history and applications of the discipline.
The new edition features new art, more diversified
applications, and a new icon system. And to better
help students understand how the seemingly
disparate topics of the periodical table connect,
the book offers revised coverage of the author’s
“Network of Interconnected Ideas” on new full color
endpapers, as well as on a convenient tear-out
card. The author’s presentation does not assume
prerequisites of organic or physical chemistry.
NEW TO THIS EDITION
• INCREASED EMPHASIS ON THE “NETWORK
OF INTERCONNECTED IDEAS.” To better help
students understand how the seemingly disparate
topics of the periodical table connect, the book
 offers revised coverage of the author’s “Network
of Interconnected Ideas” including a new icon
system, full color endpapers, and a convenient
tear-out card.
• REVISED VISUALS. The text’s art program has
been revised for more clarity, and a new icon
system makes the Network of Interconnected
Ideas art better connect.
• UPDATED APPLICATIONS. The applications in
Chapter 6 have been updated and diversified, and
now cover more transition metals. In addition, the
applications in the survey of periodic table groups
chapters (12-19) have been updated.
• REORDERED APPENDIXES. The book’s
appendix have been reorganized to make them
easier to use.
FEATURES
• SELF-CONTAINED SECTIONS. Coordination,
solid state, and descriptive inorganic chemistry are
presented in self-contained sections. The reader
can begin in any one of these sections without
becoming frustrated at references to material
already learned. These self-standing chapters also
allow instructors the flexibility to present material
in any order.
• A FOCUS ON UNDERSTANDING THE PERIODIC
TABLE. The author systematically builds a
network of interconnected ideas to develop reader
confidence and to forge an understanding of the
periodic table.
• “THOUGHT” QUESTIONS. These questions,
embedded within the body of the text, encourage
students to construct and organize ideas, thought
patterns, and concepts, and to go beyond merely
memorizing groups of facts or trends. Students
must “think” their way through the material.
• A FOCUS ON PROBLEM SOLVING. Approximately
1,000 problems challenge students to apply what
they have learned to new situations and aid in
building a deeper understanding of the material. In
addition, a significant number of problems require
short explanatory paragraphs, emphasizing the
importance of writing in the discipline of chemistry.
• A HISTORICAL PERSPECTIVE. A historical
perspective is integrated throughout the text to
give students an increased appreciation of the
centuries of human endeavor that have led to
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our present understanding of the chemical world
around us.
• A WIDE RANGE OF APPLICATIONS show
students the practical uses of inorganic chemistry
through the discussion of such diverse subjects
as heavy metal poisoning and antidotes, nuclear
fusion, battery technology, fluoridation, radon as
a carcinogen, and automobile air bags.
CONTENTS
1. The Evolving Realm of Inorganic Chemistry.
PART 1: COORDINATION CHEMISTRY.2. An
Introduction to Coordination Chemistry.3. Structures
of Coordination Compounds.4. Bonding Theories for
Coordination Compounds.5. Rates and Mechanisms
of Reactions of Coordination Compounds.6.
Applications of Coordination Compounds.
PART 2: SOLID-STATE CHEMISTRY.7. Solid-
State Structures.8. Solid-State Energetics.
PART 3: DESCRIPTIVE CHEMISTRY OF THE
REPRESENTATIVE ELEMENTS.9. Building a
Network of Ideas to Make Sense of the Periodic
Table.10. Hydrogen and Hydrides.11. Oxygen,
Aqueous Solutions, and the Acid-Base Character
of Oxides and Hydroxides.12. Group 1A: The Alkali
Metals.13. Group 2A: The Alkaline-Earth Metals.14.
The Group 3A Elements.15. The Group 4A
Elements.16. Group 5A: The Pnicogens.17. Sulfur,
Selenium, Tellurium, and Polonium.18. Group 7A:
The Halogens.19. Group 8A: The Noble Gases.
© 2012, 656pp, Hardback, 9780840068460
87

INTRODUCTORY /
PREPARATORY CHEMISTRY
INTRODUCTORY CHEMISTRY, HYBRID
EDITION (WITH OWLV2 PRINTED
ACCESS CARD), 6E
Mark S. Cracolice, University of Montana; Ed Peters
Reflecting Cengage Learning’s commitment to
offering flexible teaching solutions and value for
students and instructors, this hybrid version of
INTRODUCTORY CHEMISTRY, 6e features the
instructional presentation found in the printed text
while delivering all the end-of chapter exercises
online in OWLv2.. Access to OWLv2 is included
with every new hybrid text, giving your students an
interactive learning experience with the convenience
of a text that is both brief and affordable. To provide
maximum teaching flexibility and make it easy
for you to teach chapters in the order you prefer,
the authors include necessary preview or review
information with each topic’s coverage. Even more
flexibility is provided in the new edition by the
included MindTap Reader, an electronic version
of the text that features interactivity, integrated
media, and additional algebra coverage. Known for
its question-and-answer presentation that allows
students to actively learn chemistry while studying
an assignment, this edition integrates new features
such as outstanding technological resources,
coached problems in a two-column format, and
enhanced art and photography, all of which dovetail
with the authors’ active learning approach.
NEW TO THIS EDITION
88
• A new Mindtap Reader Version combines
multimedia activities, examples, and assessments
in an interactive, fully online version of the book
that further engages students’ active learning of
chemistry, with clickable answer buttons for Active
Examples and pop-up key terms and chapter-in-
review material at point of use.
• N e w c o n t e n t i n c l u d e s u p d a t e d g e n e r a l
stoichiometry patterns in Chapters 7, 10, 14 and
16, more in-depth coverage of nomenclature in
Chapter 6, and expanded explanations of formulas
and names for ionic compounds.
• New end-of-chapter “Frequently Asked Questions”
anticipate students’ questions on the chapter’s
most challenging concepts and problems. Each
question includes an answer from the author, with
tips for remembering key concepts or solving key
problems.
• A new “Quick Quiz” feature in the Everyday
Chemistry boxes asks students to think critically
about the featured topic. (Answers are provided
in the Instructor’s Manual.)
• A new Key Terms List now appears at the end of
each chapter and is clickable in MindTap Reader.
• OWLv2, the most powerful online learning solution
for chemistry now has more flexible student
and instructor functionality, new personalized
study tools, enhanced integration with learning
management systems, and improved analytics.
OWLv2 now includes ALL quantitative end-of-
chapter questions from the book, as well as
Quick Prep, an online short course that reviews
key chemistry concepts and essential skills;
new iPad-compatible visualizations, tutorials,
and simulations; and new Adaptive Study Plans
with multiple-choice questions that expand upon
the book’s Test Yourself questions. In addition,
Tutors, Visualizations and Simulations have been
converted from Flash to HTML, allowing for easier
navigation and streamlined grading.
FEATURES
• Active Examples: Teaching core chemical skills,
these two-column examples allow students to
first actively work through and complete steps
in the right column, and then see the answer to
each step in the left column, thereby receiving
immediate feedback about their understanding of
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 the concept as it is being formed. The first frame is
labeled “Think Before You Write” and encourages
students to slow down and analyze the problem
statement before working on the solution. Each
example is titled so that students can better
identify the concept or problem-solving skill
they are learning and can easily locate specific
concepts to review when preparing for exams.
• Chapter Summaries: This section at the back of
the book includes summaries of each chapter’s
goals and key concepts, as well as chapter-
specific self-tests and answers for extra practice.
• Flexible Format: The book has been structured so
that any common sequence of topics is supported,
allowing you to present topics in any order you
prefer.
• P/Review Cross-References: A supplement to
the optional order of topics, these icons and
accompanying marginal explanations placed
at key points throughout the book are worded
carefully to serve as both a preview and a review
of key concepts, so that you may easily teach the
topics in whatever order you wish.
CONTENTS
1. Introduction to Chemistry and Introduction to Active
Learning.2. Matter and Energy.3. Measurement and
Chemical Calculations.4. Introduction to Gases.5.
Atomic Theory: The Nuclear Model of the Atom.6.
Chemical Nomenclature.7. Chemical Formula and
Relationships.8. Chemical Reactions.9. Chemical
Change.10. Quantity Relationships in Chemical
Reactions.11. Atomic Theory: The Quantum Model
of the Atom.12. Chemical Bonding.13. Structure and
Shape.14. The Ideal Gas Law and Its Applications.15.
Gases, Liquids, and Solids.16. Solutions.17. Acid-
Base (Proton-Transfer) Reactions.18. Chemical
Equilibrium.19. Oxidation-Reduction (Electron
Transfer) Reactions.20. Nuclear Chemistry.21.
Organic Chemistry.22. Biochemistry.Chapter
SummariesAppendix I: Chemical Calculations.
Appendix II: The SI System of Units.Glossary.
© 2016, 720pp, Paperback, 9781305108981
www.cengageasia.com
INTRODUCTORY CHEMISTRY, 8E
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Donald J. DeCoste, University of Illinois, Urbana-Champaign
The Eighth Edition of Zumdahl and DeCoste’s
best-selling INTRODUCTORY CHEMISTRY that
combines enhanced problem-solving structure
with substantial pedagogy to enable students to
become strong independent problem solvers in
the introductory course and beyond. Capturing
student interest through early coverage of
chemical reactions, accessible explanations and
visualizations, and an emphasis on everyday
applications, the authors explain chemical concepts
by starting with the basics, using symbols or
diagrams, and conclude by encouraging students
to test their own understanding of the solution.
This step-by-step approach has already helped
hundreds of thousands of students master chemical
concepts and develop problem-solving skills. The
book is known for its focus on conceptual learning
and for the way it motivates students by connecting
chemical principles to real-life experiences in
chapter-opening discussions and “Chemistry in
Focus” boxes. The Eighth Edition now adds a
“questioning” pedagogy to in-text examples to
help students learn what questions they should be
asking themselves while solving problems, offers
a revamped art program to better serve visual
learners, and includes a significant number of
revised end-of-chapter questions.
NEW TO THIS EDITION
• The #1 online homework and learning system
for chemistry, OWLv2, is available for this text--
89
 now with new instructor features and enhanced
functionality: a Dashboard that consolidates
all course materials; easy, intuitive assignment
creation and management; ability to preview and
select activities/questions for each assignment;
new assignment settings and options; improved
gradebook; Personalized Study tools to help
students focus their time on the key concepts and
skills; and MindTap Reader™, a new eBook with
apps and embedded video, audio, annotations,
and activities. OWLv2 courses for Gen Chem,
GOB, and Liberal Arts now include Quick Prep
essential skills assignments that can be taken
before the semester begins or during the first few
weeks, to help students succeed in the course. For
this course, OWLv2 also includes new interactive
versions of the end-of-chapter questions from
the text and new iPad-compatible visualizations,
tutorials, and simulations.
FEATURES
• The book’s full color art program has been
modified and updated as needed to better
serve visual learners. In addition, the art has
been reconfigured for better clarity, glassware
illustrations have been updated, and the orbital
art has been redesigned all according to a new art
and style program. Many new photos have been
updated to give the textbook more relevance while
also providing a contemporary look.
• The text’s hallmark problem-solving pedagogy is
enhanced by in-text examples that suggest what
questions the students should be asking as they
solve problems.
• Almost all of the in-text examples are now “
Interactive Examples” and available online. These
computer-based examples throughout the text
require students to think through the Example
step-by-step rather than simply scan the written
Example in the text as many students do.
• New “Critical Thinking” boxes have been added
at point-of-use throughout the text to emphasize
the importance of conceptual learning. These are
particularly useful for generating class discussion.
• In Section 8.4 “Learning to Solve Problems”
is written specifically to help students better
understand how to think their way through a
problem.
90 www.cengageasia.com
• In Chapter 9, the treatment of stoichiometry has
been enhanced by the addition of a new section on
limiting reactants, which emphasizes calculating
the amounts of products that can be obtained
from each reactant. Students are taught how to
select a limiting reactant both by comparing the
amounts of reactants present and by calculating
the amounts of products that can be formed by
complete consumption of each reactant.
• The authors have revised a significant number
of the end-of-chapter questions (over 10%) while
adding a new section for ChemWork problems,
which are also available online.
• The Eighth Edition is now supported by both OWL:
Online Web Learning, the number one online
learning system for chemistry, and Enhanced
WebAssign. Both are available with e-books.
• Exercises and models such as worked-out
examples, self-check exercises, and skill
development boxes support the authors’ step-
by-step problem-solving method.
CONTENTS
1. Chemistry: An Introduction.2. Measurements and
Calculations.3. Matter.4. Chemical Foundations:
Elements, Atoms, and Ions.5. Nomenclature.6.
Chemical Reactions: An Introduction.7. Reactions
in Aqueous Solutions.8. Chemical Composition.9.
Chemical Quantities.10. Energy.11. Modern Atomic
Theory.12. Chemical Bonding.13. Gases.14. Liquids
and Solids.15. Solutions.16. Acids and Bases.17.
Equilibrium.18. Oxidation–Reduction Reactions
and Electrochemistry.19. Radioactivity and Nuclear
Energy.
© 2015, 704pp, Paperback, 9781285453132

INTRODUCTORY CHEMISTRY, 8E
A Foundation, Hybrid Edition (with OWLv2 24-Months
Printed Access Card)
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Donald J. DeCoste, University of Illinois, Urbana-Champaign
Reflecting Cengage Learning’s commitment to
offering flexible teaching solutions and value for
students and instructors, this new hybrid version
features the instructional presentation found in
the printed text while delivering all the end-of
chapter exercises online in OWLv2, the leading
online learning system for chemistry. The result-
-a briefer printed text that engages students
online! Help your students improve their grades
and understanding of concepts with this value-
packed Hybrid Edition. An access code to OWLv2
with MindTap Reader, is included with the text,
providing students with powerful online resources
that include tutorials, simulations, randomized
homework questions, videos, a complete interactive
electronic version of the textbook, and more!
The Eighth Edition of Zumdahl and DeCoste’s
best-selling INTRODUCTORY CHEMISTRY: A
FOUNDATION combines enhanced problem-
solving structure with substantial pedagogy to
enable students to become strong independent
problem solvers in the introductory course and
beyond. Capturing student interest through early
coverage of chemical reactions, accessible
explanations and visualizations, and an emphasis
on everyday applications, the authors explain
chemical concepts by starting with the basics, using
symbols or diagrams, and conclude by encouraging
students to test their own understanding of the
www.cengageasia.com
solution. This step-by-step approach has already
helped numerous students master chemical
concepts and develop problem-solving skills.
The focus on conceptual learning and motivating
students by connecting chemical principles to real-
life experiences in chapter-opening discussions
and “Chemistry in Focus” boxes require students
to think through the Example step-by-step rather
than simply scan the written Example in the text
as many students do.
NEW TO THIS EDITION
• In Chapter 9, the treatment of stoichiometry has
been enhanced by the addition of a new section on
limiting reactants, which emphasizes calculating
the amounts of products that can be obtained
from each reactant. Students are taught how to
select a limiting reactant both by comparing the
amounts of reactants present and by calculating
the amounts of products that can be formed by
complete consumption of each reactant.
• Interactive Examples, new for this edition, were
added to engage students in the problem solving
process as they are reading the text. These
Interactive Examples require student input for
each step in the example. The computer asks
questions in the same way a teacher would when
explaining a new concept.
• Critical Thinking questions have been added
throughout the text to emphasize the importance
of conceptual learning. These are particularly
useful for generating class discussion.
• New ChemWork end-of chapter problems have
been added throughout the text. These problems
test students’ understanding of core concepts from
each chapter. Students who need help can get
assistance through a series of online hints. The
hints are usually in the form of interactive questions
that guide students through the problem-solving
process. Students cannot receive the correct
answer from the computer; rather, it encourages
students to continue working through the hints to
arrive at the answer. ChemWork problems in the
text can be worked using the online system or as
pencil-and-paper problems.
• Many of the Chemistry in Focus” boxes have
been revised and new ones added with up-to-date
topics such as Gorilla glass, nanocars, and using
91
 breath analysis to diagnose disease.
FEATURES
• The book’s full color art program has been
modified and updated as needed to better
serve visual learners. In addition, the art has
been reconfigured for better clarity, glassware
illustrations have been updated, and the orbital
art has been redesigned all according to a new art
and style program. Many new photos have been
updated to give the textbook more relevance while
also providing a contemporary look.
• The text’s hallmark problem-solving pedagogy is
enhanced by in-text examples that suggest what LAB MANUAL FOR ZUMDAHL/
questions the students should be asking as they DECOSTE’S INTRODUCTORY
solve problems. CHEMISTRY: A FOUNDATION, 8TH, 8E
• Almost all of the in-text examples are now John G. Little
“Interactive Examples” and available online. These
computer-based examples throughout the text Includes 35 experiments and eight appendices that
require students to think through the Example serve as useful references.
step-by-step rather than simply scan the written
© 2015, 368pp, Paperback, 9781285845166
Example in the text as many students do.
• New “Critical Thinking” boxes have been added
at point-of-use throughout the text to emphasize
the importance of conceptual learning. These are
particularly useful for generating class discussion.
• In Section 8.4 “Learning to Solve Problems”
is written specifically to help students better
understand how to think their way through a
problem.
CONTENTS
1. Chemistry: An Introduction.2. Measurements and
Calculations.3. Matter.4. Chemical Foundations:
Elements, Atoms, and Ions.5. Nomenclature.6.
Chemical Reactions: An Introduction.7. Reactions
in Aqueous Solutions.8. Chemical Composition.9.
Chemical Quantities.10. Energy.11. Modern Atomic
Theory.12. Chemical Bonding.13. Gases.14. Liquids
and Solids.15. Solutions.16. Acids and Bases.17.
Equilibrium.18. Oxidation–Reduction Reactions
and Electrochemistry.19. Radioactivity and Nuclear
Energy.20. Organic Chemistry.21. Biochemistry.
© 2015, 592pp, Paperback, 9781285459707

92 www.cengageasia.com

INTRODUCTORY CHEMISTRY, 5E
An Active Learning Approach, International Edition
Mark S. Cracolice, University of Montana; Edward I. Peters
Teach the course your way with INTRODUCTORY
CHEMISTRY, 5E, International Edition. This
text allows you to tailor the order of chapters to
accommodate your particular needs, not only
by presenting topics so they never assume prior
knowledge but also by including any and all
necessary preview or review information needed
to learn that topic. The authors’ question-and-
answer presentation allows students to actively
learn chemistry while studying an assignment.
This approach is reflected in three words of advice
and encouragement that are repeated throughout
the book: Learn It Now! This edition integrates
new features such as outstanding technological
resources, coached problems in a two-column
format, and enhanced art and photography, all
of which dovetail with the authors’ active learning
approach. Even more flexibility is provided in the
new edition by the Cengage YouBook, an electronic
version of the text that features interactivity,
integrated media, and additional algebra coverage.
NEW TO THIS EDITION
• New Active Example Format: After observing
students rush to apply an algorithm immediately
after reading a problem statement, the authors
redesigned the Active Example format. To
encourage students to be less impulsive and slow
down and analyze the problem statement before
working on the solution, the first frame in every
Active Example is labeled THINK BEFORE YOU
WRITE. Subsequent steps are labeled as PLAN
to help students consciously outline the solution
www.cengageasia.com
to a problem.
• New Two-Column Design for Active Examples:
As students actively work through and complete
the Active Example solution in the right column,
they can reveal the solution to each step in the
left column, thereby receiving immediate feedback
about their understanding of the concept as it is
being formed. Each example is also now titled so
that students can better identify the concept or
problem-solving skill they are learning and can
easily locate specific concepts to review when
preparing for exams.
• New Practice Exercises and Solutions: To solidify
the potentially fragile new knowledge that the
student just constructed during the process of
completing the Active Example, each Active
Example is now immediately followed by a
parallel Practice Exercise that covers the same
concept as the companion Active Examples, but
is typically slightly more challenging. By pairing
the Active Examples with Practice Exercises, the
book leads students toward improved conceptual
understanding and problem-solving skills.
Solutions to this edition’s 241 Practice Exercises
are provided in Appendix III.
• New End-of-Chapter Illustrations: More than 100
new photographs and line drawings have been
added to the end-of-chapter Questions, Exercises,
and Problems to better illustrate the macroscopic
aspect of chemistry and allow students to see
physical and chemical changes and common
forms of industrial manufacturing processes, as
well as better visualize the scenarios described
in the questions.
• Enhanced Features in OWL. OWL now includes
Student Self-Assessments, as well as the
interactive customizable Cengage YouBook, a
multimedia electronic version of the text.
FEATURES
• Portable Chapter-in-Review Cards: Designed to
make anywhere, anytime studying easier, these
detachable cards at the back of the book include
chapter summaries of goals and key concepts and
a chapter self-test with answers.
• Group Discussion Questions: These questions
give students the opportunity to work together
to develop their problem solving and conceptual
93
 understanding.
• Flexible Format: The book has been structured so
that any common sequence of topics is supported,
allowing professors to present topics in any order
they prefer.
• “Thinking About Your Thinking” Comments:
Designed to encourage students to think the way
chemists do and focus on critical thinking, these
features help students develop broad thinking
skills they can apply to new contexts in future
chemistry courses, other academic disciplines,
and throughout their lives.
• Section-Opening Learning Objectives: Identified
as Goals, these objectives focus attention on what
students are expected to learn or the skill they are
expected to develop while studying the section.
CONTENTS
1. Introduction to Chemistry; Introduction to Active
Learning. 2. Matter and Energy. 3. Measurement
and Chemical Calculations. 4. Introduction to Gases.
5. Atomic Theory: The Nuclear Model of the Atom.
6. Chemical Nomenclature. 7. Chemical Formula
Relationships. 8. Chemical Reactions. 9. Chemical
Change. 10. Quantity Relationships in Chemical
Reactions. 11. Atomic Theory: The Quantum Model
of the Atom. 12. Chemical Bonding. 13. Structure and
Shape. 14. The Ideal Gas Law and Its Applications.
15. Gases, Liquids, and Solids. 16. Solutions.
17. Acid-Base (Proton-Transfer) Reactions. 18.
Chemical Equilibrium. 19. Oxidation-Reduction
(Redox) Reactions. 20. Nuclear Chemistry. 21.
Organic Chemistry. 22. Biochemistry. Appendix I:
Chemical Calculations. Appendix II: The SI System
of Units. Glossary. Index.
© 2013, 848pp, Paperback, 9781133108115
94 www.cengageasia.com
A BEGINNER’S GUIDE TO SCIENTIFIC
METHOD, INTERNATIONAL EDITION,
4E
Stephen S. Carey, Portland Community College
This concise yet comprehensive guide provides an
introduction to the scientific method of inquiry as well
as detailed coverage of the many misapplications
of scientific method that define pseudoscience.
Compact enough to be used as a supplementary
book in a science class, yet thorough enough in
its coverage to be used as a core text in a class
on scientific method, this text assists students in
using the scientific method to design and assess
experiments.
NEW TO THIS EDITION
• The explanations have been thoroughly to ensure
clarity and readability for the student audience.
• The discussion of causation in Chapter 3 has been
greatly expanded.
• In Chapter 4, the basic framework for discussing
experimental design has been revised to center
on false confirmation and rejection.
• In Chapter 5, the discussion of probability and
statistical inference is greatly simplified. Each
section now begins with and explains all points
in terms of recent causal studies.
• Two new pseudoscientific fallacies have been
added and the text now contains many new and
recent illustrations of all the fallacies.
• Dozens of new exercises and examples have
been added to every chapter.
• End of chapter concept quizzes have been added.
FEATURES
• An introduction to the scientific method which
 acknowledges that good science must remain
utterly open to revision.
• Over one hundred practical, relevant exercises
and examples address common conceptual issues
and pitfalls confronted in students’ own practices
of scientific learning.
• Real-life examples from scientific literature provide
immediate practical applications of the concepts
encountered in the book.
CONTENTS
Preface.1. SCIENCE. Just What is Science? Asking
Why. Scientific Method. The Consequences of
Science. Scientific Method in Daily Life. Things
to Come. Exercises2. OBSERVATION. Making
Accurate Observations. Anomalous Phenomena.
Observing Anomalies. The Burden of Proof. Concept
Quiz. Exercises3. EXPLANATION. Explanation,
Theory and Hypothesis. Causation. Correlation.
Causal Mechanisms. Underlying Processes. Laws.
Function. The Interdependence of Explanatory
Methods. Rival Explanations and Ockham’s Razor.
Explanation and Description. Ultimate Explanations.
Concept Quiz. Exercises.4. EXPERIMENTATION.
The Basic Method. Confirmation and Rejection.
Designing a Good Test. Real World Experiments.
How Not to Design a Test. Conceptual Vagueness.
Testing Extraordinary Claims. Predictive Clarity.
Bias and Expectation. Concept Quiz. Exercises.5.
ESTABLISHING CAUSAL LINKS. Causal Studies.
Ruling Out Chance. Multiple Causal Factors.
Randomized, Prospective and Retrospective
Studies. Reading Between the Lines. Concept
Quiz. Exercises.6. FALLACIES IN THE NAME OF
SCIENCE. What is a Fallacy? False Anomalies.
Questionable Arguments by Elimination. Illicit Causal
Inferences. Unsupported Analogies and Similarities.
Untestable Explanations and Predictions. Empty
Jargon. Ad Hoc Rescues. Exploiting Uncertainty.
Science and Pseudoscience. Concept Quiz.
Exercises.FURTHER READINGINDEX
© 2012, 160pp, Paperback, 9781111726010
www.cengageasia.com
INTRODUCTION TO BASIC
CHEMISTRY, INTERNATIONAL
EDITION, 7E
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Donald J. DeCoste, University of Illinois, Urbana-Champaign
The Seventh Edition of INTRODUCTION TO BASIC
CHEMISTRY, 7e, International Edition includes
the first 16 chapters of INTRODUCTION TO
CHEMISTRY: A FOUNDATION, 7e, International
Edition. This new edition features a more explicit
problem-solving pedagogy to help students develop
critical thinking tools they can use in the introductory
course and beyond. Capturing student interest
through early coverage of chemical reactions,
accessible explanations and visualizations,
and an emphasis on everyday applications, the
authors explain chemical concepts by starting
with the basics, using symbols or diagrams, and
concluding by encouraging students to test their
own understanding of the solution. This step-by-
step approach has already helped hundreds of
thousands of students master chemical concepts
and develop problem-solving skills. The book is
known for its focus on conceptual learning and
for the way it motivates students by connecting
chemical principles to real-life experiences in
chapter-opening discussions and “Chemistry in
Focus” boxes. The Seventh Edition now adds a
“questioning” pedagogy to in-text examples to
help students learn what questions they should
be asking themselves while solving problems,
offers a revamped art program to better serve
visual learners, and includes a significant number
of revised end-of-chapter questions. The book’s
unsurpassed teaching and learning resources
95
 include a robust technology package that is now
supported by OWL: Online Web Learning.
NEW TO THIS EDITION
• A significantly improved full color art program
makes chemistry easier to understand for visual
learners.
• The text’s hallmark problem-solving pedagogy is
enhanced by in-text examples that suggest what
questions the students should be asking as they
solve problems.
• A new section in Chapter 8 explains why it is so
important to become a good problem-solver.
• The Seventh Edition is now supported by both
OWL: Online Web Learning, the number one
online learning system for chemistry.
FEATURES
• Exercises and models such as worked-out
examples, self-check exercises, and skill
development boxes support the authors’ step-
by-step problem-solving method.
• End-of-chapter material includes key terms,
a summary of important facts, questions and
problems arranged in matched pairs and keyed
to chapter sections, additional problems that
incorporate material from multiple sections, in-
class discussion questions, and “Cumulative
Reviews” that test concepts from preceding
chapters.
• The text builds and refreshes fundamental math
skills such as scientific notation, rounding, and
rearranging equations. In addition, Math Tips,
indicated by icons throughout, help students as
they perform calculations.
• The book is also available in alternative
versions: INTRODUCTION TO CHEMISTRY;
A FOUNDATION, International Edition, which
includes five additional chapters that cover
equilibrium, oxidation-reduction reactions and
electrochemistry, radioactivity and nuclear energy,
organic chemistry, and biochemistry.(Chapters
1-21) and INTRODUCTION TO CHEMISTRY,
International Edition which include additional
coverage of equilibrium, oxidation-reduction
reactions, electrochemistry, radioactivity, and
nuclear energy (Chapters 1-19).
96 www.cengageasia.com
CONTENTS
1. CHEMISTRY: AN INTRODUCTION.Chemistry:
An Introduction. Chemistry in Focus: Dr. Ruth—
Cotton Hero. What Is Chemistry? Solving Problems
Using a Scientific Approach. Chemistry in Focus:
A Mystifying Problem. The Scientific Method.
Learning Chemistry. Chemistry in Focus: Chemistry:
An Important Component of Your Education.2.
MEASUREMENTS AND CALCULATIONS.Scientific
Notation. Units. Chemistry in Focus: Critical Units!
Measurements of Length, Volume, and Mass.
Chemistry in Focus: Measurement: Past, Present,
and Future. Uncertainty in Measurement. Significant
Figures. Problem Solving and Dimensional Analysis.
Temperature Conversions: An Approach to
Problem Solving. Chemistry in Focus: Tiny
Thermometers. Density.3. MATTER.Matter.
Physical and Chemical Properties and Changes.
Elements and Compounds. Mixtures and Pure
Substances. Chemistry in Focus: Concrete—An
Ancient Material Made New. Separation of Mixtures.
Cumulative Review for Chapters 1-3.4. CHEMICAL
FOUNDATIONS: ELEMENTS, ATOMS, AND IONS.
The Elements. Chemistry in Focus: Trace Elements:
Small but Crucial. Symbols for the Elements.
Dalton’s Atomic Theory. Chemistry in Focus:
No Laughing Matter. Formulas of Compounds.
The Structure of the Atom. Chemistry in Focus:
Glowing Tubes for Signs, Television Sets, and
Computers. Introduction to the Modern Concept
of Atomic Structure. Isotopes. Chemistry in Focus:
Isotope Tales. Introduction to the Periodic Table.
Chemistry in Focus: Putting the Brakes on Arsenic.
Natural States of the Elements. Ions Compounds
That Contain Ions.5. NOMENCLATURE.Naming
Compounds. Chemistry in Focus: Sugar of Lead.
Naming Binary Compounds That Contain a Metal
and a Nonmetal (Types I and II). Naming Binary
Compounds That Contain Only Nonmetals (Type
III). Naming Binary Compounds: A Review.
Naming Compounds That Contain Polyatomic
Ions. Naming Acids. Writing Formulas from Names.
Cumulative Review for Chapters 4-5.6. CHEMICAL
REACTIONS: AN INTRODUCTION.Evidence for a
Chemical Reaction. Chemical Equations. Balancing
Chemical Equations. Chemistry in Focus: The
Beetle That Shoots Straight.7. REACTIONS IN
AQUEOUS SOLUTIONS.Predicting Whether a
Reaction Will Occur. Reactions in Which a Solid
Forms. Describing Reactions in Aqueous Solutions.
Reactions That Form Water: Acids and Bases.
Reactions of Metals with Nonmetals (Oxidation-
Reduction). Ways to Classify Reactions. Chemistry
in Focus: Do We Age by Oxidation? Chemistry in
Focus: Oxidation-Reduction Reactions Launch the
Space Shuttle. Other Ways to Classify Reactions.
Cumulative Review for Chapters 6-7.8. CHEMICAL
COMPOSITION.Counting by Weighing. Chemistry
in Focus: Plastic That Talks and Listens! Atomic
Masses: Counting Atoms by Weighing. The Mole.
Molar Mass. Percent Composition of Compounds.
Formulas of Compounds. Calculation of Empirical
Formulas. Calculation of Molecular Formulas.9.
CHEMICAL QUANTITIES.Information Given by
Chemical Equations. Mole—Mole Relationships.
Mass CalculationsChemistry in Focus: Methyl
Alcohol: Fuel with a Future? Calculations Involving
a Limiting Reactant. Percent Yield. Cumulative
Review for Chapters 8-9.10. ENERGY.The Nature
of Energy. Temperature and Heat. Exothermic
and Endothermic Processes. Thermodynamics.
Measuring Energy Changes. Chemistry in Focus:
Coffee: Hot and Quick(lime). Chemistry in Focus:
Nature Has Hot Plants. Chemistry in Focus:
Firewalking: Magic or Science? Thermochemistry
(Enthalpy). Chemistry in Focus: Methane: An
Important Energy Source. Hess’s Law. Quality
Versus Quantity of Energy. Energy and Our World.
Chemistry in Focus: Veggie Gasoline? Energy as
a Driving Force.11. MODERN ATOMIC THEORY.
Rutherford’s Atom. Electromagnetic Radiation.
Chemistry in Focus: Light as a Sex Attractant.
Chemistry in Focus: Atmospheric Effects 307.
Emission of Energy by Atoms. The Energy Levels
of Hydrogen. The Bohr Model of the Atom. The
Wave Mechanical Model of the Atom. The Hydrogen
Orbitals. The Wave Mechanical Model: Further
Development. Electron Arrangements in the First
Eighteen Atoms on the Periodic Table. Chemistry in
Focus: A Magnetic Moment. Electron Configurations
and the Periodic Table. Chemistry in Focus: The
Chemistry of Bohrium. Atomic Properties and the
Periodic Table. Chemistry in Focus: Fireworks.12.
CHEMICAL BONDING.Types of Chemical Bonds.
www.cengageasia.com
Electronegativity. Bond Polarity and Dipole Moments.
Stable Electron Configurations and Charges on
Ions. Chemistry in Focus: Composite Cars. Ionic
Bonding and Structures of Ionic Compounds. Lewis
Structures. Lewis Structures of Molecules with
Multiple Bonds. Chemistry in Focus: Hiding Carbon
Dioxide. Chemistry in Focus: Broccoli—Miracle
Food? Molecular Structure. Molecular Structure:
The VSEPR Model. Chemistry in Focus: Taste—It’s
the Structure That Counts. Molecular Structure:
Molecules with Double Bonds. Chemistry in
Focus: Minimotor Molecule. Cumulative Review for
Chapters 10-12.13. GASES.Pressure. Pressure and
Volume: Boyle’s Law. Volume and Temperature:
Charles’s Law. Volume and Moles: Avogadro’s Law.
The Ideal Gas Law. Chemistry in Focus: Snacks
Need Chemistry, Too! Dalton’s Law of Partial
Pressures. Laws and Models: A Review. The Kinetic
Molecular Theory of Gases. The Implications of the
Kinetic Molecular Theory. Gas Stoichiometry.14.
LIQUIDS AND SOLIDS.Water and Its Phase
Changes. Energy Requirements for the Changes of
State. Chemistry in Focus: Whales Need Changes
of State. Intermolecular Forces. Evaporation and
Vapor Pressure. The Solid State: Types of Solids.
Bonding in Solids. Chemistry in Focus: Metal with
a Memory.15. SOLUTIONS.Solubility. Chemistry
in Focus: Green Chemistry. Solution Composition:
An Introduction. Solution Composition: Mass
Percent. Solution Composition: Molarity. Dilution.
Stoichiometry of Solution Reactions. Neutralization
Reactions. Solution Composition: Normality.
Cumulative Review for Chapters 13-15.16. ACIDS
AND BASES.Acids and Bases. Chemistry in Focus:
Gum That Foams. Acid Strength. Chemistry in
Focus: Carbonation—A Cool Trick. Chemistry in
Focus: Plants Fight Back. Water as an Acid and a
Base. The pH Scale. Chemistry in Focus: Airplane
Rash. Chemistry in Focus: Garden-Variety Acid-
Base Indicators. Calculating the pH of Strong
Acid Solutions. Buffered Solutions.APPENDIX.
Using Your Calculator. Basic Algebra. Scientific
(Exponential) Notation. Graphing Functions. SI
Units and Conversion Factors. Solutions to Self-
Check Exercises. Answers to Even-Numbered
End-of-Chapter Questions and Exercises. Answers
to Even-Numbered Cumulative Review. Exercises.
97
 Index/Glossary. Photo Credits.
© 2011, 688pp, Paperback, 9780538736640
INTRODUCTION TO CHEMISTRY, 7E
A Foundation, International Edition
Steven S. Zumdahl, University of Illinois, Urbana-Champaign;
Donald J. DeCoste, University of Illinois, Urbana-Champaign
The Seventh Edition of Zumdahl and DeCoste’s
best-selling INTRODUCTION TO CHEMISTRY: A
FOUNDATION, International Edition that combines
enhanced problem-solving structure with substantial
pedagogy to enable students to become strong
independent problem solvers in the introductory
course and beyond. Capturing student interest
through early coverage of chemical reactions,
accessible explanations and visualizations,
and an emphasis on everyday applications, the
authors explain chemical concepts by starting
with the basics, using symbols or diagrams, and
conclude by encouraging students to test their
own understanding of the solution. This step-by-
step approach has already helped hundreds of
thousands of students master chemical concepts
and develop problem-solving skills. The book is
known for its focus on conceptual learning and
for the way it motivates students by connecting
chemical principles to real-life experiences in
chapter-opening discussions and “Chemistry in
Focus” boxes.The Seventh Edition now adds a
“questioning” pedagogy to in-text examples to
help students learn what questions they should
be asking themselves while solving problems,
offers a revamped art program to better serve
visual learners, and includes a significant number
of revised end-of-chapter questions. The book’s
98
unsurpassed teaching and learning resources
include a robust technology package that now offers
OWL: Online Web Learning.
NEW TO THIS EDITION
• The book’s full color art program has been redrawn
and reworked to make figures easier to follow and
more aesthetically pleasing. In addition, labeling
within the art has been reconfigured for better
clarity, glassware illustrations have been updated,
and the orbital art has been redesigned.
• The text’s hallmark problem-solving pedagogy is
enhanced by in-text examples that suggest what
questions the students should be asking as they
solve problems.
• A new section in Chapter 8 explains why it is so
important to become a good problem-solver.
• The Seventh Edition is now supported by
both OWL: Online Web Learning, the number
one online learning system for chemistry, and
Enhanced WebAssign. Both are available with
e-books.
FEATURES
• Exercises and models such as worked-out
examples, self-check exercises, and skill
development boxes support the authors’ step-
by-step problem-solving method.
• End-of-chapter material includes key terms,
a summary of important facts, questions and
problems arranged in matched pairs and keyed
to chapter sections, additional problems that
incorporate material from multiple sections, in-
class discussion questions, and “Cumulative
Reviews” that test concepts from preceding
chapters.
• The text builds and refreshes fundamental math
skills such as scientific notation, rounding, and
rearranging equations. In addition, Math Tips,
indicated by icons throughout, help students as
they perform calculations.
• The book is also available in alternative versions:
INTRODUCTION TO BASIC CHEMISTRY,
International Edition, which covers chemical
concepts and applications through acids and
bases (Chapters 1-16) and INTRODUCTION TO
CHEMISTRY, International Edition, which also
covers equilibrium, oxidation-reduction reactions,
www.cengageasia.com
 electrochemistry, radioactivity, and nuclear energy
(Chapters 1-19).
CONTENTS
1. CHEMISTRY: AN INTRODUCTION.Chemistry:
An Introduction. Chemistry in Focus: Dr. Ruth—
Cotton Hero. What Is Chemistry? Solving Problems
Using a Scientific Approach. Chemistry in Focus: A
Mystifying Problem. The Scientific Method. Learning
Chemistry. Chemistry in Focus: Chemistry: An
Important Component of Your Education.2.
MEASUREMENTS AND CALCULATIONS.Scientific
Notation. Units. Chemistry in Focus: Critical Units!
Measurements of Length, Volume, and Mass.
Chemistry in Focus: Measurement: Past, Present,
and Future. Uncertainty in Measurement. Significant
Figures. Problem Solving and Dimensional Analysis.
Temperature Conversions: An Approach to Problem
Solving. Chemistry in Focus: Tiny Thermometers.
Density.3. MATTER.Matter. Physical and Chemical
Properties and Changes. Elements and Compounds.
Mixtures and Pure Substances. Chemistry in Focus:
Concrete—An Ancient Material Made New.
Separation of Mixtures. Cumulative Review for
Chapters 1-3.4. CHEMICAL FOUNDATIONS:
ELEMENTS, ATOMS, AND IONS.The Elements.
Chemistry in Focus: Trace Elements: Small but
Crucial. Symbols for the Elements. Dalton’s Atomic
Theory. Chemistry in Focus: No Laughing Matter.
Formulas of Compounds. The Structure of the Atom.
Chemistry in Focus: Glowing Tubes for Signs,
Television Sets, and Computers. Introduction to the
Modern Concept of Atomic Structure. Isotopes.
Chemistry in Focus: Isotope Tales. Introduction to
the Periodic Table. Chemistry in Focus: Putting the
Brakes on Arsenic. Natural States of the Elements.
Ions Compounds That Contain Ions.5.
NOMENCLATURE.Naming Compounds. Chemistry
in Focus: Sugar of Lead. Naming Binary Compounds
That Contain a Metal and a Nonmetal (Types I and
II). Naming Binary Compounds That Contain Only
Nonmetals (Type III). Naming Binary Compounds:
A Review. Naming Compounds That Contain
Polyatomic Ions. Naming Acids. Writing Formulas
from Names. Cumulative Review for Chapters 4-5.6.
CHEMICAL REACTIONS: AN INTRODUCTION.
Evidence for a Chemical Reaction. Chemical
Equations. Balancing Chemical Equations.
www.cengageasia.com
Chemistry in Focus: The Beetle That Shoots
Straight.7. REACTIONS IN AQUEOUS SOLUTIONS.
Predicting Whether a Reaction Will Occur. Reactions
in Which a Solid Forms. Describing Reactions in
Aqueous Solutions. Reactions That Form Water:
Acids and Bases. Reactions of Metals with
Nonmetals (Oxidation-Reduction). Ways to Classify
Reactions. Chemistry in Focus: Do We Age by
Oxidation? Chemistry in Focus: Oxidation-Reduction
Reactions Launch the Space Shuttle. Other Ways
to Classify Reactions. Cumulative Review for
Chapters 6-7.8. CHEMICAL COMPOSITION.
Counting by Weighing. Chemistry in Focus: Plastic
That Talks and Listens! Atomic Masses: Counting
Atoms by Weighing. The Mole. Molar Mass. Percent
Composition of Compounds. Formulas of
Compounds. Calculation of Empirical Formulas.
Calculation of Molecular Formulas.9. CHEMICAL
QUANTITIES.Information Given by Chemical
Equations. Mole—Mole Relationships. Mass
CalculationsChemistry in Focus: Methyl Alcohol:
Fuel with a Future? Calculations Involving a Limiting
Reactant. Percent Yield. Cumulative Review for
Chapters 8-9.10. ENERGY.The Nature of Energy.
Temperature and Heat. Exothermic and Endothermic
Processes. Thermodynamics. Measuring Energy
Changes. Chemistry in Focus: Coffee: Hot and
Quick(lime). Chemistry in Focus: Nature Has Hot
Plants. Chemistry in Focus: Firewalking: Magic or
Science? Thermochemistry (Enthalpy). Chemistry
in Focus: Methane: An Important Energy Source.
Hess’s Law. Quality Versus Quantity of Energy.
Energy and Our World. Chemistry in Focus: Veggie
Gasoline? Energy as a Driving Force.11. MODERN
ATOMIC THEORY.Rutherford’s Atom.
Electromagnetic Radiation. Chemistry in Focus:
Light as a Sex Attractant. Chemistry in Focus:
Atmospheric Effects 307. Emission of Energy by
Atoms. The Energy Levels of Hydrogen. The Bohr
Model of the Atom. The Wave Mechanical Model of
the Atom. The Hydrogen Orbitals. The Wave
Mechanical Model: Further Development. Electron
Arrangements in the First Eighteen Atoms on the
Periodic Table. Chemistry in Focus: A Magnetic
Moment. Electron Configurations and the Periodic
Table. Chemistry in Focus: The Chemistry of
Bohrium. Atomic Properties and the Periodic Table.
99
 Chemistry in Focus: Fireworks.12. CHEMICAL
BONDING.Types of Chemical Bonds.
Electronegativity. Bond Polarity and Dipole Moments.
Stable Electron Configurations and Charges on Ions.
Chemistry in Focus: Composite Cars. Ionic Bonding
and Structures of Ionic Compounds. Lewis
Structures. Lewis Structures of Molecules with
Multiple Bonds. Chemistry in Focus: Hiding Carbon
Dioxide. Chemistry in Focus: Broccoli—Miracle
Food? Molecular Structure. Molecular Structure:
The VSEPR Model. Chemistry in Focus: Taste—It’s
the Structure That Counts. Molecular Structure:
Molecules with Double Bonds. Chemistry in Focus:
Minimotor Molecule. Cumulative Review for
Chapters 10-12.13. GASES.Pressure. Pressure and
Volume: Boyle’s Law. Volume and Temperature:
Charles’s Law. Volume and Moles: Avogadro’s Law.
The Ideal Gas Law. Chemistry in Focus: Snacks
Need Chemistry, Too! Dalton’s Law of Partial
Pressures. Laws and Models: A Review. The Kinetic
Molecular Theory of Gases. The Implications of the
Kinetic Molecular Theory. Gas Stoichiometry.14.
LIQUIDS AND SOLIDS.Water and Its Phase
Changes. Energy Requirements for the Changes of
State. Chemistry in Focus: Whales Need Changes
of State. Intermolecular Forces. Evaporation and
Vapor Pressure. The Solid State: Types of Solids.
Bonding in Solids. Chemistry in Focus: Metal with
a Memory.15. SOLUTIONS.Solubility. Chemistry in
Focus: Green Chemistry. Solution Composition: An
Introduction. Solution Composition: Mass Percent.
Solution Composition: Molarity. Dilution.
Stoichiometry of Solution Reactions. Neutralization
Reactions. Solution Composition: Normality.
Cumulative Review for Chapters 13-15.16. ACIDS
AND BASES.Acids and Bases. Chemistry in Focus:
Gum That Foams. Acid Strength. Chemistry in
Focus: Carbonation—A Cool Trick. Chemistry in
Focus: Plants Fight Back. Water as an Acid and a
Base. The pH Scale. Chemistry in Focus: Airplane
Rash. Chemistry in Focus: Garden-Variety Acid-
Base Indicators. Calculating the pH of Strong Acid
Solutions. Buffered Solutions.17. EQUILIBRIUM.
How Chemical Reactions Occur. Conditions That
Affect Reaction Rates. Chemistry in Focus:
Protecting the Ozone. The Equilibrium Condition.
Chemical Equilibrium: A Dynamic Condition. The
100 www.cengageasia.com
Equilibrium Constant: An Introduction.
Heterogeneous Equilibria. Le Châtelier’s Principle.
Applications Involving the Equilibrium Constant.
Solubility Equilibria. Cumulative Review for Chapters
16-17.18. OXIDATION-REDUCTION REACTIONS
AND ELECTROCHEMISTRY.Oxidation-Reduction
Reactions. Oxidation States. Oxidation-Reduction
Reactions Between Nonmetals. Balancing Oxidation-
Reduction Reactions by the Half-Reaction Method.
Electrochemistry: An Introduction. Batteries.
Corrosion. Chemistry in Focus: Stainless Steel: It’s
the Pits. Electrolysis. Chemistry in Focus: Water-
Powered Fireplace.19. RADIOACTIVITY AND
NUCLEAR ENERGY.Radioactive Decay. Nuclear
Transformations. Detection of Radioactivity and the
Concept of Half-life. Dating by Radioactivity.
Chemistry in Focus: Dating Diamonds. Medical
Applications of Radioactivity. Nuclear Energy.
Nuclear Fission. Nuclear Reactors. Chemistry in
Focus: Future Nuclear Power. Nuclear Fusion.
Effects of Radiation. Chemistry in Focus: Nuclear
Waste Disposal.20. ORGANIC CHEMISTRY.
Carbon Bonding. Alkanes. Structural Formulas and
Isomerism. Naming Alkanes. Petroleum. Reactions
of Alkanes. Alkenes and Alkynes. Aromatic
Hydrocarbons. Naming Aromatic Compounds.
Chemistry in Focus: Termite Mothballing. Functional
Groups. Alcohols. Properties and Uses of Alcohols.
Aldehydes and Ketones. Naming Aldehydes and
Ketones. Carboxylic Acids and Esters. Polymers.
Chemistry in Focus: The Chemistry of Music.
Chemistry in Focus: Polymers Are Tacky. B21.
BIOCHEMISTRY. Proteins. Primary Structure of
Proteins. Secondary Structure of Proteins. Tertiary
Structure of Proteins. Functions of Proteins.
Enzymes. Chemistry in Focus: Urine Farming.
Carbohydrates. Chemistry in Focus: Great
Expectations? The Chemistry of Placebos. Nucleic
Acids. Lipids.APPENDIX.Using Your Calculator.
Basic Algebra. Scientific (Exponential) Notation.
Graphing Functions. SI Units and Conversion
Factors. Solutions to Self-Check Exercises. Answers
to Even-Numbered End-of-Chapter Questions and
Exercises. Answers to Even-Numbered Cumulative
Review. Exercises. Index/Glossary. Photo Credits.
© 2011, 848pp, Paperback, 9780538735438

INTRODUCTION TO CHEMICAL
PRINCIPLES, 7E
A Laboratory Approach, International Edition
Susan A. Weiner, West Valley College ; Blaine Harrison
The seventh edition of this superb lab manual
offers 36 class-tested experiments, suitable
for introductory, preparatory, and health
science chemistry courses and texts, including
INTRODUCTORY CHEMISTRY: AN ACTIVE
LEARNING APPROACH, 4e, INTERNATIONAL
EDITION by Cracolice and Peters. Experiments
in this lab manual teach students to collect and
analyze experimental data and provide them with
a strong foundation for further course work in
general chemistry. This edition offers instructors
a wide variety of experiments to customize their
laboratory program, including many microscale
experiments. All experiments can be completed
in a three-hour laboratory period. As in the Sixth
Edition, there are Work Pages for each experiment
as well as Report Sheets for students to take notes
and record experimental data and results, which
facilitate instructor grading of experiments.
NEW TO THIS EDITION
• The new edition features 11 worksheets covering
the major topics of introductory chemistry. The
worksheets can be used to enhance the lab
experience or as supplementary homework.
Complete solutions are available in the Instructor’s
Manual.
• The Seventh Edition also features four
new experiments: “Experiment 27: Organic
Nomenclature,” “Experiment 30: Esters,”
“Experiment 34: Lipids,” and “Experiment 36:
Enzymes.”
www.cengageasia.com
• Several experiments have also been revised to
provide clearer direction and more detail in the
Procedure section.
FEATURES
• Duplicate Work Pages and Report Sheets for each
experiment offer a convenient and efficient way
for students to record their data as they work and
yield clean, easy-to-grade reports.
• Advance Study Assignments, to be completed
before performing the experiments, require
students to read the experiment before executing
the lab, thus enabling them to complete the
experiment in a safe and timely fashion.
• Sample Calculations are presented to acquaint
the student with the type of calculations they will
be required to perform for the experiment.
• The lab manual features a variety of experiments
for inorganic and organic chemistry so that it may
accompany many different chemistry textbooks
from introductory inorganic chemistry to allied
health chemistry.
CONTENTS
SAFETY IN THE LABORATORY.LABORATORY
PROCEDURES.EXPERIMENTS:1. Properties
and Changes of Matter (m).2. The Chemistry
of Some Household Products.3. Separation
of Cations by Paper Chromatography (m).4.
Densities of Liquids and Solids.5. Simplest
Formula of a Compound (m).6. Hydrates (m).7.
Percentage of Oxygen in Potassium Chlorate.8.
Calorimetry.9. Chemical Names and Formulas:
A Study Assignment.10. Chemical Equations: A
Study Assignment.11. Mole Ratio for a Chemical
Reaction (m).12. Types of Chemical Reactions
(m).13. Qualitative Analysis of Some Common
Ions (m).14. Separation of Cations.15. Molecular
Models: A Study Assignment.16. Molar Volume
of a Gas (m).17. Molar Mass Determination by
Freezing-Point Depression.18. The Conductivity of
Solutions: A Demonstration.19. Net Ionic Equations:
A Study Assignment.20. Titration of Acids and
Bases—I.21. Titration of Acids and Bases—II.22.
Determination of a Chemical Equation.23. A Study
of Reaction Rates.24. Chemical Equilibrium (m).25.
Measurement of pH with Indicators.26. Introduction
to Oxidation-Reduction Reactions (m).27. Organic
101
 Nomenclature.28. Hydrocarbons and Alcohols.29.
Aldehydes, Ketones, and Carboxylic Acids.30.
Esters.31. Preparation of Aspirin.32. Preparation
and Properties of a Soap.33. Carbohydrates.34.
Lipids.35. Amino Acids and Proteins.36. Enzymes.
WORKSHEETS:1. Significant Figures.2.
Dimensional Analysis.3. Avogrado’s Number-
Moles.4. Formula Writing.5. Equation Balancing-
Types of Reactions.6. Stoichiometry.7. Atomic
Structure.8. Gases.9. Solutions.10. Oxidation-
Reduction.11. Acids and Bases.Appendix.
© 2010, 480pp, Paperback, 9781439046647
SURVIVAL GUIDE FOR
INTRODUCTORY CHEMISTRY
Charles H. Atwood, University of Georgia
Straightforward, thorough, packed with examples
and exercises, and modeled after Atwood’s widely
popular CHEMISTRY SURVIVAL GUIDE, the
new SURVIVAL GUIDE FOR INTRODUCTORY
CHEMISTRY is everything your students need
to survive and thrive in an introductory course.
Designed as a reader’s guide to an introductory
textbook, the SURVIVAL GUIDE offers detailed
step-by-step problem-solving sequences, giving
students the competency—and confidence—they
need to master the material and achieve optimal
exam results. Coupled with a complementary math
review, this brief but powerful resource covers the
most fundamental aspects of introductory chemistry
in a succinct series of essential modules.
FEATURES
• Student-friendly content: Key Terms, Concepts,
102 www.cengageasia.com
and Equations highlight and clarify introductory
chemistry issues for students, helping them to
focus on essential information and to maximize
their study time.
• Sample Exercises: Providing step-by-step
instruction, Sample Exercises include detailed
explanations that guide students in gaining a
solid understanding of chemistry concepts and
principles.
• Avoiding Pitfalls: Included throughout the
text, Caution icons alert students to common
mistakes and help them avoid such missteps,
making chemistry more accessible and easier to
understand.
• Tips and Tools: Problem Solving Tips give students
additional insight for successfully working through
exercises and strengthening their analytical skills.
• You can order the SURVIVAL GUIDE FOR
INTRODUCTORY CHEMISTRY in a convenient,
money-saving package with either of these newer
texts: Zumdahl/Zumdahl, INTRODUCTORY
CHEMISTRY, 6E or Craccolice/Peters,
INTRODUCTORY CHEMISTRY: AN ACTIVE
LEARNING APPROACH, 4E.
CONTENTS
Module 1. An Approach to Problem Solving.Module
2. Metric System, Significant Figures, Dimensional
Analysis, and Density.Module 3. Matter and Energy.
Module 4. Elements, Atoms and the Periodic Table.
Module 5. Chemical Nomenclature.Module 6.
Understanding Chemical Formulas and Using the
Mole Concept.Module 7. Understanding Chemical
Reaction Equations.Module 8. Chemical Reactions
in Aqueous Solutions.Module 9. Chemical Reaction
Stoichiometry.Module 10. Electronic Structure of
Atoms.Module 11. Periodic Trends in Chemistry.
Module 12. Chemical Bonding.Module 13. Molecular
Shapes and Polarity.Module 14. Gases.Module 15.
Liquids and Solids.Module 16. Solutions.Module 17.
Acids and Bases.Module 18. Chemical Equilibrium.
Module 19. Oxidation-Reduction Reactions and
Electrochemistry.Module 20. Nuclear Chemistry.
Math Review.
© 2009, 192pp, Paperback, 9780495828266
 LIBERAL ARTS CHEMISTRY

SURVIVAL GUIDE FOR GENERAL

CHEMISTRY WITH MATH REVIEW, 2E
Charles H. Atwood, University of Georgia
Available for packaging with any CENGAGE
textbook, this survival guide focuses on helping
students practice for exams by showing them how
to solve difficult problems by dissecting them into
manageable chunks. The guide includes three
levels of proficiency questions – A, B, and minimal
– to quickly build student confidence as they master
the knowledge needed to succeed in the course.
This book is also available for students to purchase
separately at www.CENGAGEbrain.com.
CONTENTS
Module 1: Metric System, Dimensional Analysis,
Significant Figures, and Density.Module 2:
Understanding Chemical Formulas.Module 3:
Chemical Nomenclature.Module 4: The Mole
Concept.Module 5: Chemical Reaction Stoichiometry.
Module 6: Types of Chemical Reactions.Module 7:
Electronic Structure of Atoms.Module 8: Chemical
Periodicity.Module 9: Chemical Bonding.Module
10: Molecular Shapes.Module 11: Hybridization
and Polarity of Molecules.Module 12: Acids and
Bases.Module 13: States of Matter.Module 14:
Solutions.Module 15: Heat Transfer, Calorimetry,
and Thermodynamics.Module 16: Chemical
Kinetics.Module 17: Gas Phase Equilibria.Module
18: Aqueous Equilibria.Module 19: Electrochemistry.
Module 20: Nuclear Chemistry.Math Review.
© 2008, 216pp, Paperback, 9780495387510
CHEM 2, 2E
Chemistry in Your World (with OWLv2 24-Months
Printed Access Card)
John L. Hogg, Texas A&M University
Created by the continuous feedback of a “student-
tested, faculty-approved” process, CHEM2 delivers
a visually appealing, succinct print component,
tear-out review cards for students and instructors,
and a consistent online offering with OWLv2 that
includes an eBook in addition to a set of interactive
digital tools -- all at a value-based price and proven
to increase retention and outcomes. CHEM2 also
offers Go Chemistry and Thinkwell mini-video
lectures, as well as online homework available
through the OWL learning system.
NEW TO THIS EDITION
• END-OF-CHAPTER QUESTIONS have been
added to nearly every chapter.
• POWERPOINT LECTURE SLIDES, completely
customizable to your specific classroom needs,
help you prep for class faster and more efficiently.
• NEW DETACHABLE EQUATION-SPECIFIC
CARDS show students how to properly set up
conversion and stoichiometric equations while
they do their homework. Each card features a
“skeleton version” of the equation as well as an
example.
• A MORE USER-FRIENDLY, CHEMISTRY-
SPECIFIC DESIGN reflects the needs of today’s
liberal arts students.
• The #1 online homework and learning system
for chemistry, OWLv2, is available for this text--

www.cengageasia.com
103
 now with new instructor features and enhanced
functionality: a Dashboard that consolidates
all course materials; easy, intuitive assignment
creation and management; ability to preview and
select activities/questions for each assignment;
new assignment settings and options; improved
gradebook; Personalized Study tools to help
students focus their time on the key concepts
and skills; and MindTap Reader™, a new
eBook withh apps and embedded video, audio,
annotations, and activities. OWLv2 courses for
Gen Chem, GOB, and Liberal Arts now include
Quick Prep essential skills assignments that can
be taken before the semester begins or during
the first few weeks, to help students succeed in
the course. For this course, OWLv2 also includes
new interactive versions of the end-of-chapter
questions from the text, 45 new visual exercises,
and new iPad-compatible visualizations, tutorials,
and simulations.
• EXTENSIVELY REORGANIZED CHAPTERS
2 AND 16 provide a better flow of subjects to
enhance student understanding.
• THE UPDATED ART PROGRAM offers new and
more relevant instructive images.
• DETACHABLE “CHAPTER IN REVIEW” CARDS,
revised to match the text’s narrative, give students
a portable study tool packed with pertinent
information they can use to prepare for class.
• DETACHABLE “INSTRUCTOR PREP” CARDS --
now including a list of the major revisions in each
chapter -- make class prep quick and easy and
include a quick map of chapter content, a list of
corresponding PowerPoint and video resources,
additional examples, and suggested assignments
and discussion questions.
• RELEVANT, REAL LIFE APPLICATIONS have
been updated to reflect up-to-date issues affecting
the chemical world.
CONTENTS
1. Living in a World of Chemistry.2. The Chemical
View of Matter.3. Atoms and the Periodic Table.4.
The Air We Breathe.5. Chemical Bonding and States
of Matter.6. Carbon Dioxide and the Greenhouse
Effect.7. Chlorofl uorocarbons and the Ozone
Layer.8. Chemical Reactivity: Chemicals in Action.9.
Acid--Base Reactions.10. Oxidation--Reduction
104 www.cengageasia.com
Reactions.11. Water, Water Everywhere but Not
a Drop to Drink?12. Energy and Hydrocarbons.13.
Nuclear Changes and Nuclear Power.14. Organic
Chemicals and Polymers.15. The Chemistry of
Life.16. Nutrition: The Basis of Healthy Living.17.
Chemistry and Medicine.18. The Chemistry of
Useful Materials.19. Feeding the World.Appendices
(Answers to Try Its & Answers to Selected
Problems).Index.
© 2015, 496pp, Paperback, 9781133962984
CHEM
Melvin Joesten, Vanderbilt University ; John L. Hogg, Texas
A&M University; Donald R. Neu, Saint Cloud State University
CHEM delivers exactly what today’s students need
--and want. Based on student and faculty feedback
from nationwide interviews and focus groups,
CHEM was developed through a “student-tested,
faculty-approved” process. The result is a concise,
engaging, and accessible textbook that presents
the basic chemical principles faculty require within
a framework of relevant, real world applications
that liberal arts students can relate to. Delivered at
a value price, CHEM accommodates the diverse
lifestyles of today’s learners, features a modern,
open page design, and includes a wide array of
print and online learning aids, including chapter-
by-chapter study cards, self-quizzes, interactive
flash cards, Go Chemistry and Thinkwell mini-video
lectures, and online homework available through
the OWL learning system.
FEATURES
• Shorter, comprehensive chapters in a modern
design, along with a wealth of print and online
 teaching and learning aids, make this book ideal
for today’s students.
• Detachable “Chapter in Review” cards give
students a portable study tool packed with
pertinent information they can use to prepare for
class.
• Detachable “Instructor Prep” cards make class
prep quick and easy and include a quick map of
chapter content, a list of corresponding PowerPoint
and video resources, additional examples, and
suggested assignments and discussion questions.
• Learning tools designed to meet a wide range
of learning styles include interactive quizzes,
animations, videos, interactive and printable
flashcards, and additional essays.
• Relevant, real- life applications feature such topics
as the nutritional basis of healthy living, medicines
and drugs, pollution & the conservation of natural
resources, and the agricultural production of food
for an ever-expanding world population.
CONTENTS
1. Living in a World of Chemistry. 2. The Chemical
View of Matter. 3. Atoms and the Periodic Table. 4.
The Air We Breathe and Some Major Atmospheric
Pollutants. 5. Chemical Bonding and States of
Matter. 6. Carbon Dioxide and the Greenhouse
Effect. 7. Chlorofluorocarbons and the Ozone
Layer. 8. Chemical Reactivity: Chemicals in Action.
9. Acid-Base Reactions. 10. Oxidation-Reduction
Reactions. 11. Water, Water Everywhere, but Not
a Drop to Drink? 12. Energy and Hydrocarbons. 13.
Nuclear Changes and Nuclear Power. 14. Organic
Chemicals and Polymers. 15. The Chemistry of
Life. 16. Nutrition: The Basis of Healthy Living.
17. Chemistry and Medicine. 18. The Chemistry of
Useful Materials. 19. Feeding the World.
© 2011, 448pp, Paperback, 9780538738217
www.cengageasia.com
ORGANIC CHEMISTRY
A SMALL SCALE APPROACH
TO ORGANIC LABORATORY
TECHNIQUES, 4E
Donald L. Pavia, Western Washington University; George
S. Kriz, Western Washington University; Gary M. Lampman,
Western Washington University; Randall G. Engel, North
Seattle Community College
Featuring new experiments, a new essay, and new
coverage of nanotechnology, this organic chemistry
laboratory textbook offers a comprehensive
treatment of laboratory techniques including
small-scale and some microscale methods that
use standard-scale (“macroscale”) glassware
and equipment. The book is organized based
on essays and topics of current interest and
covers a large number of traditional organic
reactions and syntheses, as well as experiments
with a biological or health science focus. Seven
introductory technique-based experiments, thirteen
project-based experiments, and sections on green
chemistry and biofuels spark students’ interest and
engage them in the learning process. Instructors
may choose to offer Cengage Learning’s optional
Premium Website, which contains videos on basic
organic laboratory techniques.
NEW TO THIS EDITION
• This edition includes a new OWLv2 LabSkills
program that can be bundled with the textbook.
LabSkills provides students the opportunity to
practice skills and prepare for real laboratory
classes in a safe environment. Students work
through the assignments in advance of the lab
105
 so they can actively rehearse common practical
techniques by engaging with simulations,
videos and quizzes. Because LabSkills focuses
on techniques, instructors can customize
assignments to align with the experiments that
students will perform in any given lab session.
The online course will also offer assessment
specific to this edition’s experiments, and include
a MindTap Reader.
• New experiments in this edition: Experiment 24
- Preparation of Soap; Experiment 31 - A new
green oxidation reaction using Oxone ® in An
Oxidation-Reduction Scheme: Borneol, Camphor,
Isoborneol; Experiment 44 - Preparation of Methyl
Orange; Experiment 45 - Preparation of Indigo;
Experiment 46 - Formulation of a Paint and Art
Project.
• New essays in this edition: Soap; Dyes.
FEATURES
• OWLv2 is the most trusted online learning solution
for chemistry. Featuring chemist-developed
content, OWLv2 is the only system designed
to elevate thinking through Mastery Learning,
allowing students to work at their own pace until
they understand each concept and skill. Each
time a student tries a problem, OWLv2 changes
the chemistry, values, and sometimes even
the wording of the question to ensure students
are learning the concepts and not cheating the
system. With detailed, instant feedback and
interactive learning resources, students get the
help they need when they need it. Now with
improved student and instructor tools and greater
functionality, OWLv2 is more robust than ever.
Discover the power of OWLv2 and take learning
to a higher level.
• The textbook contains a variety of well-written,
comprehensive, and pre-tested small-scale
experiments using standard-scale (macroscale)
glassware and equipment.
• Essays and examples on contemporary topics,
such as biofuels and nanotechnology are provided
to spark student interest and engage them in the
learning process.
• Green chemistry is now better integrated due to
its importance as a topic for students.
• Infrared, proton NMR, and 13C NMR spectroscopy
106 www.cengageasia.com
is incorporated into many experiments. Some
experiments also have an option to use gas
chromatography-mass spectrometry.
• The authors include introductory, techniques-
based experiments first to meet the needs of
instructors who do not want to jump immediately
into advanced material.
CONTENTS
Introduction.WELCOME TO ORGANIC
CHEMISTRY.Laboratory Safety. Organization of the
Textbook. Advance Preparation. Budgeting Time.
Purpose.PART I: INTRODUCTION TO BASIC
LABORATORY TECHNIQUES.Experiment 1.
Solubility.Experiment 2. Crystallization.Experiment
3. Extraction.Experiment 4. A Separation and
Purification Scheme.Experiment 4A. Extractions
with a Separatory Funnel.Experiment 4B. Extractions
with a Screw-Cap Centrifuge TubeExperiment 5.
Chromatography.Experiment 5A. Thin-Layer
Chromatography.Experiment 5B. Selecting the
Correct Solvent for Thin-Layer Chromatography.
Experiment 5C. Monitoring a Reaction with Thin
Layer Chromatography.Experiment 5D. Column
Chromatography.Experiment 6. Simple and
Fractional DistillationExperiment 7. Infrared
Spectroscopy and Boiling-Point DeterminationEssay.
Aspirin.Experiment 8. Acetylsalicylic Acid.Essay.
Analgesics.Experiment 9. Acetaminophen.Essay.
Identification of Drugs.Experiment 10.TLC Analysis
of Analgesic Drugs.Essay. Caffeine.Experiment 11.
Isolation of Caffeine.Experiment 11A. Extraction of
Caffeine from Tea.Experiment 11B. Isolation of
Caffeine from a Tea Bag.Essay. Esters--Flavors and
Fragrances.Experiment 12: Isopentyl Acetate
(Banana Oil).Essay, Terpenes and Phenylpropanoids.
Experiment 13. Isolation of Eugenol from Cloves.
Essay. Stereochemical Theory of Odor.Experiment
14. Spearmint and Caraway Oil: (+)- and (-)-
Carvones.Essay.The Chemistry of Vision.
Experiment 15. Isolation of Chlorophyll and
Carotenoid Pigments from Spinach.Essay: Ethanol
and Fermentation Chemistry.Experiment 16.
Ethanol from Sucrose.PART II: INTRODUCTION
TO MOLECULAR MODELING.Essay: Molecular
Modeling and Molecular Mechanics.Experiment 17.
An Introduction to Molecular Modeling.Experiment
17A. The Conformations of n-Butane: Local Minima.
Experiment 17B. Cyclohexane Chair and Boat
Conformations.Experiment 17C. Substituted
Cyclohexane Rings (Critical Thinking Exercise).
Experiment 17D. cis- and trans-2-Butene.Essay:
Computational Chemistry - Ab initio and
Semiempirical Methods.Experiment 18.
Computational Chemistry.Experiment 18A. Heats
of Formation: Isomerism, Tautomerism, and
Regioselectivity.Experiment 18B. Heats of
Reactions: SN1 Reaction Rates.Experiment 18C.
Density-Electrostatic Potential. Maps: Acidities of
Carboxylic Acids.Experiment 18D. Density
-Electrostatic Potential Maps: Carbocations.
Experiment 18E. Density -LUMO Maps: Reactivities
of Carbonyl Groups.PART III: PREPARATIONS
AND REACTIONS OF ORGANIC COMPOUNDS.
Experiment 19. Reactivities of Some Alkyl Halides.
Experiment 20. Nucleophilic Substitution Reactions:
Competing NucleophilesExperiment 20A. Competing
Nucleophiles with 1-Butanol or 2-Butanol.Experiment
20B. Competing Nucleophiles with 2-Methyl-2-
Propanol.Experiment 20C. Analysis.Experiment 21.
Synthesis of n-Butyl Bromide and t-Pentyl Chloride.
Experiment 21A. n-Butyl Bromide.Experiment 21B.
t-Pentyl Chloride.Experiment 22.
4-MethylcyclohexenEssay. Fats and Oils.Experiment
23. Methyl Stearate from Methyl Oleate.Essay:
SoapExperiment 24. Preparation of Soap.Essay:
Petroleum and Fossil Fuels.Experiment 25. Gas
Chromatographic Analysis of Gasolines.Essay:
Biofuels.Experiment 26. Biodiesel.Experiment 26A.
Biodiesel from Coconut Oil.Experiment 26B.
Biodiesel from Other Oils.Experiment 26C. Analysis
of Biodiesel.Essay: Green Chemistry.Experiment
27. Chiral Reduction of Ethyl Acetoacetate; Optical
Purity Determination.Experiment 27A. Chiral
Reduction of Ethyl Acetoacetate.Experiment 27B.
NMR Determination of the Optical Purity of Ethyl
(S)-3-Hydroxybutanoate.Experiment 28. Nitration of
Aromatic Compounds Using a Recyclable Catalyst.
Experiment 29. Reduction of Ketones Using Carrots
as Biological Reducing AgentsExperiment 30.
Resolution of (+/-)-alpha-Phenylethylamine and
Determination of Optical Purity.Experiment 30A.
Resolution of (+/-)-alpha-Phenylethylamine.
Experiment 30B. Determination of Optical Purity
Using NMR and a Chiral Resolving Agent.Experiment
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31. An Oxidation-Reduction Scheme: Borneol,
Camphor, Isoborneol.Experiment 32. Multistep
Reaction Sequences: The Conversion of
Benzaldehyde to Benzilic Acid.Experiment 32A.
Preparation of Benzoin by Thiamine Catalysis.
Experiment 32B. Preparation of Benzil.Experiment
32C. Preparation of Benzilic Acid.Experiment 33.
Triphenylmethanol and Benzoic Acid.Experiment
33A. Triphenylmethanol.Experiment 33B. Benzoic
Acid.Experiment 34. Aqueous-Based Organozinc
Reactions.Experiment 35. Sonogashira Coupling of
Iodosubstituted Aromatic Compounds with Alkynes
Using a Palladium Catalyst.Experiment 36. Grubbs
Catalyzed Metathesis of Eugenol with 1,4-Butenediol
to Prepare a Natural Product.Experiment 37. The
Aldol Condensation Reaction: Preparation of
Benzalacetophenones (Chalcones).Experiment 38.
A Green Enantioselective Aldol Condensation
Reaction.Experiment 39. Preparation of an ,-
Unsaturated Ketone via Michael and Aldol
Condensation Reactions.Experiment 40. Preparation
of Triphenylpyridine.Experiment 41. 1,4-Diphenyl-
1,3-Butadiene.Experiment 42. Relative Reactivities
of Several Aromatic Compounds.Experiment 43.
Nitration of Methyl Benzoate.Essay: Synthetic Dyes.
Experiment 44. Preparation of Methyl Orange.
Experiment 45. Preparation of Indigo.Experiment
46. Formulation of a Paint and Art Project.Essay.
Local Anesthetics.Experiment 47. Benzocaine.
Essay. Pheromones: Insect Attractants and
Repellants.Experiment 48. N,N-Diethyl-m-
toluamide: The Insect Repellent “OFF.”Essay: Sulfa
Drugs.Experiment 49. Sulfa Drugs: Preparation of
Sulfanilamide.Essay: Polymers and Plastics.
Experiment 50. Preparation and Properties of
Polymers: Polyester, Nylon, and Polystyrene.
Experiment 50A. Polyesters.Experiment 50B.
Polyamide (Nylon).Experiment 50C. Polystyrene.
Experiment 50D. Infrared Spectra of Polymer
Samples.Experiment 51. Ring-Opening Metathesis
Polymerization (ROMP) Using a Grubbs Catalyst:
A Three Step Synthesis of a Polymer.Experiment
51A. Diels-Adler Reaction.Experiment 51B.
Conversion of the Diels-Adler Adduct to the Diester.
Experiment 51C. Synthesizing the Polymer by Ring-
Opening Metathesis Polymerization ROMP)Essay.
Diels–Alder Reaction and Insecticides.Experiment
107
 52. The Diels–Alder Reaction of Cyclopentadiene Technique 11. Crystallization: Purification of Solids.
with Maleic Anhydride.Experiment 53. Diels-Adler Technique 12. Extractions, Separations, and Drying
Reaction with Anthracine-9-Methanol.Experiment Agents.Technique 13. Physical Constants of
54. Photoreduction of Benzophenone and Liquids: The Boiling Point and Density.Technique
Rearrangement of Benzpinacol to Benzopinacolone. 14. Simple Distillation.Technique 15. Fractional
Experiment 54A. Photoreduction of Benzophenone. Distillation, Azeotropes.Technique 16. Vacuum
Experiment 54B. Synthesis of -Benzopinacolone: Distillation, Manometers.Technique 17. Sublimation.
The Acid-Catalyzed Rearrangement of Benzpinacol. Technique 18. Steam Distillation.Technique 19.
Essay. Fireflies and Photochemistry.Experiment 55. Column Chromatography.Technique 20. Thin-Layer
Luminol.Essay. The Chemistry of Sweeteners. Chromatography.Technique 21. High-Performance
Experiment 56. Carbohydrates.Experiment 57. Liquid Chromatography (HPLC).Technique 22. Gas
Analysis of a Diet Soft Drink by HPLC.Part IV: Chromatography.Technique 23. Polarimetry.
IDENTIFICATION OF ORGANIC SUBSTANCES. Technique 24. Refractometry.Technique 25.
Experiment 58. Identification of Unknowns. Infrared Spectroscopy.Technique 26. Nuclear
Experiment 58A. Solubility Tests.Experiment 58B. Magnetic Resonance Spectroscopy (Proton NMR).
Tests for the Elements (N, S, X).Experiment 58C. Technique 27. Carbon-13 Nuclear Magnetic
Tests for Unsaturation.Experiment 58D. Aldehydes Resonance Spectroscopy.Technique 28. Mass
and Ketones.Experiment 58E. Carboxylic Acids. Spectrometry.Technique 29. Guide to the Chemical
Experiment 58F. Phenols.Experiment 58G. Amines. LiteratureAppendix 1: Tables of Unknowns and
Experiment 58H. Alcohols.Experiment 58I. Esters. Derivatives.Appendix 2: Procedure for Preparing
PART V: PROJECT-BASED EXPERIMENTS. Derivatives.Appendix 3: Index of Spectra.
Experiment 59. Preparation of a C-4 or C-5 Acetate
© 2016, 1024pp, Hardback, 9781305253926
Ester.Experiment 60. Competing Nucleophiles in
SN1 and SN2 Reactions: Investigations Using
2-Pentanol and 3-Pentanol.Experiment 61. Friedel-
Crafts Acylation.Experiment 62. The Analysis of
Antihistamine Drugs by Gas Chromatography-Mass
Spectrometry.Experiment 63. Carbonation of an
Unknown Aromatic Halide.Experiment 64. The
Aldehyde Enigma.Experiment 65. Synthesis of
Substituted Chalcones: A Guided-Inquiry
Experience.Experiment 66. Green Epoxidation of
Chalcones.Experiment 67. Cyclopropanation
Reactions of Chalcones.Experiment 68. Michael
and Aldol Condensation Reactions.Experiment 69.
Esterification Reactions of Vanillin: The Use of NMR
to Determine a Structure.PART VI: THE
TECHNIQUES.Technique 1. Laboratory Safety.
Technique 2. The Laboratory Notebook, Calculations,
and Laboratory Records.Technique 3. Laboratory
Glassware: Care and Cleaning.Technique 4. How
to Find Data for Compounds: Handbooks and
Catalogues.Technique 5. Measurement of Volume
and Weight.Technique 6. Heating and Cooling
Methods.Technique 7. Reaction Methods.Technique
8. Filtration.Technique 9. Physical Constants of
Solids: The Melting Point.Technique 10. Solubility.

108 www.cengageasia.com

EXPERIMENTAL ORGANIC
CHEMISTRY, 6E
A Miniscale & Microscale Approach
John C. Gilbert, Santa Clara University, Santa Clara, CA;
Stephen F. Martin, University of Texas at Austin
Providing even more emphasis on inquiry-based
learning and student collaboration and featuring
three new green experiments and more than a dozen
newly developed experiments, this Sixth Edition
of Gilbert and Martin’s proven EXPERIMENTAL
ORGANIC CHEMISTRY contains procedures for
both miniscale (also known as small scale) and
microscale users. The book offers an early focus
on equipment, record keeping, and safety in the
laboratory, and then guides students step by step
through the theoretical and mechanistic principles
underlying the experiments and the laboratory
techniques needed to perform them with confidence.
Students learn how to use a range of experimental
techniques to synthesize compounds and analyze
their properties, complete multi-step syntheses
of organic compounds, and solve structures
of unknown compounds. New experiments in
Chapter 17 and 18 demonstrate the potential of
chiral agents in fostering enantioselectivity and of
performing solvent-free reactions. The bioorganic
experiment in Chapter 24 reflects the increasing
emphasis on bioorganic chemistry in the course
and gives students an opportunity to accomplish
a mechanistically interesting and synthetically
important coupling of two -amino acids to produce
a dipeptide.
NEW TO THIS EDITION
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• With three new green experiments and over a
dozen newly developed experiments (in chapters
3, 10, and 14-20) this edition is considerably
enhanced to provide a comprehensive lab
experience for students.
• To make room for new experiments, Chapters
25 (Identifying Organic Compounds) and 26
(The Literature of Organic Chemistry) have been
moved online.
• All images have been checked, with many revised
and updated as needed.
• New spectra have been added and are available
online.
• OWLv2 with LabSkills and MindTap Reader:
Featuring chemist-developed content, OWLv2 with
LabSkills is the only system designed to elevate
thinking through Mastery Learning. Developed to
prepare students for their lab sessions through
pre-lab assignments, this new OWLv2 course
includes LabSkills pre-lab techniques, a MindTap
Reader of the lab manual, and pre and post-
lab content specific to the experiments. With
detailed, instant feedback and interactive learning
resources, students get the help they need when
they need it.
FEATURES
• Safety is emphasized through “Safety Alerts” and
“Wrapping It Up” sections that highlight possible
hazards and proper disposal of spent chemicals.
• Fascinating “Historical Highlights” familiarize
students with the lives of chemical pioneers who
have advanced the field of chemistry.
• Accurately drawn art shows students how to set
up an experiment with confidence.
• Margin drawings of equipment remind students
about the set up for such techniques as distillation
and reflux.
• Each experiment begins with a thorough discussion
of the theory and procedures involved and lays
out experimental procedures in a clear format to
enhance student understanding.
CONTENTS
1. Introduction, Record Keeping, and Laboratory
Safety.2. Techniques and Apparatus.3. Solids:
Recrystallization and Melting Points.4. Liquids:
Distillation and Boiling Points.5. Extraction.6.
109
 Chromatography.7. Stereoisomers.8. Spectral
Methods.9. Alkanes.10. Alkenes.11. Alkynes.12.
Dienes: The Diels-Alder Reaction.13. Kinetic
and Thermodynamic Control of a Reaction.14.
Nucleophilic Aliphatic Substitution: Preparation
of Alkyl Halides.15. Electrophilic Aromatic
Substitution.16. Oxidation of Alcohols and Carbonyl
Compounds.17. Reduction Reactions of Double
Bonds: Alkenes, Carbonyl Compounds, and
lmines.18. Reactions of Carbonyl Compounds.19.
Organometallic Chemistry.20. Carboxylic Acids
and Their Derivatives.21. Multistep Organic
Synthesis.22. Polymers.23. Carbohydrates.24.
Amino Acids and Peptides.25. Identifying Organic
Compounds (ONLINE ONLY).26. The Literature of
Organic Chemistry (ONLINE ONLY).
© 2016, 960pp, Hardback, 9781305080461
ORGANIC CHEMISTRY, 9E
John E. McMurry, Cornell University
The most trusted and best-selling text for
organic chemistry just got better! Updated with
more coverage of nuclear magnetic resonance
spectroscopy, expanded with new end-of-chapter
mechanism problems and Practice Your Scientific
Reasoning and Analysis questions, and enhanced
with OWLv2, the latest version of the leading online
homework and learning system for chemistry, John
McMurry’s ORGANIC CHEMISTRY continues
to set the standard for the course. The Ninth
Edition also retains McMurry’s hallmark qualities:
comprehensive, authoritative, and clear. McMurry
has developed a reputation for crafting precise
110 www.cengageasia.com
and accessible texts that speak to the needs
of instructors and students. More than a million
students worldwide from a full range of universities
have mastered organic chemistry through his
trademark style, while instructors at hundreds of
colleges and universities have praised his approach
time and time again.
NEW TO THIS EDITION
• D i s c u s s i o n s o f N M R s p e c t r o s c o p y a n d
opportunities to practice mechanism problems
have been expanded substantially for this 9th
edition.
• Mechanism problems at the ends of chapters
are now grouped together so that they are easily
located and recognized.
• More than 200 new end-of-chapter problems
have been added, with a particular emphasis on
mechanism-drawing practice.
• Nomenclature in many figures has been updated
for consistency, so that infix numerical bonding
positions appear immediately before the suffix.
• Seven new Practice Your Scientific Analysis and
Reasoning essays and corresponding MCAT-
style questions, with topics focused on the latest
developments in the medical, pharmaceutical or
biological application of organic chemistry.
• The most powerful online learning solution for
chemistry is better than ever. OWLv2 now has
more flexible student and instructor functionality,
new personalized study tools, enhanced
integration with learning management systems,
and improved analytics. For this course, OWLv2
also includes Quick Prep (a short course to review
key chemistry concepts and essential skills),
hundreds of new interactive versions of the end-
of-chapter questions from the text with hints and
directed feedback, and Mechanism Activities,
Tutors, Visualizations and Simulations that have
been converted from Flash to HTML, allowing for
easier navigation and streamlined grading.
FEATURES
• OWLv2 is the most trusted online learning solution
for chemistry. Featuring chemist-developed
content, OWLv2 is the only system designed
to elevate thinking through Mastery Learning,
allowing students to work at their own pace until
 they understand each concept and skill. Each
time a student tries a problem, OWLv2 changes
the, chemistry, values, and sometimes even
the wording of the question to ensure students
are learning the concepts and not cheating the
system. With detailed, instant feedback and
interactive learning resources, students get the
help they need when they need it. Now with
improved student and instructor tools and greater
functionality, OWLv2 is more robust than ever.
Discover the power of OWLv2 and take learning
to a higher level.
• IMPROVED CHAPTER-ENDING PROBLEM
ORGANIZATION. End-of-chapter problems
are now grouped by type to assist professors
in assigning problems and students in solving
them. Mechanism-type problems have now been
given their own section in chapters containing
mechanism problems.
• U N I Q U E “ V I S U A L I Z I N G C H E M I S T R Y ”
PROBLEMS. These problems challenge students
to make the essential connection between typical
line-bond drawings and computer-generated
molecular models. “Visualizing Chemistry”
problems enhance your students’ ability to
bridge the gap between the microscopic level of
molecules and the macroscopic level of daily life.
• HOLISTIC OVERVIEWS. At two key points,
McMurry provides an “Overview” to help students
grasp the subject matter more holistically. The first
“Overview” offers a review of organic mechanisms,
while the second discusses the cohesiveness of
carbonyl group reactions.
CONTENTS
1. Structure and Bonding.2. Polar Covalent Bonds;
Acids and Bases.3. Organic Compounds: Alkanes
and Their Stereochemistry.4. Organic Compounds:
Cycloalkanes and Their Stereochemistry5.
Stereochemistry at Tetrahedral Centers.6. An
Overview of Organic Reactions.7. Alkenes:
Structure and Reactivity.Practice Your Scientific
Analysis and Reasoning I: The Chiral Drug
Thalidomide8. Alkenes: Reactions and Synthesis.9.
Alkynes: An Introduction to Organic Synthesis.10.
Organohalides.11. Reactions of Alkyl Halides:
Nucleophilic Substitutions and Eliminations.Practice
Your Scientific Analysis and Reasoning II: From
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Mustard Gas to Alkylating Anticancer Drugs12.
Structure Determination: Mass Spectrometry and
Infrared Spectroscopy.13. Structure Determination:
Nuclear Magnetic Resonance Spectroscopy.14.
Conjugated Compounds and Ultraviolet
Spectroscopy.15. Benzene and Aromaticity.
Practice Your Scientific Analysis and Reasoning
III: Photodynamic Therapy (PDT)16. Chemistry of
Benzene: Electrophilic Aromatic Substitution.17.
Alcohols and Phenols.18. Ethers and Epoxides;
Thiols and Sulfides.Preview of Carbonyl
Chemistry.19. Aldehydes and Ketones: Nucleophilic
Addition Reactions.Practice Your Scientific Analysis
and Reasoning IV: SSRIs 20. Carboxylic Acids and
Nitriles.21. Carboxylic Acid Derivatives: Nucleophilic
Acyl Substitution Reactions.22. Carbonyl Alpha-
Substitution Reactions.23. Carbonyl Condensation
Reactions.Practice Your Scientific Analysis and
Reasoning V: Thymine in DNA24. Amines and
Heterocycles.25. Biomolecules: Carbohydrates.26.
Biomolecules: Amino Acids, Peptides, and Proteins.
Practice Your Scientific Analysis and Reasoning VI:
Melatonin and Serotonin27. Biomolecules: Lipids.28.
Biomolecules: Nucleic Acids.29. The Organic
Chemistry of Metabolic Pathways.30. Orbitals
and Organic Chemistry: Pericyclic Reactions.31.
Synthetic Polymers.Practice Your Scientific
Analysis and Reasoning VII: The Potent Antibiotic
of Endiandric Acid C.
© 2016, 1416pp, Hardback, 9781305080485
111
 CHEMICAL PRINCIPLES FOR
ORGANIC CHEMISTRY
Robert Boikess, Rutgers, the State University of New Jersey
To help students succeed in the much tougher and
more rigorous Organic Chemistry class, CHEMICAL
PRINCIPLES FOR ORGANIC CHEMISTRY
presents all of the necessary topics from General
Chemistry in the way that organic chemists use
them. The book helps students “unlearn” some of
the approaches they learned in General Chemistry,
learn new or different ones, and successfully apply
concepts from General Chemistry to Organic
Chemistry.
FEATURES
• This relatively short ancillary text presents all of
the necessary topics from General Chemistry in
the way organic chemists use them.
• This book greatly simplifies the task of getting
students up to speed in the Organic Chemistry
course by teaching them how to apply concepts
from General Chemistry to Organic Chemistry.
CONTENTS
1. Valence Bond Theory.2. Molecular Orbital
Theory.3. Acids and Bases.4. Thermochemistry and
Thermodynamics.5. Chemical Kinetics.
© 2015, 224pp, Paperback, 9781285457697
112
ORGANIC CHEMISTRY, 3E
With Biological Applications, Hybrid Edition (with
OWLv2 24-Months Printed Access Card)
John E. McMurry, Cornell University
Renowned for its student-friendly writing style
and fresh perspective, this fully updated Third
Edition of John McMurry’s ORGANIC CHEMISTRY
WITH BIOLOGICAL APPLICATIONS provides
full coverage of the foundations of organic
chemistry--enhanced by biological examples
throughout. In addition, McMurry discusses the
organic chemistry behind biological pathways.
New problems, illustrations, and essays have been
added. Media integration with OWL for Organic
Chemistry, a customizable online learning system,
and assessment tool, reduces faculty workload,
facilitates instruction, and helps students master
concepts through tutorials, simulations, and
algorithmically-generated homework questions.
NEW TO THIS EDITION
• WHY THIS CHAPTER? now begins each chapter;
it is a brief introduction about the material being
covered, why it is important and how the organic
chemistry in the chapter relates to biological
chemistry.
• Figure and table references in the text are now
in color to help reference them. All figure legends
now begin with a boldface title to help students
easily identify their content.
• SOMETHING EXTRA essays end each chapter
and tie the chapter content to relevant real-world
material. Some new essays include, “Organic
Foods,” and “Dental Anesthetics.”
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• Many new problems have been included at the
end of chapters.
• Some new content includes: Mercury-catalyzed
alkyne hydration (Chapter 8); Enols and
tautomerization (Chapter 8); Conversion of
alcohols to alkyl fluorides (Chapter 12); Organic
coupling reactions (Chapter 12); Base-induced
epoxide cleavage (Chapter 13); Killiani-Fischer and
Whol degradation (Chapter 21); Prostaglandins
and other eicosanoids (Chapter 23).
• An increase in the number of Organic OWL
questions for the online homework system.
• The #1 online homework and learning system
for chemistry, OWLv2, is available for this text--
now with new instructor features and enhanced
functionality: a Dashboard that consolidates
all course materials; easy, intuitive assignment
creation and management; ability to preview and
select activities/questions for each assignment;
new assignment settings and options; improved
gradebook; Personalized Study tools to help
students focus their time on the key concepts and
skills; and MindTap Reader™, a new eBook with
apps and embedded video. OWLv2 courses for
Gen Chem, GOB, Organic, and Liberal Arts now
include Quick Prep essential skills assignments
that can be taken before the semester begins
or during the first few weeks, to help students
succeed in the course. For this course, OWLv2
also includes new interactive versions of the end-
of-chapter questions from the text and new iPad-
compatible visualizations and tutorials.
FEATURES
• EARLIER COVERAGE OF STEREOCHEMISTRY
AND SPECTROSCOPY. Chirality and
stereochemistry at tetrahedral centers, a topic
crucial to understanding biological chemistry,
appears early in Chapter 5.
• ENHANCED PROBLEMS. To enhance problem-
solving and visualization skills, McMurry uses
many multi-step problems and reduces the
number of drill-type problems.
• VERTICAL FORMAT FOR CHEMICAL AND
BIOCHEMICAL REACTION MECHANISMS.
Mechanisms are printed with action steps
vertically, alongside annotations for each step
next, so students can see what is occurring at each
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step in a reaction without having to jump back and
forth between the text and structures.
CONTENTS
1. Structure and Bonding.2. Polar Covalent Bonds;
Acids and Bases.3. Organic Compounds: Alkanes
and Their Stereochemistry.4. Organic Compounds:
Cycloalkanes and Their Stereochemistry.5.
Stereochemistry at Tetrahedral Centers.6. An
Overview of Organic Reactions.7. Alkenes and
Alkynes.8. Reactions of Alkenes and Alkynes.9.
Aromatic Compounds.10. Structure Determination:
Mass Spectrometry, Infrared Spectroscopy, and
Ultraviolet Spectroscopy.11. Structure Determination:
Nuclear Magnetic Resonance Spectroscopy.12.
Organohalides: Nucleophilic Substitutions and
Eliminations.13. Alcohols, Phenols, and Thiols;
Ethers and Sulfides: A Preview of Carbonyl
Chemistry 14. Aldehydes and Ketones: Nucleophilic
Addition Reactions.15. Carboxylic Acids and
Nitriles.16. Carboxylic Acid Derivatives: Nucleophilic
Acyl Substitution Reactions.17. Carbonyl Alpha-
Substitution and Condensation Reactions.18.
Amines and Heterocycles.19. Biomolecules: Amino
Acids, Peptides, and Proteins.20. Amino Acid
Metabolism.21. Biomolecules: Carbohydrates.22.
Carbohydrate Metabolism.23. Biomolecules: Lipids
and Their Metabolism.24. Biomolecules: Nucleic
Acids and Their Metabolism.e25. Secondary
Metabolites: An Introduction to Natural Products
Chemistry.e26. Orbitals and Organic Chemistry:
Pericyclic Reactions.e27. Synthetic Polymers.
© 2015, 992pp, Paperback, 9781285867847
113

CTE ORGANIC CHEMISTRY WITH CB
COURSESMART EBOOK, 7E
William H. Brown, Beloit College; Brent L. Iverson, University
of Texas, Austin; Eric Anslyn, University of Texas at Austin;
Christopher S. Foote, University of California, Los Angeles
Please note that the digital access code that comes
with the print book is valid for use in a specific Asia
territory only.CB CourseSmart eBook – The ultimate
eBook experience has arrived! Easily access our
eBooks with features that will improve your reading
experience, and tools to help you take notes and
organize your studies.Succeed in the course
with this student-friendly, proven text. Designed
throughout to help you master key concepts and
improve your problem-solving skills, CHEMISTRY,
Seventh Edition includes a running margin glossary,
end-of-chapter in-text mini study guides, a focus
on “how to” skills, and more in-chapter examples
and problems than any text on the market. To help
you understand reaction mechanisms, the authors
offset them in a stepwise fashion and emphasize
similarities between related mechanisms using
just four different characteristics: breaking a bond,
making a new bond, adding a proton, and taking
a proton away. Thoroughly updated throughout,
the book offers numerous biological examples for
premed students, unique roadmap problems, a wide
range of in-text learning tools, and integration with
an online homework and tutorial system, which now
includes an interactive multimedia eBook.
NEW TO THIS EDITION
• MCAT PROBLEMS: To better prepare students for
the upcoming new MCAT exam, the new edition
114 www.cengageasia.com
includes MCAT PRACTICE: PASSAGE AND
PROBLEMS throughout the text. First students
read the organic chemistry-related essay and
then answer a series of multiple-choice questions.
• NEW PRIMERS: Two new primers (Developing
a Reaction Mechanism before Chapter 6 and
Carboxylic Acid Derivative Reaction Mechanisms
before Chapter 18) set key and possibly difficult
concepts apart for easy reference to enhance
student understanding.
• NEWLY-DRAWN ORGANIC CHEMISTRY
REACTION ROADMAPS: Creating a cumulative,
graphical representation of the different reactions
students encounter in the context of important
functional groups, the organic chemistry roadmaps
help students visualize how to interconvert
different functional groups (which often require
different reactions from different chapters) by
simply identifying the most direct path on the
roadmap. New pull‐out cards show the roadmaps
in sequential order.
• REVISED REACTION ROADMAP PROBLEMS:
These unique problems relate to the authors’
organic chemistry roadmap (see above), which
compares organic chemistry to a roadmap, with
functional groups analogous to cities and reactions
analogous to the roads between them.
• FIVE NEW “HOW TO” BOXES: Integrated
throughout the text at strategic points, the new
boxes show students: “How To: Quickly Figure
Out Formal Charge,” “How To: Quickly Recognize
the Hybridization and Geometry of Atoms,” “How
To: Quickly Draw and Recognize Enantiomers
and Diastereomers,” “How To: Retrosynthetically
Dissect an Amine into the Proper Starting
Materials for a Reductive Amination,” and “How
To: Recognize Aromatic Compounds: Criteria
and Caveats.”
CONTENTS
1. Covalent Bonding and Shapes of Molecules.2.
Alkanes and Cycloalkanes.3. Stereochemistry and
Chirality.4. Acids and Bases.5. Alkenes.Primer I:
Reaction Mechanisms6. Reactions of Alkenes.7.
Alkynes.8. Haloalkanes, Halogenation, and
Radical Reactions.9. Nucleophilic Substitution and
B-Elimination.10. Alcohols.11. Ethers, Sulfides, and
Epoxides.12. Infrared Spectroscopy.13. Nuclear
Magnetic Resonance Spectroscopy.14. Mass
Spectrometry.15. Introduction to Organometallic
Compounds.16. Aldehydes and Ketones.17.
Carboxylic Acids.Primer II: Carboxylic Acid
Derivative Reaction Mechanisms.18. Functional
Derivatives of Carboxylic Acids.19. Enolate Anions
and Enamines.20. Dienes, Conjugated Systems,
and Pericyclic Reactions.21. Benzene and the
Concept of Aromaticity.22. Reactions of Benzene
and Its Derivatives.23. Amines.24. Catalytic Carbon–
Carbon Bond Formation.25. Carbohydrates.26:
Lipids.27. Amino Acids and Proteins.28. Nucleic
Acids.29. Organic Polymer Chemistry.Appendices:1.
Thermodynamics and the Equilibrium Constant.2.
Major Classes of Organic Acids.3. Bond Dissociation
Enthalpies.4. Characteristic 1H-NMR Chemical
Shifts.5. Characteristic 13C Chemical Shifts.6.
Characteristic IR Absorption Frequencies.7.
Electrostatic Potential Maps.8. Summary of
Stereochemical Terms.9. Summary of the Rules
of Nomenclature.10. Common Mistakes in Arrow
Pushing.11. Organic Chemistry Roadmaps.
GLOSSARY G-1.INDEX I-1.
© 2014, 920pp, Paperback, 9789814617833
www.cengageasia.com
ORGANIC CHEMISTRY, HYBRID
EDITION (WITH OWLV2 24-MONTHS
PRINTED ACCESS CARD), 7E
William H. Brown, Beloit College; Brent L. Iverson, University
of Texas, Austin; Eric Anslyn, University of Texas at Austin;
Christopher S. Foote, University of California, Los Angeles
Providing a modern introduction to organic
chemistry for students majoring in chemistry,
health, and the biological sciences, this revised and
updated edition of ORGANIC CHEMISTRY is both
student-friendly and cutting-edge and incorporates
the latest advances in the field. Professors Brown,
Iverson, and Anslyn have all won teaching awards
at their respective schools, and they use their
skills to build upon the text’s hallmarks of unified
mechanistic themes, focused problem-solving,
use of applied problems from the pharmaceutical
field, and unrivaled visuals. Thoroughly updated
throughout, the book offers numerous biological
examples for pre-med students, a wide range of
in-text learning tools, and integration with both a
homework and tutorial system and an interactive
multimedia eBook. To help students understand
reaction mechanisms, the authors offset them in
a stepwise fashion and emphasize similarities
between related mechanisms using just four
different characteristics: breaking a bond, making
a new bond, adding a proton and taking a proton
away. Organic chemistry reaction roadmaps take
a center stage in this edition with new pull-out
maps designed in a stepwise manner by chapter.
These roadmaps will help students to devise their
own reaction pathways.Numerous resources help
ensure student success in the course, including a
115
 running margin glossary, a mini end-of-chapter in-
text study guide, and more in-chapter examples than
any other text on the market. Emphasizing “how-
to” skills, this edition is packed with challenging
synthesis problems, medicinal chemistry problems,
and unique roadmap problems.
NEW TO THIS EDITION
• MCAT PROBLEMS: To better prepare students for
the upcoming new MCAT exam, the new edition
includes MCAT PRACTICE: PASSAGE AND
PROBLEMS throughout the text. First students
read the organic chemistry-related essay and
then answer a series of multiple-choice questions.
• NEW PRIMERS: Two new primers (Developing
a Reaction Mechanism before Chapter 6 and
Carboxylic Acid Derivative Reaction Mechanisms
before Chapter 18) set key and possibly difficult
concepts apart for easy reference to enhance
student understanding.
• NEWLY-DRAWN ORGANIC CHEMISTRY
REACTION ROADMAPS: Creating a cumulative,
graphical representation of the different reactions
students encounter in the context of important
functional groups, the organic chemistry roadmaps
help students visualize how to interconvert
different functional groups (which often require
different reactions from different chapters) by
simply identifying the most direct path on the
roadmap. New pull‐out cards show the roadmaps
in sequential order.
• REVISED REACTION ROADMAP PROBLEMS:
These unique problems relate to the authors’
organic chemistry roadmap (see above), which
compares organic chemistry to a roadmap, with
functional groups analogous to cities and reactions
analogous to the roads between them.
• FIVE NEW “HOW TO” BOXES: Integrated
throughout the text at strategic points, the new
boxes show students: “How To: Quickly Figure
Out Formal Charge,” “How To: Quickly Recognize
the Hybridization and Geometry of Atoms,” “How
To: Quickly Draw and Recognize Enantiomers
and Diastereomers,” “How To: Retrosynthetically
Dissect an Amine into the Proper Starting
Materials for a Reductive Amination,” and “How
To: Recognize Aromatic Compounds: Criteria
and Caveats.”
116 www.cengageasia.com
FEATURES
• P R E S E N T A T I O N O F M E C H A N I S M S :
Mechanisms are presented in a clear, stepwise
fashion with written commentary accompanying
each mechanistic step so verbal learners can learn
alongside more visually oriented learners. Many
mechanisms have been broken into more steps
to increase student understanding. In addition,
the authors emphasize similarities between
related mechanisms using just four different
characteristics: breaking a bond, making a new
bond, adding a proton, and taking a proton away. A
new primer (right before Chapter 6) on Developing
a Reaction Mechanism sets this material apart for
easy reference.
• VISUAL IMPACT: This text is distinguished by
its striking, full-color art program (250 pieces of
numbered art and over 1,000 pieces of in-text art).
The Seventh Edition paints a detailed picture of
the orbital nature of electron density in Chapter
1 by focusing on the interplay between the two
complementary approaches to orbital descriptions:
valence bond theory and molecular orbital theory.
High-quality photos show organic chemistry as
it occurs in the laboratory and in everyday life;
electrostatic potential maps illustrate structure and
reactivity; the spectra in the book reflects the latest
imagery; and the book includes state-of-the-art,
mathematically accurate molecular models.
• “HOW-TO” BOXES: To facilitate student success
in the course, insightful “How-To” boxes highlight
the survival skills necessary to learn and master
organic chemistry. Integrated throughout the text
at key points, these essential skills include “How
To: Draw Curved Arrows and Push Electrons,”
“How To: Draw Chiral Molecules,” “How To:
Solve NMR Spectral Problems,” and many more.
Five new How To boxes to this edition are, “How
To: Quickly Figure Out Formal Charge,” “How
To: Quickly Recognize the Hybridization and
Geometry of Atoms,” “How To: Quickly Draw and
Recognize Enantiomers and Diastereomers,”
“How To: Retrosynthetically Dissect an Amine
into the Proper Starting Materials for a Reductive
Amination,” and “How To: Recognize Aromatic
Compounds: Criteria and Caveats.”
• BIOLOGY CONNECTION: Although still a
 predominantly synthetic organic chemistry text,
the book explicitly links concepts to biological
chemistry topics--drawing in biology majors,
pre-med students, and others who will soon go
on to biochemistry. “Connections to Biological
Chemistry” boxes discuss the applications of
organic chemistry to biology to a wide range of
topics.
• REACTIONS IN CONTEXT: These problems
apply organic chemistry to medicinal chemistry
and the pharmaceutical sciences.
CONTENTS
1. Covalent Bonding and Shapes of Molecules.2.
Alkanes and Cycloalkanes.3. Stereochemistry and
Chirality.4. Acids and Bases.5. Alkenes.Primer I:
Reaction Mechanisms6. Reactions of Alkenes.7.
Alkynes.8. Haloalkanes, Halogenation, and
Radical Reactions.9. Nucleophilic Substitution and
B-Elimination.10. Alcohols.11. Ethers, Sulfides, and
Epoxides.12. Infrared Spectroscopy.13. Nuclear
Magnetic Resonance Spectroscopy.14. Mass
Spectrometry.15. Introduction to Organometallic
Compounds.16. Aldehydes and Ketones.17.
Carboxylic Acids.Primer II: Carboxylic Acid
Derivative Reaction Mechanisms.18. Functional
Derivatives of Carboxylic Acids.19. Enolate
Anions and Enamines.20. Dienes, Conjugated
Systems, and Pericyclic Reactions.21. Benzene
and the Concept of Aromaticity.22. Reactions
of Benzene and Its Derivatives.23. Amines.24.
Catalytic Carbon–Carbon Bond Formation.25.
Carbohydrates.26: Lipids.27. Amino Acids and
Proteins.28. Nucleic Acids.29. Organic Polymer
Chemistry.Appendices:1. Thermodynamics and
the Equilibrium Constant.2. Major Classes of
Organic Acids. 3. Bond Dissociation Enthalpies.4.
Characteristic 1H-NMR Chemical Shifts. 5.
Characteristic 13C Chemical Shifts.6. Characteristic
IR Absorption Frequencies.7. Electrostatic Potential
Maps. 8. Summary of Stereochemical Terms.9.
Summary of the Rules of Nomenclature.10.
Common Mistakes in Arrow Pushing.11. Organic
Chemistry Roadmaps. GLOSSARY G-1.INDEX I-1.
© 2014, 1072pp, Paperback, 9781285426501
www.cengageasia.com
PUSHING ELECTRONS, 4E
Daniel P. Weeks, Northwestern University
This brief supplemental guidebook assists students
in mastering the difficult concept of pushing
electrons that is essential to success in Organic
Chemistry. With an investment of only 12 to 16
hours of self-study your students will have a better
understanding of how to write resonance structures
and will become comfortable with bond-making and
bond-breaking steps in organic mechanisms. The
low-tech, paper-on-pencil approach uses active
involvement and repetition to teach students to
properly push electrons to generate resonance
structures and write organic mechanisms with a
minimum of memorization. Compatible with any
organic chemistry textbook.
NEW TO THIS EDITION
• All structures redrawn with attention to correcting
all bond lengths and angles.
• Updated and enhanced figures throughout the
book.
• A new chapter added on the mechanisms for
making synthetic polymers.
• A new section added on constitutional isomers.
• A new section added on correcting common
mechanistic mistakes.
• Textual revisions to clarify some sections.
FEATURES
• The key to the success of this book is that it
knows its place. It is a supplement that should
be assigned alongside a textbook, not as a
textbook replacement or a standalone product.
117
 The best way to market this book would be to
convince ochem instructors that this will be a
terrific 8-10 hr supplement that will be a great
investment for getting their students up to speed
with mechanisms. This step-by-step mechanistic
approach fills an important hole that textbooks
don’t cover.
• Helps students master to critical concept of
pushing electrons.
• Entire program requires only 12 to 16 hours of
students time through self-study.
• A paper-on-pencil approach uses active
involvement and repetition to teach the student.
CONTENTS
1. Lewis Structures.2. Resonance Structures.3.
Mechanisms.4. On Solving Mechanism Problems.5.
Some Reactiosn from Biochemistry.
© 2014, 224pp, Paperback, 9781133951889
A MICROSCALE APPROACH
TO ORGANIC LABORATORY
TECHNIQUES, INTERNATIONAL
EDITION, 5E
Donald L. Pavia, Western Washington University; George
S. Kriz, Western Washington University; Gary M. Lampman,
Western Washington University; Randall G. Engel, North
Seattle Community College
From biofuels, green chemistry, and nanotechnology,
this proven laboratory textbook provides the up-to-
date coverage students need in their coursework
and future careers. The book’s experiments, all
designed to utilize microscale glassware and
equipment, cover traditional organic reactions and
syntheses, the isolation of natural products, and
118 www.cengageasia.com
molecular modeling and include project-based
experiments and experiments that have a biological
or health science focus. Updated throughout with
new and revised experiments, new and revised
essays, and revised and expanded techniques,
the Fifth Edition is organized based on essays and
topics of current interest.
NEW TO THIS EDITION
• A new essay on Biofuels enhances this edition’s
“in the news” topics.
• Two new Green Chemistry experiments involve
techniques such as solid phase extraction and the
use of a microwave reaction system.
• In two experiments, chiral gas chromatography
is now included in the analysis of the products
obtained.
• Eight new experiments have been added:
Experiment 2, Solubility; Experiment 27,
Biodiesel; Experiment 34, Sonogashira Coupling
of Iodosubstituted Aromatic Compounds with
Alkynes Using a Palladium Catalyst; Experiment
35, Grubbs-Catalyzed Metathesis of Eugenol
with 1,4-Butanediol to Prepare a Natural
Product; Experiment 48: Diels-Alder Reaction
with Anthracene-9-methanol; Experiment 59,
Synthesis of Naproxen (Aleve®) by Palladium
Catalysis; Experiment 62, Green Epoxidation of
Chalcones; and Experiment 63, Cyclopropanation
of Chalcones.
• Four experiments have been revised: Experiment
31, An Oxidation-Reduction Scheme: Borneol,
Camphor, Isoborneol; Experiment 44, N,N-
Diethyl-m-toluamide: The Insect Repellant “OFF”;
Experiment 52, Identification of Unknowns; and
Experiment 56, Friedel-Crafts Acylation.
• Essays on Petroleum and Fossil Fuels and The
Chemistry of Sweeteners have been revised.
• Four Techniques have been revised and
expanded: Technique 7, Reaction Methods, has
been extensively revised to include information
on working under an inert atmosphere; Technique
12, Extractions, Separations, and Drying Agents,
now includes new material on instructions on
drawing separation schemes; Technique 25,
Infrared Spectroscopy, now includes the use of
ATR for infrared analysis of solids; and Technique
26, Nuclear Magnetic Resonance Spectroscopy,
 includes new material on analysis of diastereotopic
protons.
• A new method of obtaining boiling points and
monitoring distillations using a temperature
probe with one of the Vernier devices or a digital
thermometer has been introduced.
• The Cengage YouBook, an interactive, electronic
version of the lab manual, allows students to
print and bring to the lab bench only the parts of
the book they need, as well as to watch videos
showing how each technique is executed. Quizzes
in the YouBook test whether students understand
the technique, and results of the quiz can be
submitted to the instructor prior to entering the lab.
FEATURES
• Open-ended experiments allow students to “write”
their own experimental procedures and make their
own discoveries.
CONTENTS
PART I: INTRODUCTION TO BASIC LABORATORY
TECHNIQUES.Experiment 1: Introduction to
Microscale Laboratory.Experiment 2: Solubility.
Experiment 3: Crystallization.Experiment 4:
Extraction.Experiment 5: A Separation and
Purification Scheme.Experiment 6: Chromatography.
Experiment 7: Simple and Fractional Distillation.
Experiment 8: Infrared Spectroscopy and Boiling
Point Determination.ESSAY: Aspirin.Experiment
9: Acetylsalicylic Acid.ESSAY: Analgesics.
Experiment 10: Isolation of the Active Ingredient in
an Analgesic Drug.Experiment 11: Acetaminophen.
ESSAY: Identification of Drugs.Experiment 12: TLC
Analysis of Analgesic Drugs.ESSAY: Caffeine.
Experiment 13: Isolation of Caffeine.ESSAY:
Esters -- Flavors and Fragrances.Experiment
14: Isopentyl Acetate (Banana Oil).ESSAY:
Terpenes and Phenylpropanoids.Experiment 15:
Essential Oils: Extraction of Oil of Cloves by Steam
Distillation.Essay: Stereochemical Theory of Odor.
Experiment 16: Spearmint and Caraway Oil: (+)-
and (-)- Carvones.Essay: The Chemistry
of Vision.Experiment 17: Isolation of Chlorophyll
and Carotenoid Pigments from Spinach.Essay:
Ethanol and Fermentation Chemistry.Experiment
18 Ethanol from Sucrose.PART II: INTRODUCTION
TO MOLECULAR MODELING.ESSAY: Molecular
www.cengageasia.com
Modeling and Molecular Mechanics.Experiment
19: An Introduction to Molecular Modeling.
ESSAY: Computational Chemistry -- Ab initio
and Semiempirical Methods.Experiment 20:
Computational Chemistry.PART III: PROPERTIES
AND REACTIONS OF ORGANIC COMPOUNDS.
Experiment 21: Reactivities of Some Alkyl Halides.
Experiment 22: Nucleophilic Substitution Reactions:
Competing Nucleophiles.Experiment 23: Synthesis
of n-Butyl Bromide and t-Pentyl Chloride.Experiment
24: 4-Methylcyclohexene.ESSAY: Fats and Oils.
Experiment 25: Methyl Stearate from Methyl
Oleate.ESSAY: Petroleum and Fossil Fuels.
Experiment 26: Gas Chromatographic Analysis
of Gasolines.ESSAY: Biofuels.Experiment 27:
Biodiesel.ESSAY: Green Chemistry.Experiment
28: Chiral Reduction of Ethyl Acetoacetate; Optical
Purity Determination Using a Chiral Shift Reagent.
Experiment 29: Nitration of Aromatic Compounds
Using a Recyclable Catalyst.Experiment 30:
Resolution of (Phenylethylamine and
Determination of Optical Purity.Experiment 31: An
Oxidation-Reduction Scheme: Borneol, Camphor,
Isoborneol.Experiment 32: Multi-Step Reaction
Sequences: The Conversion of Benzaldehyde to
Benzilic Acid.Experiment 33: Triphenylmethanol
and Benzoic Acid.Experiment 34: Sonogashira
Coupling of Iodosubstituted Aromatic Compounds
with Alkynes Using a Palladium Catalyst.Experiment
35: Grubbs-Catalyzed Metathesis of Eugenol
with 1,4-Butanediol to Prepare a Natural Product.
Experiment 36: Aqueous-based Organozinc
Reactions.Experiment 37: The Aldol Condensation
Reaction: Preparation of Benzalacetophenones
(Chalcones).Experiment 38: Preparation of an
-Unsaturated Ketone via Michael and Aldol
Condensation Reactions.Experiment 39: The
Wittig Reaction: Preparation of 1,4-Diphenyl-1,3-
butadiene.Experiment 40: Relative Reactivities
of Several Aromatic Compounds.Experiment
41: Nitration of Methyl Benzoate.ESSAY: Local
Anesthetics.Experiment 42: Benzocaine.Experiment
43: Methyl Salicylate (Oil of Wintergreen).ESSAY:
Pheromones: Insect Attractants and Repellents.
Experiment 44: N,N-Diethyl-m-toluamide: The Insect
Repellent “OFF.”ESSAY: Sulfa Drugs.
Experiment 45: Sulfa Drugs: Preparation of
119
 Sulfanilamide.Essay: Polymers and Plastics. Technique 11: Crystallization: Purification of Solids.
Experiment 46: Preparation and Properties of Technique 12: Extractions, Separations, and Drying
Polymers: Polyester, Nylon, and Polystyrene.Essay: Agents.Technique 13: Physical Constants of
Diels-Alder Reactions and Insecticides.Experiment Liquids: The Boiling Point and Density.Technique
47: The Diels-Alder Reaction of Cyclopentadiene 14: Simple Distillation.Technique 15: Fractional
with Maleic Anhydride.Experiment 48: Diels-Alder Distillation, Azeotropes.Technique 16: Vacuum
Reaction with Anthracene-9-methanol.Experiment Distillation, Manometers.Technique 17: Sublimation.
49: Photoreduction of Benzophenone and Technique 18: Steam Distillation.Technique 19:
Rearrangement of Benzpinacol to Benzopinacolone. Column Chromatography.Technique 20: Thin-Layer
ESSAY:Fireflies and Photochemistry.Experiment Chromatography.Technique 21: High-Performance
50: Luminol.ESSAY: The Chemistry of Sweeteners. Liquid Chromatography (HPLC).Technique 22:
Experiment 51: Analysis of a Diet Soft Drink by Gas Chromatography.Technique 23: Polarimetry.
HPLC.PART IV: IDENTIFICATION OF ORGANIC Technique 24: Refractometry.Technique 25:
SUBSTANCES.Experiment 52: Identification Infrared Spectroscopy.Technique 26: Nuclear
of Unknowns.PART V: PROJECT-BASED Magnetic Resonance Spectroscopy.Technique
EXPERIMENTS.Experiment 53: Preparation of a 27: Carbon-13 Nuclear Magnetic Resonance
C-4 or C-5 Acetate Ester.Experiment 54: Isolation SpectroscopyTechnique 28: Mass Spectrometry.
of Essential Oils from Allspice, Cloves, Cumin, Technique 29: Guide to the Chemical Literature.
Caraway, Cinnamon, Fennel, or Star Anise. APPENDICES:Appendix 1: Tables of Unknowns
Experiment 55: Competing Nucleophiles in SN1 and and Derivatives.Appendix 2: Procedures for
SN2 Reactions: Investigations using 2-Pentanol and Preparing Derivatives.Appendix 3: Index of Spectra.
3-Pentanol.Experiment 56: Friedel-Crafts Acylation.
© 2013, 1040pp, Paperback, 9781133107415
Experiment 57: The Analysis of Antihistamine Drugs
by Gas Chromatography-Mass Spectrometry.
Experiment 58: The Use of Organozinc Reagents in
Synthesis: An Exercise in Synthesis and Structure
Proof by Spectroscopy.Experiment 59: Synthesis
of Naproxen by Palladium Catalysis.Experiment 60:
The Aldehyde Enigma.Experiment 61: Synthesis
of Substituted Chalcones: A Guided-Inquiry
Experience.Experiment 62: Green Epoxidation
of Chalcones.Experiment 63: Cyclopropanation
of Chalcones.Experiment 64: Michael and
Aldol Condensation Reactions.Experiment 65:
Esterification Reactions of Vanillin: The Use of NMR
to Solve a Structure Proof Problem.Experiment 66:
An Oxidation Puzzle.PART VI: THE TECHNIQUES.
Technique 1: Laboratory Safety.Technique 2: The
Laboratory Notebook, Calculations, and Laboratory
Records.Technique 3: Laboratory Glassware:
Care and Cleaning.Technique 4: How to Find
Data for Compounds: Handbooks and Catalogues.
Technique 5: Measurement of Volume and Weight.
Technique 6: Heating and Cooling Methods.
Technique 7: Reaction Methods.Technique 8:
Filtration.Technique 9: Physical Constants of
Solids: The Melting Point.Technique 10: Solubility.

120 www.cengageasia.com
 you. Each activity contains “The Big Picture” and
“Common Points of Confusion” sections that steer
students away from common pitfalls and toward
an expert understanding of organic chemistry.
• P R O V E N E F F E C T I V E I N I N C R E A S I N G
STUDENT LEARNING. Students learn best when
they are actively engaged and thinking in class
and working to solve problems and understand
concepts the way real scientists do, by analyzing
data and asking questions. The workbook
activities improve student understanding of
lectures and textbook reading and help them do
ORGANIC CHEMISTRY better on exams. Special “To the Student” sections
Guided Inquiry for Recitation, Volume 2, International
Edition cover the nuts and bolts of using the workbook
Andrei Straumanis, College of Charleston effectively.
CONTENTS
Add the power of guided inquiry to your course without
giving up lecture with ORGANIC CHEMISTRY: A 1. Aromaticity.2. Introduction to EAS. 3. EAS
GUIDED INQUIRY FOR RECITATION, Volume Resonance Effects.4. EAS Competing Effects.5.
II, International Edition. Slim and affordable, the EAS Synthesis Workshop.6. Grignard and Lithium
book covers key Organic 2 topics using POGIL Reagents.7. Nucleophilic Addition-Elimination. 8.
(Process Oriented Guided Inquiry Learning), a Carboxylic Acids and Derivatives.9. Acid Halides and
proven teaching method that increases learning in Anhydrides.10. Enol and Enolate Nucleophiles.11.
organic chemistry. Containing everything you need Aldol Reactions.12. Aldol Condensations.13.
to energize your teaching assistants and students Claisen & Michael Reactions.14. Amines.15. Carbon
during supplemental sessions, the workbook builds (13C) NMR.16. Proton (1H) NMR.Appendix.NW3:
critical thinking skills and includes once-a-week, Naming Aromatic Compounds.NW4: Naming
student-friendly activities that are designed for Carbonyl Compounds.
supplemental sessions, but can also be used in lab,
© 2012, 224pp, Paperback, 9781111578305
for homework, or as the basis for a hybrid POGIL-
lecture approach.
FEATURES
• EASILY ADAPTABLE TO ANY ORGANIC
CHEMISTRY COURSE. This workbook makes
it easy for you to take advantage of the benefits
of Process Oriented Guided Inquiry Learning
(POGIL) without giving up lecture.
• PERFECT FOR TEACHING ASSISTANTS OR
UNDERGRADUATE PEER LEADERS. Designed
to help you get more out of your TA or peer-led
supplemental sessions, this workbook includes
special “To the TA” sections that cover the nuts
and bolts of a successful implementation.
• A WIDE RANGE OF FLEXIBLE ACTIVITIES.
Choose from among the diverse set of
C”hemActivities “that cover key Organic 2 topics
and use them in whatever order works best for

www.cengageasia.com
121
 Confusion” sections that steer students away
from common pitfalls and toward an expert
understanding of organic chemistry.
• P R O V E N E F F E C T I V E I N I N C R E A S I N G
STUDENT LEARNING. Students learn best when
they are actively engaged and thinking in class
and working to solve problems and understand
concepts the way real scientists do, by analyzing
data and asking questions. The workbook
activities improve student understanding of
lectures and textbook reading and help them do
better on exams. Special “To the Student” sections
ORGANIC CHEMISTRY cover the nuts and bolts of using the workbook
A Guided Inquiry for Recitation, Volume 1, International
Edition effectively.
Andrei Straumanis, College of Charleston CONTENTS
Add the power of guided inquiry to your course without 1. Lewis Structures.2. Resonance.3. Constitutional
giving up lecture with ORGANIC CHEMISTRY: A Isomers.4. Cycloalkane Stereoisomers.5. Alkene
GUIDED INQUIRY FOR RECITATION, Volume Stereoisomers.6. Addition to Alkenes.7. Radical
I, International Edition. Slim and affordable, the Halogenation.8. Chiral Centers.9. Absolute
book covers key Organic 1 topics using POGIL Configuration (R/S).10. One-Step Nucleophilic
(Process Oriented Guided Inquiry Learning), a Substitution (SN2).11. Two-Step Nucleophilic
proven teaching method that increases learning in Substitution (SN1).12. Two-Step Elimination
organic chemistry. Containing everything you need (E1).13. One-Step Elimination (E2).14. Sorting out
to energize your teaching assistants and students E1, E2, SN1, SN2.15. Retrosynthesis.16. Carbon
during supplemental sessions, the workbook (13C) NMR.17. Proton (1H) NMR.Appendix.NW1-
includes once-a-week, student-friendly activities Nomenclature of Alkanes.NW2-Introduction to
that are designed for supplemental sessions, but Naming Functional Groups.
can also be used in lab, for homework, or as the
© 2012, 224pp, Paperback, 9781111578299
basis for a hybrid POGIL-lecture approach.
FEATURES
• EASILY ADAPTABLE TO ANY ORGANIC
CHEMISTRY COURSE. This workbook makes
it easy for you to take advantage of the benefits
of Process Oriented Guided Inquiry Learning
(POGIL) without giving up lecture.
• PERFECT FOR TEACHING ASSISTANTS OR
UNDERGRADUATE PEER LEADERS. Designed
to help you get more out of your TA or peer-led
supplemental sessions, this workbook includes
special “To the TA” sections that cover the nuts
and bolts of a successful implementation.
• A WIDE RANGE OF FLEXIBLE ACTIVITIES.
Choose from among 18 “ChemActivities” covering
key Organic 1 topics and use them in whatever
order works best for you. Each activity contains
“The Big Picture” and “Common Points of

122 www.cengageasia.com

ORGANIC CHEMISTRY, 13E
A Brief Course, International Edition
Harold Hart, Michigan State University; Christopher M. Hadad,
Ohio State University; Leslie E. Craine, Central Connecticut
State University; David J. Hart, The Ohio State University
The only textbook designed specifically for the one-
semester short course in organic chemistry, this
market leader appeals to a range of non-chemistry
science majors through its emphasis on practical,
real-life applications, coverage of basic concepts,
and engaging visual style. In contrast to other texts
for the course that are streamlined versions of full-
year texts, this text was created from the ground
up to offer a writing style, approach, and selection
of topics that uniquely meet the needs of the
short course. The Thirteenth Edition builds on the
strengths of previous editions through an updated,
dynamic art program—online, on CD, and in the
text—new content that keeps students current with
developments in the organic chemistry field, and a
revised lab manual.
NEW TO THIS EDITION
• OWL INTEGRATION. Improve student learning
outcomes with OWL, the #1 online homework
and learning system for chemistry. Developed
by chemistry instructors for teaching chemistry,
OWL includes course management tools that
make homework management a breeze, as well
as advanced reporting and grade book features
that save time in grading homework and tracking
student progress. OWL enables you to address
students’ different learning styles through
tutorials, simulations, visualization exercises, and
algorithmically-generated homework questions
with answer-specific feedback. With OWL’s
www.cengageasia.com
mastery learning approach, students work at their
own pace until they understand each concept/
skill. OWL includes an eBook, enhanced with
multimedia learning tools.
• UPDATED ART PROGRAM. The text’s updated,
visually dynamic art program is enhanced online,
on CD, and in the text.
• UPDATED “A WORD ABOUT” ESSAYS.
These engaging essays—now assignable and
accompanied by pedagogy — motivate students
by demonstrating how chemistry relates to other
branches of science and to their everyday lives.
Many of these essays examine emerging issues
in green chemistry while others cover interesting
topics such as Quinones and the Bombadier
Beetle, Alkaloids and the Dart Poison Frog,
Prostaglandins, and Aspirin and Pain.
• UPDATED “A CLOSER LOOK AT” BOXES. These
updated boxes encourage students to develop
their Web research skills by exploring topics
ranging from mass spectrometry and carbon
dating to Nobel laureates and protein chemistry
to the polymerase chain reaction. Instructors may
assign these activities, using them as a basis for
class discussion or as a springboard for projects.
FEATURES
• VISUALLY DYNAMIC ART PROGRAM. The art
program offers beautifully designed electrostatic
potential maps to aid discussions of acid-base
chemistry, as well as ball-and-stick structures
that help students visualize molecules in three
dimensions.
• USE OF ARROW PUSHING FORMALISM. This
assists professors teaching reaction mechanisms.
• WORKED OUT EXAMPLES AND PRACTICE
PROBLEMS. These exercises and problems
guide students through learning and mastering
chapter concepts. End-of-chapter problems
gradually increase in difficulty, reinforcing basic
principles and problem-solving skills before
moving on to more challenging ones.
• ACCOMPANYING LABORATORY MANUAL.
Developed with the assistance of co-author T.K.
Vinod at Western Illinois University, the lab manual
includes an experiment on green chemistry, pre-
laboratory exercises, and safety instructions to
students.
123
 CONTENTS
1. Bonding and Isomerism.2. Alkanes and
Cyclalkanes; Conformational and Geometric
Isomerism.3. Alkenes and Alkynes.4. Aromatic
Compounds.5. Stereoisomerism.6. Organic
Halogen Compounds; Substitution and Elimination
Reactions.7. Alcohols, Phenols, and Thiols.8.
Ethers and Epoxides.9. Aldehydes and Ketones.10.
Carboxylic Acids and Their Derivatives.11. Amines
and Related Nitrogen Compounds.12. Spectroscopy
and Structure Determination.13. Heterocyclic
Compounds.14. Synthetic Polymers.15. Lipids and
Detergents.16. Carbohydrates.17. Amino Acids,
Peptides, and Proteins.18. Nucleotides and Nucleic
Acids.
© 2012, 608pp, Paperback, 9781111426248
ORGANIC CHEMISTRY,
INTERNATIONAL EDITION, 8E
John E. McMurry, Cornell University
The most trusted and best-selling text for organic
chemistry just got better! Updated with the latest
developments, expanded with more end-of-chapter
problems, reorganized to cover stereochemistry
earlier, and enhanced with OWL, the leading online
homework and learning system for chemistry,
John McMurry’s ORGANIC CHEMISTRY, 8e,
International Edition continues to set the standard
for the course. The Eighth Edition also retains
McMurry’s hallmark qualities: comprehensive,
authoritative, and clear. McMurry has developed
a reputation for crafting precise and accessible
texts that speak to the needs of instructors and
students. More than a million students worldwide
124 www.cengageasia.com
from a full range of universities have mastered
organic chemistry through his trademark style, while
instructors at hundreds of colleges and universities
have praised his approach time and time again.
NEW TO THIS EDITION
• IMPROVED CHAPTER-ENDING PROBLEM
ORGANIZATION. End-of-chapter problems are
now grouped by type to assist professors in
assigning problems and students in solving them.
• EARLIER COVERAGE OF STEREOCHEMISTRY.
Stereochemistry now appears earlier in the book
(Chapter 5) to get to this important topic sooner
in the course. In addition, Cahn–Ingold–Prelog
sequence rules are now introduced in Section 5.5.
• REVISISED COVERAGE OF FUNDAMENTAL
TOPICS. The revision of activation energies in
multistep reactions and the update of all bond
dissociation energies in Chapter 6 helps students
to better understand this fundamental topic.
• REVISED END-OF-CHAPTER QUESTIONS IN
OWL. The integrated OWL online learning system
now includes more parameterized end-of-chapter
questions, encouraging students to practice
multiple questions of the same type with different
chemicals, wording, and numbers to ensure their
mastery of the underlying chemical concepts.
OWL also includes an interactive e-version of the
textbook, enhanced with rich multimedia learning
tools and available 24/7 in OWL.
• REVISED “FOCUS ON” BOXES. These end-of-
chapter boxes now present interesting applications
of organic chemistry relevant to the particular
chapter.
• UPDATED FIGURES. To better coordinate
legends with art, step numbers have been added
to the legends of all mechanism figures. In
addition, all figure references have been more
clearly keyed to illustrations via color.
• NEW SUPPLEMENT. SPARTAN MODEL: AN
ELECTRONIC MODEL KIT is now available to
package with the Eighth Edition for those who
want to use this advanced technology resource.
FEATURES
• V E R T I C A L F O R M A T F O R R E A C T I O N
MECHANISMS. McMurry’s hallmark vertical
format is used to explain reaction mechanisms.
 The mechanisms are printed vertically while Proteins.27. Biomolecules: Lipids.28. Biomolecules:
explanations of the changes taking place in each Nucleic Acids.29. The Organic Chemistry of
step are printed next to the reaction arrow. This Metabolic Pathways.30. Orbitals and Organic
allows students to easily see what is occurring Chemistry: Pericyclic Reactions.31. Synthetic
at each step in a reaction without having to jump Polymers.
back and forth between the text and structures.
© 2012, 1376pp, Paperback, 9780840054531
• UNIQUE COVERAGE. McMurry emphasizes
organic synthesis as a teaching device to help
students organize and work with the large body
of factual information that makes up organic
chemistry. He also offers an unusually complete
treatment of the organic chemistry of nucleic acids
and an integrated treatment of polymer chemistry.
• PROBLEM-SOLVING FOCUS. Each chapter
contains many worked out examples with
“Strategy Statements” that illustrate how to solve
problems. Each practice problem and solution is
then followed by a similar problem for the student
to solve. This provides immediate problem-solving
reinforcement for the student.
TECHNIQUES LABS FOR
CONTENTS MACROSCALE AND MICROSCALE
1. Structure and Bonding.2. Polar Covalent Bonds; ORGANIC EXPERIMENTS (WITH
Acids and Bases.3. Organic Compounds: Alkanes COURSEMATE 2-SEMESTER PRINTED
and Their Stereochemistry.4. Organic Compounds: ACCESS CARD), 6E
Cycloalkanes and Their Stereochemistry.5. Kenneth L. Williamson, Mount Holyoke College, Emeritus;
Stereochemistry at Tetrahedral Centers.6. An Katherine M. Masters, Pennsylvania State University
Overview of Organic Reactions.7. Alkenes:
Succeed in your organic laboratory course with
Structure and Reactivity.8. Alkenes: Reactions and
TECHNIQUES LABS FOR MACROSCALE AND
Synthesis.9. Alkynes: An Introduction to Organic
MICROSCALE ORGANIC EXPERIMENTS,
Synthesis.10. Organohalides.11. Reactions of Alkyl
Sixth Edition. This proven, authoritative manual
Halides: Nucleophilic Substitutions and Eliminations.
emphasizes safety and features new experiments
12. Structure Determination: Mass Spectrometry and
that stress greener chemistry, as well as updated
Infrared Spectroscopy.13. Structure Determination:
NMR spectra and a Premium Website that includes
Nuclear Magnetic Resonance Spectroscopy.14.
glassware-specific videos with pre-lab, gradable
Conjugated Compounds and Ultraviolet
exercises. Using the manual’s mix of macroscale
Spectroscopy.15. Benzene and Aromaticity.16.
and microscale experiments, you’ll gain the
Chemistry of Benzene: Electrophilic Aromatic
knowledge and confidence you need to perform a
Substitution.17. Alcohols and Phenols.18. Ethers
wide variety of experiments, as well as experience
and Epoxides; Thiols and Sulfides.Preview of
working with conventionally-sized glassware.
Carbonyl Chemistry.19. Aldehydes and Ketones:
Nucleophilic Addition Reactions.20. Carboxylic NEW TO THIS EDITION
Acids and Nitriles.21. Carboxylic Acid Derivatives: • UPDATED NMR SPECTRA. The authors have
Nucleophilic Acyl Substitution Reactions.22. fully updated NMR spectra throughout the manual.
Carbonyl Alpha-Substitution Reactions.23. • NEW AND UPDATED LABS AND EXPERIMENTS.
Carbonyl Condensation Reactions.24. Amines and Many labs have been updated, and new lab
Heterocycles.25. Biomolecules: Carbohydrates.26. experiments include “A Diels-Alder Reaction
Biomolecules: Amino Acids, Peptides, and

www.cengageasia.com
125
 Puzzle: The Reaction of 2,4-Hexadien-1-ol
with Maleic Anhydride” and “Multicomponent
Reactions: The Aqueous Passerini Reaction, and
Virstatin, a Possible Treatment for Cholera.”
• NEW FOCUS ON GREEN CHEMISTRY. In
addition to providing 10 new experiments that
stress green chemistry, the authors offer tips on
how to “think green” when doing the labs.
• PREMIUM WEBSITE. A new Premium Website
includes glassware-specific videos with pre-lab,
gradable exercises.
• A D D I T I O N A L E X P E R I M E N T S O N T H E
COMPANION WEBSITE. Experiments from
the author’s best-selling MACROSCALE AND
MICROSCALE ORGANIC EXPERIMENTS not
included in this print manual are all available for
download on the companion website
FEATURES
• GREENER CHEMISTRY. Experiments that stress
greener chemistry appear throughout the manual
and are identified with a green chemistry icon. For
example, the use of household bleach is explored
as an alternative to the toxic chromium ion as an
oxidizing agent for cyclohexanol.
• AN EMPHASIS ON LABORATORY SAFETY.
The laboratory safety chapter includes material
on working with closed systems and laboratory
courtesy.
• A STRONG MASS SPECTROMETRY CHAPTER.
The chapter on mass spectrometry describes
time-of-flight and mass quadrupole analyzers and
includes sections on GC-MS and computer-aided
spectral identification, as well as ESI and MALDI
ionization.
• BIOASSAY EXPERIMENTS. The manual’s
bioassay experiments include a bioassay of
eugenol isolated from cloves.
• COMPREHENSIVE COVERAGE. Material is
offered on diffuse reflectance IR analysis, capillary
GC, and temperature programming.
CONTENTS
1. Introduction.2. Laboratory Safety, Courtesy,
and Waste Disposal.3. Melting Points and Boiling
Points.4. Recrystallization.5. Distillation.6. Steam
Distillation, Vacuum Distillation, and Sublimation.7.
Extraction.8. Thin-Layer Chromatography: Analysis
126 www.cengageasia.com
of Analgesics and Isolating Lycopene from Tomato
Paste.9. Column Chromatography: Fluorenone,
Cholesteryl Acetate, Acetylferrocene, and Plant
Pigments.10. Gas Chromatography: Analysis of
Alkene Isomers.11. Infrared Spectroscopy.12.
Nuclear Magnetic Resonance Spectroscopy.13.
Mass Spectroscopy.14. Ultraviolet Spectroscopy,
Refractive Indices, and Qualitative Instrumental
Organic Analysis.15. Computational Chemistry.
© 2012, 336pp, Paperback, 9781111430412
EXPERIMENTAL ORGANIC
CHEMISTRY, 5E
A Miniscale and Microscale Approach, International
Edition
Stephen F. Martin, University of Texas at Austin; John C.
Gilbert, Santa Clara University, Santa Clara, CA
Providing even more emphasis on inquiry-based
learning, a new green experiment, and more than a
dozen new discovery experiments, this Fifth Edition
of Martin and Gilbert’s proven Organic Chemistry Lab
Experiments: Miniscale & Microscale, International
Edition contains procedures for both miniscale (also
known as small scale) and microscale users. The
manual first covers equipment, record keeping,
and safety in the laboratory, then walks students
step by step through the laboratory techniques
they need to perform the book’s experiments with
confidence. Chapters show students how to use
the book’s techniques to synthesize compounds
and analyze their properties, complete multi-
step syntheses of organic compounds, and solve
structures of unknown compounds. A bioorganic
experiment in Chapter 24 reflects the increasing
emphasis on bioorganic chemistry in the course
and gives students an opportunity to accomplish
a mechanistically interesting and synthetically
important coupling of two a-amino acids to produce
a dipeptide.
NEW TO THIS EDITION
• This edition places even more emphasis on
inquiry-based learning, with more than a dozen
new discovery experiments.
• The fifth edition includes new and updated
Historical Highlights on Polymorphs, Performance
Enhancing Drugs, Acetylene, and Chiral Drugs.
• Offers a new green experiment on the Bromination
of (E)-Stilbene.
• Includes video demonstrations of key techniques in
the book in an optional new Premium Companion
Website. The website also contains pre-lab
exercises, proton NMR spectra for analyzing
chemical shifts, integration, and coupling
constants, IR spectra for analyzing functional
groups, MSDS (material safety data sheets) tables
for checking the safe handling of the materials in
each experiment, and derivative tables.
FEATURES
• Emphasizes safety through Safety Alerts and
Wrapping It Up sections that alert students to
possible hazards and proper disposal of spent
chemicals.
• Includes fascinating Historical Highlights, brief
essays that familiarize students with the lives of
chemical pioneers who have advanced the field
of chemistry.
• Includes accurately drawn art to show students
how to set up an experiment with confidence.
• Includes margin drawings of equipment to remind
students about the set up for such techniques as
distillation and reflux.
• This book helps students understand laboratory
techniques by beginning each experiment with a
thorough discussion of the theory and procedures
involved and laying out experimental procedures
in a clear format.
CONTENTS
1. Laboratory Overview.2. Techniques and
Apparatus.3. Recrystallization and Melting Points.4.
Distillation and Boiling Points .5. Extraction.6.
www.cengageasia.com
Chromatography.7. Stereochemistry.8. Spectral
Methods.9. Alkanes.10. Alkenes.11. Alkynes.12.
Dienes and the Diels-Alder Reaction.13. Kinetic
and Thermodynamic Control of a Reaction.14.
Nucleophilic Substitution 451.15. Electrophilic
Aromatic Substitution.16. Oxidation 525.17.
Reduction.18. Carbonyl Compounds 585.19.
Organometallic Chemistry.20. Carboxylic Acids
and Their Derivatives.21. Multistep Synthesis
.22. Polymers.23. Carbohydrates.-Amino Acids
and Peptides.24. 25. Identifying Organic
Compounds.26. The Literature of Organic Chemistry.
© 2011, 960pp, Paperback, 9781439049167
FUNDAMENTALS OF ORGANIC
CHEMISTRY, INTERNATIONAL
EDITION, 7E
John E. McMurry, Cornell University
Retaining the concise, to-the-point presentation that
has already helped thousands of students move
beyond memorization to a true understanding of the
beauty and logic of organic chemistry, this Seventh
Edition of John McMurry’s FUNDAMENTALS OF
ORGANIC CHEMISTRY brings in new, focused
content that shows students how organic chemistry
applies to their everyday lives. In addition,
redrawn chemical structures and artwork help
students visualize important chemical concepts, a
greater emphasis on biologically-related chemistry
(including new problems) helps them grasp the
enormous importance of organic chemistry in
understanding the reactions that occur in living
organisms, and new EOC problems keyed to OWL
allow them to work text-specific problems online.
127
 Finally, for this edition, John McMurry reevaluated
and revised his writing at the sentence level to
ensure that the book’s explanations, applications,
and examples are more student-friendly, relevant,
and motivating than ever before.
NEW TO THIS EDITION
• The problem sets now include additional
biologically-oriented problems in most chapters,
shortened and focused “In the Medicine Cabinet’
and “In the Field” end-of-chapter problems, and
new End of Chapter problems keyed to OWL that
match the text to online homework.
• Redrawn art and chemical structures (as well
as computer-generated Orbitals) help students
visualize chemistry processes and structures.
• Titles have been added to Worked Examples to
provide students with a frame of reference.
• New “Why This Chapter?” explanations in chapter
introductions explain the relevance of chapter
material to students.
• The book’s writing has been revised at the
sentence level to make the presentation even
more student-friendly, relevant, and motivating.
FEATURES
• Clear explanations, thought-provoking examples,
and an innovative vertical format for explaining
reaction mechanisms make the text relevant and
student-friendly.
• Applied chapter openers with associated photos
and molecular models help students see the
relevance of chapter content.
• The text’s full color presentation highlights the
reacting parts of molecules and uses computer-
generated ball-and-stick molecular models to aid
students’ three-dimensional perception.
• Nearly 100 electrostatic potential maps display the
polarity patterns in molecules and the importance
of these patterns in determining chemical
reactivity.
CONTENTS
1. Structure and Bonding; Acids and Bases.2. The
Nature of Organic Compounds: Alkanes.3. The
Nature of Organic Reactions: Alkenes.4. Reactions
of Alkenes and Alkynes.5. Aromatic Compounds.6.
Stereochemistry.7. Alkyl Halides.8. Alcohols,
128 www.cengageasia.com
Phenols, and Ethers.9. Aldehydes and Ketones:
Nucleophilic Addition Reactions.10. Carboxylic Acids
and Derivatives.11. Carbonyl Alpha-Substitution
Reactions and Condensation Reactions.12. Amines.
INTERLUDE: THE ROADMAP OF CHEMICAL
REACTIONS.13. Structure Determination.14.
Biomolecules: Carbohydrates.15. Biomolecules:
Amino Acids, Peptides, and Proteins.16.
Biomolecules: Lipids and Nucleic Acids.17. The
Organic Chemistry of Metabolic Pathways.
© 2011, 672pp, Paperback, 9781439049730
INTRODUCTION TO ORGANIC
LABORATORY TECHNIQUES, 3E
A Small-Scale Approach, International Edition
Randall G. Engel, North Seattle Community College; George
S. Kriz, Western Washington University; Gary M. Lampman,
Western Washington University; Donald L. Pavia, Western
Washington University
Featuring new experiments, a new essay, and new
coverage of nanotechnology, this organic chemistry
laboratory textbook offers a comprehensive
treatment of laboratory techniques including
small-scale and some microscale methods that
use standard-scale (“macroscale”) glassware
and equipment. The book is organized based
on essays and topics of current interest and
covers a large number of traditional organic
reactions and syntheses, as well as experiments
with a biological or health science focus. Seven
introductory technique-based experiments, thirteen
project-based experiments, and sections on green
chemistry and biofuels spark students’ interest and
engage them in the learning process. Instructors
may choose to offer Cengage Learning’s optional
Premium Website, which contains videos on basic
organic laboratory techniques.
NEW TO THIS EDITION
• The Third Edition features a new essay, “Biofuels,”
and two new experiments: Experiment 25,
“Biodiesel” and Experiment 26, “Ethanol from
Corn.”
• Nanotechnology is introduced with a new
demonstration in Experiment 1 forming a self-
assembled monolayer (SAM).
• Coverage of green chemistry is expanded and
revised; and all new spectra are included in
Technique 26 “Nuclear Magnetic Resonance
Spectroscopy (Proton NMR).”
• An expanded section of project-based experiments
now includes a new Experiment 64, “Green
Epoxidation of Chalcones” and a new Experiment
65, “Cyclopropanation Reactions on Chalcones.”
In all of these experiments, students must either
solve a significant problem or they must generate
all or part of a procedure. Intended to promote
critical thinking, these experiments not only
challenge students, but also give them a feeling
of what it is like to “do” research in chemistry.
FEATURES
• The textbook contains a variety of well-written,
comprehensive, and pre-tested small-scale
experiments using standard-scale (macroscale)
glassware and equipment.
• Essays and examples on contemporary topics,
such as biofuels and nanotechnology are provided
to spark student interest and engage them in the
learning process.
• Green chemistry is now better integrated due to
its importance as a topic for students.
• Infrared, proton NMR, and 13C NMR spectroscopy
is incorporated into many experiments. Some
experiments also have an option to use gas
chromatography-mass spectrometry.
• The authors include introductory, techniques-
based experiments first to meet the needs of
instructors who do not want to jump immediately
into advanced material.
CONTENTS
Introduction.WELCOME TO ORGANIC
www.cengageasia.com
CHEMISTRY.Laboratory Safety. Organization of the
Textbook. Advance Preparation. Budgeting Time.
Purpose.Part One: The Techniques.Technique 1:
Laboratory Safety.Technique 2: The Laboratory
Notebook, Calculations, and Laboratory Records.
Technique 3: Laboratory Glassware: Care and
Cleaning.Technique 4: How to Find Data for
Compounds: Handbooks and Catalogs.Technique
5: Measurement of Volume and Weight.Technique
6: Heating and Cooling Methods.Technique 7:
Reaction Methods.Technique 8: Filtration.Technique
9: Physical Constants of Solids: The Melting Point.
Technique 10: Solubility.Technique 11:
Crystallization: Purification of Solids.Technique 12:
Extractions, Separations, and Drying Agents.
Technique 13: Physical Constants of Liquids: The
Boiling Point and Density.Technique 14: Simple
Distillation.Technique 15: Fractional Distillation,
Azeotropes.Technique 16: Vacuum Distillation,
Manometers.Technique 17: Sublimation.Technique
18: Steam Distillation.Technique 19: Column
Chromatography.Technique 20: Thin-Layer
Chromatography.Technique 21: High-Performance
Liquid Chromatography (HPLC).Technique 22: Gas
Chromatography.Technique 23: Polarimetry.
Technique 24: Refractometry.Technique 25:
Infrared Spectroscopy.Technique 26: Nuclear
Magnetic Resonance Spectroscopy (Proton NMR).
Technique 27: Carbon-13 Nuclear Magnetic
Resonance Spectroscopy.Technique 28: 6 Mass
Spectrometry.Technique 29: Guide to the Chemical
Literature.Part Two: Introduction to Basic Laboratory
Techniques.Experiment 1: Solubility.Experiment 2:
Crystallization.Experiment 3: Extraction.Experiment
4: A Separation and Purification Scheme.Experiment
4A: Extractions with a Separatory Funnel.Experiment
5: Chromatography.Experiment 5A: Thin-Layer
Chromatography.Experiment 5B: Selecting the
Correct Solvent for Thin-Layer Chromatography.
Experiment 5C: Monitoring a Reaction with Thin
Layer Chromatography.Experiment 5D: Column
Chromatography.Experiment 6: Simple and
Fractional Distillation.Experiment 7: Infrared
Spectroscopy and Boiling-Point Determination.
Experiment 8: Acetylsalicylic Acid.Experiment 9:
Acetaminophen.Experiment 10: TLC Analysis of
Analgesic Drugs.Experiment 11: Isolation of
129
 Caffeine.Experiment 11A: Extraction of Caffeine
from Tea.Experiment 11B: Isolation of Caffeine from
a Tea Bag.Experiment 12: Isopentyl Acetate
(Banana Oil).Experiment 13: Isolation of Eugenol
from Cloves.Experiment 14: Spearmint and
Caraway Oil: (+)- and (-)-Carvones.Experiment 15:
Isolation of Chlorophyll and Carotenoid Pigments
from Spinach.Experiment 16: Ethanol from Sucrose.
Part Three: Introduction to Molecular Modeling.
Experiment 17: An Introduction to Molecular
Modeling.Experiment 17A: The Conformations of
n-Butane: Local Minima.Experiment 17B:
Cyclohexane Chair and Boat Conformations.
Experiment 17C: Substituted Cyclohexane Rings
(Critical Thinking Exercise).Experiment 17D: cis-
and trans-2-Butene.Experiment 18: Computational
Chemistry.Experiment 18A: Heats of Formation:
Isomerism, Tautomerism, and Regioselectivity.
Experiment 18B: Heats of Reaction: SN1 Reaction
Rates.Experiment 18C: Density–Electrostatic
Potential Maps: Acidities of Carboxylic Acids.
Experiment 18D: Density–Electrostatic Potential
Maps: Carbocations.Experiment 18E: Density–
LUMO Maps: Reactivities of Carbonyl Groups.Part
Four: Preparations and Reactions of Organic
Compounds.Experiment 19: Reactivities of Some
Alkyl Halides.Experiment 20: Nucleophilic
Substitution Reactions: Competing Nucleophiles.
Experiment 20A: Competitive Nucleophiles with
1-Butanol or 2-Butanol.Experiment 20B: Competitive
Nucleophiles with 2-Methyl-2-Propanol.Experiment
20C: Analysis.Experiment 21: Synthesis of n-Butyl
Bromide and t-Pentyl Chloride.Experiment 21A:
n-Butyl Bromide.Experiment 21B: t-Pentyl Chloride.
Experiment 22: 4-Methylcyclohexene.Experiment
23: Methyl Stearate from Methyl Oleate.Experiment
24: Gas-Chromatographic Analysis of Gasolines.
Experiment 25: Biodiesel.Experiment 25A: Biodiesel
from Coconut Oil.Experiment 25B: Biodiesel from
Other Oils.Experiment 25C: Analysis of Biodiesel.
Experiment 26: Ethanol from Corn.Experiment 27:
Chiral Reduction of Ethyl Acetoacetate; Optical
Purity Determination.Experiment 27A: Chiral
Reduction of Ethyl Acetoacetate.Experiment 27B:
NMR Determination of the Optical Purity of Ethyl
(S)-3-Hydroxybutanoate.Experiment 28: Nitration of
Aromatic Compounds Using a Recyclable Catalyst.
130 www.cengageasia.com
Experiment 29: Reduction of Ketones Using Carrots
as Biological Reducing Agents.Experiment 30:
Resolution of (±)-a-Phenylethylamine and
Determination of Optical Purity.Experiment 30A:
Resolution of (±)-a-Phenylethylamine.Experiment
30B: Determination of Optical Purity Using NMR
and a Chiral Resolving Agent.Experiment 31: An
Oxidation-Reduction Scheme: Borneol, Camphor,
Isoborneol.Experiment 32: Multistep Reaction
Sequences: The Conversion of Benzaldehyde to
Benzilic Acid.Experiment 32A: Preparation of
Benzoin by Thiamine Catalysis.Experiment 32B:
Preparation of Benzil.Experiment 32C: Preparation
of Benzilic Acid.Experiment 33: Triphenylmethanol
and Benzoic Acid.Experiment 33A:
Triphenylmethanol.Experiment 33B: Benzoic Acid.
Experiment 34: Aqueous-Based Organozinc
Reactions.Experiment 35: Sonogashira Coupling of
Iodosubstituted Aromatic Compounds with Alkynes
using a Palladium Catalyst.Experiment 36: Grubbs
Catalyzed Metathesis of Eugenol with 1,4-Butenediol
to Prepare a Natural Product.Experiment 37: The
Aldol Condensation Reaction: Preparation of
Benzalacetophenones (Chalcones).Experiment 38:
A Green Enantioselective Aldol Condensation
Reaction.Experiment 39: Preparation of an a,b-
Unsaturated Ketone via Michael and Aldol
Condensation Reactions.Experiment 40: Preparation
of Triphenylpyridine.Experiment 41: 1,4-Diphenyl-
1,3-Butadiene.Experiment 42: Relative Reactivities
of Several Aromatic Compounds.Experiment 43:
Nitration of Methyl Benzoate.Experiment 44:
Benzocaine.Experiment 45: N,N-Diethyl-m-
toluamide: The Insect Repellent “OFF”.Experiment
46: Sulfa Drugs: Preparation of Sulfanilamide.
Experiment 47: Preparation and Properties of
Polymers: Polyester, Nylon, and Polystyrene.
Experiment 49A: Polyesters.Experiment 49B:
Polyamide (Nylon).Experiment 49C: Polystyrene.
Experiment 49D: Infrared Spectra of Polymer
Samples.Experiment 48: Ring-Opening Metathesis
Polymerization (ROMP) Using a Grubbs Catalyst:
A Three-Step Synthesis of a Polymer.Experiment
48A: Diels-Alder Reaction of Furan and Maleic
Anhydride.Experiment 48B: Ring Opening of
Anhydride in Methanol.Experiment 48C: Ring-
Opening Metathesis Polymerization (ROMP).
Experiment 48A: Diels-Adler Reaction.Experiment of Vanillin: The Use of NMR to Determine at
48B: Conversion of the Diels-Adler Adduct to the Structure.Experiment 68: An Oxidation Puzzle.Part
Diester.Experiment 48C: Synthesizing the Polymer Seven: Essays.Essay 1: Aspirin.Essay 2: Analgesics.
by Ring-Opening Metathesis Polymerization Essay 3: Identification of Drugs.Essay 4: Caffeine.
(ROMP).Experiment 49: The Diels–Alder Reaction Essay 5: Esters—Flavors and Fragrances.Essay 6:
of Cyclopentadiene with Maleic Anhydride. Terpenes and Phenylpropanoids.Essay 7:
Experiment 50: Diels-Alder Reaction with Stereochemical Theory of Odor.Essay 8: The
Anthracene-9-methanol.Experiment 51: Chemistry of Vision.Essay 9: Ethanol and
Photoreduction of Benzophenone and Fermentation Chemistry.Essay 10: Molecular
Rearrangement of Benzpinacol to Benzopinacolone. Modeling and Molecular Mechanics.Essay 11:
Experiment 51A: Photoreduction of Benzophenone. Computational Chemistry—ab Intio and
Experiment 51B: Synthesis of b-Benzpinacolone: Semiempirical Methods.Essay 12: Fats and Oils.
The Acid-Catalyzed Rearrangement of Benzpinacol. Essay 13: Petroleum and Fossil Fuels.Essay 14:
Experiment 52: Luminol.Experiment 53: Analysis of Biofuels.Essay 15: Green Chemistry.Essay 16:
A Diet Soft Drink by HPLC.Experiment 54: Local Anesthetics.Essay 17: Pheromones: Insect
Carbohydrates.Part Four: Identification of Organic Attractants.Essay 18: Sulfa Drugs.Essay 19:
Substances.Experiment 55: Identification of Polymers and Plastics.Essay 20: Diels-Alder
Unknowns.Experiment 55A: Solubility Tests. Reaction and Insecticides.Essay 21: Fireflies and
Experiment 55B: Tests of the Elements (N, S, Photochemistry.Essay 22: The Chemistry of
X).Experiment 55C: Tests for Unsaturation. Sweeteners.Appendices.Appendix 1: Tables of
Experiment 55D: Aldehydes and Ketones. Unknowns and Derivatives.Appendix 2: Procedures
Experiment 55E: Carboxylic Acids.Experiment 55F: for Preparing Derivatives.Appendix 3 Index of
Phenols.Experiment 55G: Amines.Experiment 55H: Spectra.
Alcohols.Experiment 55I: Esters.Part Six: Project-
© 2011, 1024pp, Paperback, 9780538733281
Based Experiments.Experiment 56: Preparation of
a C-4 or C-5 Acetate Ester.Experiment 57: Isolation
of Essential Oils from Allspice, Caraway, Cinnamon,
Cloves, Cumin, Fennel, or Star Anise.Experiment
57A: Isolation of Essential Oils by Steam Distillation.
Experiment 57B: Identification of the Constituents
of Essential Oils by Gas Chromatography–Mass
Spectrometry.Experiment 57C: Investigation of the
Essential Oils of Herbs and Spices—A Mini-
Research Project.Experiment 58: Competing
Nucleophiles in SN1 and SN2 Reactions:
Investigations Using 2-Pentanol and 3-Pentanol.
Experiment 59: Friedel–Crafts Acylation.Experiment
60: The Analysis of Antihistamine Drugs by Gas
Chromatography–Mass Spectrometry.Experiment
61: Carbonation of an Unknown Aromatic Halide.
Experiment 62 The Aldehyde Enigma.Experiment
63 Synthesis of Substituted Chalcones: A Guided-
Inquiry Experience.Experiment 64: Green
Epoxidation of Chalcones.Experiment 65:
Cyclopropanation Reactions on Chalcones.
Experiment 66: Michael and Aldol Condensation
Reactions.Experiment 67: Esterification Reactions

www.cengageasia.com
131

ORGANIC EXPERIMENTS, 6E
Macroscale and Microscale, International Edition
Kenneth L. Williamson, Mount Holyoke College, Emeritus;
Katherine M. Masters, Pennsylvania State University
The market leader for the full-year organic
laboratory, this manual derives many experiments
and procedures from the classic Feiser lab text,
giving it an unsurpassed reputation for solid,
authoritative content. The Sixth Edition includes
new experiments that stress greener chemistry,
as well as updated NMR spectra and a Premium
Website that includes glassware-specific videos
with pre-lab, gradable exercises. Offering a flexible
mix of macroscale and microscale options for most
experiments, this proven manual emphasizes safety
and allows instructors to save on the purchase
and disposal of expensive, sometimes hazardous,
organic chemicals. Macroscale versions can be
used for less costly experiments, allowing students
to get experience working with conventionally-sized
glassware.
NEW TO THIS EDITION
• UPDATED NMR SPECTRA. The authors have
fully updated NMR spectra throughout the manual.
• NEW AND UPDATED LABS AND EXPERIMENTS.
Many labs have been updated, and new lab
experiments include “A Diels-Alder Reaction
Puzzle: The Reaction of 2,4-Hexadien-1-ol
with Maleic Anhydride” and “Multicomponent
Reactions: The Aqueous Passerini Reaction, and
Virstatin, a Possible Treatment for Cholera.”
• PREMIUM WEBSITE. A new Premium Website
includes glassware-specific videos with pre-lab,
gradable exercises.
132 www.cengageasia.com
FEATURES
• GREENER CHEMISTRY. Experiments that stress
greener chemistry appear throughout the manual
and are identified with a green chemistry icon. For
example, the use of household bleach is explored
as an alternative to the toxic chromium ion as an
oxidizing agent for cyclohexanol.
• AN EMPHASIS ON LABORATORY SAFETY.
The laboratory safety chapter includes material
on working with closed systems and laboratory
courtesy.
• A STRONG MASS SPECTROMETRY CHAPTER.
The chapter on mass spectrometry describes
time-of-flight and mass quadrupole analyzers and
includes sections on GC-MS and computer-aided
spectral identification, as well as ESI and MALDI
ionization.
• BIOASSAY EXPERIMENTS. The manual’s
bioassay experiments include a bioassay of
eugenol isolated from cloves.
• COMPREHENSIVE COVERAGE. Material is
offered on diffuse reflectance IR analysis, capillary
GC, and temperature programming.
CONTENTS
1. Introduction.2. Laboratory Safety, Courtesy,
and Waste Disposal.3. Melting Points and Boiling
Points.4. Recrystallization.5. Distillation.6. Steam
Distillation, Vacuum Distillation, and Sublimation.7.
Extraction.8. Thin-Layer Chromatography: Analyzing
Analgesics and Isolating Lycopene from Tomato
Paste.9. Column Chromatography: Fluorenone,
Cholesteryl Acetate, Acetylferrocene, and Plant
Pigments.10. Gas Chromatography: Analyzing
Alkene Isomers.11. Infrared Spectroscopy.12.
Nuclear Magnetic Resonance Spectroscopy.13.
Mass Spectrometry.14. Ultraviolet Spectroscopy,
Refractive Indices, and Qualitative Instrumental
Organic Analysis.15. Computational Chemistry.16.
The SN2 Reaction: 1-Bromobutane.17. Nucleophilic
Substitution Reactions of Alkyl Halides.18. Radical
Initiated Chlorination of 1-Chlorobutane.19. Alkenes
from Alcohols: Cyclohexene from Cyclohexanol.20.
Bromination and Debromination: Purification of
Cholesterol.21. Dichlorocarbene.22. Oxidation:
Cyclohexanol to Cyclohexanone; Cyclohexanone
to Adipic Acid.23. The Cannizzaro Reaction:
Simultaneous Synthesis of an Alcohol and an
Acid in the Absence of Solvent.24. Oxidative
Coupling of Alkynes: 2,7-Dimethyl-3,5-octadiyn-
2,7-diol.25. Catalytic Hydrogenation.26. Sodium
Borohydride Reduction of 2-Methylcyclohexanone:
A Problem in Conformational Analysis.27.
Epoxidation of Cholesterol.28. Nitration of
Methyl Benzoate.29. Friedel-Crafts Alkylation
of Benzene and Dimethoxybenzene; Host-
Guest Chemistry.30. Alkylation of Mesitylene.31.
The Friedel-Crafts Reaction: Anthraquinone
and Anthracene.32. Friedel-Crafts Acylation of
Ferrocene: Acetylferrocene.33. Reactions of
Triphenylmethyl Carbocation, Carbanion, and
Radical.34. 1,2,3,4-Tetraphenylnaphthalene
via Benzyne.35. Triptycene via Benzyne.36.
Aldehydes and Ketones.37. Dibenzalacetone by
the Aldol Condensation.38. Grignard Synthesis
of Triphenylmethanol and Benzoic Acid.39.
The Wittig and Wittig-Horner Reactions.40.
Esterification and Hydrolysis.41. Acetylsalicylic
Acid (Aspirin).42. Malonic Ester of a Barbiturate.43.
Amines.44. The Sandmeyer Reaction: 1-Bromo-
4-chlorobenzene, 2-Iodobenzoic Acid, and
4-Chlorotoluene.45. Synthesis and Bioassay
of Sulfanilamide and Derivatives.46. Dyes
and Dyeing.47. Martius Yellow.48. Diels-Alder
Reaction.49. Ferrocene [Bis(cyclopentadienyl)
iron].50. A Diels-Alder Reaction Puzzle: The
Reaction of 2,4-Hexadien-1-ol with Maleic
Anhydride.51. Tetraphenylcyclopentadienone.52.
Hexaphenylbenzene and Dimethyl
Tetraphenylphthalate.53. The Benzoin
Condensation: Catalysis by the Cyanide Ion and
Thiamine.54. Nitric Acid Oxidation; Preparation
of Benzil from Benzoin; and Synthesis of a
.Heterocycle: Diphenylquinoxaline.55. The
Borohydride Reduction of a Ketone: Hydrobenzoin
from Benzil.56. The Synthesis of 2,2-Dimethyl-1,5-
dioxolane; The Acetonide Derivative of a Vicinal
Diol.57. 1,4-Addition: Reductive Acetylation of
Benzil.58. The Synthesis of an Alkyne from an
Alkene; Bromination and Dehydrobromination:
Stilbene and Diphenylacetylene.59. The Perkin
Reaction: Synthesis of α-Phenylcinnamic Acid
and Its Decarboxylation to cis-Stilbene.60.
Multicomponent Reactions: The Aqueous Passerini
Reaction.61. Chemiluminescence: Syntheses of
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Cyalume and Luminol.62. Photochemistry: The
Synthesis of Benzopinacol.63. Carbohydrates and
Sweeteners.64. Virstatin, a Possible Treatment for
Cholera.65. Biosynthesis of Ethanol and Enzymatic
Reactions.66. The Synthesis of Natural Products:
Pseudopellitierene and Camphor.67. Polymers:
Synthesis and Recycling.68. Searching the
Chemical Literature.
© 2011, 880pp, Paperback, 9780538733632
UNDERSTANDING THE PRINCIPLES
OF ORGANIC CHEMISTRY
A Laboratory Course, Reprint, International Edition
Steven F. Pedersen, University of California - Berkeley; Arlyn
M. Myers, University of California - Berkeley
Class-tested by thousands of students and
using simple equipment and green chemistry
ideas, UNDERSTANDING THE PRINCIPLES
OF ORGANIC CHEMISTRY: A LABORATORY
COURSE, International Edition includes 37
experiments that introduce traditional, as well as
recently developed synthetic methods. Offering up-
to-date and novel experiments not found in other
lab manuals, this innovative book focuses on safety,
gives students practice in the basic techniques
used in the organic lab, and includes microscale
experiments, many drawn from the recent literature.
An Online Instructor’s Manual available on the
book’s instructor’s companion website includes
helpful information, including instructors’ notes, pre-
lab meeting notes, experiment completion times,
answers to end-of-experiment questions, video clips
of techniques, and more.
FEATURES
133
 • SAFETY NOTES in each experiment warn
students about potential hazards, CHEMICAL
SAFETY NOTES emphasize the proper handling
of reagents, and TECHNIQUE TIPS give students
guidelines for handling equipment and using
proper procedures.
• REFERENCES TO TOPICS IN UNDERGRADUATE
TEXTBOOKS and/or the primary literature in the
experiments reinforce the importance of what
students are learning in the lecture course and
demonstrate how text material relates to the
laboratory.
• INTRODUCTORY ESSAYS in the experiments
expose students to the history and practical
applications of laboratory science. Within many
experiments, “DID YOU KNOW?” boxes provide
a brief, interesting fact about one of the chemicals
used in the experiment.
• A CONSISTENT FORMAT for each experiment
includes Background Reading, Prelab Checklist,
Experimental Procedure, and Cleanup.
• Instructors may choose to offer the optional
PREMIUM ORGANIC CHEMISTRY
LABORATORY TECHNIQUES WEBSITE, which
contains 33 videos on basic organic laboratory
techniques. Each video has a series of questions
with instant grading and feedback, so students
can test their understanding of the concepts and
email their assessment results to their instructors.
CONTENTS
PART I: THE THEORY AND TECHNIQUES.1.
Safety in the Chemistry Lab.2. The Laboratory
Notebook and the Laboratory Period.3. Where to
Find It: Searching the Literature.4. Things You Need
to Know Before You Begin.5. Properties of Organic
Molecules.6. Characteristic Physical Properties of
Pure Compounds.7. Isolation and Purification of
Compounds.8. Structure Determination.9. Running
a Synthetic Reaction. PART II: THE EXPERIMENTS.
Experiment 1. Calibrating a Pasteur Pipette.
Experiment 2. Investigating Solubility and Acid-Base
Reactions.Experiment 3. Mixed Melting Points.
Experiment 4. Whittling Down the Possibilities:
Identifying an Unknown Using Molecular Dipole
Moment, Solubility, Density and Boiling Point
Data.Experiment 5. Recrystallization and Melting
Points: Recrystallization of Adipic and Salicylic
134 www.cengageasia.com
Acids. Experiment 6. Recrystallization and Melting
Points: Recrystallization of an Unknown Solid and
the Decolorization of Brown Sugar.Experiment 7.
Thin Layer Chromatography (TLC).Experiment 8.
Identification of an Adulterated Herb or Spice by Thin
Layer Chromatography (TLC).Experiment 9. What
Do You Take for Pain? Experiment 10. Nucleophilic
Substitution Reactions of Alkyl Halides.Experiment
11. The Isolation of Trimyristin from Nutmeg.
Experiment 12. The Magtrieve™ Oxidation of
4-Chlorobenzyl Alcohol.Experiment 13. The Sodium
Borohydride Reduction of Benzil and Benzoin.
Experiment 14. The Grignard Reaction: The
Preparation of 1,1-Diphenylethanol.Experiment 15.
The Asymmetric Dihydroxylation of trans-Stilbene.-
PineneExperiment 16. Some Chemistry of Oxide.
Experiment 17. A Dehydrogenation/Hydrogenation
Reaction.Experiment 18. The Friedel-Crafts
Reaction. Experiment 19. Microwave Heating of
Organic Compounds.Experiment 20. The Reaction
of 1,1-Diphenylethanol on Clay in the Presence of
Microwave Radiation.Experiment 21. The Wittig
Reaction.Experiment 22. The Suzuki Reaction.
Experiment 23. The Crossed-Aldol Condensation.
Experiment 24. Identifying the Structure of an
Aldehyde by Qualitative Analysis.Experiment 25.
The Benzoin Reaction.Experiment 26. The Diels-
Alder Reaction.Experiment 27. -ß-Unsaturated
Carboxylic Acid Derivative.Synthesis of an
Experiment 28. The Reaction of 2-Acetylphenyl
Benzoate with Potassium Hydroxide.Experiment
29. The Reaction of 2-Acetylphenyl Benzoate with
Potassium Hydroxide. Experiment 30. Synthesis
of 1,2,3,4-Tetrahydro-â-Carboline.Experiment 31.
Base-Catalyzed Hydrolysis of Nicotinonitrile Using
an Anion-Exchange Resin.Experiment 32. Reactions
of Salicylamide.Experiment 33. The Hunsdiecker
Reaction.Experiment 34. The Investigation of
the Mechanism of a Reaction.Experiment 35.
Monoterpenes and the Ritter Reaction.Experiment
36. Chemoselectivity in Transfer-Hydrogenation
Reactions.
© 2011, 526pp, Paperback, 9781111428174

ORGANIC CHEMISTRY, 2E
A Guided Inquiry
Andrei Straumanis, College of Charleston
Designed for use as a supplement to a traditional
text to encourage active and collaborative learning
in the classroom, this activity book incorporates new
methods for teaching chemistry that reflect current
research on how students learn. The purpose of
the guided inquiry approach is to teach you to
think analytically and collaboratively in teams,
like scientists do, rather than teaching you to
memorize important conclusions arrived at by great
scientists of the past. By looking carefully at new
problems, constructing logical conclusions based
on observations, and discussing the merits of your
conclusions with peers, you’ll develop a stronger
conceptual understanding of and appreciation for
the material. Honing your logical and empirical skills
enables you to better pursue not only chemistry, but
any other complex sets of ideas.
FEATURES
• Unique ChemActivities not found in other texts
and study guides consist of a series of Models,
Critical Thinking Questions, and Skill Development
Exercises that guide student groups in their
exploration of organic chemistry.
• These materials introduce flexibility into a
curriculum, enabling instructors to replace a
lecture with group work on a ChemActivity.
Students work in small groups while the instructor
facilitates and leads whole-class discussions.
Students deepen their scientific understanding
by explaining topics to one another.
• Scientific Models are presented throughout the
chapters in bulleted and illustrated formats,
www.cengageasia.com
assisting conceptual learning.
• Critical Thinking Questions appear after each
Model and ask students to explore the ideas
presented in a number of ways, including drawing
a molecule, completing a table, or writing an
explanation about a topic to another student who
missed class that day. This multi-faceted approach
addresses different learning styles, reinforces
concepts, and can help reveal areas of weak
understanding.
• Exercises following each Model and set of Critical
Thinking Questions are matched to certain models
presented in the chapter, and test students’ ability
to solve problem based on that model.
CONTENTS
Intro Organic Chemistry: a Guided Inquiry.1. Bond
Angles and Shape.2. Lewis Structures.3. Electron
Orbitals.4. Polar Bonds, Polar Reactions.5.
Resonance.6. Alkanes & Alkenes.7. Cycloalkanes.8.
Addition via Carbocation.9. Addition via Cyclic
Intermediate.10. Oxidation and Reduction.11.
Addition to Alkynes.12. Chirality.13. Substitution.14.
Elimination.15. Radical Reactions.16. Synthesis
Workshop 1.17. Conjugation and Molecular
Orbital (MO) Theory.18. Aromaticity.19. EAS:
Electrophilic Aromatic Substitution.20. Acidity and
pKa of Phenols.21. NAS: Nucleophilic Aromatic
Substitution.22. Synthesis Workshop 2.23. Addition
to a Carbonyl.24. Carboxylic Acids & Derivatives.25.
Enolate & Enol Nucleophiles.26. Aldol and Claisen
Reactions.27. Amines.Summary of Synthetic
Transformations.Index.Table of pKa Values by
Structure.
© 2009, 528pp, Paperback, 9780618974122
135

CTE ORGANIC CHEMISTRY WITH
BIOLOGICAL APPLICATIONS WITH CB
COURSESMART EBOOK, 3E
John E. McMurry, Cornell University
Please note that the digital access code that comes
with the print book is valid for use in a specific Asia
territory only.CB CourseSmart eBook – The ultimate
eBook experience has arrived! Easily access our
eBooks with features that will improve your reading
experience, and tools to help you take notes and
organize your studies.Renowned for its student-
friendly writing style and fresh perspective, this fully
updated Third Edition of John McMurry’s ORGANIC
CHEMISTRY WITH BIOLOGICAL APPLICATIONS
provides full coverage of the foundations of organic
chemistry--enhanced by biological examples
throughout. In addition, McMurry discusses the
organic chemistry behind biological pathways.
New problems, illustrations, and essays have been
added. Media integration with OWL for Organic
Chemistry, a customizable online learning system
and assessment tool, reduces faculty workload,
facilitates instruction, and helps students master
concepts through tutorials, simulations, and
algorithmically-generated homework questions.
NEW TO THIS EDITION
• WHY THIS CHAPTER? now begins each chapter;
it is a brief introduction about the material being
covered, why it is important and how the organic
chemistry in the chapter relates to biological
chemistry.
• Figure and table references in the text are now
in color to help reference them. All figure legends
136 www.cengageasia.com
now begin with a boldface title to help students
easily identify their content.
• SOMETHING EXTRA essays end each chapter
and tie the chapter content to relevant real-world
material. Some new essays include, “Organic
Foods,” and “Dental Anesthetics.”
• Many new problems have been included at the
end of chapters.
• Some new content includes: Mercury-catalyzed
alkyne hydration (Chapter 8); Enols and
tautomerization (Chapter 8); Conversion of
alcohols to alkyl fluorides (Chapter 12); Organic
coupling reactions (Chapter 12); Base-induced
epoxide cleavage (Chapter 13); Killiani-Fischer and
Whol degradation (Chapter 21); Prostaglandins
and other eicosanoids (Chapter 23).
• An increase in the number of Organic OWL
questions for the online homework system.
• The #1 online homework and learning system
for chemistry, OWLv2, is available for this text--
now with new instructor features and enhanced
functionality: a Dashboard that consolidates
all course materials; easy, intuitive assignment
creation and management; ability to preview and
select activities/questions for each assignment;
new assignment settings and options; improved
gradebook; Personalized Study tools to help
students focus their time on the key concepts and
skills; and MindTap Reader™, a new eBook with
apps and embedded video. OWLv2 courses for
Gen Chem, GOB, Organic, and Liberal Arts now
include Quick Prep essential skills assignments
that can be taken before the semester begins
or during the first few weeks, to help students
succeed in the course. For this course, OWLv2
also includes new interactive versions of the end-
of-chapter questions from the text and new iPad-
compatible visualizations and tutorials.
CONTENTS
1. Structure and Bonding.2. Polar Covalent Bonds;
Acids and Bases.3. Organic Compounds: Alkanes
and Their Stereochemistry.4. Organic Compounds:
Cycloalkanes and Their Stereochemistry.5.
Stereochemistry at Tetrahedral Centers.6. An
Overview of Organic Reactions.7. Alkenes and
Alkynes.8. Reactions of Alkenes and Alkynes.9.
Aromatic Compounds.10. Structure Determination:
Mass Spectrometry, Infrared Spectroscopy, and
Ultraviolet Spectroscopy.11. Structure Determination:
Nuclear Magnetic Resonance Spectroscopy.12.
Organohalides: Nucleophilic Substitutions and
Eliminations.13. Alcohols, Phenols, and Thiols;
Ethers and Sulfides: A Preview of Carbonyl
Chemistry 14. Aldehydes and Ketones: Nucleophilic
Addition Reactions.15. Carboxylic Acids and
Nitriles.16. Carboxylic Acid Derivatives: Nucleophilic
Acyl Substitution Reactions.17. Carbonyl Alpha-
Substitution and Condensation Reactions.18.
Amines and Heterocycles.19. Biomolecules: Amino
Acids, Peptides, and Proteins.20. Amino Acid
Metabolism.21. Biomolecules: Carbohydrates.22.
Carbohydrate Metabolism.23. Biomolecules: Lipids
and Their Metabolism.24. Biomolecules: Nucleic
Acids and Their Metabolism.e25. Secondary
Metabolites: An Introduction to Natural Products
Chemistry.e26. Orbitals and Organic Chemistry:
Pericyclic Reactions.e27. Synthetic Polymers.
© 2015, 816pp, Paperback, 9789814624886
www.cengageasia.com
CTE ORGANIC CHEMISTRY WITH CB
COURSESMART EBOOK, 7E
William H. Brown, Beloit College; Brent L. Iverson, University
of Texas, Austin; Eric Anslyn, University of Texas at Austin;
Christopher S. Foote, University of California, Los Angeles
Please note that the digital access code that comes
with the print book is valid for use in a specific Asia
territory only.CB CourseSmart eBook – The ultimate
eBook experience has arrived! Easily access our
eBooks with features that will improve your reading
experience, and tools to help you take notes and
organize your studies.Succeed in the course
with this student-friendly, proven text. Designed
throughout to help you master key concepts and
improve your problem-solving skills, CHEMISTRY,
Seventh Edition includes a running margin glossary,
end-of-chapter in-text mini study guides, a focus
on “how to” skills, and more in-chapter examples
and problems than any text on the market. To help
you understand reaction mechanisms, the authors
offset them in a stepwise fashion and emphasize
similarities between related mechanisms using
just four different characteristics: breaking a bond,
making a new bond, adding a proton, and taking
a proton away. Thoroughly updated throughout,
the book offers numerous biological examples for
premed students, unique roadmap problems, a wide
range of in-text learning tools, and integration with
an online homework and tutorial system, which now
includes an interactive multimedia eBook.
NEW TO THIS EDITION
• MCAT PROBLEMS: To better prepare students for
the upcoming new MCAT exam, the new edition
includes MCAT PRACTICE: PASSAGE AND
137
 PROBLEMS throughout the text. First students Spectrometry.15. Introduction to Organometallic
read the organic chemistry-related essay and Compounds.16. Aldehydes and Ketones.17.
then answer a series of multiple-choice questions. Carboxylic Acids.Primer II: Carboxylic Acid
• NEW PRIMERS: Two new primers (Developing Derivative Reaction Mechanisms.18. Functional
a Reaction Mechanism before Chapter 6 and Derivatives of Carboxylic Acids.19. Enolate Anions
Carboxylic Acid Derivative Reaction Mechanisms and Enamines.20. Dienes, Conjugated Systems,
before Chapter 18) set key and possibly difficult and Pericyclic Reactions.21. Benzene and the
concepts apart for easy reference to enhance Concept of Aromaticity.22. Reactions of Benzene
student understanding. and Its Derivatives.23. Amines.24. Catalytic Carbon–
• NEWLY-DRAWN ORGANIC CHEMISTRY Carbon Bond Formation.25. Carbohydrates.26:
REACTION ROADMAPS: Creating a cumulative, Lipids.27. Amino Acids and Proteins.28. Nucleic
graphical representation of the different reactions Acids.29. Organic Polymer Chemistry.Appendices:1.
students encounter in the context of important Thermodynamics and the Equilibrium Constant.2.
functional groups, the organic chemistry roadmaps Major Classes of Organic Acids.3. Bond Dissociation
help students visualize how to interconvert Enthalpies.4. Characteristic 1H-NMR Chemical
different functional groups (which often require Shifts.5. Characteristic 13C Chemical Shifts.6.
different reactions from different chapters) by Characteristic IR Absorption Frequencies.7.
simply identifying the most direct path on the Electrostatic Potential Maps.8. Summary of
roadmap. New pull‐out cards show the roadmaps Stereochemical Terms.9. Summary of the Rules
in sequential order. of Nomenclature.10. Common Mistakes in Arrow
• REVISED REACTION ROADMAP PROBLEMS: Pushing.11. Organic Chemistry Roadmaps.
These unique problems relate to the authors’ GLOSSARY G-1.INDEX I-1.
organic chemistry roadmap (see above), which
© 2014, 920pp, Paperback, 9789814617833
compares organic chemistry to a roadmap, with
functional groups analogous to cities and reactions
analogous to the roads between them.
• FIVE NEW “HOW TO” BOXES: Integrated
throughout the text at strategic points, the new
boxes show students: “How To: Quickly Figure
Out Formal Charge,” “How To: Quickly Recognize
the Hybridization and Geometry of Atoms,” “How
To: Quickly Draw and Recognize Enantiomers
and Diastereomers,” “How To: Retrosynthetically
Dissect an Amine into the Proper Starting
Materials for a Reductive Amination,” and “How
To: Recognize Aromatic Compounds: Criteria
and Caveats.”
CONTENTS
1. Covalent Bonding and Shapes of Molecules.2.
Alkanes and Cycloalkanes.3. Stereochemistry and
Chirality.4. Acids and Bases.5. Alkenes.Primer I:
Reaction Mechanisms6. Reactions of Alkenes.7.
Alkynes.8. Haloalkanes, Halogenation, and
Radical Reactions.9. Nucleophilic Substitution and
B-Elimination.10. Alcohols.11. Ethers, Sulfides, and
Epoxides.12. Infrared Spectroscopy.13. Nuclear
Magnetic Resonance Spectroscopy.14. Mass

138 www.cengageasia.com
 PHYSICAL CHEMISTRY
CTE PHYSICAL CHEMISTRY WITH CB
COURSESMART EBOOK, 2E
David W. Ball, Cleveland State University
Please note that the digital access code that comes
with the print book is valid for use in a specific
Asia territory only.CB CourseSmart eBook – The
ultimate eBook experience has arrived! Easily
access our eBooks with features that will improve
your reading experience, and tools to help you take
notes and organize your studies.With its easy-to-
read approach and focus on core topics, PHYSICAL
CHEMISTRY, 2e provides a concise, yet thorough
examination of calculus-based physical chemistry.
The Second Edition, designed as a learning tool for
students who want to learn physical chemistry in
a functional and relevant way, follows a traditional
organization and now features an increased focus
on thermochemistry, as well as new problems,
new two-column examples, and a dynamic new
four-color design. Written by a dedicated chemical
educator and researcher, the text also includes
a review of calculus applications as applied to
physical chemistry.
NEW TO THIS EDITION
• Chapters 1-8 have been completely revised
for a better examination of the principles of
thermochemistry.
• Design and art have been upgraded from a static
2-color display to a dynamic 4-color design.
This edition’s dynamic, four-color art and photo
program fully complements the text and visually
www.cengageasia.com
reinforces students’ conceptual understanding.
• New two-column in-text examples, where
appropriate, provide students with more
explanation on how to work problems and apply
key concepts.
• An increased number of end-of-chapter problems
provide a wider variety of difficulty.
• A stronger thermochemistry presence appears
throughout the entire book, not just in Chapters
1-8.
FEATURES
• Chapter 9, “Pre-Quantum Mechanics,” a unique
preview to Quantum Mechanics, allows students to
develop a better understanding of the importance,
conclusions, and necessity of the subject by
putting the state of classical science into a
historical context.
CONTENTS
1. Gases and the Zeroth Law of Thermodynamics.2.
The First Law of Thermodynamics.3. The Second
and Third Laws of Thermodynamics.4. Free
Energy and Chemical Potential.5. Introduction
to Chemical Equilibrium.6. Equilibria in Single-
Component Systems.7. Equilibria in Multiple-
Component Systems.8. Electrochemistry and
Ionic Solutions.9. Pre-Quantum Mechanics.10.
Introduction to Quantum Mechanics.11. Quantum
Mechanics: Model Systems and the Hydrogen
Atom.12. Atoms and Molecules.13. Introduction to
Symmetry in Quantum Mechanics.14. Rotational
and Vibrational Spectroscopy.15. Introduction
to Electronic Spectroscopy and Structure.16.
Introduction to Magnetic Spectroscopy.17.
Statistical Thermodynamics: Introduction.18.
More Statistical Thermodynamics.19. The Kinetic
Theory of Gases.20. Kinetics.21. The Solid State:
Crystals.22. Surfaces.Appendixes.Answers to
Selected Exercises.Index.
© 2015, 576pp, Paperback, 9789814624015
139

SPECTROSCOPY
CTE INTRODUCTION TO
SPECTROSCOPY WITH CB
COURSESMART EBOOK, 5E
Donald L. Pavia, Western Washington University; Gary M.
Lampman, Western Washington University; George S. Kriz,
Western Washington University; James A. Vyvyan, Western
Washington University
Please note that the digital access code that comes
with the print book is valid for use in a specific Asia
territory only.CB CourseSmart eBook – The ultimate
eBook experience has arrived! Easily access our
eBooks with features that will improve your reading
experience, and tools to help you take notes and
organize your studies.Gain an understanding
of the latest advances in spectroscopy with
INTRODUCTION TO SPECTROSCOPY. This
proven book provides a systematic introduction
to spectra and basic theoretical concepts in
spectroscopic methods and includes up-to-date
spectra; a modern presentation of one-dimensional
nuclear magnetic resonance (NMR) spectroscopy;
an introduction to biological molecules in mass
spectrometry; and coverage of modern techniques
alongside DEPT, COSY, and HECTOR.
140 www.cengageasia.com
NEW TO THIS EDITION
• NEWEST SPECTRA TECHNIQUES: You can
easily provide students with the latest spectra
techniques, found in Appendix 10, “Index of
Spectra”.
FEATURES
• A TRUSTED, PROVEN RESOURCE: For more
than 30 years, this text has proven to be an
excellent resource for spectroscopy students and
those seeking a solid introductory reference text
on spectroscopy.
• MODERN COVERAGE: The book provides a
modern presentation on one-dimensional NMR
spectroscopy.
• DETAILED COVERAGE: The mass spectrometry
material in Chapter 8 provides a detailed look at
biological molecules for the latest coverage on
this important topic.
• NEWEST SPECTRA TECHNIQUES: The latest
spectra techniques are provided in Appendix 10,
“Index of Spectra”.
• UP-TO-DATE SPECTROGRAPHS: Throughout
the text, spectrographs are created with the latest
techniques to ensure accuracy.
CONTENTS
1. Molecular Formulas and What Can Be
Learned from Them.2. Infrared Spectroscopy.3.
Nuclear Magnetic Resonance Spectroscopy
Part One: Basic Concepts.4. Nuclear Magnetic
Resonance Spectroscopy Part Two: Carbon-13
Spectra, Including Heteronuclear Coupling with
Other Nuclei.5. Nuclear Magnetic Resonance
Spectroscopy Part Three: Spin-Spin Coupling.6.
Nuclear Magnetic Resonance Spectroscopy Part
Four: Other Topics in One-Dimensional NMR.7.
Ultraviolet Spectroscopy.8. Mass Spectrometry.9.
Combined Structure Problems.10. Nuclear Magnetic
Resonance Spectroscopy Part Five: Advanced NMR
Techniques.Answers to Selected Problems.Appendix
1: Infrared Absorption Frequencies of Functional
Groups.Appendix 2: Some Representative Chemical
Shift Values for Various Types of Protons.Appendix
3: Typical Proton Coupling Constants.Appendix
4: Calculation of Proton (1H) Chemical Shifts.
Appendix 5: Calculation of Carbon-13 Chemical
Shifts.Appendix 6: 13C Coupling Constants.
Appendix 7: Tables of Precise Masses and Isotopic
Abundance Ratios for Molecular Ions Under Mass
100 Containing Carbon, Hydrogen, Nitrogen, and
Oxygen.Appendix 8: Common Fragment Ions
Under Mass 105.Appendix 9: Handy-Dandy Guide
to Mass Spectral Fragmentation Patterns.Appendix
10: Index of Spectra.
© 2015, 504pp, Paperback, 9789814624206

www.cengageasia.com
141
 Combined Author/Title Index
A Chemistry, 9e  p.71
A Beginner’s Guide to Scientific Method, International
Edition, 4e  p.78/p.95
A Microscale Approach to Organic Laboratory Techniques,
International Edition, 5e  p.118
Applications of Microsoft® Excel in Analytical Chemistry,
2e p.36
Armstrong, General, Organic, and Biochemistry  p.28
Armstrong, General, Organic, and Biochemistry, 2e  p.8
Armstrong, General, Organic, and Biochemistry, Hybrid
Edition (with OWLv2 24-Months Printed Access Card),
2e p.10
A Small Scale Approach to Organic Laboratory
Techniques, 4e  p.106
Atwood, Lab Manual for Zumdahl/Zumdahl’s Chemistry:
An Atoms First Approach, 2nd, 2e  p.59
Atwood, Survival Guide for General Chemistry with Math
Review, 2e  p.86/p.103
Atwood, Survival Guide for Introductory Chemistry  p.102
B CourseSmart eBook, 9e  p.37
Ball, CTE Physical Chemistry with CB CourseSmart
eBook, 2e  p.139
Basic Laboratory Experiments for General, Organic, and
Biochemistry p.28
Basic Laboratory Experiments for General, Organic, and
Biochemistry, 2e  p.7
Bauer/Birk/Sawyer, Laboratory Inquiry in Chemistry,
3e p.85
Bettelheim/Brown/Campbell/Farrell, Introduction to
General, Organic and Biochemistry, 11e  p.5
Bettelheim/Brown/Campbell/Farrell, Introduction to
General, Organic and Biochemistry, International
Edition, 10e  p.25
Bettelheim/Landesberg, Laboratory Experiments for
Introduction to General, Organic and Biochemistry,
International Edition, 8e  p.26
Biochemistry, International Edition, 5e  p.38
Boikess, Chemical Principles for Organic Chemistry  p.112
Brown/Holme, CTE Chemistry for Engineering Students
with CB CourseSmart eBook, 3e  p.42
Brown/Iverson/Anslyn/Foote, CTE Organic Chemistry with
CB CourseSmart eBook, 7e  p.114/p.138
Brown/Iverson/Anslyn/Foote, Organic Chemistry, Hybrid
Edition (with OWLv2 24-Months Printed Access Card),
7e p.116
C Building, 2e  p.76
Campbell/Farrell, CTE Biochemistry with CB CourseSmart
eBook, 8e  p.40
Carey, A Beginner’s Guide to Scientific Method,
International Edition, 4e  p.78/p.95
Chem p.105
Chem 2, 2e  p.104
Chemical Principles for Organic Chemistry  p.112
Chemistry p.79
Chemistry, 2e  p.57
Chemistry, 3e  p.82
Chemistry, 5e  p.64/p.66
142 www.cengageasia.com
Chemistry, 7e  p.81
Chemistry, 8e  p.58
Chemistry & Chemical Reactivity, Hybrid Edition (with
OWLv2 24-Months Printed Access Card), 9e  p.67
Chemistry for Today, 8e  p.13/p.14
Chemistry, Hybrid Edition (with OWLv2 24-Months Printed
Access Card), 9e  p.74
Chemistry, Hybrid Edition (with OWLv2 24-Months Printed
Access Card), 10e  p.72
Cracolice/Peters, Introductory Chemistry, 5e  p.93
Cracolice/Peters, Introductory Chemistry, Hybrid Edition
(with OWLv2 Printed Access Card), 6e  p.88
CTE Biochemistry with CB CourseSmart eBook, 8e  p.40
CTE Chemical Principles with CB CourseSmart eBook,
7e p.54
CTE Chemistry and Chemical Reactivity with CB
CourseSmart eBook, 9e  p.50/p.55
CTE Chemistry for Engineering Students with CB
CourseSmart eBook, 3e  p.42
CTE Chemistry with CB CourseSmart eBook, 9e  p.43
CTE Chemistry with CB CourseSmart eBook, 10e  p.48
CTE Fundamentals of Analytical Chemistry with CB
CTE General Chemistry with CB CourseSmart eBook,
10e p.47
CTE Introduction to Spectroscopy with CB CourseSmart
eBook, 5e  p.140
CTE Organic Chemistry with Biological Applications with
CB CourseSmart eBook, 3e  p.136
CTE Organic Chemistry with CB CourseSmart eBook,
7e p.114/p.138
CTE Physical Chemistry with CB CourseSmart eBook,
2e p.139
D
Descriptive Inorganic, Coordination, and Solid State
Chemistry, 3e  p.87
E
Ebbing/Gammon, CTE General Chemistry with CB
CourseSmart eBook, 10e  p.47
Engel/Kriz/Lampman/Pavia, Introduction to Organic
Laboratory Techniques, 3e  p.129
Experimental Organic Chemistry, 5e  p.127
Experimental Organic Chemistry, 6e  p.109
Experiments in General Chemistry, 2e  p.84
Experiments in General Chemistry, 6e  p.69
Experiments in General Chemistry: Inquiry and Skill
Experiments in General Chemistry, Lab Manual, 10e  p.78
F
Fundamentals of Organic Chemistry, International Edition,
7e p.128
G
Garrett/Grisham, Biochemistry, International Edition,
5e p.38

General Chemistry (with MindTap Chemistry 24-Months
Printed Access Card)  p.52
General, Organic, and Biochemistry  p.28
General, Organic, and Biochemistry, 2e  p.8
General, Organic, and Biochemistry, Hybrid Edition (with
OWLv2 24-Months Printed Access Card), 2e  p.10
General, Organic, and Biological Chemistry, 7e  p.2
General, Organic, and Biological Chemistry, Hybrid (with
OWLv2 Quick Prep for General Chemistry Printed
Access Card), 7e  p.3
General, Organic, and Biological Chemistry, International
Edition, 6e  p.20
Gilbert/Martin, Experimental Organic Chemistry, 6e  p.109
H Masterton/Hurley, Chemistry, 8e  p.58
Hart/Hadad/Craine/Hart, Organic Chemistry, 13e  p.123
Hogg, Chem 2, 2e  p.104
Holler/Crouch, Applications of Microsoft® Excel in
Analytical Chemistry, 2e  p.36
I McMurry, Organic Chemistry, 9e  p.110
Introduction to Basic Chemistry, International Edition,
7e p.96
Introduction to Chemical Principles, 7e  p.101
Introduction to Chemistry, 7e  p.98
Introduction to General, Organic and Biochemistry,
11e p.5
Introduction to General, Organic and Biochemistry,
International Edition, 10e  p.25
Introduction to Organic Laboratory Techniques, 3e  p.129
Introductory Chemistry, 5e  p.93
Introductory Chemistry, 8e  p.90/p.91
Introductory Chemistry for Today, International Edition,
7e p.31
Introductory Chemistry for Today, International Edition,
8e p.16
Introductory Chemistry, Hybrid Edition (with OWLv2
Printed Access Card), 6e  p.88
J Printed Access Card), 7e  p.116
Joesten/Hogg/Donald R. Neu, Chem  p.105
K Oxtoby/Gillis/Butler, Principles of Modern Chemistry,
Kotz/Treichel/Townsend/Treichel, Chemistry & Chemical
Reactivity, Hybrid Edition (with OWLv2 24-Months
Printed Access Card), 9e  p.67
Kotz/Treichel/Townsend/Treichel, CTE Chemistry and
Chemical Reactivity with CB CourseSmart eBook,
9e p.50/p.55
L Pavia/Kriz/Lampman/Engel, A Small Scale Approach to
Lab Manual for Stoker’s General, Organic, and Biological
Chemistry, 7th, 7e  p.6
Lab Manual for Zumdahl/DeCoste’s Introductory
Chemistry: A Foundation, 8th, 8e  p.93
Lab Manual for Zumdahl/Zumdahl’s Chemistry, 9th,
9e p.77
Lab Manual for Zumdahl/Zumdahl’s Chemistry: An Atoms
www.cengageasia.com
Combined Author/Title Index
First Approach, 2nd, 2e  p.59
Laboratory Experiments for Introduction to General,
Organic and Biochemistry, International Edition, 8e  p.26
Laboratory Inquiry in Chemistry, 3e  p.85
Landesberg, Basic Laboratory Experiments for General,
Organic, and Biochemistry  p.28
Landesberg, Basic Laboratory Experiments for General,
Organic, and Biochemistry, 2e  p.7
Little, Lab Manual for Zumdahl/DeCoste’s Introductory
Chemistry: A Foundation, 8th, 8e  p.93
M
Martin/Gilbert, Experimental Organic Chemistry, 5e  p.127
Masterton/Hurley/Neth, Chemistry, 7e  p.81
McMurry, CTE Organic Chemistry with Biological
Applications with CB CourseSmart eBook, 3e  p.136
McMurry, Fundamentals of Organic Chemistry,
International Edition, 7e  p.128
McMurry, Organic Chemistry, 3e  p.113
McMurry, Organic Chemistry, International Edition,
8e p.124
Moore/Stanitski, Chemistry, 5e  p.64/p.66
Morrison/Atwood/Caughran, Survival Guide for General,
Organic and Biochemistry  p.35
Murov, Experiments in General Chemistry, 6e  p.69
O
Organic and Biochemistry for Today, International Edition,
7e p.32
Organic and Biochemistry for Today, International Edition,
8e p.17
Organic Chemistry  p.121/p.122
Organic Chemistry, 2e  p.135
Organic Chemistry, 3e  p.113
Organic Chemistry, 9e  p.110
Organic Chemistry, 13e  p.123
Organic Chemistry, Hybrid Edition (with OWLv2 24-Months
Organic Chemistry, International Edition, 8e  p.124
Organic Experiments, 6e  p.132
Oxtoby/Gillis/Butler, Principles of Modern Chemistry,
8e p.60
Hybrid Edition (with OWLv2 Printed Access Card),
8e p.62
P
Pavia/Kriz/Lampman/Engel, A Microscale Approach to
Organic Laboratory Techniques, International Edition,
5e p.118
Organic Laboratory Techniques, 4e  p.106
Pavia/Lampman/Kriz/Vyvyan, CTE Introduction to
Spectroscopy with CB CourseSmart eBook, 5e  p.140
Pedersen/Myers, Understanding the Principles of Organic
Chemistry p.134
Principles of Modern Chemistry, 8e  p.60
Principles of Modern Chemistry, Hybrid Edition (with
143


Combined Author/Title Index

OWLv2 Printed Access Card), 8e  p.62 V

Pushing Electrons, 4e  p.118
R MindTap Chemistry 24-Months Printed Access
Reger/Goode/Ball, Chemistry, 3e  p.82
Rodgers, Descriptive Inorganic, Coordination, and Solid
State Chemistry, 3e  p.87
Rosen, The Guide to Surviving General Chemistry,
2e p.53
S Wentworth/Munk, Experiments in General Chemistry, Lab
Safety-Scale Laboratory Experiments for Chemistry for
Today, 7e  p.34
Safety-Scale Laboratory Experiments for Chemistry for
Today, 8e  p.19
Seager/Slabaugh, Chemistry for Today, 8e  p.13/p.14
Seager/Slabaugh, Introductory Chemistry for Today,
International Edition, 7e  p.31
Seager/Slabaugh, Introductory Chemistry for Today,
International Edition, 8e  p.16
Seager/Slabaugh, Organic and Biochemistry for Today,
International Edition, 7e  p.32
Seager/Slabaugh, Organic and Biochemistry for Today,
International Edition, 8e  p.17
Seager/Slabaugh, Safety-Scale Laboratory Experiments
for Chemistry for Today, 7e  p.34
Seager/Slabaugh, Safety-Scale Laboratory Experiments
for Chemistry for Today, 8e  p.19
Skoog/West/Holler/Crouch, CTE Fundamentals of
Analytical Chemistry with CB CourseSmart eBook,
9e p.37
Stanton/Zhu/Atwood, Experiments in General Chemistry,
2e p.84
Stoker, General, Organic, and Biological Chemistry,
7e p.2
Stoker, General, Organic, and Biological Chemistry,
Hybrid (with OWLv2 Quick Prep for General Chemistry
Printed Access Card), 7e  p.3
Stoker, General, Organic, and Biological Chemistry,
International Edition, 6e  p.20
Stoker, Lab Manual for Stoker’s General, Organic, and
Biological Chemistry, 7th, 7e  p.6
Straumanis, Organic Chemistry  p.121/p.122
Straumanis, Organic Chemistry, 2e  p.135
Survival Guide for General Chemistry with Math Review,
2e p.86/p.103
Survival Guide for General, Organic and Biochemistry  p.35
Survival Guide for Introductory Chemistry  p.102
Vining/Young/Day/Botch, General Chemistry (with
Card) p.52
W
Weeks, Pushing Electrons, 4e  p.118
Weiner/Harrison, Introduction to Chemical Principles,
7e p.101
Manual, 10e  p.78
Whitten/Davis/Peck/Stanley, Chemistry, Hybrid Edition
(with OWLv2 24-Months Printed Access Card), 10e  p.72
Whitten/Davis/Peck/Stanley, CTE Chemistry with CB
CourseSmart eBook, 10e  p.48
Williamson/Masters, Organic Experiments, 6e  p.132
Williamson/Masters, Techniques Labs for Macroscale
and Microscale Organic Experiments (with CourseMate
2-Semester Printed Access Card), 6e  p.126
Williamson/Peck, Experiments in General Chemistry:
Inquiry and Skill Building, 2e  p.76
Z
Zumdahl/DeCoste, CTE Chemical Principles with CB
CourseSmart eBook, 7e  p.54
Zumdahl/DeCoste, Introduction to Basic Chemistry,
International Edition, 7e  p.96
Zumdahl/DeCoste, Introduction to Chemistry, 7e  p.98
Zumdahl/DeCoste, Introductory Chemistry, 8e  p.90/p.91
Zumdahl/Zumdahl, Chemistry  p.79
Zumdahl/Zumdahl, Chemistry, 2e  p.57
Zumdahl/Zumdahl, Chemistry, 9e  p.71
Zumdahl/Zumdahl, Chemistry, Hybrid Edition (with OWLv2
24-Months Printed Access Card), 9e  p.74
Zumdahl/Zumdahl, CTE Chemistry with CB CourseSmart
eBook, 9e  p.43
Zumdahl/Zumdahl, Lab Manual for Zumdahl/Zumdahl’s
Chemistry, 9th, 9e  p.77

T
Techniques Labs for Macroscale and Microscale Organic
Experiments (with CourseMate 2-Semester Printed
Access Card), 6e  p.126
The Guide to Surviving General Chemistry, 2e  p.53

U
Understanding the Principles of Organic Chemistry  p.134

144 www.cengageasia.com


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__ 2011 9780538736640 Zumdahl Introduction to Basic Chemistry, International Edition, 7e p.96 208.95
__ 2010 9781439046647 Weiner Introduction to Chemical Principles, 7e p.101 201.95
__ 2011 9780538735438 Zumdahl Introduction to Chemistry, 7e p.98 242.95
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Chemistry, 7th, 7e
__ 2015 9781285845166 Little Lab Manual for Zumdahl/DeCoste’s Introductory p.93 151.95
Chemistry: A Foundation, 8th, 8e
__ 2014 9781133611486 Zumdahl Lab Manual for Zumdahl/Zumdahl’s Chemistry, 9th, 9e p.77 181.95
__ 2016 9781305398313 Atwood Lab Manual for Zumdahl/Zumdahl’s Chemistry: An Atoms p.59 161.95
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__ 2013 9781133113102 Bettelheim Laboratory Experiments for Introduction to General, p.26 193.95
Organic and Biochemistry, International Edition, 8e
__ 2009 9780495113454 Bauer Laboratory Inquiry in Chemistry, 3e p.85 119.95

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__ 2011 9780538734851 Seager Organic and Biochemistry for Today, International p.32 248.95
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__ 2014 9781133607496 Seager Organic and Biochemistry for Today, International p.17 273.95
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__ 2012 9781111578299 Straumanis Organic Chemistry p.122 30.95
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__ 2012 9781111426248 Hart Organic Chemistry, 13e p.123 272.95
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__ 2008 9780495387510 Atwood Survival Guide for General Chemistry with Math Review, p.86/p.103 52.95
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__ 2008 9780495554691 Morrison Survival Guide for General, Organic and Biochemistry p.35 41.95
__ 2009 9780495828266 Atwood Survival Guide for Introductory Chemistry p.102 59.95

T
__ 2012 9781111430412 Williamson Techniques Labs for Macroscale and Microscale Organic p.126 154.95
Experiments (with CourseMate 2-Semester Printed
Access Card), 6e
__ 2015 9781305391383 Rosen The Guide to Surviving General Chemistry, 2e p.53 33.95

U
__ 2011 9781111428174 Pedersen Understanding the Principles of Organic Chemistry p.134 204.95

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CATALOG 2015–2016 • HIGHER EDUCATION • CENGAGE LEARNING ASIA CLA Nov 2014

CATALOG 2015–2016 • HIGHER EDUCATION

Title Highlights
Cengage Technology Editions offer the best in print and digital content to create the kinds of blended learning
experiences that are fast gaining popularity among students. These editions provide hybrid alternatives to best-selling
titles from Cengage Learning in disciplines such as Business and Economics, Science and Mathematics, Social Sciences
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A. see page 43 B. see page 50 C. see page 42 D. see page 40

E. see page 37 F. see page 140 G. see page 136 H. see page 139

A. Chemistry 9e
Zumdahl/Zumdahl; 9789814568715
B. Chemistry and Chemical Reactivity 9e
Kotz/Trichel/Townsend/Trichel;
9789814617796
C. Chemistry for Engineering Students 3e
Brown/Holme; 9789814624862
D. Biochemestry 8e
Campbell/Farrell; 9789814624244
G. Organic Chemistry with Biological
Applications 3e
Chemistry
McMurry; 9789814624886
E. Fundamentals of Analytical Chemistry 9e
Skoog/West/Holler/Crouch; 9789814591447 H. Physical Chemistry 2E
Ball; 9789814624015
F. Introduction to Spectroscopy 5e
Pavia/Lampman/Kriz/Vyvyan;
9789814624206

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