Patrick: An Introduction to Medicinal Chemistry 5e

Chapter 1: Multiple choice questions and answers

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You have answered 13 out of 13 questions correctly.

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Question 1
What type of molecule is the following structure?

Your answer:
c) A phospholipid
Feedback:
The 'phospho' of phospholipid indicates the presence of a phosphate group. The lipid part of the name refers to the two long hydrocarbon
chains. The structure is also known as a phosphoglyceride. Proteins consist of amino acids linked by peptide bonds. Carbohydrates contain
several hydroxyl groups. Nucleic acids consist of nucleic acid bases linked to a sugar phosphate backbone.
Page reference: 3-4

Question 2
Which of the following is an accurate description of the phospholipid bilayer in cell membranes?
Your answer:
d) It is made up of two layers of phospholipid molecules with the tails interacting with each other.
Feedback:
The cell membrane is made up of a bilayer of phospholipid molecules where the hydrophobic tails interact with each other in the centre of
the membrane by van der Waals interactions. The polar head groups interact with water at the outer and inner surfaces of the membrane.
Page reference: 3-4

Question 3
Which of the following statements is true regarding the phospholipid bilayer in cell membranes?
Your answer:
b) Water and ions are unable to cross the bilayer due the hydrophobic tails of the phospholipid molecules.
Feedback:
The tails of the phospholipid molecules are hydrophobic (water hating) and repel water and ions. The polar head groups do not have any
role in preventing water or ions from crossing the cell membrane. The phospholipid molecules are certainly fluid, but no pores are formed as
a result of that.
Page reference: 3-4

Question 4
Which of the following statements is true?
Your answer:

b) Drugs are generally smaller than drug targets.

Feedback:
There are situations where a drug may be a similar size to its target if the drug is a protein, but in the vast majority of cases, drugs are much
smaller than their macromolecular targets.
Page reference: 4-5

Question 5
What is meant by a binding site?
Your answer:
a) The area of a macromolecular target that is occupied by a drug when it binds.
Feedback:
The binding site is part of the macromolecular target and not the drug. It is normally a hollow or cleft on the surface of the target. The
functional groups and regions of the drug that are involved in binding to the binding site are known as the pharmacophore.
Page reference: 4-5

Question 6
Consider the molecule in blue bound to a binding site. Identify the binding interactions taking place at i and iv shown in red.

Your answer:
a) hydrogen bonds
Feedback:
Van der Waals interactions take place between regions of molecules consisting solely of carbon and hydrogen atoms. Ionic bonds occur
between charges of opposite sign. Hydrogen bonds occur between a molecule acting as a hydrogen bond donor (RXH; where X is normally
oxygen or nitrogen), and a molecule acting as hydrogen bond acceptor where a heteroatom is present (normally oxygen or nitrogen).
Page reference: 5-8

Question 7
Consider the molecule in blue bound to a binding site. Identify the binding interactions taking place at iii shown in red.

Your answer:

c) van der Waals interactions

Feedback:
Van der Waals interactions take place between regions of molecules consisting solely of carbon and hydrogen atoms. Ionic bonds occur
between charges of opposite sign. Hydrogen bonds occur between a molecule acting as a hydrogen bond donor (RXH; where X is normally
oxygen or nitrogen), and a molecule acting as hydrogen bond acceptor where a heteroatom is present (normally oxygen or nitrogen).
Page reference: 5-8

Question 8
Consider the molecule in blue bound to a binding site. Identify the binding interactions taking place at ii shown in red.

Your answer:
b) ionic bonds
Feedback:
Van der Waals interactions take place between regions of molecules consisting solely of carbon and hydrogen atoms. Ionic bonds occur
between charges of opposite sign. Hydrogen bonds occur between a molecule acting as a hydrogen bond donor (RXH; where X is normally
oxygen or nitrogen), and a molecule acting as hydrogen bond acceptor where a heteroatom is present (normally oxygen or nitrogen).
Page reference: 5-8

Question 9
Which of the following binding interactions is likely to be the most important initial interaction when a drug enters a binding site?
Your answer:
c) ionic
Feedback:
Ionic interactions fall off in strength more slowly with distance than the other interactions, and so they are likely to be the most important
initial interaction. Van der Waals interactions are the least likely to be important as a molecule approaches its binding site.
Page reference: 5

Question 10
Which of the following underlined atoms is likely to be the strongest hydrogen bond acceptor?
Your answer:
d) carboxylate oxygen (RCO 2-)
Feedback:
Generally, the more electron rich the heteroatom, the better it will be as a hydrogen bond acceptor. Thus, a negatively charged oxygen will
be the best hydrogen bond acceptor. The amide and aniline nitrogens will be poor hydrogen bond acceptors since the lone pair of electrons
in each case interacts with a neighbouring group (carbonyl group and aromatic ring respectively). Therefore, it is not available to form
hydrogen bonds.
Page reference: 6-8

Question 11

Which of the following underlined protons is likely to be the strongest hydrogen bond donor?
Your answer:
d) ammonium ion (RNH3+)
Feedback:
The best hydrogen bond donor will be the one where the hydrogen is the most electron deficient. In the ammonium ion, the nitrogen has a
positive charge and this in turn will make the attached hydrogens electron deficient. The phenol is likely to be the next best hydrogen bond
donor since the oxygen's lone pair of electrons will interact with the aromatic ring giving it a slightly positive charge.
Page reference: 6-8

Question 12
Which of the following functional groups is most likely to participate in a dipole-dipole interaction?
Your answer:
b) Ketone
Feedback:
The ketone will have the strongest dipole moment due to the electronegative oxygen polarising the carbonyl bond. The alcohol will also
have a significant dipole moment, but less than that of the ketone. The alkene and aromatic rings may have small or negligible dipole
moments depending on their substituents.
Page reference: 8-9

Question 13
Which of the following statements is untrue?
Your answer:
d) An increase in entropy results in a greater positive value of G and a greater chance of binding.
Feedback:
An increase in entropy will result in a greater negative value of G and a greater chance of binding. This derives from the equation G = H
TS.
Page reference: 10

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