2 Protons and neutrons have the relative mass of I,
while electrons are of negligible mass.
(d) the structure of a molecule
3 Protons have a charge of +1, while electrons have
a charge ofI. Neutrons are electrically neutral.
11 1 mol is the amount of substance that contains
the same number of atoms as in 12 gof carbon-
4 Proton number is the number of protons in an
atom.
12 constant is the number of particles present in one
mole of a substance It has a salueOf 6.02 x mol-I.
5 Nucleon number is the total number of protons
and neutrons in the atom.
13 Molar mass is the mass of one mole of a
substance.
6 Isotopes are atoms of an element with the same
proton number but with different nucleon numbers
14 One mole of a gas occupies 22.4 dm' at s.t.p. and
24.4 dm' at room conditions, r.t.p.
7 The relative atomic mass is the average mass of
an element compared to 12 the mass of one atom of C-12.
Chapter 2 : Electronic Structure of Atoms
S The parts and functions of a mass spectrometer
are vaporisation chamber to vaporisc solid and liquid samples (b) ionisation chamber 'Aherepositisc ions are formed (c) acceleration chamber where ions are accelerated to high speed (d) magnetic field where ions are deflected according to mie values (e) detector where ions are detected in an ion detector (O recorder where the peaks arc recorded in a mass spectrum 9 Angle of deflection is imcrsely proportional to the m/e value. 10 A mass spectrum can bc used to determine
1 Emission spectrum is a line spectrum consisting
of discrete lines with certain frequencies. The lines in a spectrum become closer as frequency increases. 2 An electron can only occupy a certain energy level. Thus, its energy is quantised. 3 The energy levels in an atom become closer when they are further away from the nucleus and finally converge in the convergence limit. 4 When an electron absorbs energy, it is excited and moves up to higher energy levels. This is an unstable state. Thus, the electron will lose energy and falls back to lower energy levels. The energy is radiated as light with a fixed frequency, v. 5 Lyman series is formed when electrons fall from higher energy levels to n = 1. 6 Balmer series is formed when electrons fall from higher energy levels to n = 2.
7 The energy of an electronic transition can be
calculated from the equation E = hv, where v is the frequency of the line, and h is the Planck's constant. 8 The subenergy levels in an atom are designated by s, p, d and f. 9 An orbital is a region where the probability of finding an electron is maximum. 10 The s-orbitals are spherical while the p-orbitals are dumb-bell shaped. 11 The maximum number of electrons in an energy level = 2n2 12 Each electron can be identified by a set of four quantum numbers. (a) Principal quantum number, n, that determines the energy level of the electron (b) Azimuthal quantum number, l, that determines the shape of the orbitals (c) Magnetic quantum number, m, that determines the orientation of the orbitals in space (d) Electron spin quantum number, s, that determines the direction of spin of the electron 13 The Aufbau principle states that electrons will occupy orbitals of the lowest energy available first before occupying orbitals of higher energy. 14 Pauli exclusion principle states an orbital can only be occupied by two electrons with opposite spins, that is, no two electrons can have the same four quantum numbers. 15 Hund's rule states that the most stable arrangement of electrons in degenerate orbitals is the one with the greatest number of parallel spins. Chapter 3 : Chemical Bonding
1 Ionic bond (electrovalent bond) is the electrostatic
attraction between 2 An ionic bond is formed when one or more than one electrons is/are transferred from valence shell of an atom (metal) to the valence shell of another atom (non-metal). 3 The strength of an ionic bond is proportional to the charge on the ions and inversely proportional to the distance between the ions. 4 Covalent bond (single) is the bond formed when a pair of electrons are shared between two atoms. 5 The covalent bond is formed by the overlapping of atomic orbitals or hybridised orbitals of one atom with another atom. 6 The covalent bond is usually formed between non-metals. 1 The octet rule is the tendency for atoms in compounds to achieve noble gas configurations with eight valence electrons. 8 Electron-pair repulsion theory states that the geometrical arrangement of atoms or groups of atoms around a central atom is determined by electron-pair repulsion in the valence shell of the central atom. 9 The shape of a molecule can be predicted by using (a) the electron-pair repulsion theory, (b) the overlapping of hybridised orbitals. 10 The lone pair of electrons exerts a stronger repulsion effect than a bonding pair of electrons. 11 Hybridisation is the process of mixing together two or more atomic orbitals that have similar energies. 12 When s and p orbitals hybridise, the new orbitals formed are the sp, sp2 and .sp3 hybrid orbitals. 13 The geometry of hybrid orbitals are as follows: sp (linear), sp2 (trigonal planar), and sp3 (tetrahedral).
14 A single bond contains one a-bond, a double
bond contains one a-bond and one It-bond and a triple bond contains one a-bond and two It-bonds. A a-bond is stronger than a It-bond. 15 The strength of a covalent bond depends on bond length and bond strength. Thus the bond strength increases in the order: C C < C < C C. 16 Dipole is a pair of separated positive charge and negative charge in a covalent bond. 17 The presence of dipoles give ionic character to polar covalent molecules. 18 Tetrachloromethane (CC14) is a non-polar molecule eventhough the CCI bonds in it are polar because the molecule has a symmetrical structure. Consequently, the dipoles cancel one another. 19 In a covalent molecule, polarisation is the separation of electric charges in a molecule due to unequal sharing of electrons in a covalent bond. 20 In ionic bonding, polarisation also means the distortion of the charge cloud of a negative ion by
26 The presence of mobile delocalised electrons
explains the electrical conductivity and thermal conductivity of metals. 27 The strength of a metallic bond is proportional to the number of valence electrons and inversely to the atomic size. 28 Van der Waals forces (bond) are weak intermolecular forces, that include both permanent dipole-permanent dipole and temporary dipoleinduced dipole attractions. 29 The larger the molecular size, or the larger the number of electronS 1 oint of the molecule. van der Waals forces, and the higher the melting point or boiling p 30 For organic compounds, a branched chain isomer has a lower bolling point than a straight chain isomer. The more numerous the branches, the lower the boiling point 31 Hydrogen bond is a special type of dipole-dipole interaction that eX1sts between a hydrogen atom which is covalently bonded to a highly electronegative atom (e.g. N, O, F) and the lone pair electron of another highly electronegative atom.
aneighbouring positive ion.
32 The relative strengths of chemical bonds 21 The polarisation of negative ion (anion) by positive ion (cation) gives covalent character to the ionic bond.
Ionic bond covalent bond > hydrogen bond > van
der Waals forces
22 The polarisation of anion by cation increases
when (a) the charge on the cation increases, (b) the size of the cation decreases and (c) the size of the anion increases.
33 The boiling points of the covalent molecules
such as I-IF, 1-120 and NH3, are higher than expected because of hydrogen bonding between the molecules.
23 Nitrogen molecule is inert because of two factors
(a) strong triple bond (NEIN) and (b) nonpolarity of the bond.
34 Ice is less dense than water because the
arrangement of water molecules in ice as a result of extensive hydrogen bonding creates a very open structure.
24 Coordinate bond (dative bond) is a covalent
bond where both electrons in the shared pair are supplied by one of the bonded atoms. 25 Metallic bond is the electrostatic attraction between positive metal ions and the 'sea' of mobile delocalised electrons.
35 Hydrogen bonding also accounts for the
solubility of organic compounds containing the OH, COOH and NH2 groups and the dimerisation of carboxylic acids. Chapter 4:Matter
1 Kinetic theory of gas:
The volume of the gas molecules is negligible compared to the total volume of the gas. There is no intermolecular forces of attraction or repulsion. 2 Boyle's law : P (n, T constant)
collide with the walls of the container, vapour
pressure is produced. 15 A more volatile liquid has a higher vapour pressure, a lower boiling point and a lower enthalpy of vaporisation. 16 crystal lattice is the regular arrangement of particles in a crystal structure. 17 Major types of crystalline solids:
3 Charles' law :Voc T (n, P constant)
Crystalline solid Interparticle forces Example 4 Avogadro's law :Voc n (T, P constant) Ionic Electrostatic attraction NaC1 5 Ideal gas law :PV=nRT Simple molecular Van der Waals or H-bonds 12 6 Dalton's law states that the total pressure of a gas mixture (with no interaction) is the same as the sum of the partial pressures of the gaseous components.
Giant molecular Covalent bond C, Si02
Metallic Metallic bond Cu
7 Partial pressure of a gas in a mixture is the
pressure exerted by the gas if it alone occupies the container at the same temperature. 8 An ideal gas obeys the ideal gas law which states that a gas has no particle volume and no intermolecular forces between the gas molecules. 9 Real gas deviate from ideal behaviour because gas molecules have finite volume, intermolecular forces exist. 10 Real gases exhibit near ideal behaviour at low pressure and high temperature. 11 Real gases deviate significantly from ideal behaviour at high pressure and low temperature. 12 Melting point or freezing point is the temperature at which solid and liquid exist in equilibrium. 13 Boiling point is the temperature where liquid and gas exist in equilibrium, and the vapour pressure equals the external pressure.
18 Allotropes are different structural forms of an
element. 19 Diamond, graphite and fullerene are allotropes of carbon. 20 A phase diagram summarises the relationship between the solid, liquid and gaseous states of a given substance as a function of pressure and temperature. 21 Triple point describes the conditions where all three phases, solid, liquid and gas coexist in equilibrium. 22 Critical point is the temperature above which a gas will not liquefy by an increase in pressure. Beyond the critical temperature, Tc the liquid and vapour phases are indistinguishable. 23 For carbon dioxide, melting point increases as pressure increases. For water, melting point decreases as pressure increases. 24 Addition of non-volatile solute to a solvent
14 Vapour pressure is the pressure exerted by a
vapour in equilibrium with its liquid at a fixed temperature. When the molecules of a vapour
lowers the vapour pressure of the solvent
causes depression of melting point
causes elevation of boiling point
25 Colligative properties depend on the number of solute particles in a solution and not on the nature of the particles.