ZIMBABWE SCHOOL

EXAMINATIONS COUNCIL
(ZIMSEC)

ADVANCED LEVEL SYLLABUS

CHEMISTRY
(9189)

EXAMINATION SYLLABUS FOR 2013 – 2017

CHEMISTRY

CONTENTS PAGE

Introduction 2

Aims 4

Assessment Objectives 6

Scheme of Assessment 8

Structure of Syllabus 11

Subject Content 12

Practical Assessment 61

Mathematical Requirements 68

Glossary of Terms 70

2
INTRODUCTION

This syllabus is designed to give greater flexibility both to teachers and to candidates
and to place greater emphasis on the understanding and application of scientific
concepts and principles. Less emphasis is placed on factual material whilst still giving
a thorough introduction to the study of Chemistry. Teachers should use local examples
where possible to illustrate concepts.

3
AIMS

These are not in order of priority.

Many of these Aims are reflected in the Assessment Objectives which follow; others are not
readily assessed.

The syllabus aims are to:

1 provide, through well designed studies of experimental and practical chemistry, a

worthwhile educational experience for all students, whether or not they go to study
science beyond this level and, in particular, to enable them to acquire sufficient
understanding and knowledge to:

1.1 become confident citizens in a technological world, able to take or develop an

informed interest in matters of scientific import;

1.2 recognise the usefulness and limitations, of scientific method and to appreciate
its applicability in other disciplines and in everyday life;

1.3 be suitably prepared for employment and/or further studies beyond A Level.

2 develop abilities and skills that

2.1 are relevant to the study and practice of science;

2.2 are useful in everyday life;

2.3 encourage efficient and safe practice;

2.4 encourage the presentation of information and ideas appropriate for different
audiences and purposes;

2.5 develop self motivation and the ability to work in a sustained fashion.

2.6 Accuracy and Precision.

3 develop attitudes relevant to science such as

3.1 objectivity;

3.2 integrity;

3.3 enquiry;

3.4 initiativeness;

3.5 insight.

4
4 stimulate interest in, and care for, the environment.

5 promote an awareness that

5.1 the study and practice of science are co-operative and cumulative activities,
and are subject to social, economic, technological, ethical and cultural
influences and limitations;

5.2 the applications of science may be both beneficial and detrimental to the
individual, the community and the environment;

5.3 the use of information technology is important for communication, as an aid to

experiments and as a tool for interpretation of experimental and theoretical
results.

6 stimulate students, create and sustain their interest in Chemistry, and understand its
relevance to society.

5
ASSESSMENT OBJECTIVES

The assessment objectives listed below reflect those parts of the Aims which will be
assessed.

A Knowledge with understanding

Students should be able to demonstrate knowledge with understanding in relation to:

1 scientific phenomena, facts, laws, definitions, concepts, theories;

2 scientific vocabulary, terminology, conventions (including symbols, quantities and

units);

3 scientific instruments and apparatus, including techniques of operation and aspects of

safety;

4 scientific quantities and their determination;

5 scientific and technological applications with their social economic and environmental
implications;

6 present reasoned explanations for phenomena, patterns and relationships.

The Subject Content defines the factual knowledge that candidates may be required to recall
and explain. questions testing these objectives will often begin with one of the following
words: define, state, describe, explain or outline.

B Handling, applying and evaluating information

Students should be able - in words or by using symbolic, graphical and numerical forms of
presentation - to:

1 locate, select, organise and present information from a variety of sources;

2 handle information, distinguishing the relevant from the extraneous;

3 manipulate numerical and other data and translate information from one form to
another;

4 analyse and evaluate information so as to identify patterns, report trends and draw
inferences;

5 construct arguments to support hypotheses or justify a course of action;

6 apply knowledge, including principles, to novel situations;

7 evaluate information and hypotheses.

6
These assessment objectives cannot be precisely specified in the Subject Content because
questions testing such skills may be based on information which is unfamiliar to the
candidate. In answering such questions, candidates are required to use principles of
concepts that are within the syllabus and apply them in a logical, reasoned or deductive
manner to a novel situation. Questions testing these objectives will begin with one of the
following words; predict, suggest, construct, calculate or determine.

C Experimental skills and investigations

Students should be able to

1 plan investigations;

2 use techniques, apparatus and materials;

3 make and record observations, measurements and estimates;

4 interpret and evaluate observations and experimental results;

5 select techniques and materials;

6 evaluate methods and suggest possible improvements.

7
SCHEME OF ASSESSMENT

Candidates are required to enter for: Papers 1, 2, 3, 4, 5 & 6 (June and November)

Paper Type of Paper Duration Marks

1 Free Response 2h 72
Questions
2 Structured Questions 1¼h 48
3 Multiple Choice 1h 40
4 Option Topics 1¼h 40
5&6 Practical Test 2½h 50

Paper 1 (2h) (72 marks)

Section A (based mainly on physical chemistry) three questions;

Section B (based mainly on inorganic chemistry) two questions;

Section C (based mainly on organic chemistry) three questions.

Candidates will be required to answer a total of six questions, two from

Section A one from Section B, two from Section C, plus any other.

Paper 2 (1¼h) (48 marks)

A variable number of structured questions, all compulsory. Based on the core

syllabus (Section 1 to 10). Answered on the question paper.

Paper 3 (1h) (40 marks)

Forty multiple choice questions based on the core syllabus (Sections 1 to 10).
Thirty items will be of the direct choice type and ten of the multiple completion
type. All questions will include 4 responses.

Paper 4 (1¼h) (40 marks)

Testing the options. Three questions on each option (10 marks each).
Candidates to answer a total of four questions, not more than two on any
option.

Paper 5 & 6 (2½h) (50 marks)

The scope of the practical test is indicated in the Practical Chemistry syllabus.
(The paper will be marked out of 75 and scaled to a mark out of 50).

8
MARKS ALLOCATED TO ASSESSMENT OBJECTIVES AND SYLLABUS AREAS

In demonstrating what they know, understand and can do, candidates will be expected, within
the theory (other than the multiple-choice paper), to use a form of communication appropriate
to the context of the question.

Theory Papers (Papers 1, 2 and 3) (160 marks in total)

Knowledge with understanding approximately 55 marks allocated to recall and 35 marks

allocated to understanding.

Handling, applying and evaluating information approximately 70 marks.

The portion of marks allocated to Physical, Inorganic chemistry in Papers 1, 2 and 3 will be in
the approximately ratio 3:2:3.

Options Theory Paper (Paper 4) (40 marks)

This paper is designed to test appropriate aspects of objectives A1 to A6 and B1 to B7.

Whilst every effort will be made to produce questions of comparable difficulty and reasonable
spread of skills, the differing natures of the various options mean that different skills will be
required of candidates according to their choice of options and questions.

Practical Tests (Paper 5 & 6) (50 marks)

Experimental skills and investigations.

This paper is designed to test appropriate aspects of objectives C1 to C6. The practical
paper may also involve some calculations based on experimental results.

The Subject Core requires some assessment of planning/design skills – a relatively structured
example of a possible qualitative analysis format being included with the associated
specimen papers. However, the assessment of such skills will not necessarily be confined to
this particular area of practical chemistry. It is anticipated that the nature of ‘planning’
exercises within the practical examination will evolve and develop as experience is gained.

Depending on the context in which the ‘planning/design’ element is set, the number of marks
associated with this element will be in the range of 20% to 30% of the total marks available
for the practical test.

9
Data Booklet

A Data Booklet is available for use in Papers 1, 2, 3 and 4. Copies of the booklet can be
ordered from the Publication Office at ZIMSEC using the appropriate order form.

Nomenclature

The ASE proposals in Signs, Symbols and Systematics (The ASE Companion to 5 – 16
Science, 1995) will generally be adopted. In particular, the names sulphite, nitrite, sulphur
trioxide, sulphurous acid and nitrous acid will be used in question papers.

Grading Conditions

Candidates’ results are based on the aggregation of their marks in the various papers, i.e.
there are no hurdle conditions under which a prescribed level of performance in an individual
paper prevents the award of an A level result.

Skills Weighting and Distribution

Skill Paper 1 Paper 2 Paper 3 Paper 4 Paper 5 & 6

M % M % M % M % M %
Factual recall 18 25 6 12.5 10 25 10 25 9 12
and
comprehension
Handling 36 50 32 67 20 50 20 50 40 53
information and
application
Deductive 18 25 10 21 10 25 10 25 26 35
reasoning
synthesis and
evaluation
Total 72 100 48 100 40 100 40 100 75 100

10
STRUCTURE OF THE SYLLABUS

The syllabus has been constructed to allow a choice of two options out of four options.

The following options are available:

Biochemistry Environmental Transition Elements

Chemistry

Phase Equilibria

It will be noted that some of the options are specifically directed to applied chemistry. The
chosen options are also intended to illustrate the variety of contexts in which understanding of
the underlying chemistry is relevant.

The options are also intended to cater for differing interests of students, for expertise and
resources within schools and to take into account of differences in locale in which schools are
teaching chemistry, e.g. schools in rural or industrial communities/the local employment
opportunities.

Some of the options are more obviously quantitative/mathematical in nature, whereas others
have a greater descriptive content. Similarly, choice of option may also be influenced by
other subjects being studied alongside chemistry. This deliberate variety is seen as a virtue
of the complete syllabus.

Notwithstanding the different balances within the options to descriptive/quantitative aspects, it

is intended that teachers will take appropriate opportunity to incorporate practical work,
industrial and laboratory visits relevant to the content of the options chosen.

In order to specify the syllabus as precisely as possible and also to emphasise the importance
of skills other than recall, learning Outcomes have been used throughout. Each part of the
syllabus is specified by a Content followed by detailed learning outcomes. Although this
format, of necessity, makes the syllabus a lengthier document, it is hoped that the format will
be helpful to teachers and students.

It is intended that teachers should incorporate social, environmental, economic and

technological aspects of chemistry, where relevant, throughout the syllabus. Some examples
are included in the syllabus and students should be encouraged to apply the principles in
these examples to other situations introduced during the course. Inclusion of further
examples in the core of the syllabus has been avoided as this would merely increase the
amount of factual recall required of students.

11
SUBJECT CONTENT

PHYSICAL CHEMISTRY

1 ATOMS, MOLECULES AND STOICHIOMETRY

Content

i Relative masses of atoms and molecules

ii The mole, the Avogadro constant

iii The determination of relative atomic masses, Ar and relative molecular masses, Mr
from mass spectra

iv The calculation of empirical and molecular formulae

v Reacting masses and volumes (of solutions and gases)

Learning Outcomes

[the term relative formula or Mr will be used for ionic compounds]

Candidates should be able to:

(a) define the terms relative atomic, isotopic, molecular and formula masses, based on the
12
C scale

(b) define the term mole in terms of the Avogadro constant

(c) analyse mass spectra in terms of isotopic abundances and molecular fragments
[knowledge of the working of the mass spectrometer is not required]

(d) calculate the relative atomic mass of an element given the relative abundances of its
isotopes, or its mass spectrum

(e) define the terms empirical and molecular formulae

(f) calculate empirical and molecular formulae, using combustion data or composition by
mass

(g) write and/or construct balanced equations

(h) perform calculations, including use of the mole concept, involving:

(i) reacting masses (from formulae and equations)

(ii) volumes of gasses (e.g. in the burning of hydrocarbons)

(iii) volumes and concentrations of solutions

12
(i) deduce stoichiometric relationship from calculations such as those in (h)

2 ATOMIC STRUCTURE

Content

i The nucleus of the atom: neutrons and protons, isotopes, proton and nucleon numbers

ii Electrons: electronic energy levels, ionisation energies, atomic orbitals, extranuclear

structure

Learning Outcomes

Candidates should be able to:

(a) identify and describe protons, neutrons and electrons in terms of their relative charges
and relative masses

(b) deduce the behaviour of beams of protons, neutrons and electrons in electric fields

(c) describe the distribution of mass and charges within an atom

(d) deduce the numbers of protons, neutrons and electrons present in both atoms and
ions given proton and nucleon numbers (and charge)

(e) (i) describe the contribution of protons and neutrons to atomic nuclei in terms of
proton number and nucleon number.

(ii) distinguish between isotopes on the basis of different numbers of neutrons

present

(f) describe the number and relative energies of the s, p and d orbitals for the principal
quantum numbers 1, 2 and 3 and also the 4s and 4p orbitals.

(g) describe the shapes of s and p orbitals

(h) state the electronic configuration of atoms and ions given the proton number (and
charge)

(i) (i) explain and use the term ionisation energy

(ii) explain the factors influencing the ionisation energies of elements

(iii) explain the trends in ionisation energies across a period and down a group of
the Periodic Table (see also Section 9)

(j) deduce the electronic configurations of elements from successive ionisation energy
data.

13
(k) interpret successive ionisation energy data of an element in terms of the position of
that element within the Periodic Table.

3 CHEMICAL BONDING

Content

I Ionic (electrovalent) bonding

II Covalent bonding and co-ordinate (dative covalent) bonding

(i) The shapes of simple molecules

(ii) Bond energies, bond lengths and bond polarities

III Intermolecular forces, including hydrogen bonding

IV Metallic bonding

V Bonding and physical properties

Learning Outcomes

Candidates should be able to:

(a) describe ionic (electrovalent) bonding, as in sodium chloride and magnesium

oxide, including the use of 'dot-and-cross' diagrams

(b) describe, including the use of 'dot-and-cross' diagrams,

(i) covalent bonding, as in hydrogen; oxygen; chlorine; hydrogen chloride;

carbon dioxide; methane; ethene

(ii) co-ordinate (dative covalent) bonding, as in the formation of the

ammonium ion and in the Al2 Cl6 molecule

(c) explain the shapes of, and bond angles in, molecules by using the quantitative
model of electron-pair repulsion (including lone pairs), using as simple
examples: BF3 (trigonal); CO2 (linear); CH4 (tetrahedral); NH3 (pyramidal);
H2O (non-linear); SF6 (octahedral)

(Teachers may use the concept of hybridisation on shapes of some molecules

but this will not be examined).

(d) describe covalent bonding in terms of orbital overlap, giving σ and π bonds

(e) explain the shape of, and bond angles in, the ethene and benzene molecules
in terms of σ and π bonds (see also Section 10.1)

14
 (f) predict the shapes of, and bond angles in, molecules analogous to those
specified in (c) and (e)

(g) describe hydrogen bonding, using ammonia and water as simple examples of
molecules containing N-H and O-H groups

(h) explain the terms bond energy, bond length and bond polarity and use them to
compare the reactivities of covalent bonds [see also 5b(ii)]

(i) describe intermolecular forces (Van der Waals' forces), based on permanent
and induced dipoles, as in CHCl3(I); Br2(I) and the liquid noble gases

(j) describe metallic bonding in terms of a lattice of positive ions surrounded by

mobile electrons

(k) describe, interpret and/or predict the effect of different types of bonding (ionic
bonding; covalent bonding; hydrogen bonding, other intermolecular
interactions; metallic bonding) on the physical properties of substances

(l) deduce the type of bonding present from given information

(m) show understanding of chemical reactions in terms of energy transfers

associated with the breaking and making of chemical bonds

4 STATES OF MATTER

Content

I The gaseous state:

(i) Ideal gas behaviour and deviations from it

(ii) pV = nRT and its use in determining a value for Mr

II The liquid state

The kinetic concept of the liquid state and simple kinetic-molecular

descriptions of changes of state

III The solid state

Lattice structures

Learning Outcomes

Candidates should be able to:

(a) state the basic assumptions of the kinetic theory as applied to an ideal gas

(b) explain qualitatively in terms of intermolecular forces and molecular size:

15
 (i) the conditions necessary for a gas to approach ideal behaviour

(ii) the limitations of ideality at very high pressures and very low
temperatures

(c) state and use the general gas equation pV = nRT in calculations, including the
determination of Mr

(d) describe, using a kinetic-molecular model, the liquid state; melting;

vaporisation and vapour pressure

(e) describe, in simple terms, the lattice structure of a crystalline solid which is:

(i) ionic, as in sodium chloride, magnesium oxide

(ii) simple molecular, as in iodine

(iii) giant molecular, as in graphite; diamond; silicon (IV) oxide

(iv) hydrogen-bonded, as in ice

(v) metallic, as in copper

[the concept of the 'unit cell' is not required]

(f) explain the strength, high melting point, electrical insulating properties of
ceramics in terms of their giant molecular structure

(g) relate the uses of ceramics, based on magnesium oxide, aluminium oxide and
silicon (IV) oxide, to their properties (suitable examples include furnace
linings; electrical insulators; glass; crockery)

(h) describe and interpret the uses of the metals aluminium including its alloys,
and copper, including brass, in terms of their physical properties

(i) recognise that materials are a finite resource and the importance of recycling
processes

(j) outline the importance of hydrogen bonding to the physical properties of

substances, including ice and water

(k) suggest from quoted physical data the type of structure and bonding present in
a substance

16
5 CHEMICAL ENERGETICS

Content

I Enthalpy changes: ΔH of formation, combustion, hydration, solution,

neutralisation and atomisation; bond energy; lattice energy; electron affinity

II Hess' Law including Born-Haber cycles

Learning Outcomes

Candidates should be able to:

(a) explain that some chemical reactions are accompanied by energy changes,
principally in the form of heat energy; the energy changes can be exothermic
(H, negative) or endothermic (H, positive)

(b) explain and use the terms:

(i) enthalpy change of reaction and standard conditions, with particular

reference to: formation; combustion; hydration; solution; neutralisation;
atomisation

(ii) bond energy (H positive, i.e. bond breaking)

(iii) lattice energy (H negative, i.e. gaseous ions to solid lattice)

(c) calculate enthalpy changes from appropriate experimental results, including

the use of the relationship

enthalpy change = mcT

(d) explain, in qualitative terms, the effect of ionic charge and of ionic radius on
the numerical magnitude of a lattice energy

(e) apply Hess' Law to construct simple energy cycles, and carry out calculations
involving such cycles and relevant energy terms, with particular reference to:

(i) determining enthalpy changes that cannot be found by direct

experiment, e.g an enthalpy change of formation from enthalpy
changes of combustion

(ii) average bond energies

(iii) the formation of a simple ionic solid and of its aqueous solution

(iv) Born-Haber cycles (including ionisation energy and electron affinity)

17
 (f) construct and interpret a reaction pathway diagram, in terms of the enthalpy
change of the reaction and of the activation energy (see Section 8)

6 ELECTROCHEMISTRY

Content

I Redox processes: electron transfer and changes in oxidation number

(oxidation state)

II Electrode potentials

(i) Standard electrode (redox) potentials, Eθ, and their uses

(ii) Standard cell potentials, Eθcell, and their uses

(iii) Batteries and fuel cells

III Electrolysis

(i) Factors affecting the amount of substance liberated during electrolysis

(ii) The Faraday constant: the Avogadro constant: their relationship

(iii) Industrial uses of electrolysis

Learning Outcomes

Candidates should be able to:

(a) describe and explain redox processes in terms of electron transfer and/or of
changes in oxidation number (oxidation state)

(b) explain, including the electrode reactions, the industrial processes of:

(i) the electrolysis of brine, using a diaphragm cell

(ii) the extraction of aluminium from molten aluminium oxide/cryolite

(iii) the electrolytic purification of copper

(c) define the terms:

(i) standard electrode (redox) potential

(ii) standard cell potential

(d) describe the standard hydrogen electrode

18
 (e) describe methods used to measure the standard electrode potentials of:

(i) metals or non-metals in contact with their ions in aqueous solution

(ii) ions of the same element in different oxidation states

(f) calculate a standard cell potential by combining two standard electrode

potentials

(g) use standard cell potentials to:

(i) explain/deduce the direction of electron flow from a simple cell

(ii) predict the feasibility of a reaction

(h) construct redox equations using the relevant half-equations (see Section 9.4)

(i) predict qualitatively how the value of an electrode potential varies with the
concentration of the aqueous ion

(j) state the possible advantages of developing other types of cell, e.g. the H2/O2
fuel cell and improved batteries (as in electric vehicles) in terms of smaller
size, lower mass and higher voltage

(k) state the relationship, F = Le, between the Faraday constant, the Avogadro
constant and the charge on the electron

(l) predict the identity of the substance liberated during electrolysis from the state
of electrolyte (molten or aqueous), position in the redox series (electrode
potential) and concentration

(m) calculate:

(i) the quantity of charge passed during electrolysis

(ii) the mass and/or volume of substance liberated during electrolysis,

including those in the electrolysis of H2SO4(aq); Na2SO4(aq)

(n) describe the determination of a value of the Avogadro constant by an

electrolytic method

7 EQUILIBRIA

Content

I Chemical equilibria: reversible reactions; dynamic equilibrium

(i) Factors affecting chemical equilibria

19
 (ii) Equilibrium constants

(iii) The Haber process; the Contact process

II Ionic equilibria

(i) Bronsted-Lowry theory of acids and bases

(ii) Acid dissociation constants, Ka and the use of pKa

(iii) Base dissociation constants, Kb and the use of pKb.

(iv) The ionic product of water, Kw

(vi) pH: choice of pH indicators

(v) Buffer solutions

(vi) Solubility product; the common ion effect

Learning Outcomes

Candidates should be able to:

(a) explain, in terms of rates of the forward and reverse, what is meant by a
reversible reaction and dynamic equilibrium

(b) state Le Chateliers's Principle and apply it to deduce qualitatively (from

appropriate information) the effects of changes in temperature, concentration
or pressure, on a system at equilibrium

(c) deduce whether changes in concentration, pressure or temperature or the

presence of a catalyst affect the value of the equilibrium constant for a reaction

(d) deduce expressions for equilibrium constants in terms of concentrations, Kc,

and partial pressures, Kp

[treatment of the relationship between Kp and Kc is not required]

(e) calculate the values of equilibrium constants in terms of concentrations or

partial pressures from appropriate data

(f) calculate the quantities present at equilibrium, given appropriate data (such
calculations will not require the solving of quadratic equations)

(g) describe and explain the conditions used in the Haber process and Contact
process, as examples of the importance of an understanding of chemical
equilibrium in the chemical industry (see also Section 9.6)

20
 (h) show understanding of, and apply the Bronsted-Lowry theory of acids and
bases

(i) explain qualitatively the differences in behaviour between strong and weak
acids and bases in terms of the extent of dissociation

(j) explain the terms the terms pH; Ka ; pKa; pOH; Kb; pKb; Kw and apply them in
calculations

(k) calculate [H+(aq)] and pH values for strong and weak acids and strong bases

(l) explain the choice of suitable indicators for acid-base titrations, given
appropriate data

(m) describe the changes in pH during acid-base titrations and explain these
changes in terms of the strengths of the acids and bases

(n) (i) explain how buffer solutions control pH

(ii) describe and explain their uses, including the role of HCO3- in
controlling pH in blood

(o) calculate the pH and/or pOH of buffer solutions, given appropriate data

(p) show understanding of, and apply, the concept of solubility product, Ksp

(q) calculate Ksp from concentrations and vice versa

(r) show understanding of the common ion effect

8 REACTION KINETICS

Content

I Simple rate equations; order of reaction; rate constants

II Effect of temperature of rate constants; the concept of activation energy

III Homogeneous and heterogeneous catalysis

Learning Outcomes

Candidates should be able to:

(a) explain and use the terms: rate of reaction; activation energy; catalysis; rate
equation; order of reaction; rate constant; half-life of a reaction; rate-
determining step

(b) explain qualitatively, in terms of collisions, the effect of concentration changes

21
 on the rate of a reaction

(c) show understanding, including reference to the Boltzmann distribution, of what

is meant by the term activation energy

(d) explain qualitatively, in terms of both the Boltzmann distribution and of collision
frequency, the effect of temperature change on the rate of a reaction

(e) (i) explain that, in the presence of a catalyst, a reaction has a different
mechanism, i.e. one of lower activation energy

(ii) interpret this catalytic effect in terms of the Boltzmann distribution

(f) describe enzymes as biological catalysts (proteins) which may have specific
activity

(g) construct and use rate equations of the form rate = k[A]m[B]n (limited to simple
cases of single step reactions and of multi-step processes with a rate-
determining step, for which m and n are 0, 1 or 2), including:

(i) deducing the order of a reaction by the initial rates method

(ii) justifying, for zero - and first - order reactions, the order of reaction
from concentration-time graphs

(iii) verifying that a suggested reaction mechanism is consistent with the

observed kinetics

(iv) predicting the order that would result from a given reaction mechanism
(and vice versa)

(v) calculating an initial rate using concentration data

[integrated forms of rate equations are not required]

(h) (i) show understanding that the half-life of a first-order reaction is

independent of concentration

(ii) use the half-life of a first-order reaction in calculations

(i) calculate a rate constant using the initial rates method

(j) devise a suitable experimental technique for studying the rate of a reaction,
from given information

(k) outline the different modes of action of homogeneous and heterogeneous

catalysis, including:

(i) the Haber process

(ii) the catalytic removal of oxides of nitrogen in the exhaust gases from
22
 car engines (see also Section 10.3)

(iii) the catalytic role of atmospheric oxides of nitrogen in the oxidation of

atmospheric sulphur dioxide

(iv) catalytic role of Fe3+/Fe2+ in the I-/S2O82- reaction

9 INORGANIC CHEMISTRY

Statement of Aims

It is intended that the study should:

be concerned primarily with aspects of selected ranges of elements and their

compounds;

be based on a study of the patterns:

 across the third period of the Periodic Table

 in the three Groups II, IV and VII;

introduce, with examples, the transition elements and their compounds

introduce the more important everyday aspects of nitrogen, sulphur and their
compounds

apply unifying themes to inorganic chemistry, such as structure (Section 2), chemical
bonding (Section 3), redox (Section 6), the reactions of ions, acid-base behaviour,
precipitation (Section 7) and complexing behaviour (Section 9.5), where appropriate;

Include:

 the representation of reactions by means of balanced equations (molecular and/or

ionic equations, together with state symbols);

 the interpretation of redox reactions in terms of changes in oxidation state of the

species involved;

 the prediction of the feasibility of reactions from Eθ values;

 the interpretation of chemical reactions in terms of the formation of complex ions.

23
9.1 THE PERIODIC TABLE: CHEMICAL PERIODICITY

Content

I Periodicity of physical properties of the elements: variation with proton number

across the third period (sodium to argon) of:

(i) atomic radius and ionic radius

(ii) melting point

(iii) electrical conductivity

(iv) ionisation energy

II Periodicity of chemical properties of the elements in the third period

(i) Reaction of the elements with oxygen, chlorine and water

(ii) Variation in oxidation number of the oxides (sodium to sulphur only)

and of the chlorides (sodium to phosphorous only)

24
 (iii) Reactions of these oxides and chlorides with water

(iv) Acid/base behaviour of these oxides and the corresponding hydroxides

Learning Outcomes

Candidates should, for the third period (sodium to argon), be able to:

(a) describe qualitatively (and indicate the periodicity in) the variations in atomic
radius, ionic radius, melting point and electrical conductivity of the elements
(see the Data Booklet)

(b) explain qualitatively the variation in atomic radius and ionic radius

(c) interpret the variation in melting point and in electrical conductivity in terms of
the presence of simple molecular, giant molecular or metallic bonding in the
elements

(d) explain the variation in first ionisation energy

(e) describe the reactions, if any, of the elements with oxygen (to give Na2O;MgO;
Al2O3; P4O6 ; P4O10; SO2; SO3), chlorine (to give NaCl; MgCl2; Al2Cl6; SiCl4;
PCl3; PCl5), and water (Na and Mg only)

(f) state and explain the variation in oxidation number of the oxides and chlorides

25
 (g) describe the reactions of the oxides with water

[treatment of peroxides and superoxides is not required]

(h) describe and explain the acid/base behaviour of oxides and hydroxides,
including, where relevant, amphoteric behaviour in reaction with sodium
hydroxide (only) and acids

(i) describe and explain the reactions of the chlorides with water

(j) interpret the variations and trends in (f), (g), (h) and (i) in terms of bonding and
electro negativity

(k) suggest the types of chemical bonding present in chlorides and oxides from
observations of their chemical and physical properties

(l) predict the characteristic properties of an element in a given group by using

knowledge of chemical periodicity

(m) deduce the nature, possible position in the Periodic Table, and identity of
unknown elements from the given information of physical and chemical
properties.

9.2 GROUP II

Content

I Similarities and trends in the properties of the Group II metals magnesium to

barium and their compounds

II Some uses of Group II compounds

Learning Outcomes

Candidates should be able to:

(a) describe the reactions of the elements with oxygen and water

(b) describe the behaviour of the oxides with water

(c) describe the thermal decomposition of the nitrates and carbonates

(d) interpret, and make predictions from, the trends in physical and chemical
properties of the elements and their compounds

(e) explain the use of magnesium oxide as a refractory lining material and
carbonates as a building material

(f) describe the use of lime in agriculture

(g) interpret and explain qualitatively the trend in the thermal stability of the
26
 nitrates and carbonates in terms of the charge density of the cation and the
polarisability of the large anion

(h) interpret and explain qualitatively the variation in solubility of the sulphates in
terms of relative magnitudes of the enthalpy change of hydration and the
corresponding lattice energy

9.3 GROUP IV

Content

The elements carbon to lead as a group in which the physical and chemical properties
of the elements change with increase in proton number from non-metals through
metalloids to metals and their compounds

I The variation in melting points and electrical conductivities of the elements

II The bonding, molecular shape, volatility and hydrolysis of the tetrachlorides

III The bonding, acid/base nature and thermal stability of the oxides of oxidation
states II and IV

IV The relative stability of the higher and lower oxidation states for the elements
in their oxides and aqueous cations

Learning Outcomes

Candidates should be able to:

(a) outline the variation in melting point and in electrical conductivity of the
elements and interpret them in terms of structure and bonding

(b) describe and explain the bonding in, molecular shape and volatility of the
tetrachlorides

(c) describe and explain the reactions of the tetrachlorides with water in terms of
structure and bonding

(d) describe and explain the bonding, acid-base nature and thermal stability of the
oxides of exidation states II and IV

(e) describe and explain the relative stability of higher and lower oxidation states
of the elements in their oxides and aqueous cations, including, - where
relevant - Eθ values

(f) recognize the properties and uses of ceramics based on silicon (IV) oxide

27
9.4 GROUP VII

Content

The similarities and trends in the physical and chemical properties of chlorine,
bromine and iodine

I Characteristic physical properties

II The relative reactivity of the elements as oxidising agents

III Some reactions of the halide ions

IV The manufacture of chlorine

V The reactions of chlorine with aqueous sodium hydroxide

VI The important uses of the halogens and of halogen compounds (see also
Section 10.4)

Learning Outcomes

Candidates should be able to:

(a) describe the trends in volatility and colour of chlorine, bromine and iodine

(b) interpret the volatility of the elements in terms of Van der Waals’ forces

(c) describe and explain the relative reactivity of elements as oxidising agents
including their reaction with sodium thiosulphate with reference to E values.

(c) describe and explain the reactions of the elements with hydrogen

(e) (i) describe and explain the relative thermal stabilities of the hydrides,

(ii) interpret these relative stabilities in terms of bond energies

(f) describe and explain the reactions of halide ions with

(i) aqueous silver ions followed by aqueous ammonia,

(ii) concentrated sulphuric acid

(g) outline a method for the manufacture of chlorine from brine by a diaphragm
cell (see also Section 6)

(h) describe and interpret in terms of changes of oxidation number the reaction of
chlorine with cold, and with hot, aqueous sodium hydroxide

(i) explain the use of chlorine in water purification

28
 (j) recognise the industrial importance and environment significance of the
halogens and their compounds, (e.g. for bleaches; pvc; halogenated
hydrocarbons as solvents, refrigerants and in aerosols) (see also Section 10.4)

9.5 NITROGEN AND SULPHUR

Content

I Nitrogen

(i) Its unreactivity

(ii) Ammonia, the ammonium ion, nitric acid and fertilisers

(iii) The environmental impact of nitrogen oxides and nitrates

II Sulphur

(i) The formation of atmospheric sulphur dioxide, its role in acid rain
formation, the use of sulphur dioxide in food preservation

(ii) Sulphuric acid

Learning Outcomes

Candidates should be able to:

(a) explain the lack of reactivity of nitrogen

(b) describe:

(i) the formation, and structure, of the ammonium ion

(ii) the displacement of ammonia from its salts

(c) describe the Haber process for the manufacture of ammonia from its
elements, giving essential operating conditions, and interpret these conditions
(qualitatively) in terms of the principles of kinetics and equilibria (see also
Sections 7 and 8)

(d) recognise the industrial importance of ammonia and nitrogen compounds

derived from ammonia

(e) recognize the environmental consequences of the uncontrolled use of nitrate

fertilisers.

(f) describe and explain the occurrence, and catalytic removal, of oxides of
nitrogen

(g) explain why atmospheric oxides of nitrogen are pollutants, including their
29
 catalytic role in the oxidation of atmospheric sulphur dioxide

(h) describe the formation of atmospheric sulphur dioxide from the combustion of
sulphur contaminated carbonaceous fuels

(i) state the role of sulphur dioxide in the formation of acid-rain and describe the
main environmental consequences of acid-rain

(j) state the main details of the Contact process for sulphuric acid production
(k) recognize the industrial importance of sulphuric acid

(l) describe the use of sulphur dioxide in food preservation

9.6 AN INTRODUCTION TO THE CHEMISTRY OF TRANSITION ELEMENTS

Content

I General physical and characteristic chemical properties of the first set of

transition elements, titanium to copper

II Colour of complexes

Learning Outcomes

Candidates should be able to:

(a) explain what is meant by a transition, in terms of d-block elements forming one
or more stable ions with incomplete d orbitals

(b) state the electronic configuration of a first row transition element and of its ions

(c) state that the atomic radii, ionic and first ionisation energies of the transition
metals are relatively invariant

(d) contrast, qualitatively, the melting point; density, atomic radius; ionic radius;
first ionisation energy and conductivity of the transition elements with those of
calcium as a typical s-block element

(e) describe the tendency of transition elements to have variable oxidation states

(f) predict from a given electronic configuration, the likely oxidation states of a
transition element

(g) describe and explain the use of Fe3+/Fe2+, MnO4-/Mn2+ and Cr2O72-/Cr3+ as
examples of redox systems (see also Section 6)

30
 (h) (i) explain the reactions of transition elements with ligands to form
complexes, including the complexes of copper (II) ions with water and
ammonia

(ii) describe the formation, and state the colour of, these complexes

(i) predict, using Eθ values, the likelihood of redox reactions

(j) explain qualitatively that ligand exchange may occur, including CO/O2 in
haemoglobin

(k) state examples of catalysis by transition metals and/or their compounds

10 ORGANIC CHEMISTRY

Statement of Aims

Although there are features of organic chemistry that are distinctive, it is intended that
appropriate cross references with other sections/topics in the syllabus should be
made.

When describing preparative reactions, candidates will be expected to quote the

reagents, e.g. aqueous NaOH, the essential practical conditions, e.g. reflux, and the
identity of each of the major products. Detailed knowledge of practical procedures is
not required: however, candidates may be expected to suggest (from their knowledge
of the reagents, essential conditions and products) what steps may be needed to
purify/extract a required product from the reaction mixture. In equations for organic
redox reactions, the symbols [O] and [H] are acceptable.

10.1 INTRODUCTORY TOPICS

In each of the sections below, 10.1 to 10.8 candidates will be expected to be able to
predict the reaction products of a given compound in reactions that are chemically
similar to those specified.

Content

I Molecular, structural and empirical formulae

II Functional groups and the naming of organic compounds

[Candidates will be expected to recognize the shape of the benzene ring when
it is present in organic compounds]

III Characteristic organic reactions

IV Shapes of organic molecules;  and  bonds

31
V Isomerism: structural; cis-trans; optical

Structural formulae

In candidates’ answers, an acceptable response to a request for structural formulae

will be to give the minimal detail, using conventional groups, for an unambiguous
structure, e.g. CH3CH2CH2OH for propan –1-o1, not C3H7OH.

Displayed formulae

A displayed formula should show both the relative placing of atoms and the number of
bonds between them, e.g.

H O

H C C

H O H

for ethanoic acid.

The convention for representing the aromatic ring is preferred.

The symbol for cyclohexane is acceptable.

Optical Isomers

When drawing a pair of optical isomers, candidates should indicate the three-
dimensional structures according to the convention used in the example below.

CH3 CH3

C C

HO H H OH

CO2H CO2H

mirror plane

32
Learning Outcomes

Candidates should be able to:

(a) interpret, and use the nomenclature, general formulae and displayed formulae
of the following classes of compound:

(i) alkanes, alkanes and arenes

(ii) halogenoalkanes and halogenoarenes

(iii) alcohols (including primary, secondary and tertiary) and phenols

(iv) aldehydes and ketones

(v) carboxylic acids, esters and acyl chlorides

(vi) amines (primary only), nitriles, amides and amino acids

(b) interpret, and use the following terminology associated with organic reactions:

(i) functional group

(ii) homolytic and heterolytic fission

(iii) free radical, initiation, propagation, termination

(iv) nucleophile, electrophile

(v) addition, substitution, elimination, hydrolysis

(v) oxidation and reduction.

(c) (i) describe the shapes of the ethane and benzene molecules

(ii) predict the shapes of other related molecules

(d) explain the shapes of the ethane, ethene and benzene molecules in terms of 
and  carbon-carbon bonds

(e) describe structural isomerism

(f) describe cis-trans isomerism in alkenes, and explain its origin in terms of
restricted rotation due to the presence of  bonds

(g) explain what is meant by a chiral centre and that such a centre gives rise to
optical isomerism

33
 (h) deduce the possible isomers for an organic molecule of known molecular
formula

(i) identify chiral centres and/or cis-trans isomerism in a molecule of given

structural formula

10.2 HYDROCARBONS

Content

I Alkanes (exemplified by ethane)

(i) Free-radical reactions

(ii) Crude oil and ‘cracking’

II Alkenes (exemplified by ethene)

(i) Addition and oxidation reactions

(ii) Industrial importance

III Arenes (exemplified by benzene and methylbenzene)

(i) Influence of delocalised  electrons on structure and properties

(ii) Substitution reactions with electrophiles

(iii) Oxidation of side-chain

IV Hydrocarbons as fuels

Learning Outcomes

Candidates should be able to:

(a) be aware of the general unreactivity of alkanes, including towards polar

reagents

(b) describe the chemistry of alkanes as exemplified by the following reactions of

ethane:
(i) combustion

(ii) substitution by chlorine and by bromine

(c) describe the mechanism of free-radical substitution at methyl groups with

particular reference to the initiation, propagation and termination reactions

34
 (d) describe the chemistry of alkenes as exemplified, where relevant, by the
following reactions of ethene:

(i) addition of hydrogen, steam, hydrogen halides and halogens

(ii) oxidation by cold, dilute manganate (VII) ions to form the diol

(iii) oxidation by hot, concentrated manganate (VII) ions leading to the

rupture of the carbon-to-carbon double bond in order to determine the
position of alkene linkages in larger molecules

(iv) polymerisation (see also section 10.8)

(e) describe the mechanism of electrophilic addition in alkenes, using

bromine/ethene as an example

(f) explain the use of crude oil as a source of both aliphatic and aromatic
hydrocarbons

(g) suggest how ‘cracking’ can be used to obtain more useful alkanes and alkenes
of lower Mr from larger hydrocarbon molecules

(h) describe and explain how the combustion reactions of alkanes lead to their use
as fuels in industry, in the home and in transport

(i) recognise the environmental consequences of carbon monoxide, oxides of

nitrogen and unburnt hydrocarbons arising from the internal combustion
engine and of their catalytic removal

(j) describe the chemistry of arenes as exemplified by the following reactions of

benzene and methylbenzene:

(i) substitution reactions with chlorine and with bromine

(ii) nitration

(iii) oxidation of the side-chain to give a carboxylic acid

(k) (i) describe the mechanism of electrophilic substitution in arenes, using the
mono-nitration of benzene as an example

(iii) describe the effect of the delocalisation of electrons in arenes in such

reactions

(l) predict whether halogenation will occur in the side-chain or aromatic nucleus in
arenes depending on reaction conditions

(m) apply the knowledge of positions of substitution in the electrophilic substitution

of arenes

35
10.3 HALOGEN DERIVATIVES

Content

I Halogenoalkanes and halogenoarenes

(i) Nucleophilic substitution

(ii) Hydrolysis

(iii) Formation of nitriles, primary amines

(iv) Elimination

II Relative strength of the C-Hal bond

Learning Outcomes

Candidates should be able to:

(a) recall the chemistry of halogenoalkanes as exemplified by

(i) the following nucleophilic substitution reactions of bromoethane:

hydrolysis; formation of nitriles; formation of primary amines by
reaction with ammonia

(ii) the elimination of hydrogen bromide from 2-bromopropane

(b) describe the mechanism of nucleophilic substitution in halogenoalkanes

(c ) interpret the different reactivities of halogenoalkanes and chlorobenzene with

particular reference to hydrolysis and to the relative strengths of the C-Hal
bonds eg CFCs; anaesthetics; flame retardants; plastic

(d) explain the uses of fluoroalkanes and fluorohalogenoalkanes in terms of their

relative chemical inertness

(e) recognise the concern about the effect of chlorofluoroalkanes on the ozone
layer

10.4 HYDROXY COMPOUNDS

Content

I Alcohols (exemplified by ethanol)

(i) Formation of halogenoalkanes

(ii) Reaction with sodium; oxidation; dehydration; esterification; acylation

36
 (iii) The tri-iodomethane test

II Phenol

(i) Its acidity; reaction with sodium

(ii) Nitration of, and bromination of, the aromatic ring

Learning Outcomes

Candidates should be able to:

(a) recall the chemistry of alcohols, exemplified by ethanol:

(i) combustion

(ii) substitution to give halogenoalkanes

(iii) reaction with sodium

(iv) oxidation to carbonyl compounds and carboxylic acids

(v) dehydration to alkenes

(vi) ester formation

(b) classify hydroxy compounds into primary, secondary and tertiary alcohols

(c) suggest characteristic distinguishing reactions, e.g. mild oxidation

(d) deduce the presence of CH3CH(OH)– group in an alcohol from its reaction with
alkaline aqueous iodine to form tri-iodomethane

(e) recall the chemistry of phenol, as exemplified by the following reactions:

(i) with bases

(ii) with sodium

(iii) nitration of, and bromination of, the aromatic ring

(f) explain the relative acidities of water, phenol and ethanol

37
10.5 CARBONYL COMPOUNDS

Content

I Aldehydes (exemplified by ethanal)

(i) Oxidation to carboxylic acid

(ii) Reaction with hydrogen cyanide

(iii) Characteristic tests for aldehydes

II Ketones (exemplified by propanone and phenylethanone)

(i) Reaction with hydrogen cyanadie

(ii) Characteristic tests for ketones

Learning Outcomes

Candidates should be able to:

(a) describe

(i) the formation of aldehydes and ketones from primary and

secondary alcohols respectively using Cr2O72-/H+

(ii) the reduction of aldehydes and ketones using NaBH4

(b) describe the mechanism of the nucleophilic addition reactions of hydrogen

cyanide with aldehydes and ketones

(c) describe the use of 2,4-dinitrophenylhydrazine (2,4-DNPH) to detect the

presence of carbonyl compounds

(d) deduce the nature (aldehyde or ketone) of an unknown carbonyl compound

from the results of simple tests (i.e. Fehling’s and Tollens’ reagents; ease of
oxidation)

(e) describe the reaction of CH3CO- compounds with alkaline aqueous iodine to
give tri-iodomethane

38
10.6 CARBOXYLIC ACIDS AND DERIVATIVES

Content

I Carboxylic acids (exemplified by ethanoic acid and benzoic acid)

(i) Formation from primary alcohols and nitriles

(ii) Salt, ester and acyl chloride formation

II Acyl chlorides (exemplified by ethanoyl chloride)

(i) Ease of hydrolysis compared with alkyl and aryl chlorides

(ii) reaction with alcohols, phenols and primary amines

III Esters (exemplified by ethyl ethanoate and phenyl benzoate)

(i) Formation from carboxylic acids and from acyl chlorides

(ii) Hydrolysis (under acidic and under basic conditions)

(iii) Uses of esters

Learning Outcomes

Candidates should be able to:

(a) describe the formation of carboxylic acids from alcohols, aldehydes and nitriles

(b) describe the reactions of carboxylic acids in the formation of

(i) salts

(ii) esters

(iii) acyl chlorides

(c ) explain the acidity of carboxylic acids and of chlorine-substituted ethanoic

acids in terms of their structures

(d) describe the hydrolysis of acyl chlorides

(e) describe the reaction of acyl chlorides with alcohols, phenols and primary
amines

(f) explain the relative ease of hydrolysis of acyl chlorides, alkyl chlorides and aryl
chlorides

39
 (g) describe the formation of esters from carboxylic acids or acyl chlorides, using
ethyl ethanoate and phenyl benzoate as examples

(h) describe the acid and base hydrolysis of esters

(i) describe the formation of polyesters (see also Section 10.8)

(j) state the major commercial uses of esters e.g: solvents; perfumes; flavouring

10.7 NITROGEN COMPOUNDS

Content

I Primary amines (exemplified by ethylamine and phenylamine)

(i) Formation

(ii) Salt formation

(iii) Other reactions of phenylamine

II Amides (exemplified by ethanamide)

(i) Formation from acyl chlorides

(ii) Hydrolysis

III Amino acids (exemplified by aminoethanoic acid)

(i) Acid and base properties

(ii) Zwitterion formation

IV Proteins

(i) Structure, based on the peptide linkage

(ii) Hydrolysis of proteins

Learning Outcomes

Candidates should be able to:

(a) describe the formation of ethylamine (by nitrile reduction – see also Section
10.4) and of phenylamine (by the reduction of nitrobenzene)

(b) explain the basicity of amines

(c) explain the relative basicities of ammonia, ethylamine and phenylamine in

terms of their structures
40
 (d) describe the reaction of phenylamine with:

(i) aqueous bromine

(ii) nitrous acid to give the diazonium salt and phenol

(e) describe the coupling of benzenediazonium chloride and phenol and the use of
similar reactions in the formation of dyestuff

(f) describe the formation of amides from the reaction between RNH2 and RCOCl

(g) describe amide hydrolysis on treatment with aqueous alkali or acid

(h) describe the acid/base properties of amino acids and the formation of
zwitterions

(i) describe the formation of peptide bonds between amino acids and, hence,
explain protein formation

(j) describe the hydrolysis of proteins

(k) describe the formation of polyamides (see also Section 10.8)

10.8 POLYMERISATION

Content

I Addition polymerisation

II Condensation polymerisation

Learning Outcomes

Candidates should be able to:

(a) describe the characteristics of addition polymerisation as exemplified by

poly(ethene) and pvc

(b) recognise the difficulty of the disposal of polyalkenes, i.e. non-biodegradability

and harmful combustion products

( c) describe the characteristics of condensation polymerisation

(i) in polyesters as exemplified by Terylene

(ii) in polyamides as exemplified by peptides, proteins, nylon 6 and nylon

66

41
(d) predict the type of polymerisation reaction for a given monomer or pair of
monomers

(e) deduce the repeat unit of a polymer obtained from a given monomer or pair of
monomers

(f) deduce the type of polymerisation reaction which produces a given section of a
polymer molecule

(g) identify the monomer(s) present in a given section of a polymer molecule

42
 BIOCHEMISTRY OPTION

[A detailed treatment of this topic is given in the Option Booklet Biochemistry]

Statement of Aims

Biochemistry is the study of chemical processes in living organisms. Students should be

aware of the characteristics of living organisms and recognise that these characteristics are
maintained by complex chemical reactions. The basic structure of animal cells with reference
to the structure and function of sub-cellular organelles (nucleus, mitochondria, ribosomes,
endoplasmic reticulum and the membrane) is useful background but will not be examined in
this option. Students will not be expected to memorise the formulae or structures of complex
substances, such as proteins polysaccharides and nucleic acids. Students studying Biology
will inevitably have met some of the ideas in this option, but it is important to emphasise that
the course lays stress on the chemical interpretation of biological processes at the molecular
level.

1 PROTEINS

Content

I Amino acids

II Polypeptides and proteins

III Protein structure: primary; secondary; tertiary; quaternary structures

IV Denaturation of proteins

V Fibrous and globular proteins

VI Enzymes: relationship between enzymes and substrates; active sites;

reversible inhibition; coenzymes; lysozyme

Learning Outcomes

Candidates should be able to:

(a) state the general formula for -amino acids as RCH(NH2)CO2H; describe the
nature of the functional groups contained in R and be able to interpret the
properties of -amino acids in terms of their structure

(b) explain

(i) the formation of the peptide linkage between -amino acids leading to
the idea that polypeptides and proteins are condensation polymers

(ii) the term primary structure of proteins

43
(c) describe the hydrolysis of proteins and peptides and the separation of the
products by electrophoresis and ion-exchange chromatography

(d) interpret information obtained by the techniques as outlined in (c)

(e) describe the secondary structure of proteins: -helix and  - pleated sheet and
the stabilisation of these structures by hydrogen bonding

(f) state the importance of the tertiary protein structure and explain the
stabilisation of the tertiary structure with regard to the R groups in the amino
acid residues (ionic linkages, disulphide bridges, hydrogen bonds and van der
Waals’ forces)

(g) describe

(i) the quaternary structure of proteins

(ii) the protein components of haemoglobin

(h) explain denaturation of proteins by heavy metal ions, extremes of temperature

and pH changes

(i) apply the knowledge of the loss and formation of secondary and tertiary
structures to interpret common everyday phenomena

(j) describe the behaviour of enzymes as catalysts of high activity and specificity

(k) explain the relationship between enzyme and substrate concentration in

biochemical systems

(l) (i) determine the value of Vmax and Km, the Michaelis constant, by
graphical means

(iii) explain the meaning of, and use, Vmax and Km

(m) explain the significance of Km in the different physiological roles of hexokinase

and glucokinase

(n) explain the concept of the active site in enzyme structure

(o) compare competitive and non-competitive inhibition of enzymes in terms of

their effects on Vmax and Km

(p) explain competitive, including feed-back control of metabolism

(q) explain non-competitive inhibition, including by heavy metal ions

(r) explain the importance of coenzymes and cofactors with respect to enzyme
activity

44
2 CARBOHYDRATES

Content

I Monosaccharides - and -pyranose structure of glucose

II Disaccharides and polysaccharides as condensation polymers. The nature of

the glycosidic link; enzymic and acid hydrolysis of the glycosidic linkage

III Structure and function of cellulose as a structural polymer and starch and
glycogen as storage polymers

IV Consequences of hydrogen bonding on the relative solubilities of

monosaccharides and polysaccharides in water

Learning Outcomes

Candidates should be able to:

(a) describe the -and -pyranose ring structures of glucose polysaccharides and
condensation polymers

(b) predict the relative solubilities of monosaccahrides and polysaccharides on the

basis of hydrogen bonding

(c ) suggest how the structures and properties of cellulose, starch and glycogen
make them suitable for their roles as structural or storage polymers in plants
and animals

3 LIPIDS AND MEMBRANE STRUCTURE

Content

I Biological functions of lipids

II Simple structure and function of triglycerides

III Phosphoglycerides; simplified structure and function; formation of micelles and

bilayers

IV Membranes; fluid mosaic model; active transport

Learning Outcomes

Candidates should be able to:

(a) describe the structure and function of triglyceryl esters

(b) describe the structure and function of phosphoglycerides and the formation of
micelles and bimolecular layers

45
 (c) describe the fluid mosaic structure of membranes

(d) explain active transport by using the Na+/K+ pump as an example

4 NUCLEIC ACIDS

Content

I Nucleotides and nucleic acids

II DNA and RNA; base pairing

III DNA and genetic information

IV m-RNA and the triplet code

V ATP as an important example of a nucleotide; its importance in metabolic activity

Learning Outcomes

Candidates should be able to:

(a) describe, in simple terms, the structure of nucleotides and their condensation
polymers, nucleic acids

(b) describe the chemical and physical differences between DNA and RNA
molecules including the concept of base pairing and the part played by
hydrogen bonding

(c ) explain the role of DNA as the repository of genetic information, including the
triplet code

(d) describe the role of m-RNA in the transcription and translation phases in
protein synthesis

(e) describe the importance of the nucleotide ATP, with regard to the part it plays
in metabolic activity

46
 ENVIRONMENTAL CHEMISTRY OPTION

[A detailed treatment of this topic is given in the Option Booklet Environmental Chemistry]

Statement of Aims

Throughout this option, the emphasis is on the application of chemical facts and principles to
the explanation of the processes occurring in the environment, and to the solution of
problems of environmental chemical instability and pollution. In the context of this option, it is
important that students should appreciate this aspect, bearing in mind the currently
increasing concern, both national and international, for safeguarding the environment.

As standard practice, where relevant, the questions on this option will be accompanied in the
question paper with data on the nitrogen, carbon, oxygen and water cycles. Questions will be
based on this syllabus, not necessarily on the content of the publication described above.

Throughout this option, the teaching of the topics should be put into an environmental context.

1 THE ATMOSPHERE

Content

I The atmosphere and some of the processes that maintain its chemical
composition

II The carbon cycle: photosynthesis, respiration, the exchange of carbon dioxide

between air and water

III The nitrogen cycle

IV Naturally occurring free-radical reactions

V The effects on the atmosphere of the combustion of carbon-containing fuels

and of the release of pollutant gases

VI Polyatomic gases and the greenhouse effect: the control of the release of
pollutants

VII Generation of power

Learning Outcomes

Candidates should be able to:

(a) (i) apply to the carbon cycle the concepts of chemical equilibrium to describe and
explain how [CO2(atm)] depends on: photosynthesis; plant and animal
respiration; equilibrium with carbon dioxide dissolved in surface water,
including reference to other solution processes

(ii) calculate [CO2(aq)] given appropriate information

47
(b) apply to the nitrogen cycle the concepts of chemical equilibrium to describe how
[NO(atm)] and [NO2(atm)] depends on: their production as a result of lightning
discharges; the removal of NO2 by solution in water, forming acid rain

(c) apply the concepts of dynamic chemical equilibrium to describe and explain how the
stratospheric concentration of ozone is maintained by: the photodissociation of NO2,
O2 and O3 to give reactive oxygen atoms; the formation of O3 and OH by reaction of
oxygen atoms with O2 and H2O; the reaction between O3 and NO

(d) (i) apply the principles of chemical kinetics to the above reactions between free
radicals and molecules

(ii) to explain why free-radical reactions are important under the conditions
obtaining in the upper atmosphere

(e) outline the role of ozone in the stratosphere in reducing the intensity of harmful ultra-
violet radiation at the Earth’s surface

(f) show understanding that the relative rates at which a substance is supplied to and
removed from the atmosphere by various sinks leads to the concept of ‘residence
time’

(g) recognise that carbon monoxide, sulphur dioxide, oxides of nitrogen and lead
compounds may be released as a result of the combustion of hydrocarbon-based
fuels

(h) outline problems associated with the release of the pollutants specified in (g),
including acid rain and the formation by free-radical reactions of hazardous inorganic,
and organic, compounds (e.g. peroxyacetyl nitrate, pan)

(i) analyse, qualitatively, data relating to sequences of reactions, including those

involving free-radicals

(j) recognise that the manufacture of lime and cement involves the release of carbon
dioxide

(k) explain the build-up, and recognise the adverse effects, of ozone in the lower
atmosphere

(l) describe, in terms of relevant physical properties and chemistry,

(i) the use of CFCs

(ii) the role of CFCs in destroying ozone in the stratosphere (photodissociation

and free-radical chain reactions)

(m) recognise possible alternatives to the use of CFCs

(n) describe qualitatively the role of polyatomic pollutants in the greenhouse effect and
predict possible consequences of this effect
48
(o) outline the main industrial methods of controlling sulphur dioxide emission (flue
desulphurisation, removal of sulphur-containing compounds, alkaline scrubbing, use
of limestone-based fluidised beds)

(p) recognise the use of lean-burn engines and catalytic converters in reducing pollutant
emissions from petrol-driven cars

(q) (i) deduce environmental considerations related to the usage and generation of
power (with particular reference to fossil fuels and nuclear energy)

(ii) identify other potential power sources

(r) recognise the hazards associated with radon emission from uranium-bearing rocks
and with nuclear accidents

(s) outline the implications of absorption of carbon dioxide by the oceans – the
greenhouse effect and rock formation

(t) recognise other functions of the oceans in regulating climate

2 THE CHEMICAL STRUCTURE OF SOIL; PROCESSES INVOLVING SOILS AND

WATER

Content

I A general description of soil

II Ion exchange in soils

III redox processes in soil and water

IV The generation of acidity within soils, its effects and control

Learning Outcomes

Candidates should be able to:

(a) describe soil as a mixture of decomposing organic material and inorganic

compounds (with particular reference to N, P and K)

(b) explain the prevalence of oxides, carbonates and silicates as common

insoluble components in weathered soils

(c) outline the structure of layer silicates in terms of the combination of sheets of
silicon/oxygen and aluminium/oxygen

(d) compare 1:1 and 2:1 layer silicates, noting the importance of hydrogen

49
 bonding in the former

(e) describe ion substitution (Al3+ for Si4+ in Si/O layers and Mg 2+ for Al3+) within
layer silicates

(f) explain the formation of cracks in soils as a result of drying

(g) explain how ion retention occurs on the surface of silicate clays and the
importance of this for plant growth

(h) explain how absorbed hydrogen ions maintain soil acidity (see also (o), (p) and
(q) below)

(i) explain the role of oxygen in maintaining nitrogen in an oxidised form to

facilitate plant growth

(j) deduce from the electrode potentials the effects of reducing conditions in
terms of Fe2+ formation and the subsequent reduction of nitrate ions

(k) explain the formation of methane and hydrogen sulphide under extreme
reducing conditions, (e.g. from buried organic waste material)

(l) explain the importance of dissolved oxygen in rivers

(m) explain the role of oxides of carbon, sulphur and nitrogen in decreasing the pH
of water

(n) describe soil acidification as a result of respiration and growth

(o) explain the enhancement of nitrate reduction by increasing acidity and its
effect on nitrogen availability

(p) describe the replacement of cations at exchange sites by hydrogen ions as the
ambient acidity increases

(q) explain the lack of stability of silicate clays in acid solution and the consequent
release of aluminium ions

(r ) explain how the hydrated aluminium enhances acidity

(s) describe the increased solubility of heavy metal ions in acid solution

(t) explain how bedrocks containing carbonates limit the effects of acidity

(u) explain, in terms of the relevant equilibria, the buffering actions of the HCO-3
ion and humus (regarded as an organic acid, RCO2H)

(v) explain the role and limitations of liming, (e.g. as acid ice melts) in acidity
control

50
3 THE WATER CYCLE

Content

I The primary, secondary and tertiary treatment of sewage; BOD values, nitrates
and phosphates in water

II (i) The disposal of solid waste

(iii) The removal of metallic ions from industrial waste

Learning Outcomes

Candidates should be able to:

(a) explain the preparation of potable water by the separation of solid material,
precipitation by using Al3+(aq) and purification by chlorine

(b) outline the treatment of sewage as a removal of solids, organic matter,

measured by BOD, and the use of activated charcoal and selective
precipitations

(c ) recognise that chlorination can cause the formation of chlorinated organic

matter in domestic water

(d) explain the need for nitrogen – and phosphate containing fertilisers

(e) describe the leaching of nitrate and the conditions leading to the release of
nitrogen oxides and ammonia from fertilised land

(f) explain the function of phosphate additives in detergents and the disadvantage
of its presence (along with nitrates) in river water, e.g. eutrophication

4 WASTE MANAGEMENT

Content

Disposal, treatment of waste and recycling

Learning Outcomes

Candidates should be able to:

(a) outline the use of ion exchange in the treatment of industrial waste

(b) recognise the potential consequence of the use of land-filling and incineration
(including the importance of temperature control and the possible release of
dioxins) for the disposal of solid waste

51
(c ) outline the advantages and disadvantages of dumping waste at sea and in
rivers (including sewage as a source of nutrients and the problems associated
with oil spillages)

(d) recognise the problems associated with heavy metals in the environment, e.g.
lead, mercury and chromium

(e) recognise the problems associated with the disposal of radioactive waste

(f) recognise the problems associated with disposal of mine waste

(g) outline the advantages and difficulties of recycling waste materials

52
 PHASE EQUILIBRIA OPTION

[A detailed treatment of this topic is given in the Option Booklet Phase Equilibria]

Statement of Aims

This option applies equilibrium concepts within the main body of the syllabus to the
interaction between the different phases that occur in single component systems and those
that apply to multi-component systems, i.e. mixtures/solutions involving solids and liquids.

The application of these ideas to certain analytical techniques is also included.

1 PHASE DIAGRAMS

Content

I Phase diagrams of pure compounds; solutions of solids in solids and in liquids;

solutions of liquids in liquids.

II Eutectics

III Alloys

Learning Outcomes

Candidates should be able to:

(a) understand that phase diagrams are graphical plots of experimentally determined
results

(b) interpret phase diagrams as curves describing the conditions of equilibrium between
phases and as regions representing single phases

(c) predict how phases may change with changes in temperature or pressure

(d) sketch the shape of the phase diagram for water and explain the anomalous
behaviour of water

(e) understand and use the term eutectic

(f) interpret phase diagrams for two-component systems and predict how composition
and phase vary with changes in temperature

(g) sketch the shape of the phase diagram for mixtures of tin and lead

(h) state, and explain in simple terms, how the properties of common alloys differ from
those of pure metals in hardness, resistance to tarnishing, melting

(i) sketch the shape of the phase diagram for a two-component system, such as sodium
53
 chloride, or potassium nitrate, and water

(j) sketch the shape of the solubility curve of one of these salts in water.

2 RAOULT’S LAW AND DISTILLATION

Content

I Raoult’s law; its application to liquid-liquid mixtures; positive and negative deviations
from it related to intermolecular attractions or bonding.

II Boiling point/composition curves; fractional distillation; azeotropic mixtures

III Steam distillation

Learning Outcomes

Candidates should be able to:

(a) state and apply Raout’s law

(b) explain qualitatively the effect of a non-volatile solute on the vapour pressure of a
solvent and, hence, on its freezing point and boiling point

(c) outline in qualitative terms the relationship between boiling point, enthalpy change of
vaporisation and intermolecular forces

(d) interpret the boiling point/composition curves for mixtures of two miscible liquids in
terms of ‘ideal’ behaviour, or positive or negative deviations from Raoult’s Law

(e) understand and use the term azeotropic mixture

(f) explain the limitations on separating two components which form an azeotropic
mixture

(g) describe the principles of fractional distillation of ideal liquid mixtures

(h) describe a typical laboratory fractionating column

(i) demonstrate a knowledge and understanding of the packing of fractionating columns

and other means of establishing equilibrium at different temperatures between liquid
and vapour

(j) (i) explain the concept of theoretical plates in fractionating columns

(ii) deduce the number of theoretical plates by graphical means, using given data

(k) explain steam distillation of two immiscible liquids

(l) demonstrate an awareness of the applications of these methods of distillation to the

54
 laboratory separation of the components of liquid mixtures

3 DISTRIBUTION BETWEEN PHASES

Content

I Solubility of gases in liquids; Henry’s Law

II Partition coefficient; solvent extraction

Learning Outcomes

Candidates should be able to:

(a) describe and explain how the solubility of a gas in a liquid is affected by pressure,
temperature and change of chemical state

(b) state Henry’s Law and apply it in simple calculations

(c ) (i) state what is meant by a partition coefficient

(ii) calculate a partition coefficient for a system in which the solute is in the same
molecular state in the two solutions

(d) explain solvent extraction e.g. by using ether

4 SEPARATION TECHNIQUES FOR ANALYSIS: CHROMATOGRAPHY AND

ELECTROPHORESIS

Content

I Chromatography: theory and practice

II Electrophoresis: theory and practice in relation to peptide analysis and detection of

metal ions

Learning Outcomes

Candidates should be able to:

(a) describe simply and explain qualitatively, paper, high performance liquid, thin layer
and gas/liquid chromatography in terms of absorption and/or partition, based on
appropriate practical experience

(b) demonstrate an awareness of the applications of these methods of chromatography in

industry and medicine

55
(c ) describe simply the process of electrophoresis, and the effect of pH

(d) describe the hydrolysis of proteins and the separation and detection of the products by
electrophoresis

(e) outline simply the process of analysis of genes and genetic fingerprinting

56
 TRANSITION ELEMENTS OPTION

[A detailed treatment of this topic is given in the Option Booklet Transition Elements]

Statement of Aims

The material in this option is intended to build on (but be essentially independent of) the
transition elements material incorporated in the ‘core syllabus’

1 COMPLEXES

Content

I Bonding in complexes: stoichiometry, stereochemistry and isomerism of complexes

II Magnetism; colour

Learning Outcomes

Candidates should be able to:

(a) explain the terms complex, ligand, co-ordinate (dative covalent) bond

(b) explain the formation of complexes in terms of co-ordinate bonds and the splitting of d
electron energy levels

(c ) state that ligands may be neutral or anionic

(d) state that complexes typically exhibit four-fold or six-fold co-ordination

(e) describe the shape of four-fold complexes as either square planar or tetrahedral

(f) describe the shape of six-fold complexes as octahedral

(g) explain the types of isomerism that complexes (of the listed metals) may exhibit,
including those associated with polydentate ligands

(h) describe and explain ligand exchanges in terms of competing equilibria, including the
dissolving of insoluble compounds

(i) explain ligand exchange in terms of stability constants

(j) explain redox reactions of complexes in terms of E values

(k) interpret the effect of ligand exchange on E values

(l) explain, in terms of d orbital splitting, why transition element complexes are usually
coloured

57
(m) explain changes in colour of complexes as a result of ligand exchange

(n) explain the magnetic properties of transition metals and their complexes in terms of
paired and unpaired d electrons.

2 CHEMISTRY OF TRANSITION ELEMENTS

Contents

I Characteristic transition element chemistry as illustrated by vanadium, chromium,

manganese, iron, cobalt, nickel and copper.

II Some other chemistry of these metals

Learning Outcomes

Candidates should be able to describe and explain the chemistry of:

(a) vanadium, in respect of:

(i) its use in hardening steel,

(ii) the occurrence, relative stability and colour of its ions and compounds
containing the metal in the +2, +3, +4, +5 oxidation states.

(b) chromium, in respect of:

(i) its use in stainless steel and in hardening steel

(ii) the occurrence, relative stability and colour of its aqueous ions and compounds
containing the metal in the +3 and +6 oxidation states.

(iii) the use of dichromate (VI) as an oxidising agent

(iv) the chromate (VI) to dichromate (VI) interconversion

(c ) manganese, in respect of:

(i) the occurrence and relative stability and colour of its aqueous ions and
compounds containing the metal in the +2, +4, +6 and +7 oxidation states

(ii) redox reactions involving MnO2, MnO42 and MnO-4

(d) iron, in respect of:

(i) the biochemical importance of iron in haemoglobin and in cytochrome

(ii) the rusting of iron and its prevention

(iii) the use of iron, its ions or compounds in homogeneous and heterogenous

58
 catalysis, i.e. the Fe3+/Fe+ in the I-/S2O82 reaction; Fe/Fe2O3 in the Haber
process

(iv) the occurrence, relative stability and colour of its aqueous ions and compounds
containing the metal in the +2 and +3 oxidation states, including (in particular)
the effect of pH and the cyanide ligand on stability

(v) tests to distinguish between Fe2+ (aq) and Fe3+ (aq), namely
Fe(CN)63 (aq) and SCN (aq), respectively

(e) cobalt, in respect of

(i) the biochemical importance of cobalt

(ii) the occurrence, relative stability and colour of ions and compounds containing
the metal in its +2 and +3 oxidation states, including the use of anhydrous
cobalt (II) ions as a test for water and the effect of ligands and/or temperature
on the stability and geometry of cobalt complexes, using as examples

[Co(H2O)6]2+ [CoCl4]2, and

[Co(NH3)6]2+ [Co(NH3)6]3+

(iii) the use of cobalt in alloys, e.g. alnico

(f) nickel, in respect of:

(i) the production of nickel from its sulphide ore and its purification

(ii) the use of nickel in alloys, e.g. alnico

(iii) the use of nickel as a hydrogenation catalyst

(g) copper, in respect of:

(i) the production from its sulphide ores

(ii) its electrolytic purification, including reference to what happens to the metallic
impurities

(iii) its use in brass, bronze and other alloys

(iv) the occurrence and relative stability of ions and compounds containing the
metal in the +1 and +2 oxidation states, including the disproportionation and
stabilisation of Cu+ (aq)

(v) the use of alkaline aqueous Cu2+ complexes as a test for aldehydes

(vi) the Cu2+(aq)/I(aq) reaction

59
 PRACTICAL SYLLABUS (PAPER 5)

The papers in the practical paper may include the following:

(i) A volumetric analysis problem, based on one set of titrations;

A knowledge of the following volumetric determination will be assumed: acids and

alkalis using suitable indicators; iron (II), ethanedioic acid (and its salts), by
potassium manganate (VII); iodine and sodium thiosulphate. Simple titrations
involving other reagents may also be set but, where appropriate, sufficient
working details will be given.

(ii) Candidates may be required to carry out an experiment that involves the
determination of some quantity, e.g. the enthalpy change of a reaction or, the rate
of a reaction. Such experiments will depend on the simple manipulation of usual
laboratory apparatus.

(iii) An observational problem in which the candidate will be asked to investigate, by

specified experiments, an unkown substance. The substance may be an element,
a compound or a mixture.

Systematic analysis and a knowledge of traditional methods of separation will not be

required. It will be assumed that candidates will be familiar with (i) the reactions of the
following cations: NH4+; Mg2+; Al3+; Ca2+; Cr3+; Mn2+; Fe2+; Fe3+; Cu2+; Zn2+; Ba2+; Pb2+; (ii) the
reactions of the following anions: CO32; NO3; NO2; SO42; SO32; Cl; Br; I; CrO42; (iii) tests
for the following gases: NH3; CO2; Cl2; H2; O2; SO2, as detailed in the qualitative analysis
notes which will be included with the question paper.

The substances to be investigated may contain ions not included in the above list: in such
cases, candidates will not be expected to identify the ions but only to draw conclusions of a
general nature.

Candidates should not attempt tests, other than those specified, on substances, except when
it is appropriate to test for a gas.

Exercises requiring a knowledge of simple organic reactions as outlined in Section 10, e.g.
test-tube reactions indicating the presence of unsaturated, alcoholic, phenolic and carboxylic
groups, may also be set, but this would be for the testing of observation skills and drawing
general conclusions only.

Candidates are NOT allowed to refer to note books, text books or any other
information in the Practical examination.

One, or more, of the questions may incorporate some assessment of planning skills or
evaluating evidence and procedure.

Candidates may also be required to carry out calculations as detailed in the theory syllabus.

60
Practical techniques

The following notes are intended to give schools and candidates an indication of the accuracy
that is expected in quantitative exercises and general instructions for qualitative exercises.

(a) Candidates should normally record burette readings to the nearest 0.05cm3 and they
should ensure that they have carried out a sufficient number of titrations,e.g. in an
experiment with a good end-point, two titres within 0.10cm3.

(b) Candidates should normally record: weighings to the nearest 0.10g,

temperature readings to the nearest
0.5.C when using a thermometer
calibrated in 1C intervals and to the
nearest 0.1C where the interval is 0.2C.

(c ) In qualitative analysis exercises, candidates should use approximately 1cm depth of a

solution (1-2 cm3) for each test and add reagents slowly, ensuring good mixing, until
no further change is seen. Candidates should indicate at what stage a change occurs,
writing any deductions alongside the observation on which they are based. Answers
should include details of colour changes and precipitates formed and the names and
chemical tests for any gases evolved (equations are not required).

Marks for deductions or conclusions can only be gained if the appropriate observations
are recorded.

61
APPARATUS LIST

This list given below has been drawn up in order to give guidance to schools concerning the
apparatus that is expected to be generally available for examination purposes. The list is not
intended to be exhaustive: in particular, items (such as bunsen burners,tripods, glass-tubing)
that are commonly regarded as standard equipment in a chemical laboratory are not included.
Unless otherwise, the rate of allocation is “per candidate”.

Two burettes, 50cm3

Two pipettes, 25 cm3
One pipette, 10 cm3
Dropping pipette
One pipette filler
Conical flasks: three within range 150 cm3 to 250 cm3
Volumetric flask, 250 cm3
Measuring cylinders, 25 cm3 and 50 cm3
Wash bottle
Two filter funnels
Porcelain crucible, approximately 15 cm 3, with lid
Evaporating basin, at least 30 cm3
Beakers, squat form lip: 100 cm3, 250 cm3
Thermometers: -10C to +110C at 1C;
-5C to +50C at 0.2C
Plastic beaker, e.g. polystyrene, of approximate capacity 150 cm3
Test-tubes (some of which should be Pyrex or hard glass) approximately 125 mm x 16 mm
Boiling tubes, approximately 150 mm x 25 mm
Clocks (or wall-clock) to measure to an accuracy of about 1s. (Where clocks are specified,
candidates may use their own wrist watches if they prefer).
Balance, single-pan, direct reading, 0.01g or better (1 per 8-12 candidates).

Details of the requirements for a particular examination are given in the Instructions for
Supervisors which are sent to Centres several weeks prior to the examination. These
Instructions also contain advice about colour-blind candidates.

Supervisors are reminded of their responsibilities for supplying the Examiners with the
information specified in the Instructions. Failure to supply such information may cause
candidates to be unavoidably penalised.

The attention of Centres is drawn to the Handbook for Centres which contain a section on
Science Syllabuses which includes information about arrangements for practical
examinations.

62
QUALITATIVE ANALYSIS NOTES

[Key: ppt = precipitate; sol. = soluble; insol = insoluble; xs = excess.]

1 Reactions of aqueous cations

cation
reaction with
NaOH(aq) NH3(aq)

aluminium, white ppt. white ppt.

Al3+(aq) sol. in xs insol. in xs
ammonium, ammonia produced on heating
NH4+(aq)
barium no ppt. no ppt.
Ba2+(aq) (if reagents are pure)
calcium, white. Ppt. with high no ppt.
Ca2+(aq) [Ca2+(aq)]
chromium (III), grey-green ppt. sol. in xs grey-green ppt.
Cr3+(aq) giving dark green solution insol. in xs
copper(II), Cu2+(aq), pale blue ppt. blue ppt. sol. in xs
insol. in xs giving dark blue solution
iron (II), green ppt. green ppt.
Fe2+(aq) insol. in xs insol. in xs
iron (III), red-brown ppt. red-brown ppt.
Fe3+(aq) insol. in xs insol. in xs
lead (II), white ppt. white ppt.
Pb2+(aq) sol. in xs insol. in xs
magnesium, White ppt. white ppt.
Mg 2+(aq) insol. in xs insol. in xs
manganese (II), off-white ppt. off-white ppt.
Mn2+(aq) insol. in xs insol. in xs
zinc, White ppt. white ppt.
Zn2+(aq) sol. in xs sol. in xs

(Lead (II) ions can be distinguished from aluminium ions by the insolubility of lead (II)
chloride].

63
2 Reactions of anions

Ion Reaction

carbonate, CO2 liberated by dilute acids

CO32

chromate (VI) yellow soln turns orange with H+(aq);

CrO42(aq) gives yellow ppt. with Ba2+(aq);
gives bright yellow ppt. with Pb 2+(aq)
gives white ppt. with Ag+(aq) (sol. in NH3(aq))
chloride, Cl(aq) gives white ppt. with Pb2+(aq)
bromide, Gives pale cream ppt. with Ag+(aq) (partially sol. in NH3(aq));
Br(aq) gives yellow ppt. with Pb 2+(aq)
iodide, gives yellow ppt. with Ag +(aq) (insol. in NH3(aq));
I(aq) gives yellow ppt. with Pb 2+(aq)
nitrate, NO3(aq) NH3 liberated on heating with OH(aq) and Al foil
nitrite, NO2(aq) NH3 liberated on heating with OH(aq) and Al foil;
NO liberated by dilute acids
(colourless NO – (pale) brown NO2 in air)
sulphate, gives white ppt. with Ba2+(aq) or with Pb2+(aq) (insol. in xs
SO42(aq) dilute strong acids)
sulphite, SO2 liberated with dilute acids;
SO32(aq) gives white ppt. with Ba2+(aq) (sol. in dilute strong acids)

3 Test for gases

Gas Test and test result

ammonia, turns damp red litmus paper blue;

NH3
carbon dioxide, gives a white ppt. with limewater
CO2 (ppt. dissolves with xs CO2)
chlorine, bleaches damp litmus paper
Cl2
hydrogen, “pops” with a lighted splint
H2
oxygen, relights a glowing splint
O2
sulphur dioxide, turns aqueous potassium dichromate (VI) from orange to green
SO2

64
SUMMARY OF KEY QUANTITIES AND UNITS

The list below is intended as a guide to the more important quantities which might be
encountered in teaching and used in question papers. The list is not exhaustive.

Quantity Usual symbols SI unit

Base quantities
mass m kg, g
length l m
time t s
electric current I A
thermodynamic temperature T K
amount of substance n mol

Other quantities
temperature , t C
volume V, v m3, dm3
density  kg m3, g dm3,
pressure p Pa
frequency v, f Hz
wavelength  m, mm, nm
speed of electromagnetic waves c m s1
Planck constant h Js
electric potential difference V V

(standard) electrode potential (E) E V

redox
electromotive force E V
molar gas constant R JK1 mol1
half-life T½ t½ s
atomic mass ma kg
relative atomic mass Ar 
isotopic
molecular mass m kg
relative molecular mass Mr 
molar mass M kg mol-1
nucleon number A 
proton number Z 
neutron number N 
number of molecules N 
number of molecules per unit volume n m3
Avogadro constant L mol1
Faraday constant F C mol1
enthalpy change of reaction H J, kJ
standard enthalpy change of reaction H J mol1, kJ mol1
ionisation energy I kJ mol1
lattice energy  kJ mol1
bond energy  kJ mol1
electron affinity  kJ mol1
rate constant k as appropriate
65
equilibrium constant K, Kp, Kc as appropriate
acid dissociation constant Ka as appropriate
order of reaction n, m 
mole fraction x 
concentration c mol dm3
partition coefficient K 
ionic product, solubility product K, Ksp, as appropriate
ionic product of water Kw mol2 dm6
pH pH 

66
MATHEMATICAL REQUIREMENTS

It is assumed that candidates will be competent in the techniques described below.

(a) Make calculations involving addition, subtraction, multiplication and division of

quantities.

(b) Make appropriate evaluations of numerical expressions.

(c) Express small fractions as percentages, and vice versa.

(d) Calculate an arithmetic mean.

(e) Transform decimal notation to power of ten notation (standard form).

(f) Use tables or calculators to evaluate logarithms (for pH calculations), squares, square
roots, and reciprocals.

(g) Change the subject of an equation (Most such equations involve only the simpler
operations but may include positive and negative indices and square roots).

(h) Substitute physical quantities into an equation using consistent units so as to calculate
one quantity. Check the dimensional consistency of such calculations, e.g. the units of
a rate constant k.

(i) Solve simple algebraic equations.

(j) Comprehend and use the symbols/notations <, >, , , , , x , (or < x >).

(k) Test tabulated pairs of values for direct proportionality by a graphical method or by
constancy of ratio.

(l) Select appropriate variables and scales for plotting a graph, especially to obtain a
linear graph of the form y = mx + c.

(m) Determine and interpret the slope and intercept of a linear graph.

(n) Choose by inspection a straight line that will serve as the ‘least bad’ linear model for a
set of data presented graphically.

(o) Understand

(i) the slope of a tangent to a curve as a measure of the rate of change,

(ii) the ‘area’ below a curve where the area has physical significance, e.g.
Boltzmann distribution curves.

(p) Comprehend how to handle numerical work so that significant figures are neither lost
unnecessarily nor used beyond what is justified.
67
(q) Estimate orders of magnitude.

(r ) Formulate simple algebraic equations as mathematical models, e.g. construct a rate

equation, and identify failures of such models.

Calculators

If calculators are to be used, it is suggested that they should have the following functions:
+, , x, x2, x y, lgx. A memory function may be useful but is not essential.

68
GLOSSARY OF TERMS USED IN SYLLABUS/SCIENCE PAPERS

It is hoped that the glossary (which is relevant only to science subjects) will prove helpful to
candidates as a guide, i.e. it is neither exhaustive not definitive. The glossary has been
deliberately kept brief not only with respect to the number of terms included but also to the
descriptions of their meanings. Candidates should appreciate that the meaning of a term
must depend in part on its context.

1 Define (the term(s)…) is intended literally. Only a formal statement or equivalent

paraphrase being required.

2 What do you understand by/What is meant by (the term(s)…) normally implies that a
definition should be given, together with some relevant comment on the significance
or context of the term(s) concerned, especially where two or more terms are included
in the question. The amount of supplementary comment intended should be
interpreted in the light of the indicated mark value.

3 State implies a concise answer, with little or no supporting argument, e.g. a numerical
answer that can be obtained ‘by inspection’.

4 List requires a number of points, generally each of one word, with no elaboration.
Where a given number of points is specified, this should not be exceeded.

5 Explain may imply reasoning or some reference to theory, depending on the context.

6 Describe requires candidates to state in words (using diagrams where appropriate)

the main points of the topics. It is often used with reference either to particular
phenomena or to a particular experiment. In the former instance the term usually
implies that the answer should include reference to (visual) observations associated
with the phenomena.

In other contexts, describe and give an account of should be interpreted more

generally, i.e. the candidate has greater discretion about the nature and the
organisation of the material to be included in the answer. Describe and explain may
be coupled in a similar way to state and explain.

7 Discuss requires candidates to give a critical account of the points involved in the
topic.

8 Outline implies brevity, i.e. restricting the answer to giving essentials.

9 Predict or deduce implies that the candidate is not expected to produce the required
answer by recall but by making a logical connection between other pieces of
information. Such information may be wholly given in the question or may depend on
answers extracted in an earlier part of the question.

10 Comment is intended as an open-ended instruction, inviting candidates to recall or

infer points of interest relevant to the context of the question, taking account of the
number of marks available.
11 Suggest is used in two main contexts, i.e. either to imply that there is no unique
69
 answer (e.g. in chemistry, two or more substances may satisfy the given conditions
describing an ‘unknown’), or to imply that candidates are expected to apply their
general knowledge to a ‘novel’ situation, one that may be formally ‘not in the syllabus’.

12 Find is a general term that may variously be interpreted as calculate, measure,

determine etc.

13 Calculate is used when a numerical answer is required. In general, working should be

shown, especially where two or more steps are involved.

14 Measure implies that the quantity concerned can be directly obtained from a suitable
measuring instrument, e.g. length, using a rule, or angle using a protractor.

15 Determine often implies that the quantity concerned cannot be measured directly but
is obtained by calculation, substituting measured or known values of other quantities
into a formula, e.g. relative molecular mass.

16 Estimate implies a reasoned order of magnitude statement or calculation of the

quantity concerned, making such simplifying assumptions as may be necessary about
points of principle and about the values of quantities not otherwise included in the
question.

17 Sketch, when applied to graph work, implies that the shape and/or position of the
curve need only be qualitatively correct, but candidates should be aware that,
depending on the context, some quantitative aspects may be looked for, e.g. passing
through the origin, having an intercept, asymptote or discontinuity at a particular value.

In diagrams, sketch implies that a simple, freehand drawing is acceptable:

nevertheless, care should be taken over proportions and the clear exposition of
important details.

18 Construct is often used in relation to chemical equations where a candidate is

expected to write a balanced equation, not factual recall but by analogy or by using
information in the question.

19 Compare requires candidates to provide both the similarities and differences between
things or concepts.

20 Classify requires candidates to group things based on common characteristics.

Special Note

Units, significant figures. Candidates should be aware that misuse of units and/or
significant figures, i.e. failure to quote units where necessary, the inclusion of units in
quantities defined as ratios or quoting answers to an inappropriate number of significant
figures, is liable to be penalised.

70
The information contained in this document may be subject to alteration in the light of
changing circumstances.

Any alternations to previous published information will be communicated to registered

centres.
71
Any correspondence should be address to:

Zimbabwe School Examinations Council

Examinations Centre
Upper East Road
Mount Pleasant
P O Box CY 1464
Causeway
Harare

/SK
C:\MYDOCUMENTS\ADV-LEVEL-CHEMISTRY SYLLABUS

72