WAEC Chemistry Syllabus 2022 PDF Download Available
WAEC Chemistry Syllabus 2022 PDF Download Available
WAEC Chemistry Syllabus 2022 PDF Download Available
Atoms, molecules and ions. Definition of particles and treatment of particles as building
blocks of matter.
Explain physical and chemical changes with examples. Physical change- melting of solids,
magnetization of iron, dissolution of salt etc. Chemical change- burning of wood, rusting of
iron, decay of leaves etc. Detailed {electron|negatron|lepton} configurations (s,p,d) for atoms
of the first thirty elements. Origin of s,p and d orbitals as sub-energy levels; shapes of s and p
orbitals only.
(1) Aufbau Principle, Hund’s Rule of Maximum Multiplicity and Pauli Exclusion Principle.
(2) Abbreviated and {detailed|elaborate|elaborated|careful} {electron|negatron|lepton}
configuration in terms of s, p, and d WAEC {syllabus|course of study|program|programme|
curriculum|information|info} For Chemistry |
Explanation of the periodic law. Periodic properties; atomic size, ionic size, ionization
energy, {electron|negatron|lepton} affinity and {electronegativity|negativity|tendency|
inclination}. Simple discrepancies {should|ought to} be accounted for in {respect to|reference
to|regard to|relation to|relevance|relevancy} {beryllium|Be|glucinium|atomic number 4|
metallic element|metal}, boron, {oxygen|O|atomic number 8|chemical element|element|gas}
and {nitrogen|N|atomic number
(1) Period three metals (Na, Mg, Al). (2) Period four metals (K, Ca). (3) Chemical equations.
(4) {ph|pH|pH scale|hydrogen ion concentration} of solutions of the {metallic|metallic |
aluminous|aluminiferous|antimonial|argentiferous|auriferous|gold-bearing|bimetal|bimetallic|
bronze|gold|golden|gilded|silver|tinny|metallike} oxides and trioxocarbonates.
Factors influencing covalent bond formation. Electron affinity, ionization energy, atomic size
and electronegativity.
Solubility in polar and non-polar solvents, melting point, boiling point and electrical
conductivity.
Formation and difference between pure covalent and coordinate (dative) covalent bonds.
Linear, planar, tetrahedral and shapes {for some|for a few} compounds e.g.
BeCl2, BF3, CH4, NH3, CO2. Factors {should|ought to} include: atomic radius, ionization
energy and {number|variety|range} of valence electrons.
Types of specific packing not required. Typical properties {including|as well as|together
with} heat and electrical {conductivity|conduction|physical phenomenon}, {malleability|
plasticity|physical property}, lustre, ductility, {sonority|plangency|resonance|reverberance|
ringing|sonorousness|vibrancy|timbre|timber|quality|tone} and hardness.
Relative physical properties of polar and non-polar compounds. Description of formation and
nature should be treated. Dipole-dipole, {induced|induced |elicited|evoked|iatrogenic} dipole-
dipole, {induced|induced |elicited|evoked|iatrogenic} dipole-induced dipole forces {should|
ought to} be treated {under|beneath|underneath|below} van der Waal’s forces. Variation of
the melting points and boiling points of noble gases, halogens and alkanes {in the|within the}
homologous series explained in terms of van der Waal’s forces; and variation {in the|within
the} boiling points of {h2o|water|H2O|binary compound|liquid}, and H2S explained {using|
exploitation|victimization|victimisation|mistreatment} {hydrogen|H|atomic number 1|
chemical element|element|gas} bonding
Calculations involving formulae and equations will be required. Mass and volume
relationships in chemical reactions {and the|and therefore the|and also the} {stoichiometry|
ratio} of such reactions such as: calculation of {percentage|proportion|share} composition of
{element|part|component}. (1) Combustion reactions (including combustion {of simple|of
straightforward|of easy} hydrocarbons) (2) Synthesis (3) Displacement or replacement (4)
Decomposition (5) Ionic reactions (1) Laws of conservation of mass. (2) Law of constant
composition. (3) Law of multiple proportions. Explanation of the laws to balance given
equations. (4) Experimental illustration of the law of conservation of mass.
(1) Mass and volume measurements. (2) The mole as a unit of measurement; Avogadro’s
constant, L= 6.02 x 1023 entities mol-1. (3) Molar quantities and their uses. (4) Moles of
electrons, atoms, molecules, formula units etc.
Use of mole ratios in crucial ratio of chemical reactions. Simple calculations to work out the
amount of entities, quantity of substance, mass, concentration, volume and proportion yield
of product. (1) construct of an answer as created from solvent and matter. (2) Distinguishing
between dilute solution and concentrated solution. (3) Basic, acidic and neutral solutions.
Mass (g) or moles (mol) per unit volume. Emphasis on current IUPAC chemical word,
symbols and conventions. Concentration be expressed as mass concentration, g dm-3,
molarity, mol dm-3.
(1) Preparation of some primary standards e.g anhydrous Na2CO3, (COOH)2,
2H2O/H2C2O4.2H2O. (2) Meanning of the terms primary normal, secondary normal and
normal resolution.
Dilution factor
(2) Classify acids and bases into {strong|robust|sturdy} and weak. (3) Extent of dissociation
reaction with water and {conductivity|conduction|physical phenomenon}. (4) Behaviour of
weak acids and weak bases in water as example of equilibrium systems.
(1) Definition of {ph|pH|pH scale|hydrogen ion concentration} and {knowledge|information|
data} of {ph scale|pH|pH scale|hydrogen ion concentration}.
(1) Description of laboratory and industrial production of salts. (2) Mining of impure sodium
chloride and conversion into granulated salt. (3) Preparation of NaOH, Cl2 and H2.
(1) Explanation of how salts forms acidic, alkaline and neutral aqueous solutions. (2)
Behaviour of some salts (e.g NH4Cl, AlCl3, Na2CO3, CH3COONa) in water as examples of
equilibrium systems. (3) Effects of charge density of some cations and anions on the
hydrolysis of their aqueous solution. Examples to be taken from group 1, group 2, group 3
and the d-block element.
(1) Qualitative description of how acidbase indicator works. (2) Indicators as weak organic
acids or bases (organic dyes). (3) Colour of indicator at any pH dependent on relative
amounts of acid and forms. (4) Working pH ranges of methyl orange and phenolphthalein.
(1) Knowledge and correct use of relevant apparatus. (2) Knowledge of how acid-bases
indicators work in titrations.
(3) Acid-base titration experiments involving HCl, HNO3, H2SO4 and NaOH, KOH,
Ca(OH)2, CO32-, HCO3-. (4) Titration involving weak acids versus strong bases, strong
acids versus weak bases and strong acids versus strong bases using the appropriate indicators
and their applications in quantitative determination; e.g. concentrations, mole ratio, purity,
water of crystallization and composition.
(1) Meaning of Solubility. (2) Saturated and unsaturated solutions. (3) Saturated solution as
an equilibrium system. (4) Solubility expressed in terms of: mol dm-3 and g dm-3 of
solution/solvent. (5) Solubility curves and their uses. (6) Effect of temperature on solubility
of a substance. (7) Relationship between solubility and crystallization. (8)
Crystallization/recrystallization as a method of purification. (9) Knowledge of soluble and
insoluble salts of stated cations and anions. (10) Calculations on solubility.
Generalization about solubility of salts and their applications to qualitative analysis. e.g.
Pb2+, Ca2+, Al3+, Cu2+, Fe2+, Fe3+, Cl-, Br-, I-, SO42-, S2-, and CO32-, Zn2+, NH4+,
SO32- Explanation of solubility rules.
(1) Definition of reaction rate. (2) Observable physical and changes: colour, mass,
temperature, pH, formation of precipitate etc.
(1) Physical states, concentration/ pressure of reactants, temperature, catalysts, light, particle
size and nature of reactants. (2) Appropriate experimental demonstration for each factor is
required.
(1) Collision and transition state theories to be treated qualitatively only. (2) Factors
influencing collisions: temperature and concentration. (3) Effective collision. (4) Activation
energy. (5) Energy profile showing activation energy and enthalpy change.
(e) Electrolysis:
(1) Oxidation and reduction in terms of: (a) addition and removal of oxygen and hydrogen;
(b) loss and gain of electrons; (c) change in oxidation numbers/states. (2) Determination of
oxidation numbers/states.
(1) Description of oxidizing and reducing agents in terms of: (a) addition and removal of
oxygen and hydrogen; (b) loss and gain of electrons; (c) change in oxidation numbers/state.
Balancing redox equations by: (a) ion, electron or change in oxidation number/states; (b) half
reactions and overall reaction.
(1) Electrochemical cells as a combination of two half-cells. (2) The meaning of magnitude
and sign of the e.m.f.
(1) Distinction between primary and secondary cells (2) Daniell cell, lead acid battery cell,
dry cells, fuel cells and their use as generators of electrical energy from chemical reactions.
Definition.
Mechanism of electrolysis.
Limit electrolytes to molten PbBr2 and NaCl, dilute NaCl solution, concentrated NaCl
solution, CuSO4(aq), dilute H2SO4, NaOH(aq) and CaCl2(aq) (using platinum or graphite
and copper electrodes).
Simple calculations based on the relation 1F= 96,500 C and mole ratios to determine mass,
volume of gases, number of entities, charges etc. using half and overall reactions.
(1) Corrosion treated as a redox process. (2) Rusting of iron and its economic costs. (3)
Prevention based on relative magnitude of electrode potentials and preventive methods like
galvanizing, sacrificial/cathodic protection and non-redox methods (painting, greasing/oiling
etc.)
(a) Classification
(ii) Isomerism.
(f) Alkanes:
(ii) Uses.
(g) Alkenes:
(ii) Uses;
(h) Alkynes:
(i) Benzene:
(J) Alkanols:
(ii) Classification;
(vi) Uses.
(iv) Uses.
(iv) Uses
Broad classification into straight chain, branched chain, aromatic and alicyclic compounds.
(1) Composition and classification. (2) Fractional distillation and major products. (3)
Cracking and reforming. (4) Petro-chemicals: sources; uses e.g. as starting materials of
organic synthesis. (5) Quality of petrol, meaning of octane number and its importance to the
petroleum industry.
(1) Gradation in physical properties. (2) Effects on the physical properties by introduction of
active groups into the inert alkane.
(1) Examples should be limited to compounds having maximum of five carbon atoms. (2)
Differences between structural and geometric/stereo isomerism.
(1) Laboratory and industrial preparations and other sources. (2) Nomenclature and structure.
(3) Reactivity: (a) combustion; (b) substitution reactions; (c) cracking of large alkane
molecules.
As fuels, as starting materials for synthesis. Uses of haloakanes and pollution effects.
(3) Addition reactions with halogens hydrogen, bromine water, hydrogen halides and
acidified water. (4) Oxidation: hydroxylation with aqueous KMnO4. (5) Polymerization.
(1) Nomenclature and structure. (2) Industrial production of ethyne. (3) Uses of ethyne. (4)
Distinguishing test between terminal and non-terminal alkynes. (5) Test to distinguish
between alkane, alkene and alkyne.
(1) Addition reactions: hydrogenation and halogenation (mechanism not required). (2)
Compare reactions with those of alkenes
(1) Laboratory preparation including hydration of alkenes. (2) Industrial and local production
of ethanol including alcoholic beverages, (3) Harmful impurities and methods of purification
should be mentioned. (4) Recognition of the structure of mono, di- and triols.
(1) Reaction with: (a) Na; (b) alkanoic acids (esterification); (c) conc. H2SO4. (2) Oxidation
by: (a) KMnO4(aq); (b) K2Cr2O7(aq); (c) I2 in NaOH(aq).
Acid properties only i.e. reactions with H2O, NaOH, NH3, NaHCO3, Zn and Mg.
Reaction with NaHCO3, Na2CO3.
Uses of ethanoic and phenyl methanoic (benzoic) acids as examples of aliphatic and aromatic
acids respectively.
RECOMMENDED:
(c) Biotechnology.
(1) Natural resources in candidate’s won country. (2) Chemical industries in candidates own
country and their corresponding raw materials. (3) Distinction between fine and heavy
chemicals
(4) Factors that determine location of chemical industries. (5) Effect of industries on the
community.
(1) Sources, effects and control. (2) Greenhouse effect and depletion of the ozone layer. (3)
Biodegradable and non-biodegradable pollutants.
Food processing, fermentation including production of garri, bread and alcoholic beverages
e.g. Local gin.
(c) Fats/oils:
(d) Carbohydrates:
(ii) Properties;
(iv) Uses.
(i) Properties;
Physical properties e.g. solubility Chemical properties to include: (a) hydrolysis of proteins;
(b) laboratory test using Ninhydrin/Biuret reagent/Millons reagent.
(1) Nomenclature and general structure of amino acids. (2) Difunctional nature of amino
acids.
(1) Preparation of soap (saponification) from fats and oils. (2) Comparison of soap less
detergents and their action on soft and hard water.
(1) Classes of carbohydrates as: (a) monosaccharides; (b) disaccharides; (c) polysaccharides.
(2) Name and components of various classes of carbohydrates.
(1) Physical properties such as solubility of sugars. (2) Chemical properties- Hydrolysis of
disaccharides into monosaccharides. (3) Test for reducing sugars using sugar strips, Fehling’s
or Benedicts solution or Tollen’s reagent.
(1) Definition of terms: monomers, polymers and polymerization. (2) Addition and
condensation polymerization. (3) Classification and preparation based on the monomers and
comonomers.
(1) Thermoplastics and thermosets. (2) Modification of properties of polymers. (3) Plastics
and resins. (4) Chemical test on plastics using: (a) heat; (b) acids; (c) alkalis
(ii) Types and nature of radiations: alpha, beta particles and gamma radiation.
(1) Qualitative knowledge of the mass spectrometer: principles and operations of the mass
spectrometer; and its use to detect isotopes, determination of Relative atomic and molecular
masses only. (2) Wave nature of electrons. (3) Quantum numbers and their importance.
Meaning of terms: Nucleons, nuclide.
(1) Carbon dating (qualitative treatment only). (2) Use of radioactivity in agriculture,
medicine and industries. (3) Hazards associated with nuclear radiations.
Factors affecting stability of nuclides: Binding energy, neutron-proton ratio, and half life.
Calculations involving half-life
(a) Reactions between acids and metals their oxides and trioxocarbonates (IV).
(c) Physical and chemical properties of period 3 elements and their compounds.
(d) Silicon
(1) Period three metals (Na, Mg, Al) (2) Period four metals (K, Ca) (3) Chemical equations
(4) pH of solutions of the metallic oxides and trioxocarbonates.
(1) Oxides of carbon, nitrogen, sulphur, phosphorus and chlorine. (2) pH of aqueous solutions
of the oxides. (3) Chemical equations.
(1) Comparison of the physical and chemical properties of period three elements. (2)
Comparison of the physical and chemical properties of (hydrides, oxides, hydroxides and
chlorides) compounds. (3) Thermal stability of CO32- and NO3- of Li, Na, K, Mg and Ca.
(4) Experiment to compare thermal stability of Na2CO3/LiCO3/CuSO4
(1) Structures for SiO2 and CO2 account for the differences between physical and chemical
properties of the two oxides. (2) Uses of silicon and its compounds e.g. ceramics, glass, silica
gel and microchips.
(1) Inter- atomic bond energies. (2) Hydrides and their acid strength comparison of the Ka
values of the hydrogen halides. (3) Variable oxidation states of the halogens.
Definition of ligands and central ions Examples of ligands (1) Formation of coordination
compounds. (2) Nomenclature of complex ions and compounds (Cl-, F-, I-, NO3-, NH3,
H2O, SO42-).
Reactivity of the metals with air, water, acids and comparison with s-block elements (Li, Na,
Be, Mg).
(a) Formation of Ionic bonds: (i) Factors that influence ionic bond formation
(1) Ionic character (polarity) in covalent bonds based on electronegativity difference between
the species involved. (2) Effects of covalent and ionic character in ionic and covalent bonds
on the solubility, thermal stability and boiling points of ionic and covalent compounds.
Definition of Hybridization.
(1) Description of sp, sp2, sp3 hybrid orbitals. (2) Shapes of sp, sp2, sp3 and sp3d2 hybrid
orbitals. Treatment should be limited to the following molecules only. CH4, H2O, NH3,
BCl3, C2H2, BeCl2, C2H4 and SF6.
(1) Outline of steps involved in the preparation of solutions from liquid solutes. (2)
Determination of concentration of liquid solutes (stock solution) given the density, w/v,
w/w), specific gravity, relative molecular mass, molar mass, and % purity. (3) Primary
standard, secondary standard and standardized solution.
(1) Definition and understanding of the meaning of the energy terms: systems, surroundings,
open and closed. (2) Enthalpy change involved in the following processes: combustion,
atomization, sublimation, hydration/salvation and dissolution.
Explanation of Hess’s law and its application in the development of the Born-Haber cycle.
(1) Use of difference cycles to illustrate Hess’s law.
(2) Simple calculations using chemical equations, energy cycles or diagrams with given
energy changes.
Explanation of bond energy and bond dissociation energy. (1) Bond energy as an average
value. Differences in bond energy and bond dissociation energy. (2) Bond energy in
molecules and its use in assessment of bond strength, energy content and enthalpy of
reaction. (3) Calculations using summation of bond energies in reactants and products as a
measure of enthalpy of reaction.
(1) Ionic product constant of water Kw = [H+(aq)][OH(aq)] = 1.0 x 10-14 mol2dm-6. (2) pH
and pOH as a measure of acidity and alkalinity respectively pH = -log[H3O+]. (3)
Knowledge of pH scale. (4) Calculation of [H+], [OH-] and the corresponding pH and pOH
of given solutions.
Explanation of pKa and pKb of weak acids and bases. (1) Behaviour of weak acids and weak
bases in water as example of equilibrium systems. (2) Calculations involving Ka, pKa and
Kb, pKb. (3) Ka, pKa and Kb, pKb as measurements of acid and basic strengths respectively.
(1) Qualitative definition of buffers. (2) Examples of buffers from the laboratory. (3)
Preparation of buffer solutions.
Double indicator titrations (continuous and Discontinuous) and back titration. Calculations
involving concentration, composition and % purity. Graphs for acid-based titrations. Nature
of graphs of strong acid and strong base, strong acid and weak base and strong base and weak
acid
(1) Explanation of solubility products (Ksp) of sparingly soluble ionic compounds. (2)
Calculations involving solubility and solubility products. (3) Factors affecting solubility.
Explanation of the effect of lattice energy and hydration energy on crystallization and
recrystallization.
(c) Equilibrium
(1) Deduction of order and rate law from experimental data. (2) Simple relationship between
rates and concentration of zero, first and second order reactions. Graphical representation of
zero, first and second order reactions. (3) Half-life for first order reactions and its
significance. (4) General rate law equation. (5) Derivation of the rate expression from
experimentally determined rate data: R = k[A]x [B]y where k = rate constant.
(1) Mathematical expression for the determination of equilibrium constant K (2) K is constant
for a system at constant temperature. (3) Relationship between Kp and Kc. (4) Calculation of
Kp and Kc from given set of data. (5) Difference between homogeneous and heterogeneous
equilibrium systems
(d) Alkanes
Other methods should include solvent extraction and melting point determinations.
Outline of steps in: (a) Detection of N, S and the halogens. (b) Estimation of C, H and O.
(1) Inductive effect and Mesomeric effect. (2) Resonance illustrated with benzene molecule.
(3) Explanation of the terms: nucleophiles, electrophiles, free radicals and ions. homolytic
fission, heterolytic fission.
Mono substituted reactions of benzene: toluene, phenol, aniline, benzoic acid and
nitrobenzene. (IUPAC and trivial names)
Differences between the reactivity of benzene and alkenes towards certain reagents. Uses of
hexachlorocyclobezane and benzene hexachloride (BHC).
(1) Metals – gold, bauxite, manganese and iron. (2) Precious stone – diamond. (3) Industrial
mining of limestone CaCO3, clay Kaolin, solar salt (4) Processing of Au, Al, Fe as main
products (5) Uses of the metals
(1) Sources of raw materials for cement production. (2) Processes involved in the production
of cement. (3) Uses of cement. (4) Environmental impact.
(iii) Coke: I. Classification and uses; II. Manufacture of synthetic gas and uses.
(b) Oxygen: (i) Laboratory and industrial preparation; (ii) Properties and uses;
(iii) Binary compounds of oxygen: acidic, basic, amphoteric and neutral oxides.
(ii) Water as a solvent; (iii)Hardness of water, causes and methods of removing it;
(e) Halogens:
(h) Sulphur: (i) Allotropes and uses; (ii) Compound of sulphur; (iii) Trioxosulphate (IV) acids
and its salts; (iv) Tetraoxosulphate (VI) acid: industrial preparation, reactions and uses.
(1) Graphite, diamond and amorphous Carbon; (2) Structures, properties and uses. (3) The
uses of the allotropes should be correlated with their properties and structures. (4)
Combustion of allotropes.
(1) Laboratory preparation. (2) Properties and uses. (3) Test for carbon (IV) oxides.
(2) Uses.
Test for water will be required. Reference should be made to the electrolysis of acidified
water.
(1) Advantages and disadvantages of hard water and soft water. (2) Experiments to compare
the degrees of hardness in different samples of water.
Uses should include silver halide in photography and sodium oxochlorate (I) as a bleaching
agent.
Both laboratory and industrial preparations from liquefied air are required.
(1) Laboratory and industrial preparations. (2) Properties and uses. (3) Test for ammonia. (4)
Fountain experiment.
(1) Laboratory preparation. (2) Properties and uses. (1) Action of heat will be required. (2)
Test for trioxonitrate (V) ions.
(b) Alloys.
(e) Reactivity of iron and aluminium with air, water and acids. (f) Properties and uses of
copper and its compounds
(1) Raw materials, processing, main products and by-products. (2) Uses of metals.
Compounds must be limited to NaCl, NaOH, Na2CO3, NaNO3, Na2SO4 and NaClO.
The compounds must be limited to CaCO3, CaO, CaSO4, CaCl2, and Ca(OH)2
16.0 PRACTICALS
WAEC Syllabus For Chemistry | (a) GENERAL SKILLS AND PRINCIPLES
Candidates will be expected to be familiar with the following skills and principles: (i)
Measurement of mass and volume; (ii) Preparation and dilution of standard solutions; (iii)
Filtration, recrystallisation and melting point determination; (iv) Measurement of heats of
neutralization and solutions; (v) Determination of pH value of various solutions by
colorimetry;
Acid-base titrations
The use of standard solutions of acids and alkalis and the indicators; methyl orange, methyl
red and phenolphthalein to determine the following:
(i) The concentrations of acid and alkaline solutions; (ii) The molar masses of acids and bases
and water of crystallization. (iii) The solubility of acids and bases; (iv) The percentage purity
of acids and bases; (v) Analysis of Na2CO3/NaHCO3 mixture by double indicator methods
(Ghanaians only). (vi) Stoichiometry of reactions.
Redox titrations Titrations of the following systems to solve analytical problems: (i) Acidic
MnO4- with Fe2+; (ii) Acidic MnO4- with C2O42-; (iii) I2 in KI versus S2O32-.
(i) Characteristic tests of the following cations with dilute NaOH(aq) and NH3(aq);
(iii) Characteristic reaction of dilute HCl on solids or aqueous solutions and conc. H2SO4 on
solid samples of the following: Cl- ; SO32- ; CO32- ; NO3- and SO42-.
(vi) Characteristic tests for the following gases: H2; NH3; CO2; HCl and SO2.
(vii) Characteristic test tube reactions of the functional groups in the following simple
organic compounds: Alkenes; alkanols; alkanoic acids, sugars (using Fehiling’s and
Benedict’s solutions only); starch (iodine test only) and proteins (using the Ninhydrin test,
Xanthoporteic test, Biuret test and Millon’s test only).
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