GCE A/L Chemistry study plan
GCE A/L Chemistry · Give each week a clear focus.
8 weeks · About 7 hours per week
Atomic structure and periodicity & Organic chemistry: structure, nomenclature and functional groups
Draw electron configurations (including exceptions such as Cr and Cu) and assign quantum numbers for the first 36 elements without notes
Explain and predict periodic trends in atomic and ionic radius, ionisation energy, electron affinity and electronegativity using effective nuclear charge and shielding
Name and draw straight-chain and branched alkanes, alkenes, alkynes, haloalkanes and alcohols using IUPAC rules, including stereochemical descriptors (E/Z, R/S)
Identify and classify functional groups in unfamiliar structures and state the homologous series and general formula for each
Your checkpoint
A one-page annotated periodic-trend summary sheet plus a 40-structure IUPAC naming worksheet scored against a mark scheme (target 85% correct)
Chemical bonding and intermolecular forces & Organic chemistry: structure, nomenclature and functional groups
Construct dot-and-cross diagrams and predict molecular geometry and bond angles using VSEPR for molecules with 2-6 electron domains, including lone-pair distortions
Assign hybridisation and describe sigma/pi bonding in given molecules, relating shape to orbital overlap
Rank and justify intermolecular forces (London, dipole-dipole, hydrogen bonding) and predict relative boiling points and solubility
Draw and name carbonyl compounds, carboxylic acids, esters, amines, amides and nitriles, and describe their key physical properties
Your checkpoint
A comparison table of 15 molecules giving shape, bond angle, hybridisation, polarity and dominant intermolecular force, plus a written justification of three anomalous boiling points
Chemical equilibrium, acids, bases and buffers & Gases, kinetic theory and the mole concept
Apply Le Chatelier's principle to predict the direction of shift for changes in concentration, pressure, temperature and catalyst, and explain the effect on Kc and Kp
Write and manipulate Kc and Kp expressions, including units, and solve equilibrium composition problems from initial amounts
Perform mole calculations involving gases (ideal gas equation, molar volume at RTP), solutions and limiting reagents, with consistent significant figures
Calculate pH of strong and weak acids and bases and of buffer solutions from Ka and the Henderson-Hasselbalch relationship
Your checkpoint
A timed 10-question equilibrium-and-moles problem set (45 minutes) fully worked, with a written error log identifying each mistake type
Chemical equilibrium, acids, bases and buffers & Energetics and thermochemistry
Explain Brønsted-Lowry and Lewis acid-base behaviour and predict the relative strength of acids from structure and conjugate-base stability
Construct and interpret titration curves for strong/weak acid-base combinations and select suitable indicators
Calculate enthalpy changes from calorimetry data and from standard enthalpy of formation and combustion using Hess's law
Use mean bond enthalpies and Born-Haber cycles to calculate lattice enthalpy and explain deviations from ideal ionic behaviour
Your checkpoint
A full mock section on equilibrium, acids, bases and energetics (25 marks) completed under timed conditions with self-marking against a scheme
Kinetics and reaction mechanisms & Electrochemistry and redox
Derive rate equations from initial-rate and concentration-time data, determine order and rate constant with units, and deduce half-life behaviour for first-order reactions
Explain collision theory, the effect of temperature and catalysts on rate, and sketch and interpret Maxwell-Boltzmann and energy profile diagrams
Propose stepwise mechanisms consistent with a given rate equation, including SN1, SN2, E1 and E2 for haloalkanes and the role of the intermediate carbocation
Assign oxidation states, balance half-equations and full redox equations in acidic and alkaline media, and calculate cell EMF from standard electrode potentials
Your checkpoint
A mechanism-and-kinetics portfolio: 8 hand-drawn mechanisms with curly arrows and rate-law justification, plus 5 fully balanced redox equations with EMF calculations
Organic reaction mechanisms and synthesis & Electrochemistry and redox
Predict products and write balanced equations for nucleophilic substitution, elimination, addition, oxidation and reduction reactions of the functional groups covered so far
Design two- to four-step syntheses from a given starting material to a target molecule, selecting reagents and conditions and justifying each step
Explain electrophilic addition to alkenes including Markovnikov orientation and carbocation stability, and the mechanism of electrophilic substitution in arenes
Predict the products of electrolysis of molten and aqueous electrolytes and calculate masses and volumes using Faraday's laws
Your checkpoint
A synthesis map linking at least 20 interconversions between functional groups, plus three multi-step synthesis routes written out with reagents, conditions and mechanisms
Industrial, environmental and applied chemistry & Laboratory techniques, qualitative and quantitative analysis
Describe the chemistry and conditions of the Haber, Contact and Ostwald processes and explain the economic and equilibrium trade-offs in operating conditions
Explain the chemistry of greenhouse gases, acid deposition, photochemical smog and water treatment, and evaluate one mitigation strategy with data
Select and justify appropriate separation and purification techniques (filtration, recrystallisation, distillation, solvent extraction, chromatography) for given mixtures
Interpret qualitative analysis results for common cations, anions and gases, and plan a quantitative titration or gravimetric procedure including indicator and apparatus choice
Your checkpoint
A written practical-style report on one applied topic (e.g. industrial ammonia or water treatment) with calculations, plus a completed unknown-substance identification flow chart
Atomic structure and periodicity & Chemical equilibrium, acids, bases and buffers & Organic reaction mechanisms and synthesis
Complete two full timed past-paper-style papers under exam conditions and mark them strictly against the scheme
Re-derive the five highest-error topics identified in earlier error logs and solve two fresh questions on each
Consolidate a single revision sheet of formulas, constants, reagents and conditions for all eleven domains
Practise structuring extended written answers with correct terminology, units and significant figures within time limits
Your checkpoint
Two completed timed papers with a final error analysis and a personal one-page formula-and-reagents sheet covering all domains
Milestones
Week 2: Score at least 80% on a self-made 30-question test on atomic structure, periodicity, bonding and nomenclature; if below, redo the week 1-2 worksheets before starting week 3
Week 4: Complete the timed 25-mark equilibrium/acids/energetics section in under 35 minutes with at least 70% of marks and a written error log
Week 6: Draw all 8 mechanisms and 5 redox equations from memory with correct curly arrows and balancing; achieve at least 75% on a mixed kinetics/electrochemistry/organic synthesis set
Week 8: Achieve at least 65% on both full timed papers with no domain scoring below 50%, and confirm every error-log item has been re-tested