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A-Level Chemistry Revision

Organic Chemistry

Functional groups and reaction mechanisms, isomerism, polymers and organic synthesis.

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How do alkenes typically react with bromine?

Organic Chemistry is a core part of A-Level Chemistry. Revise the key concepts and common mistakes below, then lock them in with the free games.

Key concepts

Homologous seriesA family of compounds with the same functional group and general formula.
Functional groupThe reactive part of a molecule that determines its reactions.
IsomerismMolecules with the same formula but different structures or arrangements.
Reaction mechanismStep-by-step electron movement showing how a reaction proceeds.
Alkanes & alkenesSaturated and unsaturated hydrocarbons.
AlcoholsOrganic compounds containing the -OH group.
AlkaneC-C single bonds; CnH(2n+2).
AlkeneContains C=C; CnH2n.
HaloalkaneHalogen replaces H; R-X.
AlcoholContains -OH; R-OH.
Carboxylic acidContains -COOH; weak acid.
EsterContains -COO-R'; formed from acid + alcohol.
Primary alcoholR-CH2OH; oxidises to aldehyde then acid.
Secondary alcoholR2CHOH; oxidises to ketone.

What your exam board covers

Where Organic Chemistry sits in each exam board's specification. Tap a board to see what it lists.

AQAIntroduction to organic chemistrySpec 7405

Part of: Organic chemistry

Source: AQA A-level Chemistry (7405) specification — Subject content, accessed 23 June 2026.

AQAOrganic synthesis (A-level only)Spec 7405

Part of: Organic chemistry

Source: AQA A-level Chemistry (7405) specification — Subject content, accessed 23 June 2026.

CCEAA2 1 — Further physical and organic chemistrySpec 1110
  • Lattice enthalpy
  • Enthalpy, entropy and free energy
  • Rates of reaction
  • Equilibrium
  • Acid-base equilibria
  • Isomerism
  • Aldehydes and ketones
  • Carboxylic acids
  • Derivatives of carboxylic acids
  • Aromatic chemistry

Source: CCEA A-Level Chemistry specification, accessed 23 June 2026.

Eduqas/WJECOA1 — Higher concepts in organic chemistrySpec A410QS (QAN 601/5645/4)
  • Stereoisomerism
  • Aromaticity

Source: Eduqas/WJEC A-Level Chemistry specification (from 2015), accessed 24 June 2026.

Eduqas/WJECOA4 — Organic synthesis and analysisSpec A410QS (QAN 601/5645/4)
  • Synthetic routes, practical techniques and combined instrumental analysis

Source: Eduqas/WJEC A-Level Chemistry specification (from 2015), accessed 24 June 2026.

OCRModule 4 — Core organic chemistrySpec H432
  • Basic concepts
  • Hydrocarbons
  • Alcohols and haloalkanes
  • Organic synthesis
  • Analytical techniques (IR and MS)

Source: OCR A Level Chemistry A (H432) specification, accessed 23 June 2026.

OCRModule 6 — Organic chemistry and analysisSpec H432
  • Aromatic compounds
  • Carbonyl compounds
  • Carboxylic acids and esters
  • Nitrogen compounds
  • Polymers
  • Organic synthesis
  • Chromatography and spectroscopy (NMR)

Source: OCR A Level Chemistry A (H432) specification, accessed 23 June 2026.

Common mistakes to avoid

Questions where students often pick the tempting wrong answer — make sure you know the right one:

How do alkenes typically react with bromine?✗ Bromine substitutes for a hydrogen on the alkene, releasing HBr.   ✓ By electrophilic addition — bromine adds across the double bond to form a dibromoalkane.
What is the product of mild oxidation of a primary alcohol?✗ A primary alcohol is oxidised directly to a ketone.   ✓ An aldehyde (which can be further oxidised to a carboxylic acid).
Members of a homologous series share:✗ The same molecular mass   ✓ The same functional group and general formula
Why do tertiary halogenoalkanes typically react via SN1 rather than SN2?✗ Tertiary halogenoalkanes react via SN1 because they are more reactive in every way.   ✓ The tertiary carbocation intermediate is stabilised by three alkyl groups (positive inductive effect), making the SN1 pathway favourable.

Practise Organic Chemistry — free games

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