AQA A-level Chemistry — Organic Chemistry 1 flashcards
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AS organic chemistry for AQA 7404/7405: naming and isomerism, alkanes and cracking, free-radical substitution, halogenoalkanes, alkenes and addition polymers, alcohols, and functional-group tests, mass spectrometry and IR.
Learn deck · part of AQA A-level Chemistry · written against: AQA AS and A-level Chemistry (7404/7405) specification, version 1.2, July 2026 (physical, inorganic and organic). Updated 2026-10-10.
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What features do the members of a homologous series share?The same functional group and general formula, with each member differing from the next by CH₂.Organic Chemistry › Introduction to Organic Chemistry
They have similar chemical reactions and show a gradual trend in physical properties such as boiling point. -
What does a skeletal formula show, and what does it leave out?It shows the carbon skeleton as lines and functional groups, leaving out carbon atoms and the hydrogens bonded to them.Organic Chemistry › Introduction to Organic Chemistry
Each line end and each junction is a carbon atom carrying enough hydrogens to make four bonds. -
What is the IUPAC name of CH₃CH(CH₃)CH₂CH₃?2-methylbutaneOrganic Chemistry › Introduction to Organic Chemistry
The longest chain has four carbons, and the methyl branch is on carbon 2 when numbered from the nearer end. -
What is the IUPAC name of CH₃CH(OH)CH₃?Propan-2-olOrganic Chemistry › Introduction to Organic Chemistry
Three carbons with the OH group on the middle carbon; the position number goes before the -ol suffix. -
What is the IUPAC name of CH₃CHBrCH₂CH₃?2-bromobutaneOrganic Chemistry › Introduction to Organic Chemistry
Halogens are named as prefixes, and the chain is numbered to give the bromine the lowest possible number. -
What is a structural isomer, and which three kinds are there?Compounds with the same molecular formula but different structural formulas: chain, position and functional group isomers.Organic Chemistry › Introduction to Organic Chemistry
Example: butan-1-ol and butan-2-ol are position isomers; butan-1-ol and 2-methylpropan-1-ol are chain isomers. -
Propanal and propanone are both C₃H₆O. What type of isomers are they?Functional group isomersOrganic Chemistry › Introduction to Organic Chemistry
Propanal is an aldehyde (CHO at the chain end) and propanone is a ketone (C=O in the middle), so they belong to different homologous series. -
What is a stereoisomer?A compound with the same structural formula but a different arrangement of atoms in space.Organic Chemistry › Introduction to Organic Chemistry
AQA covers two kinds: E–Z isomerism about a C=C bond, which is AS content, and optical isomerism at a chiral centre, which is A-level only. -
Which two conditions must hold for an alkene to show E–Z isomerism?There is restricted rotation about the C=C bond, and each carbon of the double bond carries two different groups.Organic Chemistry › Introduction to Organic Chemistry
But-1-ene has no E–Z isomers because one carbon of its C=C carries two hydrogens. -
In CHBr=C(Cl)CH₃, the Br and the Cl are on the same side of the double bond. Is this the E or the Z isomer?ZOrganic Chemistry › Introduction to Organic Chemistry
By the CIP rules Br outranks H on one carbon and Cl outranks CH₃ on the other (higher atomic number wins); the two higher-priority groups are on the same side.
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About these cards
Review status: Second-reader reviewed, with corrections applied.
Checked against:
- Topic outline follows the AQA AS and A-level Chemistry (7404/7405) specification, version 1.2 (July 2026) (outline only; no specification text reproduced).
- OpenStax Chemistry 2e and OpenStax Organic Chemistry: A Tenth Edition, consulted as references; no text copied.
- Infrared ranges checked against the AQA AS Chemistry data sheet (Table A, June 2025 issue); isotope masses against NIST's Atomic Weights and Isotopic Compositions; names, formulas and boiling points against PubChem; reaction conditions, tests and observations against AQA mark schemes, the AQA Chemistry required practical handbook (version 2.2) and chemguide.co.uk (reference only; no text copied).
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