A Level Chemistry CIE: Organic Chemistry (A Level Only) Revision Notes

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Comprehensive vocabulary flashcards covering functional groups, nomenclature, reaction terminology, isomerism, and polymerisation topics from A Level Chemistry CIE Section 7 (Organic Chemistry).

Last updated 11:33 AM on 7/16/26
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28 Terms

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Functional group

An atom or group of atoms in an organic molecule that determines its characteristic chemical and physical properties.

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Arenes

Aromatic compounds that contain a benzene ring.

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Halogenoarenes

Aromatic compounds that contain a halogen bonded to a benzene ring; also known as aryl halides.

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Phenols

Aromatic compounds containing a hydroxide group bonded to a benzene ring.

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Acyl chlorides

Carboxylic acid derivatives containing a chlorine atom attached to a C=OC=O group, also known as 'acid' chlorides.

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Amines

Compounds with the NH2-NH_2 (primary), NH-NH (secondary), or N-N (tertiary) group which act as basic compounds due to the lone pair of electrons on the nitrogen.

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Amides

Compounds containing an amine (NH2-NH_2) group and a carbonyl group (C=OC=O), resulting in the CONH2-CONH_2 group.

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Amino Acids

Organic compounds that contain both a basic amino (NH2-NH_2) group and an acidic carboxylic acid (COOH-COOH) group; they serve as the building blocks of proteins.

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Electrophilic substitution

Reactions in which an atom or group of atoms is replaced by an electrophile after an initial attack by the electron-deficient species.

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Addition reaction

A reaction where two or more molecules combine to give a single product only.

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Elimination reaction

The reverse of an addition reaction, where a small molecule such as H2OH_2O or HClHCl is removed from an organic molecule.

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Stereoisomers

Molecules that have the same structural formula but have the atoms arranged differently in space.

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Chiral carbon

A carbon atom that has four different atoms or groups of atoms attached to it; also called a chiral centre.

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Enantiomers

Optical isomers that are non-superimposable mirror images of each other.

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Racemic mixture

A mixture containing equal amounts of enantiomers in a solution, making it optically inactive.

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Stereoselectivity

The preference of a reaction to form one enantiomer over the other.

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Friedel-Crafts alkylation

An electrophilic substitution reaction where an alkyl chain is substituted into the benzene ring in the presence of an AlCl3AlCl_3 catalyst.

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Electron-withdrawing substituents

Groups that remove electron density from the π\pi system making the benzene ring less reactive and directing incoming electrophiles to the 33 and/or 55 positions.

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Electron-donating substituents

Groups that donate electron density into the π\pi system making the benzene ring more reactive and directing incoming electrophiles to the 22, 44, and/or 66 positions.

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pKapK_a

A measure of the acidity of a substance; the smaller the value, the stronger the acid.

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Zwitterion

An ion with both a positive (NH3+-NH_3^+) and a negative (COO-COO^-) charge, characteristic of amino acids depending on pHpH.

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Isoelectric point

The pHpH at which an amino acid exists as a neutral zwitterion.

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Peptide bond

The new amide bond formed between two amino acids in a condensation reaction.

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Electrophoresis

An analytical technique used to separate ions, such as amino acids, by placing them in an electrical field.

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Condensation polymerisation

A reaction used to make polyesters and polyamides where a small molecule, typically H2OH_2O or HClHCl, is lost when monomers join.

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Kevlar

A strong and flexible polymer material with fire-resistance properties, made from 1,4-diaminobenzene1,4\text{-diaminobenzene} and benzene-1,4-dicarboxylic acidbenzene\text{-}1,4\text{-dicarboxylic acid}.

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Photodegradation

The breakdown of polymers using energy absorbed from the Electromagnetic Spectrum, specifically Ultraviolet (UV) light.

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Azo compounds

Organic compounds characterized by an R1N=NR2R_1-N=N-R_2 group, often used as dyes and formed through coupling reactions.