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Organic

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Total cards: 22•Content version: v3•Public deck•Updated: 8/1/2026

Card preview (22)

#1
Front (Question)

Define empirical formula.

Back (Answer)

A formula that shows the simplest ratio of the number of atoms of the elements present in 1 molecule of compound.

#2
Front (Question)

Define molecular formula.

Back (Answer)

A formula that shows the actual number of atoms of the elements present in 1 molecule of the compound.

#3
Front (Question)

Define structural formula.

Back (Answer)

A formula that shows how the constituent atoms of a molecule are joined together.

#4
Front (Question)

Define homolytic fission.

Back (Answer)

The breaking of a covalent bond such that one electron goes to each of the atoms, forming free-radicals.

#5
Front (Question)

Define a free-radical.

Back (Answer)

An atom or a group of atoms with an unpaired electron formed from the homolytic fission of a covalent bond and are very reactive.

#6
Front (Question)

Define heterolytic fission.

Back (Answer)

The breaking of a covalent bond such that both the electrons go to the same atom, forming positive and negative ions.

#7
Front (Question)

Define carbocation and carbanion.

Back (Answer)

A carbocation is a carbon species that carries a positive charge while a carbanion is a carbon species that carries a negative charge.

#8
Front (Question)

Define nucleophile.

Back (Answer)

A negatively-charged species or a species with a lone pair of electrons seeking a positively-charged region.

#9
Front (Question)

Define electrophile.

Back (Answer)

A positively-charged species seeking a negatively-charged region.

#10
Front (Question)

Define isomerism.

Back (Answer)

2 or more compounds have the same molecular formula but different arrangement of the atoms in the molecules.

#11
Front (Question)

Define structural isomers

Back (Answer)

Have the same molecular formula but different structural formula.

#12
Front (Question)

Define stereoisomerism.

Back (Answer)

Have the same molecular and structural formulae but different arrangement of their atoms in space. Consist of cis-trans and optical isomerism

#13
Front (Question)

Define optical isomerism.

Back (Answer)

Arises because of the ability of compounds to rotate the plane of polarisation of plane-polarized light.

#14
Front (Question)

Define chiral carbon.

Back (Answer)

A carbon to which 4 different groups are attached.

#15
Front (Question)

Define racemic mixture.

Back (Answer)

A mixture which contains equal quantities of each optical isomer.

#16
Front (Question)

Define an enantiomer.

Back (Answer)

A form of an optical isomer.

#17
Front (Question)

Define homologous series.

Back (Answer)

A family of compounds containing the same functional group and differing by a CH2 between one member and the next.

#18
Front (Question)

Define substitution reaction.

Back (Answer)

An atom or group of atoms replaces another.

#19
Front (Question)

Define addition reaction.

Back (Answer)

2 molecules combine to form a single product. Usually in unsaturated compounds where the double bond is broken to form a saturated compound.

#20
Front (Question)

Define elimination reaction.

Back (Answer)

involves removal of atoms or groups of atoms from 2 adjacent atoms to form a multiple bond.

#21
Front (Question)

Define hydrolysis reaction.

Back (Answer)

Reaction with water, catalysed by acid or base.

#22
Front (Question)

Define stereochemical formula.

Back (Answer)

A formula that shows the spatial arrangement of bonds, atoms and groups in molecules as a 3D formula.