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Addition

polymerisation Alkane

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Alcohol Alicyclic
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Aliphatic Alkene

Q-5 Q-6
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A hydrocarbon that A long chain formed
only has single bonds of repeating units,
in it. eg alkenes
A-2 A-1
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A compound with a A compound that


ring structure contains an -OH
group
A-4 A-3
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A compound that has A compound in a


at least one double branched or straight
bond chain
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Alkyl group Aromatic

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Alkynes Carbonyl
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Carboxylic acid CFC

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A compound that A side chain that has been
formed from an alkane by
contains a benzene removing a hydrogen
ring
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A Compound that A compound that has


contains a C=O group a least one triple
bond
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Chlorofluorocarbon, a A Compound that


compound that is made up
contains a -COOH
from carbon, chlorine and
fluorine. group
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Cis-trans isomerism Displayed formula

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Dative covalent bond


(coordinate bond) Delocalised electrons
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Empirical Formula E/Z isomerism

Q-17 Q-18
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This shows the position Subset of E/Z isomers
of all atoms and the where two groups attached
bonding between them to each C=C are the same

A-14 A-13
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Electrons that are Covalent bond where both


of the electrons are
being shared by provided by one of the
more than 2 atoms elements
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A form of stereoisomerism A formula showing the


where there are different lowest whole number ratios
groups around the C=C, and the of elements in a compound.
C=C prevents free rotation

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Electron
configuration Electrophile

Q-19 Q-20
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Elimination reaction Ester


Q-21 Q-22
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Esterification Functional group

Q-23 Q-24
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Electron pair Where the electrons
acceptor. are arranged in
space.
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A Compound that has A set of reactions where a


small molecule (usually, but
a -COO group not always water) is a
product.
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The part of an organic Formation of an


compound that is
ester
responsible for the
properties
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General Formula Hydrocarbon

Q-1 Q-2
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Halogenation Haloalkanes
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Homologous series Heterolytic fission

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A compound that is The simplest
made from hydrogen algebraic formula for
and carbon only a compound
A-2 A-1
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Alkanes that contain A halogen is added to a


compound across the
a halogen
C=C, an addition reaction.
A-4 A-3
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Separation of a bonded pair Set of organic compounds that


have the same functional group,
of atoms where one atom
and an increasing number of
receives both electrons
carbons and hydrogens

A-6 A-5
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Homolytic fission Hydration

Q-7 Q-8
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Hydrogenation Hydrolysis
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Infrared
Hydrogen bond spectroscopy

Q-11 Q-12
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Separation of a bonded pair of
A reaction that has
atoms where each atom
water as a reactant receives an electron, leading to
the formation of radicals.

A-8 A-7
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A reaction that has water A reaction where


as a reactant, or where an
alkali provides a -OH for
hydrogen is added
the reaction across the C=C
A-10 A-9
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A bond resulting from the


Analytical technique that
permanent dipole that arises when
can be used to identify hydrogen is bonded to either
oxygen, nitrogen or fluorine.
functional groups

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London (dispersion)
force Lone pair

Q-13 Q-14
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Mass spectrometry Molecular formula


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Molecular ion Nucleophile

Q-17 Q-18
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A pair of electrons Attraction that is formed
when an instantaneous
that are not forming dipole induces a dipole.
a bond
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Gives the number of Analytic technique that


determines the
each type of element mass/charge ratio of
in a compound fragments of a compound.
A-16 A-15
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M+ the positive ion resulting from


Electron pair donor the fragmentation of a compound
for mass spectrometry, this is the
result of one electron being lost.

A-18 A-17
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Nucleophilic
substitution Oxidising agent

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Organic pathway Ozone layer


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Primary alcohol Radical

Q-23 Q-24
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[O] reactant that is added A reaction mechanism
to a reaction to remove where part of a compound is
elections, to oxidise. replaced by a nucleophile.

A-20 A-19
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A part of the atmosphere A route that has been


where ozone (O3) is in high designed to turn on organic
concentration. compound into another.

A-22 A-21
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A compound where the


An element or
alcohol group is attached to
compound that has a carbon that also has 2
an unpaired electron hydrogens attached to it
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Radical substitution Reaction mechanism

Q-1 Q-2
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Structural Formula Saturated


Q-3 Q-4
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Secondary alcohol Skeletal formula

Q-5 Q-6
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Diagram that shows the A reaction mechanism
intermediates and where part of a compound is
movement of electrons in a replaced by a radical.
reaction.
A-2 A-1
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The minimal amount of detail


A compound that
needed to determine the
only has single bonds special arrangement of
elements in a compound
A-4 A-3
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A representation of a A compound where the alcohol


group is attached to a carbon
compound without drawing
that also has 1 hydrogen
any hydrogen or carbons
attached to it

A-6 A-5
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Stereoisomers Structural isomer

Q-7 Q-8
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Tertiary alcohol Unsaturated


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Van der Waals’ empty


forces

Q-11 Q-12
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A set of compounds that A set of compounds that
have the molecular formula have the molecular formula
but a different structure but a different
arrangement in space
A-8 A-7
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A compound where the alcohol


A compounds that
group is attached to a carbon
has double or triple that also has no hydrogens
attached to it
bonds
A-10 A-9
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Intermolecular bond that


empty covers London forces, and
permanent dipole - permanent
dipole interactions.

A-12 A-11
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