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AQA AS Organic Chemistry Exam | Questions And Answers | Newest Exam

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AQA AS Organic Chemistry Exam | Questions And Answers | Newest Exam

Institución
AQA AS Organic Chemistry
Grado
AQA AS Organic Chemistry

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AQA AS Organic Chemistry Exam |
Questions And Answers | Newest
Exam 2026-2027 |
Define the term 'Homologous series' -ANSWER A family of organic compounds that have
the same general formula and similar chemical properties

Define the term 'Structural isomer' -ANSWER A molecule with the same molecular
formula as, but different structural formula to another molecule

Define the term 'Stereoisomerism' -ANSWER A molecule which has the same structural
formula as another molecule, but has its atoms arranged differently in space

Define the term 'E-isomer' -ANSWER A stereoisomer of an alkene that had the two
highest priority groups on opposite sides of the carbon-carbon double bond

Define the term 'Z-isomer' -ANSWER A stereoisomer of an alkene that has the two
highest priority groups on the same side of the carbon-carbon double bond

(To help you remember it: Zee Zame Zide).

Define the term 'E/Z isomerism' -ANSWER A type of stereoisomerism that is cause ld by
the restricted rotation about a carbon-carbon double bond, each of he carbon atoms
must have two different groups attached

Define the term 'Alkanes' -ANSWER A saturated hydrocarbon with the general formula
CnH2n+2

Define the term 'Petroleum' -ANSWER A mixture consisting mainly of alkane
hydrocarbons that can be separated into different fractions

Define the term 'Cracking' -ANSWER Long chain hydrocarbons are broken down into
shorter chain hydrocarbons. This produces a mixture of alkanes and alkenes

Describe thermal cracking. Include conditions in your ANSWER. -ANSWER Temperatures
between 700k and 1200k
Pressure of up to 7000 KPa.

1) Carbon-carbon breaks to produce two free radicals.

2) Free radicals are highly reactive and react to produce many alkenes and some
alkanes.

,Why are long chain hydrocarbons not kept under high temperatures for long amounts of
time? -ANSWER At higher temperatures, these chains decompose. Given enough time,
this will eventually result in products which are only hydrogen gas and solid carbon.

Describe catalytic cracking. Include conditions in your ANSWER. -ANSWER Zeolite
catalyst.
720K.
Low pressure.

Hydrocarbons are mixed with a catalyst which has been ground into a fine powder.

Produces lots of branched alkanes and aromatic hydrocarbons

Describe a zeolite catalyst -ANSWER A substance which has a honeycomb structure with
an enormous surface area. They are usually acidic.

What type of products are usually formed from catalytic cracking? -ANSWER Branched
alkanes
Cycloalkanes (rings)
Aromatic compounds (e.g. benzene)

Define the term 'Halogenoalkanes' -ANSWER An alkane with at least one halogen atom
in place of a hydrogen atom

Define the term 'Ozone layer' -ANSWER A layer of ozone (O3) found in the earth's upper
atmosphere which protects the earth from ultra violet radiation

Define the term 'Alkenes' -ANSWER An unsaturated hydrocarbon with the general
formula CnH2n, containing at least one carbon-carbon double bond

How can we test for the presence of a C=C double bond? -ANSWER Add bromine water
(an orange solution) to the unknown solution. If a C=C double bond is present then the
solution will decolourise (turn colourless).

What conditions are needed for an alcohol to be made from an alkene? -ANSWER Steam
High temperature
High pressure
Acid catalyst

How many sigma bonds and pi bonds are in a single bond? -ANSWER 1 sigma
0 pi

How many sigma and pi bonds are in a double bond? -ANSWER 1 sigma
1 pi

, How many sigma and pi bonds in a triple bond? -ANSWER 1 sigma
2 pi

Why can double bonds not rotate? -ANSWER Two p-orbitals have overlapped to make a
pi orbital.

Why are alkenes more chemically reactive than alkanes? -ANSWER The double bond is
electron rich.

Why are the physical properties of alkenes similar to those of the alkanes? -ANSWER
Van der Waals forces are the only type of intermolecular forces that act between both
alkanes and alkenes.

Why can single bonds rotate? -ANSWER Two p-orbitals have not overlapped. There are
no pi orbitals.

Define the term 'Bonding in alkenes' -ANSWER Involves double covalent bonds, a centre
of high electron density

Define the term 'Addition polymers' -ANSWER A long chain molecule formed by an
addition reaction. They are formed from monomers which have a carbon-carbon double
bond.

Define the term 'monomer'. -ANSWER An individual molecule that is repeated n times to
make a polymer.

Define the term 'polymer backbone' -ANSWER The longest series of covalently bonded
atoms that together create the continuous chain of the molecule

Define the term 'repeating unit' -ANSWER The smallest group of atoms that produce the
polymer when repeated over and over

State one use for poly(ethene) or polythene -ANSWER Carrier bags or washing up bowls

State one use for poly(propene) or polypropylene -ANSWER Yoghurt containers or car
bumpers

State one use for poly(chloroethene) or poly(vinyl chloride) -ANSWER Aprons or
drainpipes

State one use for poly(propenenitrile) or acrylic -ANSWER Clothing fabrics

State one use for poly(phenylethene) or polystyrene -ANSWER Packing materials or
electrical insulation

Escuela, estudio y materia

Institución
AQA AS Organic Chemistry
Grado
AQA AS Organic Chemistry

Información del documento

Subido en
28 de junio de 2026
Número de páginas
16
Escrito en
2025/2026
Tipo
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