Lesson 3.3.11.1
3.3.11.1 Preparation Quiz: AQA Chemistry, Unit 3
20 questions
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Lesson 3.3.11.1, Preparation: 20 multiple choice questions for the AQA Chemistry (7405), Unit 3: Organic chemistry, written with Revision Ninja.
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The 20 questions
-
Which reaction prepares a primary aliphatic amine from ammonia and a halogenoalkane?
- Nucleophilic substitution
- Electrophilic addition
- Condensation polymerisation
- Free-radical substitution
-
Which type of reaction converts a nitrile into a primary aliphatic amine?
- Oxidation
- Reduction
- Hydrolysis
- Substitution
-
Which compound is reduced to prepare phenylamine in industrial synthesis?
- Benzonitrile
- Nitroethane
- Nitrobenzene
- Chlorobenzene
-
What is the product when propanenitrile, CH3CH2CN, is reduced with 4[H]?
- Propan-1-ol, CH3CH2CH2OH
- Propanoic acid, CH3CH2COOH
- Propanal, CH3CH2CHO
- Propylamine, CH3CH2CH2NH2
-
What is the main product when excess ammonia reacts with bromoethane?
- Ethylamine
- Triethylamine
- Diethylamine
- Tetraethylammonium bromide
-
How many moles of hydrogen atoms, [H], are needed to reduce one mole of nitrobenzene to phenylamine?
- 6
- 2
- 4
- 8
-
Which product forms when ethanenitrile is reduced fully?
- Ethylamine
- Ethanamide
- Methylamine
- Propylamine
-
What is the relative molecular mass of phenylamine, C6H5NH2, using C = 12, H = 1, N = 14?
- 77
- 91
- 95
- 93
-
In the reduction of nitrobenzene, which group is formed from the -NO2 group?
- -OH
- -CH3
- -NH2
- -CN
-
What role does the primary amine product act as to cause further substitution?
- Electrophile
- Catalyst
- Free radical
- Nucleophile
-
Which nitrile is reduced to produce a pure sample of ethylamine?
- Ethanenitrile
- Methanenitrile
- Propanenitrile
- Butanenitrile
-
If 0.10 mol of ethanenitrile is fully reduced, how many moles of ethylamine are formed?
- 0.10 mol
- 0.40 mol
- 0.05 mol
- 0.20 mol
-
How many hydrogen atoms are added when a nitrile is reduced to a primary amine?
- 4
- 2
- 6
- 3
-
Which amine is a primary aliphatic amine?
- Propylamine
- Phenylamine
- Triethylamine
- N-methylpropylamine
-
Why is sodium hydroxide added after reducing nitrobenzene with tin and acid?
- Oxidise product
- Precipitate catalyst
- Liberate free amine
- Neutralise nitrobenzene
-
What is the product from 1-chloropropane and excess ammonia?
- Propan-2-amine
- Dipropylamine
- Tripropylamine
- Propylamine
-
Which compound would react fastest with ammonia by nucleophilic substitution?
- Iodoalkane
- Chloroalkane
- Alkane
- Fluoroalkane
-
What is the main industrial use of phenylamine according to the specification?
- Manufacture of soap
- Production of biodiesel
- Manufacture of dyes
- Production of polyethene
-
What is the by-product of the reduction of nitrobenzene to phenylamine?
- Water
- Carbon dioxide
- Ammonia
- Hydrogen gas
-
How does carbon chain length change when reducing a nitrile to an amine?
- Decreases by one
- Increases by one
- Remains the same
- Doubles in length
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