Lesson 18B.2
18B.2 Preparing amines and amides Quiz: Pearson Edexcel Chemistry, Unit 18
20 questions
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Lesson 18B.2, Preparing amines and amides: 20 multiple choice questions for the Pearson Edexcel Chemistry (9CH0), Unit 18: Organic Chemistry III, written with Revision Ninja.
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The 20 questions
-
Which metal is used with concentrated hydrochloric acid to reduce nitrobenzene to phenylamine?
- Copper
- Zinc
- Iron
- Tin
-
What is the product of reducing nitrobenzene with tin and concentrated hydrochloric acid, followed by alkali?
- Phenol, C6H5OH
- Phenylamine, C6H5NH2
- Benzoic acid, C6H5COOH
- Benzene-1,4-diamine
-
Which reagent converts a halogenoalkane directly into a primary amine?
- Potassium cyanide
- Dilute nitric acid
- Ethanolic ammonia
- Aqueous sodium hydroxide
-
What organic product is formed when an acyl chloride reacts with a primary amine?
- Secondary amine
- N-substituted amide
- Carboxylic acid
- Nitrile
-
Which compound is a primary amine?
- Ethanamide, CH3CONH2
- Trimethylamine, (CH3)3N
- Propan-1-amine, CH3CH2CH2NH2
- N-methylethanamine, CH3NHCH2CH3
-
Calculate the relative molecular mass of phenylamine, C6H7N, using Ar: C 12, H 1, N 14.
- 94
- 77
- 107
- 93
-
What is the by-product when ethanoyl chloride reacts with ammonia to form an amide?
- Sodium chloride
- Water
- Ammonium chloride
- Ethanoic acid
-
Which reagent is used alongside hydrogen gas to reduce nitriles to primary amines?
- Nickel catalyst
- Sodium hydroxide
- Sulfuric acid
- Potassium manganate
-
Calculate the relative molecular mass of N-butylethanamide, C6H13NO, using Ar: C 12, H 1, N 14, O 16.
- 113
- 115
- 129
- 101
-
Which amide forms from ethanoyl chloride and methylamine?
- N-methylethanoate, CH3COOCH3
- Ethanenitrile, CH3CN
- Methylethanamine, CH3CH2NHCH3
- N-methylethanamide, CH3CONHCH3
-
What is the main role of hydrochloric acid in the tin reduction of nitrobenzene?
- Oxidises the tin
- Dehydrates the product
- Provides hydrogen ions
- Acts as catalyst
-
Which functional group is reduced to a primary amine using tin and concentrated hydrochloric acid?
- Nitrile group
- Carbonyl group
- Amide group
- Nitro group
-
Why is excess ammonia used when preparing a primary amine from a halogenoalkane?
- Prevents amine oxidation
- Increases activation energy
- Prevents further substitution
- Increases reaction temperature
-
Why is sodium hydroxide added after reducing nitrobenzene with tin and hydrochloric acid?
- Precipitate the tin
- Oxidise phenylamine
- Neutralise unreacted nitrobenzene
- Liberate free amine
-
Why are acyl chlorides preferred over carboxylic acids when preparing amides?
- Less toxic
- Higher boiling point
- More reactive
- Cheaper reagents
-
Calculate the mass of phenylamine from 0.0200 mol of nitrobenzene at 100% yield, using Mr = 93 for phenylamine.
- 3.72 g
- 0.93 g
- 2.46 g
- 1.86 g
-
Which reagent mixture is used to reduce butanenitrile to butylamine?
- Tin and HCl
- LiAlH4 in ether
- NaBH4 in ethanol
- Acidified KMnO4
-
Why does using aqueous ammonia rather than concentrated ammonia lower amide yield?
- Acyl chloride polymerises
- Ammonia evaporates rapidly
- Acyl chloride hydrolyses
- Amide decomposes quickly
-
For ethanoyl chloride with excess ammonia, how many moles of ammonia are needed per mole of amide formed?
- 0.5
- 2
- 1
- 3
-
What is the relative molecular mass of 1-bromobutane, C4H9Br, using Ar: C 12, H 1, Br 79.9?
- 152.9
- 120.9
- 135.0
- 136.9
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