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

  1. Which metal is used with concentrated hydrochloric acid to reduce nitrobenzene to phenylamine?

    • Copper
    • Zinc
    • Iron
    • Tin
  2. 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
  3. Which reagent converts a halogenoalkane directly into a primary amine?

    • Potassium cyanide
    • Dilute nitric acid
    • Ethanolic ammonia
    • Aqueous sodium hydroxide
  4. What organic product is formed when an acyl chloride reacts with a primary amine?

    • Secondary amine
    • N-substituted amide
    • Carboxylic acid
    • Nitrile
  5. Which compound is a primary amine?

    • Ethanamide, CH3CONH2
    • Trimethylamine, (CH3)3N
    • Propan-1-amine, CH3CH2CH2NH2
    • N-methylethanamine, CH3NHCH2CH3
  6. Calculate the relative molecular mass of phenylamine, C6H7N, using Ar: C 12, H 1, N 14.

    • 94
    • 77
    • 107
    • 93
  7. What is the by-product when ethanoyl chloride reacts with ammonia to form an amide?

    • Sodium chloride
    • Water
    • Ammonium chloride
    • Ethanoic acid
  8. Which reagent is used alongside hydrogen gas to reduce nitriles to primary amines?

    • Nickel catalyst
    • Sodium hydroxide
    • Sulfuric acid
    • Potassium manganate
  9. Calculate the relative molecular mass of N-butylethanamide, C6H13NO, using Ar: C 12, H 1, N 14, O 16.

    • 113
    • 115
    • 129
    • 101
  10. Which amide forms from ethanoyl chloride and methylamine?

    • N-methylethanoate, CH3COOCH3
    • Ethanenitrile, CH3CN
    • Methylethanamine, CH3CH2NHCH3
    • N-methylethanamide, CH3CONHCH3
  11. 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
  12. Which functional group is reduced to a primary amine using tin and concentrated hydrochloric acid?

    • Nitrile group
    • Carbonyl group
    • Amide group
    • Nitro group
  13. 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
  14. Why is sodium hydroxide added after reducing nitrobenzene with tin and hydrochloric acid?

    • Precipitate the tin
    • Oxidise phenylamine
    • Neutralise unreacted nitrobenzene
    • Liberate free amine
  15. Why are acyl chlorides preferred over carboxylic acids when preparing amides?

    • Less toxic
    • Higher boiling point
    • More reactive
    • Cheaper reagents
  16. 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
  17. Which reagent mixture is used to reduce butanenitrile to butylamine?

    • Tin and HCl
    • LiAlH4 in ether
    • NaBH4 in ethanol
    • Acidified KMnO4
  18. Why does using aqueous ammonia rather than concentrated ammonia lower amide yield?

    • Acyl chloride polymerises
    • Ammonia evaporates rapidly
    • Acyl chloride hydrolyses
    • Amide decomposes quickly
  19. For ethanoyl chloride with excess ammonia, how many moles of ammonia are needed per mole of amide formed?

    • 0.5
    • 2
    • 1
    • 3
  20. 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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