Lesson 3.3.9.2

3.3.9.2 Acylation Quiz: AQA Chemistry, Unit 3

20 questions

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Lesson 3.3.9.2, Acylation: 20 multiple choice questions for the AQA Chemistry (7405), Unit 3: Organic chemistry, written with Revision Ninja.

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The 20 questions

  1. What is the functional group of an acyl chloride?

    • -CONH2
    • -COOCH3
    • -COOH
    • -COCl
  2. What is the usual by-product when ethanoic anhydride reacts with water?

    • Hydrogen chloride
    • Ethanol
    • Ethanal
    • Ethanoic acid
  3. What organic product forms when ethanoyl chloride reacts with water?

    • Ethanol
    • Ethanal
    • Ethanamide
    • Ethanoic acid
  4. What organic product forms when ethanoyl chloride reacts with ethanol?

    • Methyl ethanoate
    • Ethanoic acid
    • Ethyl ethanoate
    • Ethanamide
  5. What acidic by-product is avoided by using ethanoic anhydride instead of ethanoyl chloride?

    • Hydrogen chloride
    • Nitric acid
    • Ethanoic acid
    • Sulfuric acid
  6. What organic product forms when ethanoyl chloride reacts with ammonia?

    • Ethylamine
    • N-methylethanamide
    • Ethanamide
    • Ethanoic acid
  7. What is the name of the product when ethanoyl chloride reacts with phenylamine?

    • Ethanoic phenylanhydride
    • Phenylethanoic acid
    • N-phenylethanamide
    • Phenyl ethanoate
  8. In the acylation mechanism of ethanoyl chloride, which atom is attacked by the nucleophile?

    • Carbonyl oxygen
    • Methyl carbon
    • Carbonyl carbon
    • Chlorine atom
  9. In the nucleophilic addition-elimination reaction of an acyl chloride, which species is eliminated?

    • Hydroxide ion
    • Chloride ion
    • Methoxide ion
    • Hydride ion
  10. Which compound is 2-ethanoyloxybenzoic acid, the active ingredient of aspirin?

    • Phenylethanone
    • Benzoic acid
    • Aspirin
    • Salicylic acid
  11. Which reagent is used industrially to acylate salicylic acid to make aspirin?

    • Methanoic acid
    • Ethanoic anhydride
    • Ethyl ethanoate
    • Ethanal
  12. What is the relative molecular mass of aspirin, C9H8O4?

    • 164
    • 152
    • 180
    • 192
  13. Why is the carbonyl carbon in acyl chlorides extremely reactive towards nucleophiles?

    • Non-polar
    • Strongly delta positive
    • Highly electron rich
    • Strongly delta negative
  14. Which product forms when ethanoyl chloride reacts with methylamine?

    • Ethanamide
    • Methyl ethanoate
    • Ethanoic acid
    • N-methylethanamide
  15. What organic by-product is formed alongside ethyl ethanoate when ethanoic anhydride reacts with ethanol?

    • Water
    • Hydrogen chloride
    • Ethanoic acid
    • Ethanal
  16. What class of compound is formed when an acyl chloride reacts with ammonia?

    • Amide
    • Primary amine
    • Ester
    • Ketone
  17. How does excess amine act when removing the hydrogen chloride formed during acylation?

    • As a catalyst
    • As a base
    • As an acid
    • As an electrophile
  18. Which feature makes acyl chlorides more reactive than carboxylic acids towards nucleophiles?

    • Non-polar C=O bond
    • Lower reaction rate
    • More electrophilic carbon
    • More nucleophilic carbon
  19. Ethanoyl chloride reacts with ethanol. If 0.20 mol of ethanol reacts completely, how many moles of ethyl ethanoate form?

    • 0.05 mol
    • 0.20 mol
    • 0.40 mol
    • 0.10 mol
  20. How does the presence of significant impurities affect the melting point of a solid?

    • Raises and broadens it
    • Lowers and broadens it
    • Raises and sharpens it
    • No effect

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