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Amines and amidesEdexcel A-Level Chemistry: Mind map

What this mind map covers

  • Functional groups
  • Butylamine reactions
  • Basicity
  • Making amines
  • Making amides

Exam questions on Amines and amides

  1. Butylamine, CH₃(CH₂)₃NH₂, is a primary aliphatic amine. It dissolves in water to give an alkaline solution and it neutralises dilute hydrochloric acid.
    A student adds butylamine dropwise, and then in excess, to aqueous copper(II) sulfate. Describe what is observed and explain the change seen in excess.2 marks
  2. A student compares the strengths of three bases at 298 K using their pKb values. A lower pKb means a stronger base. Ammonia, NH₃, has pKb = 4.75, butylamine, CH₃(CH₂)₃NH₂, has pKb = 3.39 and phenylamine, C₆H₅NH₂, has pKb = 9.13.
    Explain why butylamine is a stronger base than ammonia.2 marks
  3. Primary aliphatic amines can be prepared from halogenoalkanes or by reduction of nitriles. Butylamine, CH₃(CH₂)₃NH₂, can be made from 1-bromobutane, and it can also be made by reducing the nitrile butanenitrile, CH₃CH₂CH₂CN.
    State the reagent and conditions for converting 1-bromobutane into butylamine, and explain why a large excess of the reagent is used.3 marks
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Written by the Exaim team, led by Shaun Daswani (Head of Upper Secondary, Improve ME Institute; MSc Financial Mathematics, Imperial College London; BSc, UCL) and Jason Daswani (operational lead, Improve ME Institute; LSE).