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
- 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
- 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
- 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
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).