Lawrie Ryan and Roger Norris Solutions for Chapter: Carboxylic Acids and their Derivatives, Exercise 9: REFLECTION

Author:Lawrie Ryan & Roger Norris

Lawrie Ryan Chemistry Solutions for Exercise - Lawrie Ryan and Roger Norris Solutions for Chapter: Carboxylic Acids and their Derivatives, Exercise 9: REFLECTION

Attempt the practice questions on Chapter 26: Carboxylic Acids and their Derivatives, Exercise 9: REFLECTION with hints and solutions to strengthen your understanding. Chemistry for Cambridge International AS & A Level Coursebook with Digital Access (2 Years) solutions are prepared by Experienced Embibe Experts.

Questions from Lawrie Ryan and Roger Norris Solutions for Chapter: Carboxylic Acids and their Derivatives, Exercise 9: REFLECTION with Hints & Solutions

HARD
AS and A Level
IMPORTANT
Chemistry for Cambridge International AS & A Level Coursebook with Digital Access (2 Years)>Chapter 26 - Carboxylic Acids and their Derivatives>REFLECTION>Q 1

Discuss the mechanism of nucleophilic addition-elimination in the reaction between ethanoyl chloride and dimethylamine. Then try showing the mechanism using curly arrows.

MEDIUM
AS and A Level
IMPORTANT
Chemistry for Cambridge International AS & A Level Coursebook with Digital Access (2 Years)>Chapter 26 - Carboxylic Acids and their Derivatives>REFLECTION>Q 2

Which nucleophile you would expect to be most effective: ammonia, a primary amine or a secondary amine. Explain the inductive effect of alkyl groups.