Essential Organic Chemistry, Global Edition
Essential Organic Chemistry, Global Edition
3rd Edition
ISBN: 9781292089034
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 13.1, Problem 4P
Interpretation Introduction

Interpretation: Remove a proton from the alpha carbon of N,N-dimethylethanamide but not from the alpha carbon of either N-methylethanamide or ethanamide has to be explained.

Concept introduction: The electrons left behind when a proton is removed from the alpha carbon of an amide are not readily delocalized.  This is because the nitrogen of the NR group of an amide also has a lone-pair that can be delocalized on to the carbonyl oxygen.

Thus the lone pair on the alpha carbon and the lone pair on the nitrogen compete for the delocalization onto the same oxygen.

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Students have asked these similar questions
Isomer of N-Butyl-N-Ethyl-Hexenamide   A.) Dodecanamide       B.) N,N-Dibutyl-butanamide       C.) N-ethyl-4-cyclopentyl-petanamide       D.) N-Ethyl-N-Butyl-Hexenamide       E.) None of the given choices
Explain why a proton can be removed from the 'alpha-carbon of N,N-dimethylethanamide but not from the alpha-carbon of either N-methylethanamide or ethanamide.
Explain why a base can remove a proton from the a-carbon of N,N-dimethylethanamide but not from the α-carbon of either N-methylethanamide or ethanamide.

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Essential Organic Chemistry, Global Edition

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