Essential Organic Chemistry (3rd Edition)
Essential Organic Chemistry (3rd Edition)
3rd Edition
ISBN: 9780321937711
Author: Paula Yurkanis Bruice
Publisher: PEARSON
Question
Book Icon
Chapter 13.4, Problem 11P
Interpretation Introduction

Interpretation:

Alkylation of α carbon is more favored when the alkyl halide is primary and not when alkyl halide is tertiary.

Concept introduction:

Alkylation of α carbon atom in a carbonyl compound proceeds via the SN2 mechanism.  The SN2 reaction involves only one step in which the carbonyl compound and alkyl halide combine to form a transition state.  If the alkyl halide is bulky the transition state cannot be formed due to steric hindrance and instead an elimination product is formed.

Blurred answer
Students have asked these similar questions
Show the products when the following reagents react.
In the following reaction, which chemical species is acting like a nucleophile?
What explains why many aldehydes and ketones can undergo self- condensation reactions in basic conditions? The alpha carbon can lose a proton and act like a nucleophile and the carbonyl carbon a an electrophile O The alpha carbon can gain a proton and act like an electrophile and the carbonyl carbon is a nucleophile O The oxygen of the carbonyl group can attack the carbon of the carbonyl group Only esters can undergo self-condensation reactions

Chapter 13 Solutions

Essential Organic Chemistry (3rd Edition)

Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning