Organic Chemistry As a Second Language: First Semester Topics
Organic Chemistry As a Second Language: First Semester Topics
4th Edition
ISBN: 9781119110668
Author: David R. Klein
Publisher: WILEY
Question
Book Icon
Chapter 9.2, Problem 9.2P
Interpretation Introduction

Interpretation:

The reaction through which, the given substrate more likely to participate has to be identified.

Concept Introduction:

The compound that is been attacked by nucleophile is known as electrophile.  Usually electrophile is referred as substrates.  Valency of carbon atom is four.  Therefore, carbon atom has four bonds.  Hence, apart from the bond that is with the leaving group, the carbon atom contains three other bonds also.

Out of the three bonds that are present apart from the leaving group, if one is an alkyl group, then the substrate is known as “primary”.  If there are two alkyl groups, then the substrate is known as “secondary”.  If there are three alkyl groups, then the substrate is known as “tertiary”.  This is represented as shown below,

Organic Chemistry As a Second Language: First Semester Topics, Chapter 9.2, Problem 9.2P

In SN2 reaction, the alkyl groups are more crowded.  Hence, the nucleophile cannot attack the electrophilic center easily if there are three alkyl groups.  Therefore, for SN2 reaction, the primary substrate is more susceptible for nucleophilic attack, while the tertiary substrate is unreactive.

In SN1 reaction, the first step is the loss of leaving group to form a carbocation.  The second step is the attack of nucleophile on carbocation.  In this case, the stability of the carbocation formed is the major issue.  As we know that the alkyl groups are electron donating groups, the more the alkyl groups substituted, the more the carbocation formed will be stabilized.  Hence, tertiary is more stable than the secondary, and the primary is the worst as it contains only one alkyl group.

In simple words, we can say that, if the substrate is a primary or secondary one, then the reaction will proceed through SN2 mechanism.  The final product has inversion of configuration.  If the substrate is tertiary means, then the reaction will proceed through SN1 mechanism and the final product is racemic.

Blurred answer
Knowledge Booster
Background pattern image
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY