Organic Chemistry, Binder Ready Version
Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118454312
Author: David R. Klein
Publisher: WILEY
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Chapter 7.9, Problem 35CC
Interpretation Introduction

Interpretation: The mechanism for the given substrate should be determined under given conditions.

Concept Introduction:

SN2 Reaction: It is a nucleophilic substitution reaction in which the rate determining step depends on both of the molecules involved. The bond making and the bond breaking process happens simultaneously in this reaction which results the product with inversed configuration with respect to the reactant.

Structure of the substrate plays major role in the reactivity of SN2 reaction. If the substrate is more substituted then the rate of the reaction becomes slower. Since the mechanism of SN2 reaction proceeds through backside attack on the substrate, it depends on steric factor that if more groups attached near the leaving group the reactivity becomes slower.

The SN2 reactivity increases in molecule with better leaving group.

Intramolecular SN2 Reaction: It is a type of substitution chemical reaction in which both nucleophile and the leaving group present with in the same molecule.

Leaving group: It is a fragment that leaves substrate with a pair of electrons via heterolytic bond cleavage.

Nucleophile: Donates pair of electrons to positively charged substrate resulting in the formation of chemical bond.

Example:

Organic Chemistry, Binder Ready Version, Chapter 7.9, Problem 35CC

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