Organic Chemistry, Loose-leaf Version
Organic Chemistry, Loose-leaf Version
8th Edition
ISBN: 9781305865549
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
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Chapter 9, Problem 9.19P
Interpretation Introduction

Interpretation:

The hybridization best describes the reacting carbon in the SN2 transition state has to be given.

Concept Introduction:

  • SN2 reaction: It is a nucleophilic substitution reaction in which the rate determining step depends on both alkyl halide and the nucleophile present. The bond making and the bond breaking process happens simultaneously in this reaction, which results in the inversion of configuration.
  • Rate= k[alkylhalide]×[nucleophile]
  • Structure of the substrate plays a major role in SN2 reaction. If the substrate is more substituted 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 of reactant and nucleophile.

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