Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Chapter 6, Problem 45P
Interpretation Introduction

Interpretation:

The wedge-dashed wedge-line formulas of both A and B are to be drawn and the change in configuration is to be determined.

Concept introduction:

Reaction sequences involve conversion of one functional group to another, which may also require addition or loss of carbon from the reactant.

These sequences involve a number of steps carried out by different reagents. Sometimes different reagents give the same products.

Electrophiles are electron-deficient species, which has positive or partially positive charge. Lewis acids are electrophiles, which accept electron pair.

Nucleophiles are electron-rich species, which has negative or partially negative charge. Lewis bases are nucleophiles, which donate electron pair.

Substitution reaction: A reaction in which one of the hydrogen atoms of a hydrocarbon or a functional group is substituted by any other functional group is called substitution reaction.

Nucleophilic substitution reaction is a reaction in which an electron-rich nucleophile attacks the positive or partial positive charge of an atom or a group of atoms to replace a leaving group.

An SN2 reaction is the nucleophilic substitution reaction in which two components are involved in the rate determining step. SN2 reaction occurs in one step.

An SN1 reaction is the nucleophilic substitution reaction in which one component is involved in the rate determining step. SN1 reaction occurs in two step.

The involvement of nearby nucleophile substituent to the reaction center in the substitution process is known as neighboring group participation.

Such participation results in an increase of rate of reaction. The phenomenon is described as Anchimeric assistance.

In this participation, two SN2 reactions are occurred which results in two inversion of configuration, that is, overall retention of configuration.

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