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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1. At what position and on what ring would you expect the following substances to undergo electrophilic substitution? (b) CH3 Br lel CH3 2. Rank the compounds in each group according to their reactivity toward electrophilic substitution. (a) Chlorobenzene, o-dichlorobenzene, benzene (b) p-Bromonitrobenzene, nitrobenzene, phenol (c) Fluorobenzene, benzaldehyde, 0-xylene (d) Benzonitrile, p-methylbenzonitrile, p-methoxybenzonitrile
PLEASE HELP WITH THIS QUESTION, ONLY CORRECT ANSWERS WOULD BE UPVOTED!
NaH HO HO PBR3 A (a) Name the functional groups in compounds A and B, including, if relevant, whether they are primary (1°), secondary (2°) or tertiary (3'). (b) Propose a reagent that could be used to convert A into B. (c) Draw the structure of the intermediate C formed by reaction of compound A with NaH. (d) Propose the structure of the organic compound D formed by reaction with PB.3. (e) Could HBr be used for the conversion of A into D? Explain very briefly.
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