Chapter 20, Problem 60PP

(a)

Interpretation Introduction

Interpretation:

The given reagents used to accomplish the target products (major product) transformation should be draw and identified.

Concept introduction:

$S_{N}1$Reaction: The $S_{N}1$ reaction is twostep process, leaving group leaves the molecule is first step and forms the more stable carbocation. Further, nucleophile attacks the carbocation and forms the final product in the second step. The rate of the reaction depends on the stability of the carbocation.

$S_{N}2$Reaction: The $S_{N}2$ reaction is single step process, leaving group leaves the molecule and nucleophiles attack the molecule is single step process which is simultaneous process.

LAH Reduction: The saturated/unsaturated aldehyde and ketones in the presence of sodium metal in LAH and carbonyl compound produced saturated alcohols. The keto group involves in the reduction process of LAH, this end up reducing to give the alcohols.

Grignard Reaction: This is a organometallic reaction in different alkyl, aryl-magnesium halides add to a carbonyl group in an aldehyde and ketone. This reaction is an important for the conversion of carbon-carbon single $\left(\text{-C-C-}\right)$ bond. Moreover the addition of a reagent to an aster, lactone gives a tertiary alcohol in which two alkyl groups are the same and the addition of a Grignard reagent to a nitrile produces an unsymmetrical ketone.

Wittig reaction: This process allows the preparation of an alkene by the reaction of an aldehyde ( $\text{-CHO}$) or ketone ( $\text{-C=O}$) with ylides generated from a phosphonium salt. The geometry of the resulting cis, trans alkene depends on the reactivity of the ylide.

To identify: The reagents used to accomplish the given transformation

(b)

Interpretation Introduction

Interpretation:

The given reagents used to accomplish the target products (major product) transformation should be draw and identified.

Concept introduction:

$S_{N}1$Reaction: The $S_{N}1$ reaction is twostep process, leaving group leaves the molecule is first step and forms the more stable carbocation. Further, nucleophile attacks the carbocation and forms the final product in the second step. The rate of the reaction depends on the stability of the carbocation.

$S_{N}2$Reaction: The $S_{N}2$ reaction is single step process, leaving group leaves the molecule and nucleophiles attack the molecule is single step process which is simultaneous process.

LAH Reduction: The saturated/unsaturated aldehyde and ketones in the presence of sodium metal in LAH and carbonyl compound produced saturated alcohols. The keto group involves in the reduction process of LAH, this end up reducing to give the alcohols.

Grignard Reaction: This is a organometallic reaction in different alkyl, aryl-magnesium halides add to a carbonyl group in an aldehyde and ketone. This reaction is an important for the conversion of carbon-carbon single $\left(\text{-C-C-}\right)$ bond. Moreover the addition of a reagent to an aster, lactone gives a tertiary alcohol in which two alkyl groups are the same and the addition of a Grignard reagent to a nitrile produces an unsymmetrical ketone.

Wittig reaction: This process allows the preparation of an alkene by the reaction of an aldehyde ( $\text{-CHO}$) or ketone ( $\text{-C=O}$) with ylides generated from a phosphonium salt. The geometry of the resulting cis, trans alkene depends on the reactivity of the ylide.

To identify: The reagents used to accomplish the given transformation

(c)

Interpretation Introduction

Interpretation:

The given reagents used to accomplish the target products (major product) transformation should be draw and identified.

Concept introduction:

$S_{N}1$Reaction: The $S_{N}1$ reaction is twostep process, leaving group leaves the molecule is first step and forms the more stable carbocation. Further, nucleophile attacks the carbocation and forms the final product in the second step. The rate of the reaction depends on the stability of the carbocation.

$S_{N}2$Reaction: The $S_{N}2$ reaction is single step process, leaving group leaves the molecule and nucleophiles attack the molecule is single step process which is simultaneous process.

LAH Reduction: The saturated/unsaturated aldehyde and ketones in the presence of sodium metal in LAH and carbonyl compound produced saturated alcohols. The keto group involves in the reduction process of LAH, this end up reducing to give the alcohols.

Grignard Reaction: This is a organometallic reaction in different alkyl, aryl-magnesium halides add to a carbonyl group in an aldehyde and ketone. This reaction is an important for the conversion of carbon-carbon single $\left(\text{-C-C-}\right)$ bond. Moreover the addition of a reagent to an aster, lactone gives a tertiary alcohol in which two alkyl groups are the same and the addition of a Grignard reagent to a nitrile produces an unsymmetrical ketone.

Wittig reaction: This process allows the preparation of an alkene by the reaction of an aldehyde ( $\text{-CHO}$) or ketone ( $\text{-C=O}$) with ylides generated from a phosphonium salt. The geometry of the resulting cis, trans alkene depends on the reactivity of the ylide.

To identify: The reagents used to accomplish the given transformation