Essential Organic Chemistry (3rd Edition)
Essential Organic Chemistry (3rd Edition)
3rd Edition
ISBN: 9780321937711
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 12, Problem 39P

(a)

Interpretation Introduction

Interpretation: Using cyclohexanone as the starting material, the given compound has to be synthesized.

Concept Introduction:

Hydride reduction using NaBH4:

 NaBH4 - Sodium borohydride is a reducing agent.

 It reduces aldehydes, ketones and carboxylic acids into alcohols.

 General scheme:

Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  1

(b)

Interpretation Introduction

Interpretation: Using cyclohexanone as the starting material, the given compound has to be synthesized.

Concept Introduction:

Hydride reduction using NaBH4:

 NaBH4 - Sodium borohydride is a reducing agent.

 It reduces aldehydes, ketones and carboxylic acids into alcohols.

 General scheme:

  Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  2

 Dehydration of alcohol using concentrated acid:

 Alcohols get converted into alkene by the treatment of concentrated acid such as sulfuric acid. In this reaction, the alcohol gets eliminated as water molecule and forms the alkene double bond.

 General scheme:

 Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  3

(c)

Interpretation Introduction

Interpretation: Using cyclohexanone as the starting material, the given compound has to be synthesized.

Concept Introduction:

Hydride reduction using NaBH4:

 NaBH4 - Sodium borohydride is a reducing agent.

 It reduces aldehydes, ketones and carboxylic acids into alcohols.

 General scheme:

  Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  4

Conversion of alcohol into alkyl halide:

In this conversion, the alcohol gets converted into alkyl halide using hydrogen halide and with the elimination of a water molecule.

Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  5

(d)

Interpretation Introduction

Interpretation: Using cyclohexanone as the starting material, the given compound has to be synthesized.

Concept Introduction:

Imine formation:

Aldehyde or ketone reacts with a primary amine and forms imine in mildly acidic conditions.

Example for the formation of imine is shown here:

  Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  6

  • Imines contain C=N .
  • Imines are also called as Schiff bases, named after Hugo Schiff who described their formation.

Reduction of imine:

Imine when undergoes hydrogenation reaction, it gets converted into amine.

Example

  Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  7

(e)

Interpretation Introduction

Interpretation: Using cyclohexanone as the starting material, the given compound has to be synthesized.

Concept Introduction:

Wittig reaction:

It is the conversion of a ketone or an aldehyde into alkene using the ylide of phosphorus.

General Scheme

Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  8

  Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  9

Reduction of alkene:

Alkene when undergoes hydrogenation reaction, it gets converted into alkane.

Example

  Essential Organic Chemistry (3rd Edition), Chapter 12, Problem 39P , additional homework tip  10

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Students have asked these similar questions
Indicate how the following compounds can be synthesized from cyclohexanone and any other necessary reagents:
Describe how the following compounds could be prepared from cyclohexanone using an enamine intermediate:
2) How would you synthesize the following compounds from cyclohexanone?: a) b) CO₂H
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How to Design a Total Synthesis; Author: Chemistry Unleashed;https://www.youtube.com/watch?v=9jRfAJJO7mM;License: Standard YouTube License, CC-BY