Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure is to be shown. Concept introduction: Lower alkynes are converted into higher alkynes by converting them into the alkynides and then treating with the alkyl halide required. The alkyne obtained can be reduced to an alkene using Lindlar catalyst. The alkene when oxidized with peracids will yield the epoxide . To show: Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure.

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Answer 1

Question

Chapter 18.SE, Problem 64GP

Interpretation Introduction

Interpretation:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure is to be shown.

Concept introduction:

Lower alkynes are converted into higher alkynes by converting them into the alkynides and then treating with the alkyl halide required. The alkyne obtained can be reduced to an alkene using Lindlar catalyst. The alkene when oxidized with peracids will yield the epoxide.

To show:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure.

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Answer 2

Question

Chapter 18.SE, Problem 64GP

Interpretation Introduction

Interpretation:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure is to be shown.

Concept introduction:

Lower alkynes are converted into higher alkynes by converting them into the alkynides and then treating with the alkyl halide required. The alkyne obtained can be reduced to an alkene using Lindlar catalyst. The alkene when oxidized with peracids will yield the epoxide.

To show:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 18.SE, Problem 64GP

Interpretation Introduction

Interpretation:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure is to be shown.

Concept introduction:

Lower alkynes are converted into higher alkynes by converting them into the alkynides and then treating with the alkyl halide required. The alkyne obtained can be reduced to an alkene using Lindlar catalyst. The alkene when oxidized with peracids will yield the epoxide.

To show:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure.

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 18.SE, Problem 64GP

Interpretation Introduction

Interpretation:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure is to be shown.

Concept introduction:

Lower alkynes are converted into higher alkynes by converting them into the alkynides and then treating with the alkyl halide required. The alkyne obtained can be reduced to an alkene using Lindlar catalyst. The alkene when oxidized with peracids will yield the epoxide.

To show:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure.

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 5

Chapter 18.SE, Problem 64GP

Interpretation Introduction

Interpretation:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure is to be shown.

Concept introduction:

Lower alkynes are converted into higher alkynes by converting them into the alkynides and then treating with the alkyl halide required. The alkyne obtained can be reduced to an alkene using Lindlar catalyst. The alkene when oxidized with peracids will yield the epoxide.

To show:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure.

Answer 6

Chapter 18.SE, Problem 64GP

Interpretation Introduction

Interpretation:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure is to be shown.

Concept introduction:

Lower alkynes are converted into higher alkynes by converting them into the alkynides and then treating with the alkyl halide required. The alkyne obtained can be reduced to an alkene using Lindlar catalyst. The alkene when oxidized with peracids will yield the epoxide.

To show:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure.

Answer 7

Chapter 18.SE, Problem 64GP

Interpretation Introduction

Interpretation:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure is to be shown.

Concept introduction:

Lower alkynes are converted into higher alkynes by converting them into the alkynides and then treating with the alkyl halide required. The alkyne obtained can be reduced to an alkene using Lindlar catalyst. The alkene when oxidized with peracids will yield the epoxide.

To show:

Starting from compounds having ten or fewer carbons how to synthesize racemic disparlure.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 18.1 - Name the following ethers:Ch. 18.2 - Why do you suppose only symmetrical ethers are...Ch. 18.2 - How would you prepare the following ethers using a...Ch. 18.2 - Review the mechanism of oxymercuration shown in...Ch. 18.2 - How would you prepare the following ethers? Use...Ch. 18.2 - Prob. 6P Ch. 18.3 - Prob. 7P Ch. 18.3 - Write the mechanism of the acid-induced cleavage...Ch. 18.3 - Why are HI and HBr more effective than HCl in...Ch. 18.4 - What product would you expect from Claisen...

Solution Summary: The author explains how to synthesize racemic disparlure from compounds having ten or fewer carbons.

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Chapter 18 Solutions