Organic Chemistry
Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
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Question
Chapter 10.SE, Problem 47AP
Interpretation Introduction

a)

Organic Chemistry, Chapter 10.SE, Problem 47AP , additional homework tip  1

Interpretation:

How the biaryl compound shown can be prepared using Suzuki-Miyaura reaction is to be shown.

Concept introduction:

In Suzuki-Miyaura reaction biaryl compounds are prepared by a coupling reaction between aromatic or vinyl substituted boronic acid with an aromatic or vinyl organo-halide in the presence of Pd catalyst.

To show:

How the biaryl compound shown can be prepared using Suzuki-Miyaura reaction.

Interpretation Introduction

b)

Organic Chemistry, Chapter 10.SE, Problem 47AP , additional homework tip  2

Interpretation:

How the biaryl compound shown can be prepared using Suzuki-Miyaura reaction is to be shown.

Concept introduction:

In Suzuki-Miyaura reaction biaryl compounds are prepared by a coupling reaction between aromatic or vinyl substituted boronic acid with an aromatic or vinyl organo-halide in the presence of Pd catalyst.

To show:

How the biaryl compound shown can be prepared using Suzuki-Miyaura reaction.

Interpretation Introduction

c)

Organic Chemistry, Chapter 10.SE, Problem 47AP , additional homework tip  3

Interpretation:

How the biaryl compound shown can be prepared using Suzuki-Miyaura reaction is to be shown.

Concept introduction:

In Suzuki-Miyaura reaction biaryl compounds are prepared by a coupling reaction between aromatic or vinyl substituted boronic acid with an aromatic or vinyl organo-halide in the presence of Pd catalyst.

To show:

How the biaryl compound shown can be prepared using Suzuki-Miyaura reaction.

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Chapter 10 Solutions

Organic Chemistry

Ch. 10.7 - How would you carry out the following...Ch. 10.8 - Rank both sets of compounds in order of increasing...Ch. 10.8 - Tell whether each of the following reactions is an...Ch. 10.SE - Prob. 14VCCh. 10.SE - Prob. 15VCCh. 10.SE - Prob. 16VCCh. 10.SE - Draw the electron-pushing mechanism for each...Ch. 10.SE - Draw the electron-pushing mechanism for the...Ch. 10.SE - The formation of Br2 from NBS first involves the...Ch. 10.SE - In light of the fact that tertiary alkyl halides...Ch. 10.SE - Alkyl halides can be reduced to alkanes by a...Ch. 10.SE - Name the following alkyl halides:Ch. 10.SE - Prob. 23APCh. 10.SE - Draw and name all of the monochlorination products...Ch. 10.SE - How would you prepare the following compounds,...Ch. 10.SE - Prob. 26APCh. 10.SE - A chemist requires a large amount of...Ch. 10.SE - What product(s) would you expect from the reaction...Ch. 10.SE - What product(s) would you expect from the reaction...Ch. 10.SE - What product would you expect from the reaction of...Ch. 10.SE - Rank the compounds in each of the following series...Ch. 10.SE - Which of the following compounds have the same...Ch. 10.SE - Tell whether each of the following reactions is an...Ch. 10.SE - Prob. 34APCh. 10.SE - Alkylbenzenes such as toluene (methylbenzene)...Ch. 10.SE - Prob. 36APCh. 10.SE - Prob. 37APCh. 10.SE - Prob. 38APCh. 10.SE - Prob. 39APCh. 10.SE - Prob. 40APCh. 10.SE - The syntheses shown here are unlikely to occur as...Ch. 10.SE - Why do you suppose its not possible to prepare a...Ch. 10.SE - Prob. 43APCh. 10.SE - Identify the reagents a–c in the following...Ch. 10.SE - Prob. 45APCh. 10.SE - Prob. 46APCh. 10.SE - Prob. 47APCh. 10.SE - The relative rate of radical bromination is...Ch. 10.SE - Prob. 49APCh. 10.SE - Predict the product and provide the entire...
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