Organic Chemistry
Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
bartleby

Concept explainers

Question
Book Icon
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.

Blurred answer
Students have asked these similar questions
Reaction of p-nitroaniline with sodium nitrite and hydrochloric acid at 0°C, followed by treatment with N,N-diethylaniline.
The following diol is prepared from propanal (CH3CH2CHO) and 3-bromopropanol. Which derivatives will be among intermediate products in this transformation? ОН HO
how to synthesize 2-phenylclohexanone from cyclohexanone?

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...
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning