Log out Go to App
Go to App

Learning Materials

Features

Discover

Chapter 10: Q47E (page 308)

How might you use a Suzuki–Miyaura reaction to prepare the biarylcompounds below? In each case, show the two potential reactionpartners.

Short Answer

Expert verified

(a)

(b)

(c)

Step by step solution

01

Suzuki–Miyaura reaction

Suzuki miyaura reaction is an organic reaction, classified as a cross coupling reaction, where the coupling partners are boronic acid and an organohalide and the catalyst is a palladium complex.

02

Preparing Bi-aryl compounds by Suzuki miyaura reaction

The Suzuki- Miyaura reaction is Pd-catalyzed coupling reaction between an aromatic boronic acid and an aromatic vinyl halide. Two possible coupling reaction can yield the target product.

(a)

Preparation of Bi-aryl (a)

(b)

Preparation of Bi-aryl (b)

(c)

Preparation of Bi-aryl (c)

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Start your free trial

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Give IUPAC names for the following alkyl halide (d):

Name the following alkyl halides:

How would you carry out the following syntheses?

Identify the reagents a–c in the following scheme:

Draw resonance structures for the following species:
See all solutions

Recommended explanations on Chemistry Textbooks

Organic Chemistry

Read Explanation

Chemical Reactions

Read Explanation

Making Measurements

Read Explanation

Nuclear Chemistry

Read Explanation

Chemistry Branches

Read Explanation

Physical Chemistry

Read Explanation
View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free