Organic Chemistry, Loose-leaf Version
Organic Chemistry, Loose-leaf Version
8th Edition
ISBN: 9781305865549
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
Question
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Chapter 20, Problem 20.22P

(a)

Interpretation Introduction

Interpretation: The thermodynamic and kinetic products that are expected to be formed on addition of one mole of Br2 to the given diene have to be found.

Concept Introduction:

Kinetic and Thermodynamic products:

  • • If the reactants gives a product via small activationenergy(Ea), then the resulted product will be readily formed from the reactants and it is known as  Kinetically controlled product.
  • • If the reactants gives a product via large activationenergy(Ea), then the resulted product will be least energetic than the reactants and it is known as Thermodynamically controlled product.

 Example:

The reaction of HBr and 1,3-butadiene takes place as shown in the following mechanism. The mechanism shows the intermediates and the corresponding products.

Organic Chemistry, Loose-leaf Version, Chapter 20, Problem 20.22P , additional homework tip  1

Product A is formed from more stable intermediate. So, it would have been formed with less expense of energy and it would have been formed readily. Therefore, product A is the kinetically controlled product.

Product B is formed from less stable intermediate. So, it would have been formed with more expense of energy. Hence, product B would have not been formed readily and it will be with more energy than that of the reactant. Therefore, product B is the thermodynamically controlled product.

(b)

Interpretation Introduction

Interpretation: The thermodynamic and kinetic products that are expected to be formed on addition of one mole of Br2 to the given diene have to be found.

Concept Introduction:

Kinetic and Thermodynamic products:

  • • If the reactants gives a product via small activationenergy(Ea), then the resulted product will be readily formed from the reactants and it is known as  Kinetically controlled product.
  • • If the reactants gives a product via large activationenergy(Ea), then the resulted product will be least energetic than the reactants and it is known as Thermodynamically controlled product.

 Example:

The reaction of HBr and 1,3-butadiene takes place as shown in the following mechanism. The mechanism shows the intermediates and the corresponding products.

Organic Chemistry, Loose-leaf Version, Chapter 20, Problem 20.22P , additional homework tip  2

Product A is formed from more stable intermediate. So, it would have been formed with less expense of energy and it would have been formed readily. Therefore, product A is the kinetically controlled product and it has been formed from 1,2-addition.

Product B is formed from less stable intermediate. So, it would have been formed with more expense of energy. Hence, product B would have not been formed readily and it will be with more energy than that of the reactant. Therefore, product B is the thermodynamically controlled product and it has been formed from 1,4-addition.

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Chapter 20 Solutions

Organic Chemistry, Loose-leaf Version

Ch. 20.6 - Prob. 20.11PCh. 20.6 - Prob. 20.12PCh. 20 - If an electron is added to 1,3-butadiene, into...Ch. 20 - Prob. 20.15PCh. 20 - Predict the structure of the major product formed...Ch. 20 - Predict the major product formed by 1,4-addition...Ch. 20 - Predict the structure of the major 1,2-addition...Ch. 20 - Prob. 20.19PCh. 20 - Prob. 20.20PCh. 20 - Prob. 20.21PCh. 20 - Prob. 20.22PCh. 20 - Prob. 20.23PCh. 20 - Pyridine exhibits a UV transition of the type n at...Ch. 20 - Prob. 20.25PCh. 20 - Prob. 20.26PCh. 20 - Prob. 20.27PCh. 20 - Write the frontier molecular orbital analysis for...Ch. 20 - Prob. 20.29PCh. 20 - Draw structural formulas for the products of...Ch. 20 - Propose structural formulas for compounds A and B...Ch. 20 - Under certain conditions, 1,3-butadiene can...Ch. 20 - Prob. 20.33PCh. 20 - Prob. 20.34PCh. 20 - The following triene undergoes an intramolecular...Ch. 20 - Prob. 20.36PCh. 20 - Prob. 20.37PCh. 20 - Prob. 20.38PCh. 20 - Prob. 20.39PCh. 20 - The Diels-Alder reaction is not limited to making...Ch. 20 - The first step in a synthesis of dodecahedrane...Ch. 20 - Bicyclo-2,5-heptadiene can be prepared in two...Ch. 20 - Prob. 20.43PCh. 20 - Prob. 20.44PCh. 20 - Following is a retrosynthetic scheme for the...Ch. 20 - Prob. 20.46PCh. 20 - Prob. 20.47PCh. 20 - Prob. 20.48PCh. 20 - Prob. 20.49PCh. 20 - Prob. 20.50PCh. 20 - What reaction presented in this chapter is...Ch. 20 - Claisen rearrangement of an allyl phenyl ether...Ch. 20 - Prob. 20.53PCh. 20 - Prob. 20.54PCh. 20 - We now continue the use of organic chemistry...Ch. 20 - Write the products of the following sequences of...
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