Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781305580350
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, 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, 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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Students have asked these similar questions
Consider the following 2 dienes. When treated with HBr, one of these dienes yields four products while the other diene yields only two products. Explain.
3. What is the difference between the reaction conditions to obtain kinetic and thermodynamic products in the reactions of dienes?
A2 What is the inverse electron demand Diels–Alder reaction? Please pick a pair of a diene and a dienophile from the following dienes and dienophile that will undergo this type of reaction. Please show how this reaction works using Frontier Molecular Orbitals. What is the reaction product?

Chapter 20 Solutions

Organic Chemistry

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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