Organic Chemistry
Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
Question
Book Icon
Chapter 23.11, Problem 19P
Interpretation Introduction

a)

Organic Chemistry, Chapter 23.11, Problem 19P , additional homework tip  1

Interpretation:

The product that will be produced when the enamine obtained by reacting cyclopentanone and pyrrolidone with α, β- unsaturated acceptor, ethyl acrylate, is to be identified.

Concept introduction:

The enamine obtained by reacting a ketone with cyclic amine reacts with α, β- unsaturated acceptor to yield a substituted enamine as the intermediate which upon hydrolysis gives the product.

To identify:

The product that will be produced when the enamine obtained by reacting cyclopentanone and pyrrolidone with α, β- unsaturated, ethyl acrylate, is hydrolyzed.

Interpretation Introduction

b)

Organic Chemistry, Chapter 23.11, Problem 19P , additional homework tip  2

Interpretation:

The product that will be produced when the enamine obtained by reacting cyclopentanone and pyrrolidone with α, β- unsaturated acceptor, acrolein is to be identified.

Concept introduction:

The enamine obtained by reacting a ketone with cyclic amine reacts with α, β- unsaturated acceptor, acrolein, to yield a substituted enamine as the intermediate which upon hydrolysis gives the products.

To identify:

The product that will be produced by the hydrolysis of the enamine obtained by reacting cyclopentanone and pyrrolidone with α, β- unsaturated acceptor, acroline.

Interpretation Introduction

c)

Organic Chemistry, Chapter 23.11, Problem 19P , additional homework tip  3

Interpretation:

The product that will be produced when the enamine obtained by reacting cyclopentanone and pyrrolidone with α, β- unsaturated acceptor, pent-3-ene-2-one, is to be identified.

Concept introduction:

The enamine obtained by reacting a ketone with cyclic amine reacts with an α, β- unsaturated acceptor to yield a substituted enamine as the intermediate which upon hydrolysis gives the products.

To identify:

The product that will be produced by the hydrolysis of the enamine obtained by reacting cyclopentanone and pyrrolidone with α, β- unsaturated acceptor, pent-3-ene-2-one.

Blurred answer
Students have asked these similar questions
Give detailed mechanism Solution with explanation needed. Don't give Ai generated solution
Show work with explanation needed....don't give Ai generated solution
1. 6. Draw the products for the following reaction: 2. Diels-Aider reaction NOH O OH

Chapter 23 Solutions

Organic Chemistry

Ch. 23.7 - Show the products you would expect to obtain by...Ch. 23.7 - Prob. 12PCh. 23.8 - What product would you expect from the following...Ch. 23.9 - What product would you expect From the following...Ch. 23.9 - Prob. 15PCh. 23.10 - Prob. 16PCh. 23.10 - Prob. 17PCh. 23.10 - Prob. 18PCh. 23.11 - Prob. 19PCh. 23.11 - Show how you might use an enamine reaction to...Ch. 23.12 - Prob. 21PCh. 23.12 - How would you prepare the following compound using...Ch. 23.SE - Prob. 23VCCh. 23.SE - Prob. 24VCCh. 23.SE - Prob. 25VCCh. 23.SE - The following molecule was formed by a Robinson...Ch. 23.SE - Prob. 27MPCh. 23.SE - Prob. 28MPCh. 23.SE - Predict the product(s) and provide the mechanism...Ch. 23.SE - Predict the product(s) and provide the mechanism...Ch. 23.SE - Predict the product(s) and provide the mechanism...Ch. 23.SE - Knoevenagel condensation is a reaction involving...Ch. 23.SE - Azlactones are important starting materials used...Ch. 23.SE - Prob. 34MPCh. 23.SE - Isoleucine, another of the twenty amino acids...Ch. 23.SE - The first step in the citric acid cycle of food...Ch. 23.SE - Prob. 37MPCh. 23.SE - The Knoevenagel reaction is a carbonyl...Ch. 23.SE - The Darzens reaction invoIves a two-step,...Ch. 23.SE - The following reaction involves a hydrolysis...Ch. 23.SE - Prob. 41MPCh. 23.SE - Prob. 42MPCh. 23.SE - Prob. 43MPCh. 23.SE - Propose a mechanism for the following...Ch. 23.SE - Prob. 45MPCh. 23.SE - Prob. 46MPCh. 23.SE - Prob. 47MPCh. 23.SE - Prob. 48APCh. 23.SE - Prob. 49APCh. 23.SE - Prob. 50APCh. 23.SE - Prob. 51APCh. 23.SE - Prob. 52APCh. 23.SE - Prob. 53APCh. 23.SE - Prob. 54APCh. 23.SE - Prob. 55APCh. 23.SE - Prob. 56APCh. 23.SE - Prob. 57APCh. 23.SE - Prob. 58APCh. 23.SE - In the mixed Claisen reaction of cyclopentanone...Ch. 23.SE - Ethyl dimethylacetoacetate reacts instantly at...Ch. 23.SE - Prob. 61APCh. 23.SE - Prob. 62APCh. 23.SE - The so-called Wieland-Miescher ketone is a...Ch. 23.SE - Prob. 64APCh. 23.SE - Prob. 65APCh. 23.SE - Prob. 66APCh. 23.SE - What condensation products would you expect to...Ch. 23.SE - The following reactions are unlikely to provide...Ch. 23.SE - Fill in the missing reagents a-h in the following...Ch. 23.SE - Prob. 70APCh. 23.SE - Prob. 71APCh. 23.SE - Prob. 72APCh. 23.SE - Prob. 73AP
Knowledge Booster
Background pattern image
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
    Introduction to General, Organic and Biochemistry
    Chemistry
    ISBN:9781285869759
    Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
    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
Text book image
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning