Skip to main content

Science Chemistry EBK ORGANIC CHEMISTRY STUDY GUIDE AND S

The structure of the intermediate A , dimedone and curved arrow mechanism for compound B formation are to be stated. Concept introduction: In Claisen condensation reaction two esters or one ester and a carbonyl compound react together to form β ketoester and β -diketone compound in the presence of a base. Michael addition reaction is a nucleophilic addition reaction of an anion to α , β -unsaturated carbonyl compound and results in the formation of conjugate addition product. When ester undergoes basic hydrolysis, it results in the formation of carboxylate salt and an alcohol which is the reversible step of ester formation.

The structure of the intermediate A , dimedone and curved arrow mechanism for compound B formation are to be stated. Concept introduction: In Claisen condensation reaction two esters or one ester and a carbonyl compound react together to form β ketoester and β -diketone compound in the presence of a base. Michael addition reaction is a nucleophilic addition reaction of an anion to α , β -unsaturated carbonyl compound and results in the formation of conjugate addition product. When ester undergoes basic hydrolysis, it results in the formation of carboxylate salt and an alcohol which is the reversible step of ester formation.

Solution Summary: The author explains the structure of the intermediate A, dimedone, and curved arrow mechanism for compound B formation.

EBK ORGANIC CHEMISTRY STUDY GUIDE AND S

EBK ORGANIC CHEMISTRY STUDY GUIDE AND S

6th Edition

ISBN: 9781319385415

Author: PARISE

Publisher: VST

See similar textbooks

Question

Chapter 22, Problem 22.83AP

Interpretation Introduction

Interpretation:

The structure of the intermediate A, dimedone and curved arrow mechanism for compound B formation are to be stated.

Concept introduction:

In Claisen condensation reaction two esters or one ester and a carbonyl compound react together to form β ketoester and β-diketone compound in the presence of a base. Michael addition reaction is a nucleophilic addition reaction of an anion to α,β-unsaturated carbonyl compound and results in the formation of conjugate addition product. When ester undergoes basic hydrolysis, it results in the formation of carboxylate salt and an alcohol which is the reversible step of ester formation.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

Blurred answer

Chapter 22, Problem 22.82AP

Chapter 22, Problem 22.84AP

Students have asked these similar questions

(EXM 2, PRBLM 3) Here is this problem, can you explain it to me and show how its done. Thank you I need to see the work for like prbl solving.

can someone draw out the reaction mechanism for this reaction showing all bonds, intermediates and side products Comment on the general features of the 1H-NMR spectrum of isoamyl ester provided below

What would be the best choices for the missing reagents 1 and 3 in this synthesis? 1. PPh3 3 2. n-BuLi • Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like. • Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is. • Note: if one of your reagents needs to contain a halogen, use bromine. Click and drag to start drawing a structure.

Chapter 22 Solutions

EBK ORGANIC CHEMISTRY STUDY GUIDE AND S

Ch. 22 - Prob. 22.1P Ch. 22 - Prob. 22.2P Ch. 22 - Prob. 22.3P Ch. 22 - Prob. 22.4P Ch. 22 - Prob. 22.5P Ch. 22 - Prob. 22.6P Ch. 22 - Prob. 22.7P Ch. 22 - Prob. 22.8P Ch. 22 - Prob. 22.9P Ch. 22 - Prob. 22.10P

Ch. 22 - Prob. 22.11P Ch. 22 - Prob. 22.12P Ch. 22 - Prob. 22.13P Ch. 22 - Prob. 22.14P Ch. 22 - Prob. 22.15P Ch. 22 - Prob. 22.16P Ch. 22 - Prob. 22.17P Ch. 22 - Prob. 22.18P Ch. 22 - Prob. 22.19P Ch. 22 - Prob. 22.20P Ch. 22 - Prob. 22.21P Ch. 22 - Prob. 22.22P Ch. 22 - Prob. 22.23P Ch. 22 - Prob. 22.24P Ch. 22 - Prob. 22.25P Ch. 22 - Prob. 22.26P Ch. 22 - Prob. 22.27P Ch. 22 - Prob. 22.28P Ch. 22 - Prob. 22.29P Ch. 22 - Prob. 22.30P Ch. 22 - Prob. 22.31P Ch. 22 - Prob. 22.32P Ch. 22 - Prob. 22.33P Ch. 22 - Prob. 22.34P Ch. 22 - Prob. 22.35P Ch. 22 - Prob. 22.36P Ch. 22 - Prob. 22.37P Ch. 22 - Prob. 22.38P Ch. 22 - Prob. 22.39P Ch. 22 - Prob. 22.40P Ch. 22 - Prob. 22.41P Ch. 22 - Prob. 22.42P Ch. 22 - Prob. 22.43P Ch. 22 - Prob. 22.44P Ch. 22 - Prob. 22.45P Ch. 22 - Prob. 22.46P Ch. 22 - Prob. 22.47P Ch. 22 - Prob. 22.48P Ch. 22 - Prob. 22.49P Ch. 22 - Prob. 22.50P Ch. 22 - Prob. 22.51P Ch. 22 - Prob. 22.52P Ch. 22 - Prob. 22.53P Ch. 22 - Prob. 22.54P Ch. 22 - Prob. 22.55AP Ch. 22 - Prob. 22.56AP Ch. 22 - Prob. 22.57AP Ch. 22 - Prob. 22.58AP Ch. 22 - Prob. 22.59AP Ch. 22 - Prob. 22.60AP Ch. 22 - Prob. 22.61AP Ch. 22 - Prob. 22.62AP Ch. 22 - Prob. 22.63AP Ch. 22 - Prob. 22.64AP Ch. 22 - Prob. 22.65AP Ch. 22 - Prob. 22.66AP Ch. 22 - Prob. 22.67AP Ch. 22 - Prob. 22.68AP Ch. 22 - Prob. 22.69AP Ch. 22 - Prob. 22.70AP Ch. 22 - Prob. 22.71AP Ch. 22 - Prob. 22.72AP Ch. 22 - Prob. 22.73AP Ch. 22 - Prob. 22.74AP Ch. 22 - Prob. 22.75AP Ch. 22 - Prob. 22.76AP Ch. 22 - Prob. 22.77AP Ch. 22 - Prob. 22.78AP Ch. 22 - Prob. 22.79AP Ch. 22 - Prob. 22.80AP Ch. 22 - Prob. 22.81AP Ch. 22 - Prob. 22.82AP Ch. 22 - Prob. 22.83AP Ch. 22 - Prob. 22.84AP Ch. 22 - Prob. 22.85AP Ch. 22 - Prob. 22.86AP Ch. 22 - Prob. 22.87AP Ch. 22 - Prob. 22.88AP Ch. 22 - Prob. 22.89AP Ch. 22 - Prob. 22.90AP Ch. 22 - Prob. 22.91AP Ch. 22 - Prob. 22.92AP Ch. 22 - Prob. 22.93AP Ch. 22 - Prob. 22.94AP Ch. 22 - Prob. 22.95AP Ch. 22 - Prob. 22.96AP Ch. 22 - Prob. 22.97AP Ch. 22 - Prob. 22.98AP

Knowledge Booster

Background pattern image

Similar questions

SEE MORE QUESTIONS

Recommended textbooks for you

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:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:Cengage Learning

SEE MORE TEXTBOOKS