ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
ORGANIC CHEMISTRY SAPLING ACCESS + ETEX
6th Edition
ISBN: 9781319306977
Author: LOUDON
Publisher: INTER MAC
bartleby

Concept explainers

Question
Book Icon
Chapter 24, Problem 24.18P
Interpretation Introduction

Interpretation:

The reason as to why the acetals hydrolyze more rapidly than ordinary ethers is to be stated.

Concept introduction:

Ketones react with diols to form acetals. This reaction is generally used as a way of protecting the carbonyl group in reactions. The carbonyl group can be generated back by hydrolysis of the acetal.

Aldehydes react with diols to form hemiacetals. The reaction takes place in the presence of an acid.

The formation of acetals and hemiacetals is a type of nucleophilic substitution reaction.

Blurred answer
Students have asked these similar questions
None
Draw a Newman projection from carbon 3 to carbon 2 in the highest energy conformation for the following molecule. What is this conformation called? What kind of strain is present? Br
Which of the following dienophiles is most reactive in a Diels-Alder reaction:  Please explain why the correct answer to this question is option 5. Please provide a detailed explanation.
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
Text book image
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning