Here in Chapter 19, we learned that converting a ketone or aldehyde to an acetal is a good way to protect the carbonyl group, because an acetal is composed of ether linkages. In Problem 17.57, we saw that a ketone or aldehyde can be converted into an epoxide, which is a cyclic ether. Why would an epoxide be a poor choice as a protecting group?
Here in Chapter 19, we learned that converting a ketone or aldehyde to an acetal is a good way to protect the carbonyl group, because an acetal is composed of ether linkages. In Problem 17.57, we saw that a ketone or aldehyde can be converted into an epoxide, which is a cyclic ether. Why would an epoxide be a poor choice as a protecting group?
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter11: Ethers, Epoxides, And Sulfides
Section: Chapter Questions
Problem 11.41P: Aldehydes and ketones react with one molecule of an alcohol to form compounds called hemiacetals, in...
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Here in Chapter 19, we learned that converting a
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