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: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter25: Enolate & Enol Nucleophiles
Section: Chapter Questions
Problem 16E
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Here in Chapter 19, we learned that converting a
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