Which of the following statements about carbonyl derivatives is FALSE?

Introduction to General, Organic and Biochemistry
11th Edition
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Chapter18: Carboxylic Acids
Section: Chapter Questions
Problem 18.54P
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Which of the following statements about carbonyl derivatives is FALSE?
O Formation of an amide from an acyl chloride requires use of two equivalents of the
amine.
O The product of the base-promoted saponification of an ester is a carboxylate
anion.
O Acetals are great protecting groups for aldehydes and ketones because they are
stable to acidic conditions.
O Despite being a terrible leaving group, H2N¯ is indeed the leaving group in the
base-promoted hydrolysis of an amide.
O Transesterification can occur under either acidic or basic reactions conditions.
Transcribed Image Text:Which of the following statements about carbonyl derivatives is FALSE? O Formation of an amide from an acyl chloride requires use of two equivalents of the amine. O The product of the base-promoted saponification of an ester is a carboxylate anion. O Acetals are great protecting groups for aldehydes and ketones because they are stable to acidic conditions. O Despite being a terrible leaving group, H2N¯ is indeed the leaving group in the base-promoted hydrolysis of an amide. O Transesterification can occur under either acidic or basic reactions conditions.
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