1. Write a mechanism for the formation of oximes from aldehydes and hydroxylamine. 2. Reaction of unsymmetrical ketones with hydroxylamine gives a mixture of oxime isomers. Describe how you might distinguish the two possible products. 3. Compare and contrast the IR spectra of benzaldehyde and benzaldoxiome.
1. Write a mechanism for the formation of oximes from aldehydes and hydroxylamine. 2. Reaction of unsymmetrical ketones with hydroxylamine gives a mixture of oxime isomers. Describe how you might distinguish the two possible products. 3. Compare and contrast the IR spectra of benzaldehyde and benzaldoxiome.
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
Chapter18: Functional Derivatives Of Carboxylic Acids
Section: Chapter Questions
Problem 18.14P
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1. Write a mechanism for the formation of oximes from
2. Reaction of unsymmetrical
3. Compare and contrast the IR spectra of benzaldehyde and benzaldoxiome.
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