18.2 Which of the following nitrile groups is activated toward nucleophilic attack? ENH 18.1 Draw the mechanism for the reaction below under (a) neutral conditions and (b) basic conditions. Under which conditions do you think the hydration reaction will proceed faster? Why? HO OH + H20 Cyclohexanone Cyclohexanone hydrate

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
Chapter23: Amines
Section: Chapter Questions
Problem 23.38P: (S)-Glutamic acid is one of the 20 amino acid building blocks of polypeptides and proteins (Chapter...
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18.2 Which of the following nitrile groups is activated toward nucleophilic attack?
N.
NH
18.1 Draw the mechanism for the reaction below under (a) neutral conditions and (b) basic conditions.
Under which conditions do you think the hydration reaction will proceed faster? Why?
HO
OH
+ H20
Cyclohexanone
Cyclohexanone hydrate
Transcribed Image Text:18.2 Which of the following nitrile groups is activated toward nucleophilic attack? N. NH 18.1 Draw the mechanism for the reaction below under (a) neutral conditions and (b) basic conditions. Under which conditions do you think the hydration reaction will proceed faster? Why? HO OH + H20 Cyclohexanone Cyclohexanone hydrate
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Nucleophilic substitution reaction is one of the ost usable reaction . 

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