NH2 ད་ཡིན་ན། ༄ ོ་ད༥- ་ ཡི་ རྩ བྱིས་རྩ NH3 the acidity of the amine ion drives the reaction to shift toward the conjugate base of the carboxylic acid product. the resulting carboxylic acid ion is a weaker base than an acetate ion. O aldehydes are more reactive toward nucleophiles than ketones. nucleophilic attack occurs preferentially at the less hindered carbon of the formyl group.

NH2 ད་ཡིན་ན། ༄ ོ་ད༥- ་ ཡི་ རྩ བྱིས་རྩ NH3 the acidity of the amine ion drives the reaction to shift toward the conjugate base of the carboxylic acid product. the resulting carboxylic acid ion is a weaker base than an acetate ion. O aldehydes are more reactive toward nucleophiles than ketones. nucleophilic attack occurs preferentially at the less hindered carbon of the formyl group.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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