CH₂CH₂CN 3-phenylpropanenitrile Electrophilic bromination of 3- phenylpropanenitrile occurs preferentially at the ortho and para positions. Assuming substitution at the para position, draw the structure of the most important resonance contributor of the carbocation intermediate.
CH₂CH₂CN 3-phenylpropanenitrile Electrophilic bromination of 3- phenylpropanenitrile occurs preferentially at the ortho and para positions. Assuming substitution at the para position, draw the structure of the most important resonance contributor of the carbocation intermediate.
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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Transcribed Image Text:CH₂CH₂CN
3-phenylpropanenitrile
Electrophilic bromination of 3-
phenylpropanenitrile occurs preferentially at the
ortho and para positions. Assuming substitution at
the para position, draw the structure of the most
important resonance contributor of the
carbocation intermediate.
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