The following reaction scheme shows that the intermediate carbocation from addition of an electrophile to benzene undergoes attack by a base to give the final product. This is because that process (a) gives a more stable carbocation, (b) restores the aromaticity in the product that was lost in the initial addition step, (c) avoids forming a conjugated diene, (d) does not require a strong nucleophile. z: + HZ

The following reaction scheme shows that the intermediate carbocation from addition of an electrophile to benzene undergoes attack by a base to give the final product. This is because that process (a) gives a more stable carbocation, (b) restores the aromaticity in the product that was lost in the initial addition step, (c) avoids forming a conjugated diene, (d) does not require a strong nucleophile. z: + HZ

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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