AICI, НC

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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Draw a stepwise mechanism for the following reaction.

AICI,
НC
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Expert Solution
Step 1

First the given alkyl halide reacts with AlCl3 and forms carbocation. Then, electrophilic alkyl carbocation is formed from loss of halide to AlCl3. The pi electrons on benzene acts as nucleophile, which reacts with the electrophilic carbocation. This results in formation of cyclohexadienyl cation intermediate. Finally the proton in C present in alkyl group gets removed and results in formation of given product.

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