The image shows a chemical reaction involving the Friedel-Crafts alkylation mechanism. This reaction uses a catalyst, aluminum chloride (AlCl₃), to facilitate the alkylation of an aromatic compound, specifically an alkylbenzene.**Reactants:**- An alkylbenzene ring (with an isopropyl group attached).- A chloroalkane (1-chloropropane).A catalyst, AlCl₃, is used in the reaction.**Possible Products:**There are four possible product structures labeled from (a) to (d):a) The benzene ring with three substituents: one isopropyl and a propyl group in the para position relative to the isopropyl. b) The benzene ring with three substituents: one isopropyl and a propyl group in the meta position relative to the isopropyl. c) The benzene ring with three substituents: one isopropyl and a propyl group in the ortho position relative to the isopropyl. d) The benzene ring with three substituents: one isopropyl and a propyl group, positioned differently from options a, b, and c.The reaction showcases regioselectivity in Friedel-Crafts alkylation, where the position at which the electrophile substitutes on the aromatic ring can vary, resulting in different isomers.

Carbocation always have tendency to rearrangement.

Answered: AICI3 a) d)

Science

Chemistry

AICI3 a) d)

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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