1. Consider the electrophilic aromatic substitution reaction below. Provide the major product and complete curved arrow mechanism (including activation of the electrophile). CH3 NO₂ FeBr3 Br₂ Draw three resonance structures of the arenium intermediate (provide curved arrows between resonance forms). Of these three, indicate one which would be the relatively most stable resonance contributor. Provide a brief explanation on how/why the arenium ion intermediate resonance supports the formation of your product.

1. Consider the electrophilic aromatic substitution reaction below. Provide the major product and complete curved arrow mechanism (including activation of the electrophile). CH3 NO₂ FeBr3 Br₂ Draw three resonance structures of the arenium intermediate (provide curved arrows between resonance forms). Of these three, indicate one which would be the relatively most stable resonance contributor. Provide a brief explanation on how/why the arenium ion intermediate resonance supports the formation of your product.

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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