Please indicate which ONE specific structure is the answer. Thank you!! During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the benzene ring, that direct ortho/parafurther stabilize this intermediate by participating in the resonance delocalization of the positive charge.Assume that the following group is present on a benzene ring at position 1 and that you are brominating the ring at positon 4. In the box below draw the structureof the resonance contributor that shows this group actively participating in the charge delocalization.-NH2You do not have to consider stereochemistry.• You do not have to explicitly draw H atoms.• Do not include lone pairs in your answer. They will not be considered in the grading.C Popy asteChemDoodle

Answered: During electrophilic aromatic…

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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Please indicate which ONE specific structure is the answer. Thank you!!

During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed. Groups, already present on the benzene ring, that direct ortho/para
further stabilize this intermediate by participating in the resonance delocalization of the positive charge.
Assume that the following group is present on a benzene ring at position 1 and that you are brominating the ring at positon 4. In the box below draw the structure
of the resonance contributor that shows this group actively participating in the charge delocalization.
-NH2
You do not have to consider stereochemistry.
• You do not have to explicitly draw H atoms.
• Do not include lone pairs in your answer. They will not be considered in the grading.
C P
opy aste
ChemDoodle

Expert Solution

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An electrophile attacks at more nucleophilic site. In case of electron donating group, ortho and para positions are the one carrying negative charge in resonating structure and therefore they are ortho para directing.

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