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. resonance 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 rese contributor that shows this group actively participating in the charge delocalization. H₂C • 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.
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. resonance 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 rese contributor that shows this group actively participating in the charge delocalization. H₂C • 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.
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter21: Nas: Nucleophilic Aromatic Substitution
Section: Chapter Questions
Problem 8E
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![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.
resonance
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 rese
contributor that shows this group actively participating in the charge delocalization.
H₂C
• 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.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fed07e6d7-5565-4362-9c55-0d05e0f82a2a%2F1733bd66-a354-4e03-84ab-2698e57d6b0f%2Fh2c4sw_processed.jpeg&w=3840&q=75)
Transcribed Image Text: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.
resonance
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 rese
contributor that shows this group actively participating in the charge delocalization.
H₂C
• 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.
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