Aniline reacts with bromine in the absence of a Lewis acid to give monosubstitution products. Draw a resonance form that explains this greater reactivity to electrophilic aromatic substitution, and give a brief explanation. NH2 NH2 NH2 NH2 Br Br2 NaHCO3 Br Br

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions
Section19.SE: Something Extra
Problem 28VC
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Question 6

Aniline reacts with bromine in the absence of a Lewis acid to give
monosubstitution products. Draw a resonance form that explains this greater
reactivity to electrophilic aromatic substitution, and give a brief explanation.
NH2
NH2
NH2
NH2
Br
Br2
NaHCO3
`Br
Br
Transcribed Image Text:Aniline reacts with bromine in the absence of a Lewis acid to give monosubstitution products. Draw a resonance form that explains this greater reactivity to electrophilic aromatic substitution, and give a brief explanation. NH2 NH2 NH2 NH2 Br Br2 NaHCO3 `Br Br
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