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Why does compound X undergo bromination with Br2 in the absence of FeBr3 whereas bromination of benzene requires the presence of FeBr3? OCH3 Compound x Benzene the methoxy group of compound x is an inductive electron withdrawing substituent O compound x is a better nucleophile than benzene O Br2 is a good nucleophile the reaction is accelerated by light

Why does compound X undergo bromination with Br2 in the absence of FeBr3 whereas bromination of benzene requires the presence of FeBr3? OCH3 Compound x Benzene the methoxy group of compound x is an inductive electron withdrawing substituent O compound x is a better nucleophile than benzene O Br2 is a good nucleophile the reaction is accelerated by light

Organic Chemistry
Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution
Section16.SE: Something Extra
Problem 47AP
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Why does compound X undergo bromination with Br2 in the absence of FeBr3 whereas bromination of benzene requires the presence of FeBr3? OCH3 Compound x Benzene the methoxy group of compound x is an inductive electron withdrawing substituent O compound x is a better nucleophile than benzene O Br2 is a good nucleophile the reaction is accelerated by light
Transcribed Image Text:Why does compound X undergo bromination with Br2 in the absence of FeBr3 whereas bromination of benzene requires the presence of FeBr3? OCH3 Compound x Benzene the methoxy group of compound x is an inductive electron withdrawing substituent O compound x is a better nucleophile than benzene O Br2 is a good nucleophile the reaction is accelerated by light
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