Shown here are the resonance contributors for the cationic intermediate in the electrophilic addition of bromine to the ortho position of 4-methylphenol. For each of the first three resonance structures, add one double-barbed curved arrow to show the delocalization of the electron pair to form the structure to the right. Br: LBr: The final structure is the major resonance contributor and explains why the - OH group is... a deactivator and an ortho/para director. (Continued from above.) an activator and a meta director. a deactivator and a meta director. an activator and an ortho/para director.
Shown here are the resonance contributors for the cationic intermediate in the electrophilic addition of bromine to the ortho position of 4-methylphenol. For each of the first three resonance structures, add one double-barbed curved arrow to show the delocalization of the electron pair to form the structure to the right. Br: LBr: The final structure is the major resonance contributor and explains why the - OH group is... a deactivator and an ortho/para director. (Continued from above.) an activator and a meta director. a deactivator and a meta director. an activator and an ortho/para director.
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter19: Eas: Electrophilic Aromatic Substitution
Section: Chapter Questions
Problem 32CTQ
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