OCH3 LOCH3 1. Br2 HBr Br 2. Br Na NaBr h = Syl Nucleophilic substitution i= Sy2 Nucleophilic substitution j = Electrophilic aromatic substitution a = Proton transfer e = Electrophilic addition b=Lewis acid/base f= E1 Elimination c = Radical chain substitution d = Radical chain addition g = E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your answers. 1. 2.

OCH3 LOCH3 1. Br2 HBr Br 2. Br Na NaBr h = Syl Nucleophilic substitution i= Sy2 Nucleophilic substitution j = Electrophilic aromatic substitution a = Proton transfer e = Electrophilic addition b=Lewis acid/base f= E1 Elimination c = Radical chain substitution d = Radical chain addition g = E2 Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - j for your answers. 1. 2.

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 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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