OH 1. aqueous H2SO4 CH3 CH3 2. H2SO4 OH H2O 130° a = Proton transfer d = El Elimination f= SN1 Nucleophilic substitution b = Lewis acid/base e = E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers.

OH 1. aqueous H2SO4 CH3 CH3 2. H2SO4 OH H2O 130° a = Proton transfer d = El Elimination f= SN1 Nucleophilic substitution b = Lewis acid/base e = E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers.

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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