1. HC=C: Li HC=CH LICI 2. HO HO-S -CH3 Aqueous -CH3 acetone d = Electrophilic a = Proton transfer g = SN1 Nucleophilic substitution addition h = SN2 Nucleophilic substitution b = Lewis acid/base e = El Elimination c = Radical chain f= E2 Elimination substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2.

1. HC=C: Li HC=CH LICI 2. HO HO-S -CH3 Aqueous -CH3 acetone d = Electrophilic a = Proton transfer g = SN1 Nucleophilic substitution addition h = SN2 Nucleophilic substitution b = Lewis acid/base e = El Elimination c = Radical chain f= E2 Elimination substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i 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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