of 1. conc. HBr HO. Br 2. (Ph),C-OH HCI (Ph)3C-CI H20 f = Sy1 Nucleophilic substitution d = E1 Elimination e = E2 Elimination a = Proton transfer b= Lewis acid base c = Electrophilic addition g= SN2 Nucleophilic substitution 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.

of 1. conc. HBr HO. Br 2. (Ph),C-OH HCI (Ph)3C-CI H20 f = Sy1 Nucleophilic substitution d = E1 Elimination e = E2 Elimination a = Proton transfer b= Lewis acid base c = Electrophilic addition g= SN2 Nucleophilic substitution 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

Chapter10: Organohalides

Section10.2: Preparing Alkyl Halides From Alkanes: Radical Halogenation

Problem 4P: Taking the relative reactivities of 1Â°, 2Â°, and 3Â° hydrogen atoms into account, what product(s)...

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