From the table of available reagents select the one(s) you would use to convert 1-phenylethanol to acetophenone (PHCOCH3) Use the minimum number of steps; in no case are more than two steps necessary. List reagents by letter in the order that they are used; example: fa. Reagents available g. а. ВНз, ТHF; then H2O2, - OH d. PhMgBr; KMN04, H20 then H3O+ e. LIAIH4; h. РОCI3, pyridine b. Br2, FeBr3 then H3O+ c. CH3MGB%; then H3 O+ f. РС, CH2 Cl2

From the table of available reagents select the one(s) you would use to convert 1-phenylethanol to acetophenone (PHCOCH3) Use the minimum number of steps; in no case are more than two steps necessary. List reagents by letter in the order that they are used; example: fa. Reagents available g. а. ВНз, ТHF; then H2O2, - OH d. PhMgBr; KMN04, H20 then H3O+ e. LIAIH4; h. РОCI3, pyridine b. Br2, FeBr3 then H3O+ c. CH3MGB%; then H3 O+ f. РС, CH2 Cl2

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter16: Aldehydes And Ketones

Section: Chapter Questions

Problem 16.47P: The base-promoted rearrangement of an -haloketone to a carboxylic acid, known as the Favorskii...

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