Can i get help with these problems 1a.Give a detailed, stepwise mechanism for the Fischer esterification of aceticacid with methanol.1b.prepared from toluene. One of your intermediates must be a carboxylic acid.Suggest a sequence of synthetic steps through which 2-phenylethanol can be

Reaction involves following steps: Protonation Attack if nucleophile Deprotonation Dehydration

1a. Give a detailed, stepwise mechanism for the Fischer esterification of acetic acid with methanol. 1b. Suggest a sequence of synthetic steps through which 2-phenylethanol can be prepared from toluene. One of your intermediates must be a carboxylic acid.

1a. Give a detailed, stepwise mechanism for the Fischer esterification of acetic acid with methanol. 1b. Suggest a sequence of synthetic steps through which 2-phenylethanol can be prepared from toluene. One of your intermediates must be a carboxylic acid.

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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Can i get help with these problems

1a.
Give a detailed, stepwise mechanism for the Fischer esterification of acetic
acid with methanol.
1b.
prepared from toluene. One of your intermediates must be a carboxylic acid.
Suggest a sequence of synthetic steps through which 2-phenylethanol can be

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