a) Show the reaction mechanism for the following multistep transformations. Show allreagents and the intermediate structures.BrOHfromandb) Propose a correct retrosynthetic analysis of (E)-1,3-di(furan-2-yl)prop-2-en-1-onefollowing an aldol condensation reaction.

Answered: Image /qna-images/answer/9aaedae0-fa17-4631-b546-9762a55e9329.jpg

a) Show the reaction mechanism for the following multistep transformations. Show all reagents and the intermediate structures. OH and b) Propose a correct retrosynthetic analysis of (E)-1,3-di(furan-2-yl)prop-2-en-1-one following an aldol condensation reaction.

a) Show the reaction mechanism for the following multistep transformations. Show all reagents and the intermediate structures. OH and b) Propose a correct retrosynthetic analysis of (E)-1,3-di(furan-2-yl)prop-2-en-1-one following an aldol condensation reaction.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter23: Carbonyl Condensation Reactions

Section23.SE: Something Extra

Problem 56AP

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Concept explainers

Diol

In chemistry there are so many chemical compounds that have a hydroxyl group but a chemical compound having two hydroxyl groups (-OH) is termed as a diol. It also implies the presence of two alcohols whereas polyols contain two or more than two hydroxyl groups (-OH). Glycol or 1,2-diol is an aliphatic diol that has two alcohol groups on adjacent carbon atoms. In industries, the most commonly used diol is ethylene glycol.

Question

a) Show the reaction mechanism for the following multistep transformations. Show all
reagents and the intermediate structures.
Br
OH
from
and
b) Propose a correct retrosynthetic analysis of (E)-1,3-di(furan-2-yl)prop-2-en-1-one
following an aldol condensation reaction.

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