A ketone was converted to an alkene using a Wittig reaction. As part of this synthesis, the ylide was prepared from an alkyl bromide. What is the alkyl bromide that was used to prepare the ylide for this synthesis? O 2-bromopentane 1-bromopropane bromoethane 3-bromopentane

A ketone was converted to an alkene using a Wittig reaction. As part of this synthesis, the ylide was prepared from an alkyl bromide. What is the alkyl bromide that was used to prepare the ylide for this synthesis? O 2-bromopentane 1-bromopropane bromoethane 3-bromopentane

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

Chapter19: Enolate Anions And Enamines

Section: Chapter Questions

Problem 19.61P: Following are the steps in one of the several published syntheses of frontalin, a pheromone of the...

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help

A ketone was converted to an alkene
using a Wittig reaction. As part of this
synthesis, the ylide was prepared from an
alkyl bromide. What is the alkyl bromide
that was used to prepare the ylide for this
synthesis?
2-bromopentane
O 1-bromopropane
bromoethane
3-bromopentane

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