[1] CH3LI [2] CH3I H NMR of Y 6 H 2H 2H ЗН 1H 4 3 ppm 2.

EBK A SMALL SCALE APPROACH TO ORGANIC L
4th Edition
ISBN:9781305446021
Author:Lampman
Publisher:Lampman
Chapter61: Friedel–crafts Acylation
Section: Chapter Questions
Problem 8Q
icon
Related questions
icon
Concept explainers
Question

Treatment of W with CH3Li, followed by CH3I, affords compound Y (C7H14O) as the major product. Y shows a strong absorption in its IR spectrum at 1713 cm−1, and its 1H NMR spectrum is given below. (a) Propose a structure for Y. (b) Draw a stepwise mechanism for the conversion of W to Y.

[1] CH3LI
[2] CH3I
H NMR of Y
6 H
2H
2H
ЗН
1H
4
3
ppm
2.
Transcribed Image Text:[1] CH3LI [2] CH3I H NMR of Y 6 H 2H 2H ЗН 1H 4 3 ppm 2.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 3 images

Blurred answer