Can the final answer be a skelton structure if possible Compound A gives the product(s) below on oxidative cleavage with KMnO4 in acidic solution.Propose a structure for A.Compound AFO+(CH3)₂C O• You do not have to consider stereochemistry.• You do not have to explicitly draw H atoms.• If a group is achiral, do not use wedged or hashed bonds on it.

Compound A gives the product(s) below on oxidative cleavage with KMnO4 in acidic solution. Propose a structure for A. Compound A + (CH3)2C=O • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If a group is achiral, do not use wedged or hashed bonds on it.

Compound A gives the product(s) below on oxidative cleavage with KMnO4 in acidic solution. Propose a structure for A. Compound A + (CH3)2C=O • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If a group is achiral, do not use wedged or hashed bonds on it.

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

Chapter9: Nucleophilic Substitution And Β-elimination

Section: Chapter Questions

Problem 9.39P: Following are diastereomers (A) and (B) of 3-bromo-3,4-dimethylhexane. On treatment with sodium...

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