The reaction of 4-methylcyclohexanone with CH3MgBr followed by neutralization gives two alcohols. These two alcohols are A. enantiomers formed in equal amounts. B. diastereomers. C. constitutional isomers. D. enantiomers formed in unequal amounts.

The reaction of 4-methylcyclohexanone with CH3MgBr followed by neutralization gives two alcohols. These two alcohols are A. enantiomers formed in equal amounts. B. diastereomers. C. constitutional isomers. D. enantiomers formed in unequal amounts.

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter13: Alcohols, Phenols, And Ethers

Section: Chapter Questions

Problem 13.15E: Classify the following alcohols as primary, secondary, or tertiary: a. b. CH3CH2CH2CH2OH c.

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Question

The reaction of 4-methylcyclohexanone with CH₃MgBr followed by neutralization gives two alcohols. These two alcohols are

	A.	enantiomers formed in equal amounts.
	B.	diastereomers.
	C.	constitutional isomers.
	D.	enantiomers formed in unequal amounts.

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