Limited access

Upgrade to access all content for this subject

A chiral chair conformation of trans-1,2-cyclohexanediol and its mirror image cannot be interconverted (see the scheme below) at room temperature by conformational changes.

What is the consequence of this?

Grigoriy Sereda. Created for Albert.io. Copyright 2016. All rights reserved.

A

trans-1,2-cyclohexanediol can be separated at room temperature into two enantiomers.

B

trans-1,2-cyclohexanediol cannot be separated at room temperature into two enantiomers.

C

trans-1,2-cyclohexanediol has a higher acidity than an alkyne.

D

trans-1,2-cyclohexanediol has a lower acidity than an alkyne.

Select an assignment template