Draw 1,2,3,4,5,6-hexamethylcyclohexane with all the methyl groups
a. in axial positions.

Draw 1,2,3,4,5,6-hexachlorocyclohexane with

a. all the chloro groups in axial positions.

b. all the chloro groups in equatorial positions.

a. Draw Newman projections of the two conformers of trans-1,3-dimethylcyclohexane.

b. Which of the conformers predominates at equilibrium?

This is a Newman projection of a substituted cyclohexane.

c. Give the IUPAC name.

Draw the two chair conformers for each of the stereoisomers of trans-1-tert-butyl-3-methylcyclohexane.

Draw 1,2,3,4,5,6-hexamethylcyclohexane with all the methyl groups

b. in equatorial positions.

In the lowest energy chair conformation of $\mathrm{methylcyclohexane}$, how many methyl groups are in the axial position?

Which of the following best describes the orientation of axial bonds in a chair conformation of $\mathrm{cyclohexane}$?

This is a Newman projection of a substituted cyclohexane.

b. Draw the equivalent structure using wedge and dash notation on a cyclohexane hexagon.