Explain why one diastereomer is thermodynamically more stable than the other. To do so, draw both chair conformations for cis-4-tert-butylcyclohexanol. Do the same for trans-4-tert- butylcyclohexanol. Label all 1,3-diaxial interactions for these four species. Indicate the most stable chair conformation of cis-4-tert-butylcyclohexanol. Do the same for trans-4-tert-butyl- cyclohexanol. Which of these latter two species is the most stable