Consider the two stereo isomers of 1, 4-dimethyl cyclohexane: (a) Explain whether each methyl is axial or
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Consider the two stereo isomers of 1, 4-dimethyl cyclohexane:
(a) Explain whether each methyl is axial or equatorial in the conformations of the cis-isomer.
(b) Explain whether each methyl is axial or equatorial in the conformations of the trans-isomer.
(c) Explain which stereo isomer is more stable.
(d) Draw the more stable conformation of the more stable stereo isomer.
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This flat representation of a cyclohexane ring shows the relation of axial and equatorial bonds The ...View the full answer
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