The most stable conformation of the following compound has A. An axial methyl group and an axial ethyl group.
B. An axial methyl group and an equatorial ethyl group.
C. An axial tert-butyl group.
D. An equatorial methyl group and an equatorial ethyl group.
E. An equatorial methyl group and an axial ethyl group.

The most stable conformation of the following compound has

A. An axial methyl group and an axial ethyl group.

B. An axial methyl group and an equatorial ethyl group.

C. An axial tert-butyl group.

D. An equatorial methyl group and an equatorial ethyl group.

E. An equatorial methyl group and an axial ethyl group.

Explanation:

The most stable conformation in the cyclohexane ring is the one in which both the substituents are in the equatorial position.

Among the given options,

option D  An equatorial methyl group and an equatorial ethyl group.

When the substituents in the cyclohexane ring are in equatorial positions then, the steric repulsions will be reduced.

Answer is option D.

< > according to newton's third law of motion, forces always act in equal but opposite pairs. another way of saying this is for every action, there is an equal but opposite reaction.< >