Substituents at equatorial positions are most stable.In both the conformations one methyl group is at equatorial and axial position. So the equilibrium ...

Both the chair conformations of cis - 1,4 - dimethylcyclohexane have the same stability because one methyl group will always be in equatorial position.

6 июл. 2023 г. · The most stable conformation for trans-1,4-dimethylcyclohexane is when both methyl groups are equatorial.

The stable conformers of trans-1,4-dimethyl cyclohexane is 1-equatorial-4-equatorial form. 1,4-diequatorial conformation is most stable as the steric ...

15 мая 2019 г. · Substituents at equatorial positions are most stable. In both the conformations one methyl group is at equatorial and axial position. So the ...

16 февр. 2024 г. · To achieve the lowest energy conformation for cis-1,4-dimethylcyclohexane, one methyl group would be axial and the other equatorial in one chair ...

Оценка 5,0 (81) 1 день назад · In the most stable conformation of cis-1,4-dimethylcyclohexane, the methyl groups are:______. Answer : VIEW ALL ANSWERS ( 14+ ). Other ...

Identify the given conformers of cis-1,4-dimethylcyclohexane and compare their potential energy based on axial and equatorial positions of the methyl groups ...

7 февр. 2017 г. · The upper trace shows the cis-isomer; i.e. one methyl is axial, and one methyl is equatorial.