Cyclohexane exist as two chair conformations in rapid equilibrium at room temperature.
Each carbon atom on a cyclohexane ring has one axial and one equatorial bydrogen. Rind-flipping converts axial H's to equatorial H's and vice-versa`

In substituted cyclohexane, groups larger than hydrogen ar more stable in the equatorial position.
The cis isomers has two groups on the same side of the ring, eithere both up or both down.
The trans isomer has two groups on opposite side of the ring one up and one down.
Find out most stable substituted cyclohexane among the following:

Cyclohexane exist as two chair conformations in rapid equilibrium at room temperature. Each carbon atom on a cyclohexane ring has one axial and one equatorial bydrogen. Rind-flipping converts axial H's to equatorial H's and vice-versa In substituted cyclohexane, groups larger than hydrogen ar more stable in the equatorial position. The cis isomers has two groups on the same side of the ring, eithere both up or both down. The trans isomer has two groups on opposite side of the ring one up and one down. Find out most stble conformer of cis-3-fluorocyclojexanol:

Cyclohexane exist as two chair conformations in rapid equilibrium at room temperature. Each carbon atom on a cyclohexane ring has one axial and one equatorial bydrogen. Rind-flipping converts axial H's to equatorial H's and vice-versa In substituted cyclohexane, groups larger than hydrogen ar more stable in the equatorial position. The cis isomers has two groups on the same side of the ring, eithere both up or both down. The trans isomer has two groups on opposite side of the ring one up and one down. Which of the following is most stable conformer of 1,2-dichlorocyclohexane?

The most stable conformation of cyclohexane is

The least energetic conformation of cyclohexane is:

The most stable conformation of cyclohexane is :

Assertion: Trans isomers are more stable than cis isomers Reason: The cis isomer is the one in which two similar group are on the same side of double bond.