Draw the two chair conformers for each of the following and indicate which conformer is more stable:
a)cis-1-ethyl-3-methylcyclohexane
b)trans-1-ethyl-2-methylcyclohexane
c)trans-1-ethyl-2-isopropylcyclohex ane
d)cis-1,2-diethylcyclohexane
e)cis-1-ethyl-3-isopropylcyclohexan e
ecis-1-ethyl-4-isopropylcyclohexane

For the drawings, please refer to the attached picture.

Explanation:

Stability of the conformers depends on the location of the groups attached to the main ring. The position of the bulkier (bigger) groups plays the most important role in conformer’s stability. If the conformer contains the bulkier group in the equatorial position, that conformer will be more stable than his twin brother with the bulkier group in the axial position. These are also drawn and attached below.

it forms an anion that has a larger radius. anions have a negative charge and are larger than the original atom.

the cold front replaces the warmer air at the ground level changing the wind to be breezy and denser.there is also an immediate drop in the temperature.