Why can't 1−methylcyclohexanol be prepared from a carbonyl compound by reduction? select the single best answer?

1−methylcyclohexanol is a tertiary alcohol. Tertiary Alcohols are synthesized by either reacting Ketone with Organometallic compounds like Grignard reagent or by hydration of substituted alkenes. 1−methylcyclohexanol can not be synthesized by reduction of carbonyl compound because it is not possible to have a starting carbonyl compound having carbonyl group along with three other alkyl groups (as carbon can only form 4 bonds).

Result:
           Tertiary alcohols don't contain a hydrogen atom at carbon attached to hydroxyl group that is why it is not possible to synthesize 1−methylcyclohexanol by reduction of carbonyl compound.

Ch4 is nonpolar and insoluble in water. since all of the hydrogen atoms are evenly spread around the carbon atom even through the c h bond is polar all the poles cancel each other out.