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(A) The reaction involves the acid-catalyzed dehydration of $cis-4-methylcyclohexanol$ using $H^+$ and heat $(\Delta)$.This process proceeds via an $E

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Racemic

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(A) The reaction involves the acid-catalyzed dehydration of $cis-4-methylcyclohexanol$ using $H^+$ and heat $(\Delta)$.This process proceeds via an $E1$ mechanism involving the formation of a carbocation intermediate.The dehydration leads to the formation of $4-methylcyclohexene$.Since the product $4-methylcyclohexene$ has a chiral center at the $C4$ position,the reaction produces a pair of enantiomers in equal amounts,which is known as a racemic mixture.

The products obtained in the following reaction are:

Similar Questions

Which one of the following is a secondary alcohol?

Which of the following alcohols is least soluble in water?

The order of ease of dehydration of the following alcohols is:
$I$: $CH_3-CH_2-CH_2-OH$
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$IV$: $CH_3-CH_2-OH$

Glycerol is a trihydric alcohol. It contains . . . . . .

Identify the major product of the following reaction:
$(CH_3)_3C-CH(OH)-CH_3 \xrightarrow[\Delta]{\text{conc. } H_2SO_4} \text{Major product}$

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