Which of the following reactions is not feasi | vedclass

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(B) The dehydration of alcohols to alkenes requires specific conditions depending on the degree of substitution of the alcohol.Primary $(1^{\circ})$ a

Vedclass · Accepted Answer

$CH_3-CH_2-CH_2-CH_2-OH \xrightarrow{75\% \ H_2SO_4, \ 300 \ K} CH_3-CH_2-CH=CH_2$

Vedclass · Answer

(B) The dehydration of alcohols to alkenes requires specific conditions depending on the degree of substitution of the alcohol.Primary $(1^{\circ})$ alcohols,like butan$-1-$ol in option $(B)$,are the least reactive towards dehydration and typically require concentrated acid (e.g.,$95\% \ H_2SO_4$) and high temperatures (around $443 \ K$) to proceed.Option $(B)$ suggests the dehydration of a primary alcohol at a very low temperature $(300 \ K)$ with a lower concentration of acid $(75\% \ H_2SO_4)$,which is insufficient to drive the elimination reaction.Secondary and tertiary alcohols are more reactive and can undergo dehydration under milder conditions,making options $(C)$ and $(D)$ feasible.

Which of the following reactions is not feasible?

Similar Questions

Alcohols are comparatively more soluble in water than hydrocarbons of comparable molecular masses. Explain this fact.

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