When 3 chloro-1-butene is subjected to hydrolysis by H2O it results into the formation of an unsaturated alcohol [x].The correct statement is

Question

When 3 chloro-1-butene is subjected to hydrolysis by H2O it results into the formation of an unsaturated alcohol [x].The correct statement is (A) Reaction predominantly proceed through SN1 mechanism (B) [x] consists of four isomers (C) Final product mixture will be optical inactive in nature consist 5 pairs of diastereomers (D) Reactivity of 3 chloro-1-butene towards SN1 and SN2 is more than that of 2 chlorobutane

Tardigrade Admin · Accepted Answer

Reaction is SN1 The intermediate alicyclic cation is achiral and therefore, reacts with water to give enantiomer 3 butene-2-ol and to give some of the achiral 2 butene-1-ol. <img class="img-fluid question-image" alt="Solution" src="https://cdn.tardigrade.in/q/nta/c-8sanqacjxrkiclb9.jpg" />

Q. When 3 chloro-1-butene is subjected to hydrolysis by H₂O it results into the formation of an unsaturated alcohol [x].The correct statement is

Reaction predominantly proceed through $S_{N} 1$ mechanism

[x] consists of four isomers

Final product mixture will be optical inactive in nature consist 5 pairs of diastereomers

Reactivity of 3 chloro-1-butene towards $S_{N} 1$ and $S_{N} 2$ is more than that of 2 chlorobutane

Reaction is $S_{N} 1$ The intermediate alicyclic cation is achiral and therefore, reacts with water to give enantiomer 3 butene-2-ol and to give some of the achiral 2 butene-1-ol.

Q. When 3 chloro-1-butene is subjected to hydrolysis by H2O it results into the formation of an unsaturated alcohol [x].The correct statement is

Reaction predominantly proceed through SN​1 mechanism