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
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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
answer is A.
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Detailed Solution
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.