When 1 -chloro butane is treated with aqueous KOH it gives P . However, when it is treated with alcoholic…
Solution
In presence of aqueous KOH, 1-chlorobutane undergoes nucleophilic substitution(mechansim) to from butan-1-ol
Alcoholic KOH dissociates in water to give RO- ion which is a strong base. It abstracts hydrogen, giving rise to elimination in reaction.
Hence in the presence of alcoholic KOH, dehydro halogenation(beta elimination) takes place to form but-1-ene, where the cabocation intermediate is formed.
Asked in: AP EAMCET 2022 (04 Jul Shift 1)




