1.

Write equations for the steps in SN^1 mechanism of the conversion of tert.butyl bromide into tert.butyl alcohol.

Answer»

Solution :When t-buty BROMIDE REACTS with aqueous potassium HYDROXIDE, t-butyl alcohol

Step 1: The alkyl HALIDE undergoes slow ionisation to form a carbocation and bromide ion.

Step 2: The nucleophite `OH^-` attacks the carbocation to form TERTIARY buty alcohol.


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