Saved Bookmarks
| 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.
|
|