draw a step-wise mechanism for the reaction of 2- methyl-2-butanol
with hydrochloric acid, which includes transition states.
Solution :-
When the 2-methyl-2-butanol is reacted with the HCl then in the forst step alcohol is get protonated then it removes the water to form the carbocation then carbocation is attakced by the Cl- to form the halide product.
Following image shows the reactions mechanism steps.
draw a step-wise mechanism for the reaction of 2- methyl-2-butanol with hydrochloric acid, which includes transition...
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Draw the detailed SN1 mechanism for the reaction between 2-methyl-2-butanol and HCl to produce 2-chloro-2-methylbutane. 1. Draw the detailed Sn1 mechanism for the reaction between 2-methyl-2-butanol and HCl to produce 2-chloro-2-methylbutane. (3 pts)
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