Answer:
D
Explanation:
you can see it from the beginning its developing
Answer:
See explanation
Explanation:
The first step in this reaction is a unimolecular reaction. It involves the formation of the carbocation. This is so because tertiary alkyl halides only undergo substitution by SN1 mechanism due to sterric crowding.
The second step in the reaction is bi molecular. In this step, the carbocation now combines with the OH^- to yield the alcohol.
Net equation of the reaction is;
(CH3)3CBr + OH^- -------> (CH3)3COH + Br^-
The intermediate here is the carbocation, (CH3)3C^+
Answer:
Yep, this is my new pick up line
Explanation:
