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Fudgin [204]
3 years ago
9

Through what basic mechanism is 2-methylcyclohexanol converted to 1-bromo-1-methylcyclohexane when treated with HBr

Chemistry
1 answer:
evablogger [386]3 years ago
8 0

Answer:

Sn1 mechanism reaction

Explanation:

In this case, we have to start with the <u>protonation</u> of the "OH" group by the attack of the lone pairs in the alcohol group to the "H" in the HBr producing a <u>positive charge in the oxygen</u>. Then, water is produced and a <u>carbocation</u> is generated. This carbocation can be stabilized by a <u>hydride shift</u>. We can move a hydrogen atom to the positive charge and we will obtain a <u>tertiary carbocation</u>. Finally, the Br^- will attack to produce the final <u>halide</u>.

See figure 1.

I hope it helps!

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