Write the mechanism of the acid-induced cleavage of tert-butyl cyclohexyl ether to yield cyclohexanol and 2-methylpropene.

In acid-induced cleavage of ether, ether is treated with strong acid.It generates oxonium ion, collapsing to form an alcohol and a tertiary carbocation which further forms an alkene.

In the acid-catalyzed ether cleavage, the first step is the protonation of ether oxygen, forming an intermediate oxonium ion. This ion collapses to form an alcohol and a tertiary carbocation.

An alkene 2-methylpropene is formed when a carbocation loses a proton. This reaction is an example of E1 elimination. The acid used for the cleavage is often trifluoroacetic acid. The products obtained arecyclohexanol and 2-methylpropene.

The mechanism of the acid-induced cleavage of tert-butyl cyclohexyl ether is shown below,

The mechanism of the reaction