Heating tert-butyl methyl ether with HI gives | vedclass

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(B) The reaction of tert-butyl methyl ether with $HI$ proceeds via an $S_N1$ mechanism because the tert-butyl carbocation is highly stable. $CH_3-C(CH

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tert-Butyl iodide and methanol

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(B) The reaction of tert-butyl methyl ether with $HI$ proceeds via an $S_N1$ mechanism because the tert-butyl carbocation is highly stable. $CH_3-C(CH_3)_2-OCH_3 + HI 	o CH_3-C(CH_3)_2-I + CH_3OH$. The protonation of the ether oxygen is followed by the cleavage of the $C-O$ bond to form the stable tert-butyl carbocation,which then reacts with the iodide ion to form tert-butyl iodide and methanol.

Heating tert-butyl methyl ether with $HI$ gives which of the following mixtures?

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