Tert-butyl methyl ether on treatment with hyd | vedclass

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Question

(D) The reaction of $Tert$-butyl methyl ether with $HI$ in cold conditions follows an $S_N1$ mechanism. Since the $Tert$-butyl group can form a stable

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$Tert$-butyl iodide and methyl alcohol

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(D) The reaction of $Tert$-butyl methyl ether with $HI$ in cold conditions follows an $S_N1$ mechanism. Since the $Tert$-butyl group can form a stable $Tert$-butyl carbocation,the $C-O$ bond between the $Tert$-butyl group and the oxygen atom breaks. The reaction proceeds as follows: $(CH_3)_3C-O-CH_3 + HI \xrightarrow{	ext{cold}} (CH_3)_3C-I + CH_3OH$ Thus,the products formed are $Tert$-butyl iodide and methanol (methyl alcohol).

$Tert$-butyl methyl ether on treatment with hydrogen iodide in cold gives

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