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(C) The reaction of $1$-methylcyclobutene with $D-Cl$ follows Markovnikov's rule.In this addition,the electrophile $D^+$ attacks the double bond to fo

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(C) The reaction of $1$-methylcyclobutene with $D-Cl$ follows Markovnikov's rule.In this addition,the electrophile $D^+$ attacks the double bond to form the more stable carbocation.The $D^+$ adds to the carbon atom that has more hydrogen atoms (the $CH$ group),resulting in a tertiary carbocation at the carbon bearing the $CH_3$ group.Subsequently,the nucleophile $Cl^-$ attacks the tertiary carbocation.This leads to the formation of $1$-chloro-$1$-methyl-$2$-deuteriocyclobutane.Comparing the given options,the structure corresponding to this addition is represented in option $C$.

What is the major product expected from the following reaction?

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