Would you please check my work, the question is posted below. I belive this is a

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Would you please check my work, the question is posted below. I belive this is a SN1 reaction with a methyl shift (the question hinted towards a rearagment. (it could also be an elimination I know less about those so I am not sure if that is more likely) My understanding is that the Cl will leave creating a carbocation on C2 then one of the methyl groups from C3 will shit to C2 moving the carbocation to C3 where the H2O will bond and be deprotonated by the Cl- ion, creating an alchole there. If I am correct please explain why a SN1 is more likley than an E1 or E2, If I am incorrect please demonstrate the correct answer and how to arrive at it. Thanks alot!!

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Would you please check my work, the question is posted below. I belive this is a

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