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In SN1 reactions done in the solvent ethanol (CH3CH2OH), the intermediate carbocations can eliminate a proton to yield alkenes or react with the...

In SN1 reactions done in the solvent ethanol (CH3CH2OH), the intermediate carbocations can eliminate a proton to yield alkenes or react with the solvent to yield ethers. Draw the structure of the byproducts that would be derived from the reaction of the carbocation derived from 2-bromo-2-methylbutane inethanol.

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