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Starting with 2-methylcyclohexanol, ethyne, and 2 equivalents of methanol (all of which do not necesarily need to be used in the first step, of course), we need to form a cyclohexanone with a methyl group at the 6 position and a 2,3-butanediol group (with both OH groups at the back (dashed lines)) at the 2 position. All carbons on the target need to come from the starting materials, but other than that we can use whatever other compounds and however many steps we need. I don't want someone to do this all for me, but any tips at all would be great.
Show all the steps in the mechanism for the following reaction, When benzene is mixed with deuterated sulfuric acid, deuterium is slowly incorporated onto the ring. Show the mechanism for this reaction and explain how this relates the sulfonation of ..
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