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Problem- Part 1) Compounds Y and Z both have the formula C9H18. Both Y and Z react with one molar equivalent of hydrogen in the presence of a palladium catalyst to form 2-methyloctane. The heat of hydrogenation of Y is less than that of Z. Y and Z each undergo hydroboration/oxidation to give a primary alcohol (OH attached to a primary carbon). What is the structure of Y?
Part 2) Compound X has the formula C8H12. X reacts with two molar equivalents of hydrogen in the presence of a palladium catalyst to form cyclooctane. Treatment of X with ozone followed by zinc in aqueous acid gives two molar equivalents of the same dialdehyde. What is the structure of X
Please show me how work it out above problem
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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