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(a) Carry out an elimination experiment using alcoholic pottasium hydroxide on 2-bromo-2-methylbutane. Define how the results would differ if you use potassium tert-butoxide as the base instead of pottasium hydroxide. Define how the results would differ and why the result would differ.
(b) The elimination reaction involving the utilizing of alcoholic pottasium hydroxide is E2 elimination. (1) State out the mechanism of the reaction done that leads to the two products formed (2) Define the factors that favor an E2 mechanism over E1 mechanism.
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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