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(R)-3-chloro-2-methylhexane may undergo a nucleophilic substitution reaction in the presence of sodium ethoxide and ethanol. Complete the mechanism as well as draw the products of the reaction. Depict all missing reactants and/or products in the appropriate boxes by placing atoms on the grid as well as connecting them with bonds and including charges where needed. Point out the mechanism by drawing the electron-flow arrows on the molecules. Arrows must start on an atom or a bond and should end on an atom, bond or where a new bond should be created.
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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