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You have learned in class that addicion of an alcohol such as MeOH to this reaction results in a monobromide product instead of a dibromide. Draw the mechanism and all products obtained if you were to react trans-cinnamic acid with Br2 and MeOH. The reaction previously done was just having trans-cinnamic acid reacted with Br2 forming all the isomers with the double bond being broken and Br put into place.
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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