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The subsequent molecule contains two different nitrogen longe pairs, one of which is considerably more basic than the others. a) Depict the two possible conjugate acids arising from the protonation of these lone pairs. b) Find out which conjugate acid is more stable. c) Offer a structure based rationale for the observed difference in basicity. d) Circle the more basic nitrogen in the structure below.
The structure is 4-Dimethylaminopyridine.
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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