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Describe procedures for preparing each of the following compounds, using ethanol as the source for all of their carbon atoms (you can use any reagent you like, but every carbon in every product below must have originated in ethanol; once you prepare a compound, you need not repeat its synthesis in a subsequent part of this problem):
a. ethylamine
b. N-ethylacetamide (CH3CH2NHCOCH3)
c. diethylamine (make sure to use a RELIABLE method)
d. tetraethylammonium iodide
e. CH3CH2N=CH2CH3 (this compound is a Schiff Base)
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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