Unformatted text preview: H 3 C CH H 3 C NH O CH 2 CH 3 NH O H 3 C IUPAC: N-ethyl-2-methylpropanamide___ _ Common:_ N-ethylisobutyramide _____ IUPAC: _____ N-methylbenzamide_____ __ Common:____ N-methylbenzamide ______ (3) 3. Draw the structures of the following compounds: 1 pt each Pyridine N-methylcyclohexanamine N-phenylpropionamide N NH NH O (2) 4. Draw the structures of the products formed by acid hydrolysis of the following amide. Be sure to show the proper protonated form of each product, and its charge, if any. N O H + H 2 O OH O NH 2 H 3 C + 1 pt each (-0.3 if wrong charge, -0.3 if wrong number of protons)...
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- Spring '08
- Evolution, Amine, Amide, common names, N-ethyl-N-methyl-1-butanamine_ IUPAC, proper protonated form