Draw the structures of the organic products in each reaction of thefollowing two-step synthesis. (Hint: Thenucleophilic amine attacks the electrophilic carbonyl carbon, andthe resulting intermediate undergoes a proton shift anddehydration. Recall what is eliminated in a dehydration process.The second step is a reduction reaction; the reducing agent isNaBH3CN (or H2, metal catalyst). The aromatic ring is unaffected bythese reagents. Look at the product of the first reaction andconsider what can be easily reduced.)

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Draw the structures of the organic products in each reaction of the following two-step synthesis. + NH₂ H* (trace) heat (neutral form) NaBH3CN or H2, metal cat. (Pd/C, Ni, or Raney Ni) ΝΗ _H 0 Draw the structures of the organic products in each reaction of the following two-step synthesis. + NH₂ H* (trace) heat (neutral form) NaBH3CN or H2, metal cat. (Pd/C, Ni, or Raney Ni) ΝΗ _H 0