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Draw the structure of the organic product of each reaction in the following two-step synthesis.
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This concept is used to solve the problem. It involves the understanding of the nucleophilic reaction on the carbonyl carbon.
The electrophilic carbon is the carbonyl carbon and is made up of the nucleophilic acid which produces the nucleophilic additive product.
The nucleophile attacks [katex]{{\rm{\pi }}^*}[/katex]
The proton attacks the one oxygen pair in the given reactant, which then proceeds with the intramolecular attack by [katex]{\rm{N}}{{\rm{H}}_{\rm{2}}}[/katex].
Below is the mechanism for this reaction:
When the cyclic iine reacts to a reducing agent like [katex]{\rm{NaB}}{{\rm{H}}_{\rm{3}}}{\rm{CN or }}{{\rm{H}}_2}/{\rm{Pd or Ni}}[/katex]
This is the reaction to reduction of cyclic iine
Ans:
These are the structures of the organic products of each reaction in the two-step synthesizer: