10) Predict the product for the following reactions: NH₂ NH₂ 7 H₂SO4 7 H₂SO4 NaBH3CN

Chemistry
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Chapter1: Chemical Foundations
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The image presents a two-part question asking to predict the product of chemical reactions. 

1) **First Reaction:**
   - **Reactants:** 
     - A cyclohexanone molecule.
     - A pyrrolidine molecule (a five-membered ring with an NH2 group).
     - Sulfuric acid (H2SO4).
   - **Process:** 
     - The reaction typically involves the formation of an imine intermediate where the amine group from pyrrolidine attacks the carbonyl carbon of the cyclohexanone, with sulfuric acid acting as a catalyst.

2) **Second Reaction:**
   - **Reactants:**
     - The same initial reactants as in the first reaction (cyclohexanone, pyrrolidine, H2SO4).
     - Sodium borohydride cyanoborohydride (NaBH3CN).
   - **Process:**
     - After the formation of the imine intermediate, sodium cyanoborohydride is used for reductive amination, resulting in the formation of a secondary amine.

These reactions illustrate the concept of reductive amination, a method used to introduce or modify amine functionality in organic molecules. The diagram does not include visual data like graphs but focuses on the structural formula of the reactants and reagents.
Transcribed Image Text:The image presents a two-part question asking to predict the product of chemical reactions. 1) **First Reaction:** - **Reactants:** - A cyclohexanone molecule. - A pyrrolidine molecule (a five-membered ring with an NH2 group). - Sulfuric acid (H2SO4). - **Process:** - The reaction typically involves the formation of an imine intermediate where the amine group from pyrrolidine attacks the carbonyl carbon of the cyclohexanone, with sulfuric acid acting as a catalyst. 2) **Second Reaction:** - **Reactants:** - The same initial reactants as in the first reaction (cyclohexanone, pyrrolidine, H2SO4). - Sodium borohydride cyanoborohydride (NaBH3CN). - **Process:** - After the formation of the imine intermediate, sodium cyanoborohydride is used for reductive amination, resulting in the formation of a secondary amine. These reactions illustrate the concept of reductive amination, a method used to introduce or modify amine functionality in organic molecules. The diagram does not include visual data like graphs but focuses on the structural formula of the reactants and reagents.
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