Does the reductive amination only make secondry and tertiary amine? Bc i draw the mechanism and primary amine is not possible since one or two hydrogen on N should be removed during the rxn

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Chapter1: Chemical Foundations
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Does the reductive amination only make secondry and tertiary amine? Bc i draw the mechanism and primary amine is not possible since one or two hydrogen on N should be removed during the rxn 

The image contains several structural representations of chemical compounds with a cyclohexane ring and various substituents:

1. **Cyclohexanamine**: A cyclohexane ring with an amine group (-NH₂) attached.
2. **Phenylcyclohexylamine**: A cyclohexane ring with an amine group attached to a phenyl group (Ph).
3. **Cyclohexylmethylamine**: A cyclohexane ring with an amine group bonded to a methyl group and a phenyl group on the nitrogen atom.
4. **Phenylcyclohexylamine Ion (N⁺H₂Ph)**: A cyclohexane ring with an ionized nitrogen (indicated by the positive charge) bonded to an amine group and a phenyl group.
5. **Triaryl Ammonium Ion**: A cyclohexane ring with a positively charged nitrogen atom bonded to three phenyl groups.

These representations illustrate variations of cyclohexane compounds with nitrogen and phenyl group attachments, showcasing different nitrogen bonding forms and charges.
Transcribed Image Text:The image contains several structural representations of chemical compounds with a cyclohexane ring and various substituents: 1. **Cyclohexanamine**: A cyclohexane ring with an amine group (-NH₂) attached. 2. **Phenylcyclohexylamine**: A cyclohexane ring with an amine group attached to a phenyl group (Ph). 3. **Cyclohexylmethylamine**: A cyclohexane ring with an amine group bonded to a methyl group and a phenyl group on the nitrogen atom. 4. **Phenylcyclohexylamine Ion (N⁺H₂Ph)**: A cyclohexane ring with an ionized nitrogen (indicated by the positive charge) bonded to an amine group and a phenyl group. 5. **Triaryl Ammonium Ion**: A cyclohexane ring with a positively charged nitrogen atom bonded to three phenyl groups. These representations illustrate variations of cyclohexane compounds with nitrogen and phenyl group attachments, showcasing different nitrogen bonding forms and charges.
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