Product of cyclohexanone/benzaldehyde with a substituted amine?
You should get an imine:
Additionally, using a ketone:
The formation of an imine from a ketone to give a ketimine is a little bit harder; you may have heat under reflux and remove the water produced; the carbonyl on the ketone is much more sterically hindered than the aldehyde. Both unsaturated nitrogen compounds tend to be a little bit unstable, so they are usually used directly. Reaction (i) is usually very facile; sometimes you do not even need to use solvent, and you just add amine to aldehyde and remove the water.
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The product of the reaction between cyclohexanone/benzaldehyde and a substituted amine would be an imine or Schiff base.
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When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

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