Draw the taustomeric forms of azepines and compare their stabilities.
Azepines are heterocyclic compounds containing a seven-membered ring with one nitrogen atom. They are similar to piperines, except they have a nitrogen atom in place of a carbon atom. Azepines exhibit two tautomeric forms, which are based on the position of the double bond and the proton in the structure.
1. Azepine (Keto form): In this form, the nitrogen atom is sp2 hybridized, and _____ _________ _________ _____ _________ __________ __________ _______.
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