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Cyclohexane-1,4-dione.

this reaction mechanism follows Baldwin's rule of ring formation, when the hydroxide attacks the alpha carbon on hexane-2,5-dione, it gives the product a double bond on the alpha carbon and puts a negative charge on the oxygen, the electrons from the double bond are then used to create a bond between Carbon-1 and Carbon-6. Giving you a carbonyl group on each end of the ring. It helps when you're writing out the mechanism to draw the hexane-2,5-dione in the formation of an aromatic ring!

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