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why is the nucleophile attacking the 4.position, the beta C . can someone explain the attacks in this mechism of 1,4 nucleophilic addition ( conjugated)?

why is the nucleophile attacking the 4.position, the beta C .

can someone explain the attacks in this mechism of 1,4 nucleophilic addition ( conjugated)?

small amount of alkoxide produced in base protonation of enolate +HO

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