Is 2,4-Pentanedione a Ring or Hydrocarbon Chain in the Iodoform Test Reaction?

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The discussion centers on the chemical structure of 2,4-Pentanedione, clarifying that it is not a ring structure but rather a hydrocarbon chain with carbonyl groups (double-bonded oxygen) at positions 2 and 4. Participants explore the Iodoform test reaction, specifically how it operates with two carbonyl groups. The chemical equation for the reaction is presented, indicating that the reaction with sodium hydroxide (NaOH) and iodine (I2) leads to the formation of sodium carboxylates and iodoform (CHI3) derivatives. There is consensus that multiple products can result from the reaction, including carboxylate salts.
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Is 2,4-Pentanedione a ring structure or just a hydrocarbon chain with double-bonded O's on C 2 and 4? When showing the reaction with the Iodoform test what would the chemical equation be? I know it is

2,4-Pentanedione

NaOH
--> I know how this would work with a single double-bonded O but how
I2 would it work with two? Would the result be...

CH3CIONaCIOCH3 with 2 CHI3 (iodoform) derivatives in the solution? Please help. Thanks. :bugeye:
 
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I believe there may be two products possible, but I'm only guessing here :

H_3C-C(=O)-CH_2-C(=O)-CH_3 \xrightarrow {NaOH, ~I_2} NaO-C(=O)-CH_2-C(=O)-ONa + H_3C-C(=O)-CH_2-C(=O)-ONa
 
Yes, Gokul is right; the products are carboxylates and iodoform, aka CHI_3.
 
Thank you! :)
 
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