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    • https://espanol.libretexts.org/Quimica/Libro%3A_Qu%C3%ADmica_Org%C3%A1nica_con_%C3%A9nfasis_Biol%C3%B3gico_(Soderberg)/13%3A_Reacciones_con_intermediados_de_carbaniones_estabilizados_I/13.2%3A_Taut%C3%B3meros
      In the formation of an enol, a base abstracts an a-proton from a carbonyl compound, and that same proton (or a proton on a nearby acid group) is transferred to the carbonyl oxygen. There are a few spe...In the formation of an enol, a base abstracts an a-proton from a carbonyl compound, and that same proton (or a proton on a nearby acid group) is transferred to the carbonyl oxygen. There are a few special cases where the enol form predominates at equilibrium: 2,4-pentane dione exists mostly in its enol form (76%), due to the extra stability of the conjugated double bonds that are present in the enol form, and due also to a favorable hydrogen bonding interaction.

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