Complete the mechanism for the keto-enol tautomerization below using bonds, charges, nonbonding electron pairs, and curved arrows (forward reaction only). Do not remove any pre-drawn bonds/lone pairs.

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enol form H- HO H keto form HOTH H3C- X :8-H Ö: 1L 1L H-8: H-8: (b) The tautomer that predominates in aqueous solution is the: H H3C- H₂C- I keto form. enol form. :8-H 8-H Map o (Scroll down for more) enol form H- HO H keto form HOTH H3C- X :8-H Ö: 1L 1L H-8: H-8: (b) The tautomer that predominates in aqueous solution is the: H H3C- H₂C- I keto form. enol form. :8-H 8-H Map o (Scroll down for more)

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