What is the correct order of stability for the following tautomeric compounds?(I) ${\text{CH}}_2=\text{C}(\text{OH})-{\text{CH}}_2-\text{C}(=\text{O}){\text{CH}}_3$ (II) ${\text{CH}}_3-\text{C}(=\text{O})-{\text{CH}}_2-\text{C}(=\text{O}){\text{CH}}_3$ (III) ${\text{CH}}_3-\text{C}(\text{OH})=\text{CH}-\text{C}(=\text{O}){\text{CH}}_3$

- III (Enol): Most stable because of extensive conjugation and intramolecular hydrogen bonding forming a 6-membered ring.II (Keto): Generally keto forms are stable, but less so than a conjugated, H-bonded enol in $\beta$ -dicarbonyls.I (Enol): Least stable as it lacks the specific stabilization factors of III.Correct order: III > II > I.