KINETICS AND MECHANISM FOR THE IODINATION OF METHYLMALONIC ACID

The reactiondocumentclass{article}pagestyle{empty}begin{document}$ CHleft({CH_3 } right)left({COOH} right)_2 + I_2 rightleftharpoons CI(CH_3)left({COOH} right)_2 + H^ + + I^ - $end{document} was followed spectrophotometrically at 353 nm and 470 nm at 25°C under various conditions of pH and methylmalonic acid concentration. The equilibrium constant for the reaction is 0.11 ± 0.02. An iterative technique was used to integrate postulated rate equations. Agreement between experimental and calculated absorbance versus time curves was generally better than 0.005 A (approximately 5% of maximum) at both wavelengths for a mechanism where the rate‐determining step is formation of an enolate (k = 1.63 Θ 10−4 ± 0.03 Θ 10−4 sec−1). The enolate may be rapidly transformed to the enol or enol carboxylate anion depending on the pH. All three forms are rapidly iodinated. The mechanism of general base catalysis is supported by rate increases proportional to base concentration in buffer solutions. The bases, acetate ion, chloracetate ion, sulfate ion, dichloracetate ion, and water, follow a Brønsted relationship with β = 0.7. Copyright © 1979 John Wiley & Sons, Inc.