posted on 2005-04-04, 00:00authored byValbona Celo, Susannah L. Scott
The kinetics and mechanism of the reaction of aqueous Hg(II) with methyl iodide have been investigated. The
overall reaction is best described as Hg(II)-assisted hydrolysis, resulting in quantitative formation of methanol and,
in the presence of excess methyl iodide, ultimately, HgI2 via the intermediate HgI+. The kinetics are biexponential
when methyl iodide is in excess. At 25 °C, the acceleration provided by Hg2+ is 7.5 times greater than that caused
by HgI+, while assistance of hydrolysis was not observed for HgI2. Thus, the reactions are not catalytic in Hg(II).
The kinetics are consistent with an SN2-M+ mechanism involving electrophilic attack at iodide. As expected, methylation
of mercury is not a reaction pathway; traces of methylmercury(II) are artifacts of the extraction/preconcentration
procedure used for methylmercury analysis.