Kinetics and mechanism of the iodine oxidation of hydroxylamine
✍ Scribed by Robert T. Wang; Gyula Rábai; Kenneth Kustin
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 405 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
Studies of the stoichiometry and kinetics of the reaction between hydroxylamine and iodine, previously studied in media below pH 3, have been extended to pH 5.5. The stoichiometry over the pH range 3.4-5.5 is 2NHzOH
and k l , kz, Kp, and KI are (6.5 2 0.6) x lo5 M-' s-', (5.0 2 0.5) s-', 1 x lo6 M-', and 725 M-', respectively. A mechanism taking into account unprotonated hydroxylamine (NHZOH) and molecular iodine (Iz) as reactive species, with intermediates NHzOIz-, HNO, NH20, and 12-, is proposed.
📜 SIMILAR VOLUMES
## Abstract Kinetics of the hydrolytic disproportionation of I~2~ equation image was studied by UV–VIS spectrophotometry at 298 K and at the ionic strength 0.2 M (NaClO~4~) in buffered solutions in the pH range 8.91–10.50 at different initial iodide concentrations. The characterization of this re
## Abstract The kinetics and mechanism by which monochloramine is reduced by hydroxylamine in aqueous solution over the pH range of 5–8 are reported. The reaction proceeds via two different mechanisms depending upon whether the hydroxylamine is protonated or unprotonated. When the hydroxylamine is