𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Kinetic investigation on the oxidation of nitrite by oxochromium(V) ion in aqueous and micellar systems

✍ Scribed by Mookandi Kanthimathi; Balachandran Unni Nair


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
129 KB
Volume
36
Category
Article
ISSN
0538-8066

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The kinetics of oxidation of nitrite by [O = Cr^V^ (5‐chlorosalen)]^+^ complex has been studied spectrophotometrically at [Cr^V^] = 0.5 × 10^−3^ M, [NO~2~^−^] = 0.01–0.1 M, [H^+^] = 0.0001–0.05 M, I = 0.15 M, and T = 25°C in the presence of cationic surfactant, cetyl pyridium chloride (CPC), and anionic surfactant, sodium dodecyl sulfate (SDS),in aqueous acidic medium. The oxygen atom transfer reaction from O = Cr^V^ to nitrite ion is influenced by the ionic nature of the micelle. The redox reaction is accelerated in presence of CPC and slowed down by 40 times in presence of SDS. The mechanism of the reaction involves an inner‐sphere process involving the formation of an intermediate followed by oxo transfer process. © 2003 Wiley Periodicals, Inc. Int J Chem Kinet 36: 79–86 2004


📜 SIMILAR VOLUMES


Micellar effect on quinquivalent vanadiu
✍ Bidyut Saha; Sucharita Sarkar; Kiran M. Chowdhury 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 227 KB 👁 2 views

## Abstract Vanadium(V) oxidation of D‐glucose shows first‐order dependence on D‐glucose, vanadium(V), H^+^, and HSO. These observations remain unaltered in the presence of externally added surfactants. The effect of the cationic surfactant (i.e., __N__‐cetylpyridinium chloride [CPC]), anionic surf

Kinetics and mechanism of the electroche
✍ J.A. Wargon; A.J. Arvía 📂 Article 📅 1972 🏛 Elsevier Science 🌐 English ⚖ 993 KB

The kinetics of the electrochemical oxidation of NO,-ion dissolved in DMSO has been studied on Pt electrodes at temperature ranging from 25 to 44'C, by means of potentiostatic E/Icurves and by relaxation techniques. The oxidation reaction is explained in terms of a consecutive reaction scheme which

Kinetics and mechanism of the oxidation
✍ Evan R. Moore; Andrew E. Bourne; Todd J. Hoppe; Philip J. Abode; Steven R. Boone 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 262 KB 👁 2 views

## Abstract The mechanism by which an excess of iron(II) ion reacts with aqueous chlorine dioxide to produce iron(III) ion and chloride ion has been determined. The reaction proceeds via the formation of chlorite ion, which in turn reacts with additional iron(II) to produce the observed products. T

Studies on kinetics and mechanism of oxi
✍ Asim K. Das; Monirul Islam; Ruhidas Bayen 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 260 KB 👁 2 views

## Abstract The kinetics and mechanism of cerium(IV) oxidation of hexitols, i.e. D‐sorbitol and D‐mannitol, in aqueous sulfuric acid media have been studied in the presence and absence of surfactants. Under the kinetic conditions, [S]~T~ ≫ [Ce(IV)]~T~, where [S]~T~ is the total substrate (D‐sorbito

Kinetic and Mechanistic Studies on the O
✍ Amit Das; Subrata Mukhopadhyay 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 German ⚖ 124 KB 👁 2 views

## Abstract The kinetics of a net two‐electron transfer between an authentic Mn^IV^ complex, [Mn(bigH)~3~]^4+^ (__Fig. 1__; bigH = biguanide = C~2~N~5~H~7~), and nitrite in aqueous solution in the pH interval 2.00–3.60 is described. Stoichiometric data for the reaction clearly indicates Δ[Mn^IV^]/Δ

Mechanistic Studies on the Oxidation of
✍ Jhimli Bhattacharyya; Subrata Mukhopadhyay 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 German ⚖ 147 KB 👁 1 views

## Abstract Examined in this study is the kinetics of a net 2e^−^ transfer between [Fe~2~(__μ__‐O)(phen)~4~(H~2~O)~2~]^4+^ (1) and its hydrolytic derivatives [Fe~2~(__μ__‐O)(phen)~4~(H~2~O)(OH)]^3+^ (2) and [Fe~2~(__μ__‐O)(phen)~4~(OH)~2~]^2+^ (3) with $\rm{{{NO}}\_{{2}}^ - }$ in aqueous media and