Pseudo-first-order rate constants (k obs ) for alkaline hydrolysis of 4-nitrophthalimide (NPTH) decreased by nearly 8-and 6-fold with the increase in the total concentration of cetyltrimethyl-ammonium bromide ([CTABr] T ) from 0 to 0.02 M at 0.01 and 0.05 M NaOH, respectively. These observations are
Kinetics of the alkaline hydrolysis of isoproturon in CTAB and NaLS micelles
✍ Scribed by S. K. Gangwar; M. Z. A. Rafiquee
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 209 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Abstract
Kinetics of the alkaline hydrolysis of isoproturon has been studied in the absence and presence of cetyltrimethylammonium bromide (CTAB) and sodium lauryl sulfate (NaLS) micelles. CTAB micelles were found to enhance the rate of reaction, while NaLS micelles inhibited the reaction rate. The reaction obeyed first‐order kinetics in [isoproturon] and was linearly dependent on [NaOH] at lower concentration. The rate of reaction became independent at higher [NaOH]. At lower [NaOH] the reaction proceeded via formation of hydroxide ion addition complex, while at higher [NaOH] the reaction occurred via deprotonation of NH, leading to the formation of isocyanate. The values of k~w~, k~m~, and K~s~ were determined by considering the pseudophase ion exchange model. The activation parameters have also been reported. The effect of added salts (NaCl and KNO~3~) on the reaction rate has also been studied. © 2006 Wiley Periodicals, Inc. Int J Chem Kinet 39: 39–45, 2007
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