## Abstract This work reports the results of a kinetic and mechanistic investigations of the addition reaction of triphenylphosphine to __para__‐naphtoquinone in 1,2‐dichloromethane as solvent. The order of reaction with respect to the reactants was determined using initial rate method, and the rat
Kinetics and mechanism study of aniline addition to ethyl propiolate
✍ Scribed by Davood Nori-Shargh; Bita Soltani; Nasrin Saroogh-Farahani; Farzad Deyhimi
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 206 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Abstract
The kinetics of the addition reaction of aniline to ethyl propiolate in dimethylsulfoxide (DMSO) as solvent was studied. Initial rate method was used to determine the order of the reaction with respect to the reactants, and pseudo‐first‐order method was used to calculate the rate constant. This reaction was monitored by UV–Vis spectrophotometer at 399 nm by the variable time method. On the basis of the experimental results, the Arrhenius equation for this reaction was obtained as log k = 6.07 ‐ (12.96/2.303 RT). The activation parameters, E~a~, Δ__H__^#^, Δ__G__^#^, and Δ__S__^#^ at 300 K were 12.96, 13.55, 23.31 kcal mol^−1^ and −32.76 cal mol^−1^ K^−1^, respectively. The results revealed a first‐order reaction with respect to both aniline and ethyl propiolate. In addition, based on the experimental results and using also density functional theory (DFT) at B3LYP/6‐31G* level, a mechanism for this reaction was proposed. © 2005 Wiley Periodicals, Inc. Int J Chem Kinet 38: 144–151, 2006
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