𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Solvent and structural effects on the kinetics of the reactions of 2-substituted cyclohex-1-enylcarboxylic and 2-substituted benzoic acids with diazodiphenylmethane

✍ Scribed by J. B. Nikolić; G. S. Ušćumlić; I. O. Juranić


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
214 KB
Volume
39
Category
Article
ISSN
0538-8066

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The rate constants for the reaction of 2‐methyl‐cyclohex‐1‐enylcarboxylic, 2‐phenylcyclohex‐1‐enylcarboxylic, and 2‐methylbenzoic and 2‐phenylbenzoic acids with diazodiphenyl‐methane were determined in 14 various solvents at 30°C. To explain the kinetic results through solvent effects, the second‐order rate constants of the examined acids were correlated using the Kamlet–Taft solvatochromic equation. The correlations of the kinetic data were carried out by means of multiple linear regression analysis, and the solvent effects on the reaction rates were analyzed in terms of initial and transition state contributions. The quantitative relationship between the molecular structure and the chemical reactivity has been discussed, as well as the effect of geometry on the reactivity of the examined molecules. The geometric data of all the examined compounds corresponding to the energy minima in solvent, simulated as dielectric continuum, obtained using semiempirical MNDO‐PM3 energy calculations. © 2007 Wiley Periodicals, Inc. Int J Chem Kinet 39: 664–671, 2007


📜 SIMILAR VOLUMES


Solvent and structural effects on the ki
✍ J. B. Nikolić; G. S. Ušćumlić; V. V. Krstić 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 102 KB

## Abstract The rate constants for the reaction of different cycloalkenylcarboxylic, cycloalkenylacetic acids, and phenylacetic acid with diazodiphenylmethane were determined in 12 aprotic solvents at 30°C. In order to explain the kinetic results through solvent effects, the second‐order rate const

A comparative LSER study of the reactivi
✍ J. B. Nikolić; G. S. Ušćumlić; Ivan O. Juranić 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 173 KB

## Abstract The rate constants for the reaction of 2‐substituted cyclohex‐1‐eneacetic and 2‐substituted phenylacetic acids with diazodiphenylmethane were determined in various aprotic solvents at 30°C. To explain the kinetic results through solvent effects, the second‐order rate constants of the ex

A linear solvation energy relationship s
✍ J. B. Nikolić; G. S. Ušćumlić; I. O. Juranić 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 346 KB

## Abstract The reactivities of 2‐(4‐substituted phenyl)‐cyclohex‐1‐enecarboxylic acids, 2‐(4‐substituted phenyl)‐benzoic acids, and 2‐(4‐substituted phenyl)‐acrylic acids with diazodiphenylmethane in various solvents were investigated. To explain the kinetic results through solvent effects, the se

Solvent and substituent effects on the r
✍ Basim H. M. Asghar; Magda F. Fathalla; Ezzat A. Hamed 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 135 KB 👁 2 views

## Abstract The solvent effect on a nucleophilic substitution reaction of 2‐ and 4‐chloro‐3,5‐dinitrobenzotrifluoride with substituted anilines was studied in methanol, acetonitrile, and toluene at 25°C. This reaction is of second order, except 2‐chloro‐3,5‐dinitrobenzotrifluoride in toluene shows

Kinetic investigation on the reactions o
✍ Subbiah Ananthalakshmi; M. Nallu 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 112 KB 👁 1 views

## Abstract Second‐order rate constants of the reactions of __p__‐toluenesulfonyl chloride with __p__‐substituted benzoic acids in the presence of triethylamine in acetonitrile/acetone under equimolar and pseudo‐first‐order conditions have been determined by the conductometric method using the Gugg