Cargando…
Use of Empirical Correlations to Determine Solvent Effects in the Solvolysis of S-Methyl Chlorothioformate
The specific rates of solvolysis of S-methyl chlorothioformate (MeSCOCl) are analyzed in 20 solvents of widely varying nucleophilicity and ionizing power at 25.0 °C using the extended Grunwald-Winstein Equation. A stepwise S(N)1 (D(N) + A(N)) mechanism is proposed in the more ionizing solvents inclu...
Autores principales: | D’Souza, Malcolm J., Hailey, Stefan M., Kevill, Dennis N. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2885106/ https://www.ncbi.nlm.nih.gov/pubmed/20559514 http://dx.doi.org/10.3390/ijms11052253 |
Ejemplares similares
-
Analysis of the Nucleophilic Solvation Effects in Isopropyl Chlorothioformate Solvolysis
por: D’Souza, Malcolm J., et al.
Publicado: (2010) -
Kinetic evaluation of the solvolysis of isobutyl chloro- and chlorothioformate esters
por: D’Souza, Malcolm J, et al.
Publicado: (2011) -
A Study of Solvent Effects in the Solvolysis of Propargyl Chloroformate
por: D'Souza, Malcolm J., et al.
Publicado: (2011) -
Mechanistic studies of the solvolysis of alkanesulfonyl and arenesulfonyl halides
por: D’Souza, Malcolm J, et al.
Publicado: (2022) -
Correlation of the Rates of Solvolysis of Neopentyl Chloroformate—A Recommended Protecting Agent
por: D’Souza, Malcolm J., et al.
Publicado: (2011)