Grunwald-Winstein Analysis - Isopropyl Chloroformate Solvolysis Revisited

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Grunwald-Winstein Analysis - Isopropyl Chloroformate Solvolysis Revisited

Specific rates of solvolysis at 25 degrees C for isopropyl chloroformate (1) in 24 solvents of widely varying nucleophilicity and ionizing power, plus literature values for studies in water and formic acid, are reported. Previously published solvolytic rate constants at 40.0 degrees C are supplemented with two additional values in the highly ionizing fluoroalcohols. These rates are now are anal...

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Extended Grunwald-Winstein Analysis - LFER Used to Gauge Solvent Effects in p-Nitrophenyl Chloroformate Solvolysis

Specific rates of solvolysis at 25 degrees C for p-nitrophenyl chloroformate (1) are analyzed using the extended (two-term) Grunwald-Winstein equation. For 39 solvents, the sensitivities (l = 1.68+/-0.06 and m = 0.46+/-0.04) towards changes in solvent nucleophilicity (l) and solvent ionizing power (m) obtained, are similar to those previously observed for phenyl chloroformate (2) and p-methoxyp...

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Corrrelation of the Specific Rates of Solvolysis of Ethyl Fluoroformate Using the Extended Grunwald-Winstein Equation

The specific rates of solvolysis of ethyl fluoroformate have been measured at 24.2 degrees C in 21 pure and binary solvents. These give a satisfactory correlation over the full range of solvents when the extended Grunwald-Winstein equation is applied. The sensitivities to changes in the N(T) solvent nucleophilicity scale and the Y(Cl) solvent ionizing power scale, and the k(F)/k(Cl) values are ...

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Detailed Analysis for the Solvolysis of Isopropenyl Chloroformate.

The specific rates of solvolysis (including those obtained from the literature) of isopropenyl chloroformate (1) are analyzed using the extended Grunwald-Winstein equation, involving the N(T) scale of solvent nucleophilicity (S-methyldibenzothiophenium ion) combined with a Y(Cl) scale based on 1-adamantyl chloride solvolysis. A similarity model approach, using phenyl chloroformate solvolyses fo...

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Analysis of the Nucleophilic Solvation Effects in Isopropyl Chlorothioformate Solvolysis

Correlation of the solvent effects through application of the extended Grunwald-Winstein equation to the solvolysis of isopropyl chlorothioformate results in a sensitivity value of 0.38 towards changes in solvent nucleophilicity (l) and a sensitivity value of 0.72 towards changes in solvent ionizing power (m). This tangible l value coupled with the negative entropies of activation observed indi...

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ژورنال

عنوان ژورنال: International Journal of Molecular Sciences

سال: 2009

ISSN: 1422-0067

DOI: 10.3390/ijms10030862