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Int J Mol Sci. 2009 Mar;10(3):862-79. doi: 10.3390/ijms10030862. Epub 2009 Mar 2.

Grunwald-Winstein analysis: isopropyl chloroformate solvolysis revisited.

Author information

1
Department of Chemistry, Wesley College, Dover, Delaware 19901-3875, USA. dsouzama@wesley.edu <dsouzama@wesley.edu>

Abstract

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 analyzed using the one and two-term Grunwald-Winstein Equations. In the more ionizing solvents including ten fluoroalcohols negligible sensitivities towards changes in solvent nucleophilicity (l) and very low sensitivities towards changes in solvent ionizing power (m) values are obtained, evocative to those previously observed for 1-adamantyl and 2-adamantyl chloroformates 2 and 3. These observations are rationalized in terms of a dominant solvolysis-decomposition with loss of the CO(2) molecule. In nine of the more nucleophilic pure alchohols and aqueous solutions an association-dissociation mechanism is believed to be operative. Deficiencies in the acid production indicate 2-33% isopropyl chloride formation, with the higher values in less nucleophilic solvents.

KEYWORDS:

Grunwald-Winstein Equation; Linear Free Energy Relationships; Solvolysis; chloroformates; ionizing power; isopropyl chloroformate; nucleophilicity; solvolysis-decomposition

PMID:
19399225
PMCID:
PMC2672006
DOI:
10.3390/ijms10030862
[Indexed for MEDLINE]
Free PMC Article

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