Application of the extended Grunwald-Winstein equation to solvolyses of n-propyl chloroformate

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SCOPUS

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초록

Application of the extended Grunwald-Winstein equation to solvolyses of n-propyl chloroformate in a variety of pure and binary solvents indicates an addition-elimination pathway in the majority of the solvents but an ionization pathway in the solvents of highest ionizing power and lowest nucleophilicity. For methanolysis, a solvent deuterium isotope effect of 2.17 is compatible with the incorporation of general-base catalysis into the substitution process. Activation parameters are consistent with the duality of mechanism. Very modest positive salt effects are observed on adding chloride or bromide salts to the ethanolysis.

키워드

n-propyl chloroformate; addition-elimination; ionization; solvent isotope effect; Grunwald-Winstein equation; SOLVENT NUCLEOPHILICITY SCALE; TERT-BUTYL CHLORIDE; SN2-SN1 SPECTRUM; NITROBENZOYL CHLORIDE; DUAL PATHWAYS; RATES; MECHANISM; PRODUCT; ATTACK; PHOSPHOROCHLORIDATE
제목
Application of the extended Grunwald-Winstein equation to solvolyses of n-propyl chloroformate
저자
Kyong, Jin Burm; Won, Hoshik; Kevill, Dennis N.
DOI
10.3390/i6010087
발행일
2005-01
유형
Article
저널명
International Journal of Molecular Sciences
권
6
호
1-2
페이지
87 ~ 96