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Journal of the American Chemical Society

Volumn 123, Issue 44, 2001, Pages 10877-10883

Is the tert-butyl chloride solvolysis the most misunderstood reaction in organic chemistry? Evidence against nucleophilic solvent participation in the tert-butyl chloride transition state and for increased hydrogen bond donation to the 1-adamantyl chloride solvolysis transition state

(1) Gajewski, J J a

a INDIANA UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SOLVOLYSIS;

ETHANOL; PERMITTIVITY; POSITIVE IONS;

HYDROGEN BONDS;

1 ADAMANTYLCHLORIDE; ALCOHOL; CHLORIDE; HYDROXYL GROUP; SOLVENT; TERT BUTYL CHLORIDE; UNCLASSIFIED DRUG;

AQUEOUS SOLUTION; ARTICLE; CALCULATION; CHEMICAL REACTION; CHEMICAL REACTION KINETICS; DIELECTRIC CONSTANT; ENERGY; GAS; HYDROGEN BOND; MOLECULAR INTERACTION; ORGANIC CHEMISTRY; REACTION ANALYSIS; SOLVATION; STEREOSPECIFICITY; THEORY;

EID: 0035823833 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja010600d Document Type: Article

Times cited : (50)

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