Kinetic hydrogen isotope effects in the concerted mechanism for the hydrolysis of acetals, ketals, and ortho esters
- Southwest State Univ., Marshall, MN
The hydrolysis of many ortho esters, and some acetals and ketals, is general acid catalyzed, and in some examples these generate linear Bronsted plots over substantial ranges of catalyst acidity. This suggests that the reaction coordinate is primarily a reorganization of heavy atoms since proton transfer from one oxygen to another has been shown to generate strongly curved Bronsted plots. However, the isotopic fractionation factor for the catalytically active proton in these transition states is substantially less than 1.0; in several examples it is less than 0.5. Such values have been thought to require that the reaction coordinate be largely a motion of the hydrogen giving the low fractionation factor. This dilemma has been resolved by the observation and rationalization of fractionation factors as low as 0.28 for stable, hydrogen bridge-bonded complexes, AHA/sup -/. A similar, bounded coordinate is now suggested for the catalytically active protons in question. This permits the reaction coordinate to be pictured. 3 figures, 2 tables.
- OSTI ID:
- 6425868
- Journal Information:
- J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 100:22; ISSN JACSA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
400302* -- Organic Chemistry-- Isotope Effects-- (-1987)
ACETALS
AQUEOUS SOLUTIONS
BARYONS
CARBOXYLIC ACIDS
CATALYSTS
CATALYTIC EFFECTS
CHARGED PARTICLES
CHEMICAL REACTION KINETICS
CHEMICAL REACTIONS
DECOMPOSITION
DEUTERIUM
DIOXANE
DISPERSIONS
ELEMENTARY PARTICLES
ESTERS
ETHERS
FERMIONS
FRACTIONATION
HADRONS
HEAVY WATER
HETEROCYCLIC COMPOUNDS
HYDROGEN COMPOUNDS
HYDROGEN ISOTOPES
HYDROLYSIS
IONS
ISOTOPE EFFECTS
ISOTOPES
KETONES
KINETICS
LIGHT NUCLEI
LYSIS
MIXTURES
MOLECULAR IONS
NUCLEI
NUCLEONS
ODD-ODD NUCLEI
ORGANIC ACIDS
ORGANIC COMPOUNDS
ORGANIC OXYGEN COMPOUNDS
OXONIUM IONS
OXYGEN COMPOUNDS
PROTONS
PYRANS
REACTION INTERMEDIATES
REACTION KINETICS
SEPARATION PROCESSES
SOLUTIONS
SOLVOLYSIS
STABLE ISOTOPES
WATER