Walden Inversion and Reaction Mechanism: Walden Inversion in the Acid Hydrolysis of Carboxylic Esters by Unimolecular Alkyl Fission
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Dynamical barrier and isotope effects in the simplest substitution reaction via Walden inversion mechanism
Reactions occurring at a carbon atom through the Walden inversion mechanism are one of the most important and useful classes of reactions in chemistry. Here we report an accurate theoretical study of the simplest reaction of that type: the H+CH4 substitution reaction and its isotope analogues. It is found that the reaction threshold versus collision energy is considerably higher than the barrie...
متن کاملStepwise walden inversion in nucleophilic substitution at phosphorus.
We have studied the mechanism of S(N)2@P reactions in the model systems X(-) + PMe(2)Y and X(-) + POR(2)Y (with R=Me, OH, OMe; and X, Y=Cl, OH, MeO) using density functional theory at OLYP/TZ2P. Our main purpose is to analyze the nature of the Walden inversion in our model nucleophilic substitution reactions. Walden inversion is well-known to proceed, in general, as a concerted umbrella motion ...
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The reaction kinetics of the isomerization 3,4-dichlorobutene-1 to 1,4-dichlorobutene-2 was investigated by using gas-liquid chromatography method in the presence of Fe2O3/MgO as solid catalyst in the temperature range 25-55°C. Fe2O3/MgO has been prepared by the support saturation method, tested in the isomerization of 3, 4-dichlorobutene-1 into 1, 4-dichlorobutene-2. This catalyst shows a high...
متن کاملKinetics inversion of chloro-olefine in the solid acid system
The reaction kinetics of the isomerization 3,4-dichlorobutene-1 to 1,4-dichlorobutene-2 was investigated by using gas-liquid chromatography method in the presence of Fe2O3/MgO as solid catalyst in the temperature range 25-55°C. Fe2O3/MgO has been prepared by the support saturation method, tested in the isomerization of 3, 4-dichlorobutene-1 into 1, 4-dichlorobutene-2. This catalyst shows a high...
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ژورنال
عنوان ژورنال: Nature
سال: 1950
ISSN: 0028-0836,1476-4687
DOI: 10.1038/166680a0