Awesome Chemistry Experiments For 3-Hydroxytetrahydrofuran

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 453-20-3

Related Products of 453-20-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.453-20-3, Name is 3-Hydroxytetrahydrofuran, molecular formula is C4H8O2. In a Article,once mentioned of 453-20-3

Theoretical insights into H-abstraction by ozone from saturated species have been virtually nonexistent, in sharp contrast to the situation for reactions with unsaturated species. Our computed rate constants for reactions with tetrahydrofuran and its methyl derivatives, obtained at various levels of theory, show that abstraction occurs primarily at the carbons situated beside the heterocyclic oxygen, with least likely reaction from the methyl groups. All of the methods tested are in broad relative agreement with this conclusion and with recent experiments although they do differ widely in terms of their absolute values. Abstraction leads variously to the formation of hydrotrioxides, ROOOH, or more directly to R – OH + O2(1Deltag). To understand some of the observed behaviors, dimethyl and diethyl acyclic ethers, methyl and ethyl hydroperoxides, and the alcohols methanol and ethanol were also included in this study. For the simplest system, CH3OH + O3 ? H2C=O + H2O2, an all-electron scalar relativistic CCSD(T)/CBS approach yields a barrier height that differs by >5 kJ mol-1 when an additional multireference treatment up to CCSDT(Q) is considered.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 453-20-3

Reference:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem