One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Safety of 3-Methyldihydrofuran-2(3H)-one, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 1679-47-6, Name is 3-Methyldihydrofuran-2(3H)-one, molecular formula is C5H8O2
Evidence for Extensive Recombination of the Ring-opened to the Original Cyclic Molecular Ions of 2-Substituted Piperidines and Pyrrolidines after Electron Impact
The unusually preferred formation of (M-alkyl)(1+) ions by alpha-fission of 2,2-dialkyl-substituted N-ethyl-piperidines (2) and -pyrrolidines (3) and the virtual absence of ring degradation products is caused by facile recombination of the ring-opened to the original cyclic molecular ions.Suppression of ring opening of the initially formed molecular ions or conversion of the ring-opened into other isomeric molecular ions as explanations of the mass spectrometric behaviour of (2) and (3) are excluded.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Safety of 3-Methyldihydrofuran-2(3H)-one, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 1679-47-6, in my other articles.
Reference£º
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem