Reference of 16859-59-9, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.16859-59-9, Name is 3-Hydroxyisobenzofuran-1(3H)-one, molecular formula is C8H6O3. In a article£¬once mentioned of 16859-59-9
Selectivity in catalytic diol electrooxidation using a polypyridine ru(iv) complex
1,2-, 1,3-, and 1,4-Butanediols and phthatic alcohol were oxidized electrocatalytically using the polypyridine [(bpy)(trpy)RuO]2+ complex (1) as oxidant under different conditions: concentration of 1, pH, and temperature. By controlling the number of coulombs passed through the electrolytic cell, it was possible to obtain selective reactions. 1-Hydroxy-2-butanone,1-hydroxy-3-butanone, gamma-butyrolactone, phthalide, phtalic aldehyde, and phthalic acid were the products obtained by controlled potential electrolysis from these substrates, with yields ranging from 41 to 89%.
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 16859-59-9
Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H1483O – PubChem