Extracurricular laboratory:new discovery of Quinoxaline-2,3-diamine

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Computed Properties of C8H8N4, you can also check out more blogs about6640-47-7

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Computed Properties of C8H8N4. Introducing a new discovery about 6640-47-7, Name is Quinoxaline-2,3-diamine

Ground- and Excited-State Protonation of Aminoquinoxalines

Excited-state second protonation of 2-aminoquinoxaline occurs in aqueous perchloric acid at a rate of 1.1×1010 L.mol-1.s-1.The reaction is very sensitive to solvent structure and is blocked in acidic poly(vinyl alcohol) and heptane solutions of trifluoroacetic acid.Calculations of effective valence electron potentials provide a good reactivity index for pKa changes in excited 2-aminoquinoxaline and 2,3-diaminoquinoxaline.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Computed Properties of C8H8N4, you can also check out more blogs about6640-47-7

Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N263 | ChemSpider