s1·S1 + .. + snS·SnS <-> p1·P1 + .. + pnP·PnP
By redefinition of stoichometry as vi = -si, Ai = Si for i=1..nS vi = pi-nS, Ai = Pi-nS for i=nS+1..nS+nP
So the reaction can be written also as 0 = ∑ (vi · Ai)
| K = product(a(S).^s) / product( a(P).^s ) = product(a(A).^v) | dissociation constant | 
| ΔrG = ∑ (vi · ΔfGi) = ΔrH - T·ΔrS = -R·T·log(K) | molar Gibb's energy of the reaction | 
| ΔrH = ∑ (vi · ΔfHi) | molar enthalpy of the reaction | 
| molar entropy of the reaction | 
| Ai | i-th substance | 
| vi | stochiometric coefficients of i-th substance | 
| K | dissociation constant (activity based) | 
| a(Ai)=fi*xi | activity of the substance A | 
| fi | activity coefficient of the substance A | 
| xi | mole fraction of the substance A | 
| ΔfHi | molar enthalpy of formation of i-th substance | 
| ΔfGi | molar Gibbs energy of formation of i-th substance | 
| ΔfSi | molar entropy of formation of i-th substance | 
| Δrω | change of number of microstates of particles by reaction | 
2013-2015 by Marek Matejak, Charles University, Prague, Czech Republic