The reaction which is in dynamic equilibrium, ensured us, that the reaction is reversible . But if that the reaction is in equilibrium. The reaction quotient predict either the reversible reaction is in equilibrium or tries to achieve equilibrium. In those reactions which have not achieved equilibrium, we obtain reaction quotient `Q_(c)` in place of equilibrium constant `(K_(c))` by substituting the concentration of reactant and product at the time, at whih we have to calculate the value of `Q_(c)` . To determine the direction at which the net reaction will proceed to achieve equilibrium, we compare values of `Q_(c)` and `K_(c)`. The three possible cases are shown as comparison of `K_(c)` and `Q_(c)` in the following figures. Change in Gibbs free energy, i.e., `Delta G` is the driving force of any reaction. For spontaneous reaction , `Delta G =-ve` For non-spontaneous reaction , `Delta G=+ve` For reaction at equilibrium , `Delta G =0` Thermodynamically, we know that `Delta G= Delta G^(@)+ RT ln Q`, where `Q` is reaction quotient and `Delta G^(@)=` change in Gibbs energy at standard condition. For equilibrium `A(g) hArr B(g) (K_(eq) =1.732)` If the pressure of the system [varied by introducing a stream of `A (g)` and B (g) is represented by the curve at constant temperature T. If A and B are enclosed in the cylinder and piston of the cylinder be moved downward so that volume of cylinder becomes half, then what will be the effect in `K_(c)` at constant temeprature ?A. `K_(c)` will increaseB. `K_(c)` will decreaseC. `K_(c)` has no relation with `K_(p)`D. No effect in `K_(c)`