What is Gibbs free energy ? Derive the relation, `Delta_G = DeltaH - T Delta S`. Discuss the free energy criterion for the spontaneity of a process.

Derive the equation, DeltaG = DeltaH - T DeltaS .

What is the free energy criterion for a process to occur spontaneously?

How does T DeltaS determine the spontaneity of process?

What is significance of T DeltaS in DeltaG = DeltaH - T DeltaS ?

Gibbs free energy G, enthalpy H and entropy S are related as

The Gibbs free energy (DeltaG) is related with cell potential ( E ) by DeltaG=-nFE , the cell reaction will be spontaneous if

Define Gibb.s free energy and free energy change.

Free enegry , G = H - TS , is state function that indicates whther a reaction is spontaneous or non-spontaneous. If you think of TS as the part of the system's enegry that is disordered already, then (H -TS) is the part of the system's energy that is still ordered and therefore free to cause spontaneous change by becoming disordered. Also, DeltaG = DeltaH - T DeltaS From the second law of thermodynamics, a reaction is spontaneous if Delta_("total")S is positive, non-spontaneous if Delta_("total")S is negative, and at equilibrium if Delta_('total")S is zero. Since, -T DeltaS = DeltaG and since DeltaG and DeltaS have opposite sings, we can restate the thermodynamic criterion for the spontaneity of a reaction carried out a constant temperature and pressure. IF DeltaG lt 0 , the reaction is spontaneous. If DeltaG gt 0 , the reaction is non-spontaneous. If DeltaG = 0 , the reaction is at equilibrium. Read the above paragraph carefully and answer the following questions based on the above comprehension. For the spontaneity of a reaction, which statement is true?

Free enegry , G = H - TS , is state function that indicates whther a reaction is spontaneous or non-spontaneous. If you think of TS as the part of the system's enegry that is disordered already, then (H -TS) is the part of the system's energy that is still ordered and therefore free to cause spontaneous change by becoming disordered. Also, DeltaG = DeltaH - T DeltaS From the second law of thermodynamics, a reaction is spontaneous if Delta_("total")S is positive, non-spontaneous if Delta_("total")S is negative, and at equilibrium if Delta_('total")S is zero. Since, -T DeltaS = DeltaG and since DeltaG and DeltaS have opposite sings, we can restate the thermodynamic criterion for the spontaneity of a reaction carried out a constant temperature and pressure. IF DeltaG lt 0 , the reaction is spontaneous. If DeltaG gt 0 , the reaction is non-spontaneous. If DeltaG = 0 , the reaction is at equilibrium. Read the above paragraph carefully and answer the following questions based on the above comprehension. A particular reaction has a negative value for the free energy change. Then at ordinary temperature

Free enegry , G = H - TS , is state function that indicates whther a reaction is spontaneous or non-spontaneous. If you think of TS as the part of the system's enegry that is disordered already, then (H -TS) is the part of the system's energy that is still ordered and therefore free to cause spontaneous change by becoming disordered. Also, DeltaG = DeltaH - T DeltaS From the second law of thermodynamics, a reaction is spontaneous if Delta_("total")S is positive, non-spontaneous if Delta_("total")S is negative, and at equilibrium if Delta_('total")S is zero. Since, -T DeltaS = DeltaG and since DeltaG and DeltaS have opposite sings, we can restate the thermodynamic criterion for the spontaneity of a reaction carried out a constant temperature and pressure. IF DeltaG lt 0 , the reaction is spontaneous. If DeltaG gt 0 , the reaction is non-spontaneous. If DeltaG = 0 , the reaction is at equilibrium. Read the above paragraph carefully and answer the following questions based on the above comprehension. Which of the following is true for the reaction? H_(2)O(l) hArr H_(2)O(g) at 100^(@)C and 1 atmosphere