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Question: The equilibrium constant \({K_P}\) for the reaction: ![](https://www.vedantu.com/question-sets/dfe...

The equilibrium constant KP{K_P} for the reaction:

Varies with temperatures according to the equation:
log10(KPbar1)=7.554844(TK1)1{\log _{10}}({K_P}ba{r^{ - 1}}) = 7.55 - 4844{(T{K^{ - 1}})^{ - 1}}
Calculate KP,ΔGo,ΔHo{K_P},\Delta {G^o},\Delta {H^o} and ΔSo\Delta {S^o} at 11 bar and 400C{400^\circ }C.

Explanation

Solution

As we know that Gibbs free energy is the energy that should be supplied to a system and only a small portion of it is converted to useful work which is our free energy, entropy is the randomness of the system and the enthalpy is the amount of heat supplied at constant pressure.

Complete answer:
We know that Gibbs free energy is the energy that should be supplied to a system and only a small portion of it is converted to useful work which is our free energy, entropy is the randomness of the system and the enthalpy is the amount of heat supplied at constant pressure and the equilibrium constant is that value where the reaction has no tendency to move forward or backward.
Now, We are given that the temperature is 400C{400^\circ }C, we will first convert it into kelvin so we will get:
400+273=673K400 + 273 = 673K
Then we are provided with the equation:
log10(KPbar1)=7.554844(TK1)1{\log _{10}}({K_P}ba{r^{ - 1}}) = 7.55 - 4844{(T{K^{ - 1}})^{ - 1}}
We will first solve this equation for finding out the equilibrium constant KP{K_P} and after solving this equation we will get:
logKP=7.554844673\log {K_P} = 7.55 - \dfrac{{4844}}{{673}}
logKP=0.352\Rightarrow \log {K_P} = 0.352
KP=antilog(0.352) KP=2.25 \Rightarrow {K_P} = anti\log (0.352) \\\ \Rightarrow {K_P} = 2.25
Now we can use this value of equilibrium constant KP{K_P}to calculate the Gibbs free energy using the formula:
ΔG=RT  In  KP\Delta {G^\circ } = - RT\;In\;{K_P}
ΔG=2.303×8.314×673×0.352\Rightarrow\Delta {G^\circ } = - 2.303 \times 8.314 \times 673 \times 0.352
=4535.8  J= - 4535.8\;J or in terms of kilojoules it will be 4.54  kJ - 4.54\;kJ.
Now, we will solve for change in enthalpy ΔHo\Delta {H^o}using the formula:
lnKP=ΔHRT\Rightarrow\ln {K_P} = - \dfrac{{\Delta {H^\circ }}}{{RT}}
\Rightarrow2.303  logKP=ΔH6732.303\;\log {K_P} = - \dfrac{{\Delta {H^\circ }}}{{673}}
ΔH=2.303×0.352×673×8.314 ΔH=4.536  kJ \Rightarrow \Delta {H^\circ } = 2.303 \times 0.352 \times 673 \times 8.314 \\\ \Rightarrow \Delta {H^\circ } = 4.536\;kJ
Therefore the value of change in enthalpy is ΔH=4.536  kJ\Delta {H^\circ } = 4.536\;kJ.
Now we can calculate the change in entropy using the formula:
ΔG=ΔHTΔS\Delta {G^\circ } = \Delta {H^\circ } - T\Delta {S^\circ }
4.54=4.536673×ΔS- 4.54 = 4.536 - 673 \times \Delta {S^\circ }
13.49Jmol1=ΔS13.49\,Jmo{l^{ - 1}} = \Delta {S^\circ }
Hence the value of change in entropy is 13.49Jmol113.49Jmo{l^{ - 1}}.

**Therefore the values of KP=2.25{K_P} = 2.25, ΔG4.54  kJ\Delta {G^\circ } - 4.54\;kJ, ΔH=4.536  kJ\Delta {H^\circ } = 4.536\;kJ and 13.49Jmol1=ΔS13.49Jmo{l^{ - 1}} = \Delta {S^\circ }.

Note:**
Always remember that for a reaction to be spontaneous, Gibbs free energy is always spontaneous when its value is present in negative, similarly change in enthalpy should also be negative and change in entropy should be always positive and for a non spontaneous reaction to occur, Gibbs free energy is always positive, change in enthalpy is also positive and change in entropy is always negative. At equilibrium all these dimensions are zero.