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Question: Solid \(Ca{{\left( HC{{O}_{3}} \right)}_{2}}\) decomposes as \[Ca{{\left( HC{{O}_{3}} \right)}_{2}...

Solid Ca(HCO3)2Ca{{\left( HC{{O}_{3}} \right)}_{2}} decomposes as
Ca(HCO3)2(s)CaCO3(s)+CO2(g)+H2O(g)Ca{{\left( HC{{O}_{3}} \right)}_{2}}\left( s \right)\rightleftharpoons CaC{{O}_{3}}\left( s \right)+C{{O}_{2}}\left( g \right)+{{H}_{2}}O\left( g \right)
If the total pressure is 0.2 bar at 420 K, what is the standard free energy change for the given reaction(ΔrGo)\left( {{\Delta }_{r}}{{G}^{o}} \right)?
(A) 840 KJ/molKJ/mol
(B) 3.86 KJ/molKJ/mol
(C) 6.98 KJ/molKJ/mol
(D) 16.083 KJ/molKJ/mol

Explanation

Solution

When calcium bicarbonate is subjected to heating it is decomposed to give calcium carbonate, carbon dioxide and water. The calcium bicarbonate is soluble in water whereas calcium carbonate is insoluble in water.

Complete step by step solution:
- By looking at the stoichiometry of the reaction of decomposition of Ca(HCO3)2Ca{{\left( HC{{O}_{3}} \right)}_{2}}, we can assume that the partial pressure of carbon dioxide is equal to the partial pressure of water. And hence we can write as follows
PCO2=PH2O{{P}_{C{{O}_{2}}}}={{P}_{{{H}_{2}}O}}
It’s given that the total pressure is 0.2 bar. Thus we can write as follows
PCO2+PH2O=0.2bar{{P}_{C{{O}_{2}}}}+{{P}_{{{H}_{2}}O}}=0.2 bar
We can modify the above relation as follows
2PCO2=2PH2O=0.2bar2{{P}_{C{{O}_{2}}}}=2{{P}_{{{H}_{2}}O}}=0.2 bar
At equilibrium the relation becomes,
PCO2=PH2O=0.1bar{{P}_{C{{O}_{2}}}}={{P}_{{{H}_{2}}O}}=0.1 bar
Keq=PCO2×PH2O=0.1bar2{{K}_{eq}}={{P}_{C{{O}_{2}}}}\times {{P}_{{{H}_{2}}O}}=0.1 ba{{r}^{2}}
Keq=0.01bar2{{K}_{eq}}=0.01 ba{{r}^{2}}
We are asked to find the ΔrGo{{\Delta }_{r}}{{G}^{o}} value. The relation between Gibbs energy and standard free energy change can be written as follows
ΔG=ΔGo+RTlnKeq\Delta G=\Delta {{G}^{o}}+RT\ln {{K}_{eq}}
At equilibrium ΔG\Delta G is zero and the above relation can be modified as follows
ΔGo=RTlnKeq\Delta {{G}^{o}}=-RT\ln {{K}_{eq}}
As we know R is the universal gas constant and its value is 8.314Jmol1K18.314Jmo{{l}^{-1}}{{K}^{-1}}. T is the temperature in kelvin and the value is given in the question as 420 K. We have found the value of Keq{{K}_{eq}} as 0.01. Let’s substitute this values in the above equation
ΔGo=8.314×420×ln(0.01)=16081.6688Jmol1\Delta {{G}^{o}}=-8.314\times 420\times \ln (0.01)=16081.6688Jmo{{l}^{-1}}
We know that 1J=103KJ1J=1{{0}^{-3}}KJ. Thus by converting the above values in joules into kilojoules we get a follows
ΔrGo=16.082KJ/mol{{\Delta }_{r}}{{G}^{o}}=16.082 KJ/mol
Thus the standard free energy change for the given reaction ΔrGo{{\Delta }_{r}}{{G}^{o}} is 16.083 KJ/molKJ/mol.

Therefore the answer is option (D) 16.083 KJ/molKJ/mol

Note: The standard-state free energy of formation can be defined as the variation in free energy which happens when a compound is formed from its elements at standard-state conditions in their most thermodynamically stable states. It can also be defined as the difference between the free energies of constituent elements and the free energy of its substance at standard-state condition.