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Question: Given that \(\Delta G(HI:g) \equiv + 1.7kJ\) What is the equilibrium constant at \({25^0}C\) for \(2...

Given that ΔG(HI:g)+1.7kJ\Delta G(HI:g) \equiv + 1.7kJ What is the equilibrium constant at 250C{25^0}C for 2HI(g)H2(g)+I2(g)2HI(g) \rightleftarrows {H_{2\left( g \right)}} + {I_{2\left( g \right)}} ?
A. 24.024.0
B. 3.93.9
C. 2.02.0
D. 0.50.5

Explanation

Solution

We have to remember that an equilibrium constant is expressed by KK , the number which expresses the relationship between the products and reactants present at equilibrium in a reversible chemical reaction.
Here, we use change in free energy for a reaction at any conditions other than standard can be calculated as,
ΔG0=ΔG+RTlnK\Delta {G^0} = \Delta G + RT\ln K , for standard conditions
T=250CT = {25^0}C ,
R and K are constants.

Complete step by step answer:
Given, ΔG(HI:g)+1.7kJ\Delta G(HI:g) \equiv + 1.7kJ
T=250CT = {25^0}C ,
2HI(g)H2(g)+I2(g)2HI(g) \rightleftarrows {H_{2\left( g \right)}} + {I_{2\left( g \right)}} .
Rearranging the above change in free energy equation, we get
ΔG=2.303×RTlog10K(eq)\Delta G^\circ = - 2.303 \times RT{\log _{10}}{K_{\left( {eq} \right)}}
Where,
ΔG=\Delta G = Change in Gibbs free energy
RR is the gas Constant, value is 8.314JK1mol18.314J{K^{ - 1}}mo{l^{ - 1}} or 0.008314kJmol1K10.008314kJmo{l^{ - 1}}{K^{ - 1}} .
TTis the temperature in kelvin.
KKis the equilibrium Constant.
In equilibrium, the temperature in Kelvin, but in question, given in Celsius form, so, degree Celsius is converted to kelvin,
K=T+273K = T + 273
K=25+273K = 25 + 273
K=298K = 298
At equilibrium,
R=8.314R = 8.314.
ΔG0=2.303×RTlog10K\Delta {G^0} = - 2.303 \times RT{\log _{10}}K
On substituting the known values we get,
1.73×103=2.303×8.314×log10(Keq)×298\Rightarrow 1.73 \times {10^3} = - 2.303 \times 8.314 \times {\log _{10}}({K_{eq}}) \times 298
1700=2.303×8.314×log10(Keq)×298\Rightarrow 1700 = - 2.303 \times 8.314 \times {\log _{10}}({K_{eq}}) \times 298
On simplification we get,
1700=5705×log10(Keq)1700 = - 5705 \times {\log _{10}}({K_{eq}})
Rearranging the above equation,
17005705=log10(Keq)\dfrac{{1700}}{{ - 5705}} = {\log _{10}}({K_{eq}})
On simplification we get,
0.297=log10(Keq)- 0.297 = {\log _{10}}\left( {{K_{eq}}} \right)
Rearranging the above equation we get,
Keq=10(0.297)\Rightarrow {K_{eq}} = {10^{( - 0.297)}}
Keq=0.5\Rightarrow {K_{eq}} = 0.5

So, the correct answer is Option D.

Additional information:
In the above calculation we see Gibbs free energy, called “Available energy”-Gibbs free energy, was developed by Josiah Willard Gibbs, an American scientist. It is defined by Josiah Willard Gibbs, developer, “a certain substance in a given initial state give the greatest amount of mechanical work which can be obtained from a given quantity, allowing heat to pass or from external bodies or without increasing its total volume, except such as at the close of the process are left in their initial condition.

Note: In ΔG=\Delta G = Change in Gibbs free energy, the mean “available in the form of useful work”. ΔG0\Delta {G^0} indicates all reactants and products are in their standard states. And also for standard conditions ΔG=0\Delta G = 0 , for a system at equilibrium. Not confusing with Helmholtz free energy, which is represented by the symbolA0 - {A^0} , which gives maximum work obtainable from a system. But ΔG - \Delta G , which gives maximum useful work obtainable from the system.