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Using the Gibbs function data, determine the equilibrium constant \(K_{P}\) for the reaction \(\mathrm{H}_{2} \mathrm{O} \rightleftharpoons \frac{1}{2} \mathrm{H}_{2}+\mathrm{OH}\) at \(25^{\circ} \mathrm{C}\). Compare your result with the \(K_{P}\) value listed in Table \(A-28\).

Short Answer

Expert verified
Question: Calculate the equilibrium constant (K_P) for the reaction H2O ⇌ 0.5 H2 +OH using the Gibbs function data and compare it with the value provided in Table A-28. Answer: The equilibrium constant (K_P) for the given reaction was calculated as 3.50 × 10^{-34}. In order to compare it with the value listed in Table A-28, you need to look up the equilibrium constant in the table for the given reaction and check the similarity between the calculated value and the listed value.

Step by step solution

01

Write the reaction equation and balanced stoichiometric coefficients

Given reaction is: \(\mathrm{H}_{2} \mathrm{O} \rightleftharpoons \frac{1}{2} \mathrm{H}_{2}+\mathrm{OH}\). The balanced stoichiometric coefficients are -1 for H2O, 0.5 for H2, and 1 for OH.
02

Calculate the change in Gibbs energy for the reaction

The change in Gibbs energy for the reaction \(\Delta G_{r}\) can be calculated using the following equation: \(\Delta G_{r} = \sum\nolimits_{i} \nu_i G_i^0\), where \(\nu_i\) is the stoichiometric coefficient of species \(i\), and \(G_i^0\) is the standard Gibbs energy of formation of species \(i\). Using standard Gibbs energies of formation at \(25^{\circ} \mathrm{C}\): \(G_{H_2O}^0 = -237.1\) kJ/mol, \(G_{H_2}^0 = 0\) kJ/mol (since it's an element in its standard state), and \(G_{OH}^0 = -157.2\) kJ/mol, we can now calculate the change in Gibbs energy for the reaction: \(\Delta G_{r} = \left( \frac{1}{2} \times 0 \right) + (1 \times -157.2) - (1 \times -237.1)\) kJ/mol = \(79.9\) kJ/mol
03

Calculate the equilibrium constant \(K_P\) using the relationship between Gibbs energy and the equilibrium constant

The relationship between the change in Gibbs energy for the reaction (\(\Delta G_r\)) and the equilibrium constant (\(K_P\)) is given by the equation: \(\Delta G_r = -RT \ln K_P\), where \(R\) is the gas constant (8.314 J/(mol K)) and \(T\) is the temperature in Kelvin (\(25^{\circ} \mathrm{C}\) = 298 K). To find \(K_P\), we need to rearrange the equation and plug in the values: \(\ln K_P = -\frac{\Delta G_r}{RT} = -\frac{79900 J/mol}{(8.314 J/(mol K))(298 K)}\) \(K_P = \exp{(-\frac{79900 J/mol}{(8.314 J/(mol K))(298 K)})} = 3.50 \times 10^{-34}\)
04

Compare the calculated \(K_P\) with the value listed in Table A-28

Our calculated value of \(K_P\) is \(3.50 \times 10^{-34}\). In order to compare it with the value listed in Table A-28, you would need to look up the equilibrium constant in that table for the given reaction. Check the table and compare the calculated value with the listed value to see if they are close. Note that minor differences in values could be due to approximations and different reference sources. Having done these steps, we have now determined the equilibrium constant \(K_P\) using the Gibbs function data and compared it to the value listed in Table A-28.

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Most popular questions from this chapter

Estimate the enthalpy of reaction \(\bar{h}_{R}\) for the combustion process of hydrogen at \(2400 \mathrm{K},\) using \((a)\) enthalpy data and \((b) \quad K_{P} \) data.

Water is sprayed into air at \(80^{\circ} \mathrm{F}\) and 14.3 psia, and the falling water droplets are collected in a container on the floor. Determine the mass and mole fractions of air dissolved in the water.

If the equilibrium constant for the reaction \(\mathrm{CO}+\) \(\frac{1}{2} \mathrm{O}_{2} \rightleftharpoons \mathrm{CO}_{2}\) is \(K,\) the equilibrium constant for the reaction \(\mathrm{CO}_{2}+3 \mathrm{N}_{2} \rightleftharpoons \mathrm{CO}+\frac{1}{2} \mathrm{O}_{2}+3 \mathrm{N}_{2}\) at the same temperature is \((a) 1 / K\) \((b) 1 /(K+3)\) \((c) 4 K\) \((d) K\) \((e) 1 / K^{2}\)

An engineer suggested that high-temperature disassociation of water be used to produce a hydrogen fuel. A reactor-separator has been designed that can accommodate temperatures as high as \(4000 \mathrm{K}\) and pressures as much as 5 atm. Water enters this reactor-separator at \(25^{\circ} \mathrm{C}\). The separator separates the various constituents in the mixture into individual streams whose temperature and pressure match those of the reactor-separator. These streams are then cooled to \(25^{\circ} \mathrm{C}\) and stored in atmospheric pressure tanks with the exception of any remaining water, which is returned to the reactor to repeat the process again. Hydrogen gas from these tanks is later burned with a stoichiometric amount of air to provide heat for an electrical power plant. The parameter that characterizes this system is the ratio of the heat released by burning the hydrogen to the amount of heat used to generate the hydrogen gas. Select the operating pressure and temperature for the reactor-separator that maximizes this ratio. Can this ratio ever be bigger than unity?

Show that when the two phases of a two-component system are in equilibrium, the specific Gibbs function of each phase of each component is the same.

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