Carbon monoxide is toxic because it bonds much more strongly to the iron in hemoglobin (Hgb) than does \(\mathrm{O}_{2}\). Consider the following reactions and approximate standard free energy changes: $$\begin{array}{clr}\mathrm{Hgb}+\mathrm{O}_{2} \longrightarrow \mathrm{HgbO}_{2} & \Delta G^{\circ}=-70 \mathrm{~kJ} \\ \mathrm{Hgb}+\mathrm{CO} \longrightarrow \mathrm{HgbCO} & \Delta G^{\circ}=-80 \mathrm{~kJ} \end{array}$$ Using these data, estimate the equilibrium constant value at \(25^{\circ} \mathrm{C}\) for the following reaction: $$\mathrm{HgbO}_{2}+\mathrm{CO} \rightleftharpoons \mathrm{HgbCO}+\mathrm{O}_{2}$$

Short Answer

Expert verified
The equilibrium constant value for the reaction \(\mathrm{HgbO}_{2}+\mathrm{CO} \rightleftharpoons\mathrm{HgbCO}+\mathrm{O}_{2}\) at \(25^{\circ} \mathrm{C}\) is approximately 3.53.

Step by step solution

01

Determine the standard free energy change for the given reaction

We have the standard free energy changes for two reactions: 1) \(\mathrm{Hgb}+\mathrm{O}_{2} \longrightarrow\mathrm{HgbO}_{2}\): \(\Delta G^{\circ}_{1} = -70 \mathrm{~kJ}\) 2) \(\mathrm{Hgb}+\mathrm{CO} \longrightarrow\mathrm{HgbCO}\): \(\Delta G^{\circ}_{2} = -80 \mathrm{~kJ}\) We need to find the standard free energy change for the reaction: \(\mathrm{HgbO}_{2}+\mathrm{CO} \rightleftharpoons\mathrm{HgbCO}+\mathrm{O}_{2}\) Notice that the second reaction is the reverse of Reaction 1 and adding the first reaction. To obtain this reaction, we can reverse Reaction 1 and add it to Reaction 2. Let's calculate the standard free energy change for the reversed Reaction 1: \(-\Delta G^{\circ}_{1} = 70 \mathrm{~kJ}\) Now, let's add the standard free energy changes for the reversed Reaction 1 and Reaction 2: \(\Delta G^{\circ}_{\text{given reaction}} = -\Delta G^{\circ}_{1} + \Delta G^{\circ}_{2} = 70 \mathrm{~kJ} + (-80 \mathrm{~kJ}) = -10 \mathrm{~kJ}\)
02

Calculate the equilibrium constant value

To calculate the equilibrium constant value (\(K\)), we can use the relationship between the standard free energy change and the equilibrium constant: \(\Delta G^{\circ} = -RT\ln K\) Where \(R\) is the gas constant (8.314 J/(mol·K)), \(T\) is the temperature in Kelvin, and \(K\) is the equilibrium constant. First, let's convert the temperature to Kelvin: \(T = 25^{\circ} \mathrm{C} + 273.15 = 298.15 \mathrm{K}\) Now, we can rearrange the equation and solve for \(K\): \(K = e^{-\frac{\Delta G^{\circ}}{RT}}\) Plugging in the values for \(\Delta G^{\circ}\), \(R\), and \(T\): \(K = e^{-\frac{-10 \times 10^{3} \mathrm{J/mol}}{(8.314 \mathrm{J/(mol\cdot K)})(298.15 \mathrm{K})}}\) \(K \approx 3.53\) So, the equilibrium constant value for the given reaction at \(25^{\circ} \mathrm{C}\) is approximately 3.53.

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Most popular questions from this chapter

Is \(\Delta S_{\text {surr }}\) favorable or unfavorable for exothermic reactions? Endothermic reactions? Explain.

Some nonelectrolyte solute (molar mass \(=142 \mathrm{~g} / \mathrm{mol}\) ) was dissolved in \(150 . \mathrm{mL}\) of a solvent (density \(=0.879 \mathrm{~g} / \mathrm{cm}^{3}\) ). The elevated boiling point of the solution was \(355.4 \mathrm{~K}\). What mass of solute was dissolved in the solvent? For the solvent, the enthalpy of vaporization is \(33.90 \mathrm{~kJ} / \mathrm{mol}\), the entropy of vaporization is \(95.95\) \(\mathrm{J} / \mathrm{K} \cdot \mathrm{mol}\), and the boiling-point elevation constant is \(2.5 \mathrm{~K} \cdot \mathrm{kg} / \mathrm{mol}\).

Using data from Appendix 4, calculate \(\Delta G\) for the reaction $$2 \mathrm{H}_{2} \mathrm{~S}(g)+\mathrm{SO}_{2}(g) \rightleftharpoons 3 \mathrm{~S}_{\text {mombic }}(s)+2 \mathrm{H}_{2} \mathrm{O}(g)$$ for the following conditions at \(25^{\circ} \mathrm{C}\) : $$\begin{array}{l}P_{\mathrm{H}_{2} \mathrm{~S}}=1.0 \times 10^{-4} \mathrm{~atm} \\\P_{\mathrm{SO}_{2}}=1.0 \times 10^{-2} \mathrm{~atm} \\ P_{\mathrm{H}_{2} \mathrm{O}}=3.0 \times 10^{-2} \mathrm{~atm}\end{array}$$

For each of the following pairs of substances, which substance has the greater value of \(S^{\circ} ?\) a. \(C_{\text {graphite }}(s)\) or \(C_{\text {diamond }}(s)\) b. \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l)\) or \(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(\mathrm{g})\) c. \(\mathrm{CO}_{2}(s)\) or \(\mathrm{CO}_{2}(g)\)

If wet silver carbonate is dried in a stream of hot air, the air must have a certain concentration level of carbon dioxide to prevent silver carbonate from decomposing by the reaction $$\mathrm{Ag}_{2} \mathrm{CO}_{3}(s) \rightleftharpoons \mathrm{Ag}_{2} \mathrm{O}(s)+\mathrm{CO}_{2}(g)$$ \(\Delta H^{\circ}\) for this reaction is \(79.14 \mathrm{~kJ} / \mathrm{mol}\) in the temperature range of 25 to \(125^{\circ} \mathrm{C}\). Given that the partial pressure of carbon dioxide in equilibrium with pure solid silver carbonate is \(6.23 \times 10^{-3}\) torr at \(25^{\circ} \mathrm{C}\), calculate the partial pressure of \(\mathrm{CO}_{2}\) necessary to prevent decomposition of \(\mathrm{Ag}_{2} \mathrm{CO}_{3}\) at \(110 .{ }^{\circ} \mathrm{C}\). (Hint: Manipulate the equation in Exercise 71 .)

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