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The equilibrium constant \(K_{P}\) for the reaction $$ \mathrm{CO}(g)+\mathrm{Cl}_{2}(g) \rightleftharpoons \mathrm{COCl}_{2}(g) $$ is \(5.62 \times 10^{35}\) at \(25^{\circ} \mathrm{C}\). Calculate \(\Delta G_{\mathrm{f}}^{\circ}\) for \(\mathrm{COCl}_{2}\) at \(25^{\circ} \mathrm{C}\).

Short Answer

Expert verified
After calculating the expression, you would get that \(\Delta G_f^\circ \approx -289.78 \,kJ \cdot mol^{-1}\). This represents the Gibbs free energy change for the given reaction at \(25°C\).

Step by step solution

01

Convert Celsius to Kelvin

Firstly, we need to convert the temperature from Celsius to the Kelvin scale, because the formula for Gibbs free energy involves absolute temperature. It can be done by applying the formula, \(T(K) = T(°C) + 273.15\). Therefore, for \(T = 25°C\), in Kelvin it is \(298.15K\).
02

Identify Known Values

Next, recognize all known quantities from the exercise. We have the equilibrium constant \(K_P = 5.62 \times 10^{35}\), the universal gas constant \(R = 8.3145 \, JK^{-1}mol^{-1}\) or \(R = 0.0083145 \, kJ K^{-1} mol^{-1}\) for conciseness, and the temperature \(T = 298.15 K\) from the previous step.
03

Use the Formula

Now, use the relation \(\Delta G_f^\circ = -RT\ln K_P\) to calculate Gibbs free energy. Plug in the known values and compute the result.
04

Calculate the Gibbs Free Energy

By using the given equation and values, \(\Delta G_f^\circ = - (0.0083145 \, kJ K^{-1} mol^{-1}) \times (298.15 K) \times \ln(5.62 \times 10^{35})\), perform the calculation to obtain the value of \(\Delta G_f^\circ\).

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Equilibrium Constant
The equilibrium constant, often symbolized as \( K_P \) or \( K_c \), plays a pivotal role in determining the direction and extent of a chemical reaction. It is pivotal for understanding the balance between the reactants and products in a chemical equation. The equilibrium constant for the given reaction \( \mathrm{CO}(g) + \mathrm{Cl}_{2}(g) \rightleftharpoons \mathrm{COCl}_{2}(g) \) is reported as \(5.62 \times 10^{35}\), indicating a strong tendency for the formation of the product, \( \mathrm{COCl}_{2}(g) \).- **Interpreting the magnitude**: A very large \( K_P \) value signifies that, at equilibrium, the concentration of products greatly exceeds that of reactants. Hence, this reaction heavily favors the production of \( \mathrm{COCl}_{2} \).- **Dependency on temperature**: The equilibrium constant is temperature-dependent. This means any change in temperature could alter \( K_P \), affecting the balance of the equilibrium.Understanding the equilibrium constant helps predict how the system will respond to external changes, such as shifts in temperature.
Temperature Conversion
Converting temperature from Celsius to Kelvin is crucial when dealing with thermodynamic calculations, such as determining Gibbs Free Energy. This is because thermodynamic equations often require the absolute temperature, which is measured in Kelvin.- **Formula for conversion**: To convert from Celsius to Kelvin, use the formula: \[ T(K) = T(°C) + 273.15 \] This ensures that you are working with the correct temperature scale needed for accurate calculations.- **Example**: For \( T = 25^{\circ}C \), the equivalent in Kelvin is \[ 298.15 K \]Understanding and using the Kelvin scale prevents errors in thermodynamic calculations, such as those involving the Gibbs Free Energy.
Universal Gas Constant
The universal gas constant, denoted as \( R \), is a fundamental constant in thermodynamics that appears in various equations, including the formula for Gibbs Free Energy. Its values, depending on the units used, are:- **\(8.3145\, JK^{-1}mol^{-1}\)** or - **\(0.0083145\, kJ K^{-1} mol^{-1}\)**This constant relates energy scales to temperature scales, facilitating the conversion between different forms of energy. In the context of the Gibbs Free Energy calculation, \( R \) helps link the equilibrium constant \( K_P \) with the temperature \( T \), through the formula:\[\Delta G_f^\circ = -RT \ln K_P\]The choice of unit for \( R \) should match the units of the other parameters in the equation to ensure consistency and accuracy. It simplifies complex relationships, making calculations manageable and understandable.

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Most popular questions from this chapter

The standard enthalpy of formation and the standard entropy of gaseous benzene are \(82.93 \mathrm{~kJ} / \mathrm{mol}\) and \(269.2 \mathrm{~J} / \mathrm{K} \cdot\) mol, respectively. Calculate \(\Delta H^{\circ}, \Delta S^{\circ}\) and \(\Delta G^{\circ}\) for the process at \(25^{\circ} \mathrm{C}\). Comment on your answers. $$ \mathrm{C}_{6} \mathrm{H}_{6}(l) \longrightarrow \mathrm{C}_{6} \mathrm{H}_{6}(g) $$

Ammonium nitrate \(\left(\mathrm{NH}_{4} \mathrm{NO}_{3}\right)\) dissolves spontaneously and endothermically in water. What can you deduce about the sign of \(\Delta S\) for the solution process?

Describe two ways that you could measure \(\Delta G^{\circ}\) of a reaction.

Consider two carboxylic acids (acids that contain the \(-\mathrm{COOH}\) group \(): \mathrm{CH}_{3} \mathrm{COOH}\) (acetic acid, \(K_{\mathrm{a}}=1.8 \times 10^{-5}\) ) and \(\mathrm{CH}_{2} \mathrm{ClCOOH}\) (chloroacetic acid, \(K_{\mathrm{a}}=1.4 \times 10^{-3}\) ). (a) Calculate \(\Delta G^{\circ}\) for the ionization of these acids at \(25^{\circ} \mathrm{C}\) (b) From the equation \(\Delta G^{\circ}=\Delta H^{\circ}-T \Delta S^{\circ},\) we see that the contributions to the \(\Delta G^{\circ}\) term are an enthalpy term \(\left(\Delta H^{\circ}\right)\) and a temperature times entropy term \(\left(T \Delta S^{\circ}\right)\). These contributions are listed below for the two acids: Which is the dominant term in determining the value of \(\Delta G^{\circ}\) (and hence \(K_{\mathrm{a}}\) of the acid)? (c) What processes contribute to \(\Delta H^{\circ} ?\) (Consider the ionization of the acids as a Bronsted acid-base reaction.) (d) Explain why the \(T \Delta S^{\circ}\) term is more negative for \(\mathrm{CH}_{3} \mathrm{COOH}\).

(a) Over the years there have been numerous claims about "perpetual motion machines," machines that will produce useful work with no input of energy. Explain why the first law of thermodynamics prohibits the possibility of such a machine existing. (b) Another kind of machine, sometimes called a “perpetual motion of the second kind," operates as follows. Suppose an ocean liner sails by scooping up water from the ocean and then extracting heat from the water, converting the heat to electric power to run the ship, and dumping the water back into the ocean. This process does not violate the first law of thermodynamics, for no energy is created-energy from the ocean is just converted to electrical energy. Show that the second law of thermodynamics prohibits the existence of such a machine.

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