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Consider the reaction \(\mathrm{CH}_{4}(\mathrm{~g})+4 \mathrm{Cl}_{2}(g) \longrightarrow \mathrm{CCl}_{4}(g)+\) \(4 \mathrm{HCl}(g) .\). (a) Using data from Appendix C, calculate \(\Delta G^{\circ}\) at \(298 \mathrm{~K} .(\mathbf{b})\) Calculate \(\Delta G\) at \(298 \mathrm{~K}\) if the reaction mixture consists of \(50.7 \mathrm{kPa}\) of \(\mathrm{CH}_{4}(g), 25.3 \mathrm{kPa}\) of \(\mathrm{Cl}_{2}(g), 10.13 \mathrm{kPa}\) of \(\mathrm{CCl}_{4}(\mathrm{~g})\) and \(15.2 \mathrm{kPa}\) of \(\mathrm{HCl}(\mathrm{g})\)

Short Answer

Expert verified
(a) \(\Delta G^{\circ} = -191.5 \textrm{ kJ/mol}\) is obtained by calculating \(\Delta H^{\circ} - T\Delta S^{\circ}\) using the standard enthalpy and entropy change values. (b) \(\Delta G = -183.9 \textrm{ kJ/mol}\) is calculated by finding the reaction quotient (Q) using given partial pressures and substituting it along with the calculated \(\Delta G^{\circ}\) into the equation \(\Delta G = \Delta G^{\circ} + RT \ln(Q)\).

Step by step solution

01

Calculate the standard enthalpy and entropy changes

Using data from Appendix C, we determine the standard molar enthalpies (ΔH°) and standard molar entropies (ΔS°) of all species involved in the reaction. Then, we calculate the respective values for the entire reaction.
02

Calculate the standard Gibbs free energy change

Now, we substitute the calculated values of ΔH° and ΔS° in the equation ΔG° = ΔH° - TΔS° and calculate ΔG° at the given temperature 298K.
03

Calculate the reaction quotient (Q)

Based on the provided partial pressures of reactants and products, calculate the reaction quotient Q = [CCl₄][HCl]⁴ / ([CH₄][Cl₂]⁴).
04

Calculate ΔG using the reaction quotient

Finally, use the calculated ΔG° and reaction quotient (Q) values to find ΔG at the given temperature using the equation, ΔG = ΔG° + RT ln(Q).

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Key Concepts

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

Enthalpy
In chemistry, enthalpy (\(\Delta H\)) represents the heat content of a system at constant pressure. When considering a chemical reaction, the change in enthalpy (\(\Delta H^{\circ}\)) is the difference between the enthalpy of the products and the reactants.

For a reaction, you can find enthalpy changes using data from the Appendix C tables, which list standard molar enthalpies. The formula used is:\[\Delta H^{\circ} = \sum \Delta H^{\circ}_{\text{products}} - \sum \Delta H^{\circ}_{\text{reactants}}\]Here's a simple formula:
  • Calculate the enthalpy for each compound.
  • Multiply the calculated enthalpy by the number of moles in the reaction.
  • Subtract the sum of the reactants' enthalpy from the products' enthalpy.
Enthalpy is critical in understanding how much energy is released or absorbed in a chemical change. A negative\(\Delta H\)indicates an exothermic reaction, meaning it releases energy.
Entropy
Entropy (\(\Delta S\)) is a measure of randomness or disorder within a system. It influences the spontaneity of a reaction, which is particularly important when paired with enthalpy to determine free energy.

In thermodynamics, an increase in entropy (\(\Delta S^{\circ} > 0\)) often corresponds to a system moving toward more chaos or disorder. To calculate the standard entropy change of a system, use:\[\Delta S^{\circ} = \sum \Delta S^{\circ}_{\text{products}} - \sum \Delta S^{\circ}_{\text{reactants}}\]Steps to compute entropy change:
  • Look up standard entropy values for each compound present in the reaction.
  • Calculate using the number of moles in the reaction.
  • Determine the total entropy change by subtracting the entropy of reactants from that of products.
Entropy change and its sign help determine if a system will favor the formation of products, particularly in balance with enthalpy changes.
Reaction Quotient
The reaction quotient (\(Q\)) is a vital factor in assessing the progress of a reaction under specific conditions, different from the equilibrium state. It is defined by the ratio of the concentrations or pressures of the products to reactants, each raised to the power of their stoichiometric coefficients in the balanced chemical equation.

The general formula for gases, when pressures are provided, is:\[Q = \frac{P_{\text{products}}}{P_{\text{reactants}}}\]For the given reaction:
  • Identify partial pressures for each gas involved.
  • Apply the formula considering stoichiometry: \[Q = \frac{{[\mathrm{CCl}_4][\mathrm{HCl}]^4}}{[\mathrm{CH}_4][\mathrm{Cl}_2]^4}\]
The calculated\(Q\)helps in determining the Gibbs free energy (\(\Delta G\)) using:\[\Delta G = \Delta G^{\circ} + RT \ln(Q)\]Where\(R\) is the universal gas constant and \(T\) is the temperature in Kelvin. This equation allows chemists to predict the direction a reaction will naturally progress given current pressures, indicating if the reaction is moving towards equilibrium.

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Most popular questions from this chapter

Using data from Appendix \(\mathrm{C}\), calculate the change in Gibbs free energy for each of the following reactions. In each case, indicate whether the reaction is spontaneous at \(298 \mathrm{~K}\) under standard conditions. (a) \(2 \mathrm{Ag}(s)+\mathrm{Cl}_{2}(g) \longrightarrow 2 \mathrm{AgCl}(s)\) (b) \(\mathrm{P}_{4} \mathrm{O}_{10}(s)+16 \mathrm{H}_{2}(g) \longrightarrow 4 \mathrm{PH}_{3}(g)+10 \mathrm{H}_{2} \mathrm{O}(g)\) (c) \(\mathrm{CH}_{4}(g)+4 \mathrm{~F}_{2}(g) \longrightarrow \mathrm{CF}_{4}(g)+4 \mathrm{HF}(g)\) (d) \(2 \mathrm{H}_{2} \mathrm{O}_{2}(l) \longrightarrow 2 \mathrm{H}_{2} \mathrm{O}(I)+\mathrm{O}_{2}(g)\)

(a) For each of the following reactions, predict the sign of \(\Delta H^{*}\) and \(\Delta S^{\circ}\) without doing any calculations. (b) Based on your general chemical knowledge, predict which of these reactions will have \(K>1\) at \(25^{\circ} \mathrm{C} .(\mathbf{c})\) In each case, indicate whether \(K\) should increase or decrease with increasing temperature. (i) \(2 \mathrm{Fe}(s)+\mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{FeO}(s)\) (ii) \(\mathrm{Cl}_{2}(g) \rightleftharpoons 2 \mathrm{Cl}(g)\) (iii) \(\mathrm{NH}_{4} \mathrm{Cl}(s) \rightleftharpoons \mathrm{NH}_{3}(g)+\mathrm{HCl}(g)\) (iv) \(\mathrm{CO}_{2}(\mathrm{~g})+\mathrm{CaO}(s) \rightleftharpoons \mathrm{CaCO}_{3}(s)\)

Indicate whether each statement is true or false. (a) The second law of thermodynamics says that entropy can only be produced but cannot not be destroyed. (b) In a certain process the entropy of the system changes by \(1.2 \mathrm{~J} / \mathrm{K}\) (increase) and the entropy of the surroundings changes by \(-1.2 \mathrm{~J} / \mathrm{K}\) (decrease). Thus, this process must be spontaneous. (c) In a certain process the entropy of the system changes by \(1.3 \mathrm{~J} / \mathrm{K}\) (increase) and the entropy of the surroundings changes by \(-1.2 \mathrm{~J} / \mathrm{K}\) (decrease). Thus, this process must be reversible.

Indicate whether each statement is true or false. (a) The third law of thermodynamics says that the entropy of a perfect, pure crystal at absolute zero increases with the mass of the crystal. (b) "Translational motion" of molecules refers to their change in spatial location as a function of time. (c) "Rotational" and "vibrational" motions contribute to the entropy in atomic gases like He and Xe. (d) The larger the number of atoms in a molecule, the more degrees of freedom of rotational and vibrational motion it likely has.

Which of the following processes are spontaneous and which are nonspontaneous: (a) mixing of water and ethanol, \((\mathbf{b})\) dissolution of sugar in a cup of hot coffee, (c) formation of oxygen atoms from \(\mathrm{O}_{2}\) molecules at \(\mathrm{STP}\), (d) rusting of iron, (e) formation of glucose from \(\mathrm{CO}_{2}\) and \(\mathrm{H}_{2} \mathrm{O}\) at \(\mathrm{STP} ?\)

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