The value of \(K_{a}\) for nitrous acid \(\left(\mathrm{HNO}_{2}\right)\) at \(25^{\circ} \mathrm{C}\) is given in Appendix D. (a) Write the chemical equation for the equilibrium that corresponds to \(K_{a}\). (b) By using the value of \(K_{a}\), calculate \(\Delta G^{\circ}\) for the dissociation of nitrous acid in aqueous solution. (c) What is the value of \(\Delta G\) at equilibrium? (d) What is the value of \(\Delta G\) when \(\left[\mathrm{H}^{+}\right]=5.0 \times 10^{-2} \mathrm{M}\) \(\left[\mathrm{NO}_{2}^{-}\right]=6.0 \times 10^{-4} \mathrm{M},\) and \(\left[\mathrm{HNO}_{2}\right]=0.20 \mathrm{M} ?\)

Short Answer

Expert verified
(a) The chemical equation for the equilibrium corresponding to Kₐ is: HNO₂(aq) ⇌ H⁺(aq) + NO₂⁻(aq). (b) By using the value of Kₐ, we can calculate ΔG° for the dissociation of nitrous acid using the formula ΔG° = -RT ln(Kₐ), and it gives approximately 29.86 kJ/mol. (c) At equilibrium, the value of ΔG is 0. (d) With the given concentrations, we first calculate the reaction quotient Q and then find ΔG using the formula ΔG = ΔG° + RT ln(Q). The value of ΔG will be approximately -7.80 kJ/mol.

Step by step solution

01

a) Chemical equation for equilibrium corresponding to Kₐ

Firstly, we should understand what Kₐ is. Kₐ is the acid dissociation constant for an acid, which shows the strength of the acid. We're dealing with nitrous acid (HNO₂) as our given acid in this exercise. The chemical equation for the dissociation of HNO₂ in water can be written as: HNO₂(aq) ⇌ H⁺(aq) + NO₂⁻(aq) From the equation, we can express Kₐ: Kₐ = \(\frac{[H^+][NO_2^-]}{[HNO_2]}\)
02

b) Calculate the standard Gibbs free energy change (ΔG°)

Next, we will relate Kₐ with the standard Gibbs free energy change (ΔG°) via the following equation: ΔG° = -RT ln(Kₐ) where R is the gas constant (8.314 J/mol·K), T is the temperature in Kelvin, and Kₐ is the acid dissociation constant for nitrous acid. First, we must convert the temperature given (25°C) to Kelvin: T = 25 + 273.15 = 298.15 K Now, use the given Kₐ value (4.50 x 10⁻⁴) to calculate ΔG°: ΔG° = - (8.314 J/mol·K) (298.15 K) ln(4.50 x 10⁻⁴) This will give you the value for the standard Gibbs free energy change.
03

c) Value of ΔG at equilibrium

At equilibrium, the reaction quotient Q is equal to the equilibrium constant Kₐ. Therefore, the value of ΔG at equilibrium is 0, as it indicates that the reaction is in equilibrium and there is no net change in the system.
04

d) Calculate the value of ΔG with given concentrations

Now, we are given concentrations for H⁺, NO₂⁻, and HNO₂ in the solution. We first need to calculate the reaction quotient Q: Q = \(\frac{[H^+][NO_2^-]}{[HNO_2]}\) Q = \(\frac{(5.0 \times 10^{-2}M)(6.0 \times 10^{-4}M)}{0.20 M}\) Next, we calculate ΔG based on the reaction quotient Q using the following formula: ΔG = ΔG° + RT ln(Q) By substituting the values of ΔG°, R, and T calculated earlier, and the newly calculated value of Q, we can now find the value of ΔG.

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Most popular questions from this chapter

The oxidation of glucose \(\left(\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}\right)\) in body tissue produces \(\mathrm{CO}_{2}\) and \(\mathrm{H}_{2} \mathrm{O} .\) In contrast, anaerobic decomposition, which occurs during fermentation, produces ethanol \(\left(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}\right)\) and \(\mathrm{CO}_{2} .\) (a) Using data given in Appendix \(\mathrm{C}\), compare the equilibrium constants for the following reactions: $$ \begin{aligned} \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s)+6 \mathrm{O}_{2}(g) & \rightleftharpoons 6 \mathrm{CO}_{2}(g)+6 \mathrm{H}_{2} \mathrm{O}(l) \\ \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s) & \rightleftharpoons 2 \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{OH}(l)+2 \mathrm{CO}_{2}(g) \end{aligned} $$ (b) Compare the maximum work that can be obtained from these processes under standard conditions.

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