The standard Gibbs energy change for the reaction $$\mathrm{NH}_{3}(\mathrm{aq})+\mathrm{H}_{2} \mathrm{O}(1) \rightleftharpoons \mathrm{NH}_{4}^{+}(\mathrm{aq})+\mathrm{OH}^{-}(\mathrm{aq})$$ is \(29.05 \mathrm{kJ} \mathrm{mol}^{-1}\) at \(298 \mathrm{K}\). Use this thermodynamic quantity to decide in which direction the reaction is spontaneous when the concentrations of \(\mathrm{NH}_{3}(\mathrm{aq})\) \(\mathrm{NH}_{4}^{+}(\mathrm{aq}),\) and \(\mathrm{OH}^{-}(\mathrm{aq})\) are \(0.10 \mathrm{M}, 1.0 \times 10^{-3} \mathrm{M}\) and \(1.0 \times 10^{-3} \mathrm{M},\) respectively.

Short Answer

Expert verified
After comparing \( Q \) and \( K \), the direction of the spontaneous reaction is determined.

Step by step solution

01

Calculation of Equilibrium Constant from Gibbs Energy Change

Using the formula \( \Delta G = -RT \ln K \), where \(\Delta G\) is the standard Gibbs energy change (-29050 J/mol), \(R\) is the universal gas constant (8.314 J/(mol K)), and \(T\) is the temperature (298 K), one isolates \(K\) to find that \( K = \exp(-\Delta G / RT) \).
02

Calculation of Reaction Quotient

The reaction quotient is defined as \( Q = [NH_{4}^{+}][OH^{-}] / [NH_{3}][H_{2}O] \). As the concentration of water is essentially constant and large, it is usually neglected in the reaction quotient, so it simplifies to \( Q = [NH_{4}^{+}][OH^{-}] / [NH_{3}] \). The provided concentrations are then inserted into \( Q \) to calculate its value.
03

Determine Spontaneity of Reaction

The spontaneity of the reaction is determined by comparing \( Q \) and \( K \). If \( Q < K \), the reaction will proceed in the forward direction to reach equilibrium, because equilibrium lies to the right. If \( Q > K \), the reverse reaction is spontaneous, as equilibrium lies to the left. If \( Q = K \), the reaction is in equilibrium, and no net change occurs.

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Most popular questions from this chapter

Comment on the difficulties of solving environmental pollution problems from the standpoint of entropy changes associated with the formation of pollutants and with their removal from the environment.

At room temperature and normal atmospheric pressure, is the entropy of the universe positive, negative, or zero for the transition of carbon dioxide solid to liquid?

For one of the following reactions, \(K_{c} K_{p}=K .\) Identify that reaction. For the other two reactions, what is the relationship between \(K_{c}, \bar{K}_{\mathrm{p}},\) and \(K ?\) Explain. (a) \(2 \mathrm{SO}_{2}(\mathrm{g})+\mathrm{O}_{2}(\mathrm{g}) \rightleftharpoons 2 \mathrm{SO}_{3}(\mathrm{g})\) (b) \(\mathrm{HI}(\mathrm{g}) \rightleftharpoons \frac{1}{2} \mathrm{H}_{2}(\mathrm{g})+\frac{1}{2} \mathrm{I}_{2}(\mathrm{g})\) (c) \(\mathrm{NH}_{4} \mathrm{HCO}_{3}(\mathrm{s}) \rightleftharpoons \mathrm{NH}_{3}(\mathrm{g})+\mathrm{CO}_{2}(\mathrm{g})+\mathrm{H}_{2} \mathrm{O}(1)\)

If a reaction can be carried out only by electrolysis, which of the following changes in a thermodynamic property must apply: (a) \(\Delta H>0 ;\) (b) \(\Delta S>0\) (c) \(\Delta G=\Delta H ;\) (d) \(\Delta G>0 ?\) Explain.

Use the following data to estimate the standard molar entropy of gaseous benzene at \(298.15 \mathrm{K} ;\) that is, \(S^{\circ}\left[\mathrm{C}_{6} \mathrm{H}_{6}(\mathrm{g}, 1 \mathrm{atm})\right] .\) For \(\mathrm{C}_{6} \mathrm{H}_{6}(\mathrm{s}, 1 \mathrm{atm})\) at its melting point of \(5.53^{\circ} \mathrm{C}, S^{\circ}\) is \(128.82 \mathrm{Jmol}^{-1} \mathrm{K}^{-1}\). The enthalpy of fusion is \(9.866 \mathrm{kJ} \mathrm{mol}^{-1} .\) From the melting point to 298.15 K, the average heat capacity of liquid benzene is \(134.0 \mathrm{JK}^{-1} \mathrm{mol}^{-1} .\) The enthalpy of vaporization of \(\mathrm{C}_{6} \mathrm{H}_{6}(1)\) at \(298.15 \mathrm{K}\) is \(33.85 \mathrm{kJ} \mathrm{mol}^{-1},\) and in the vapor- ization, \(\mathrm{C}_{6} \mathrm{H}_{6}(\mathrm{g})\) is produced at a pressure of 95.13 Torr. Imagine that this vapor could be compressed to 1 atm pressure without condensing and while behaving as an ideal gas. Calculate \(S^{\circ}\left[\mathrm{C}_{6} \mathrm{H}_{6}(\mathrm{g}, 1 \text { atm) }] .[ \text { Hint: Refer to }\right.\) Exercise \(88,\) and note the following: For infinitesimal quantities, \(d S=d q / d T ;\) for the compression of an ideal gas, \(d q=-d w ;\) and for pressure-volume work, \(d w=-P d V\).

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