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Given that \(\Delta H_{\mathrm{t}}^{\circ}\) for \(\mathrm{HF}(a q)\) is \(-320.1 \mathrm{~kJ} / \mathrm{mol}\) and \(S^{\circ}\) for \(\mathrm{HF}(a q)\) is \(88.7 \mathrm{~J} / \mathrm{mol} \cdot \mathrm{K},\) find \(K_{\mathrm{a}}\) for \(\mathrm{HF}\) at \(25^{\circ} \mathrm{C}\)

Short Answer

Expert verified
Answer: The acid dissociation constant (Ka) for hydrofluoric acid (HF) at 25°C is approximately 1.2 x 10^6.

Step by step solution

01

Convert the temperature to Kelvin

In this exercise, the given temperature is 25°C, which needs to be converted to Kelvin. To do this, add 273.15 to the given temperature in Celsius: \(T(K) = 25 + 273.15 = 298.15~K\)
02

Calculate the Gibbs free energy change (ΔG°)

Now we can plug the given values of \(\Delta H_{\mathrm{t}}^{\circ}\), \(S^{\circ}\) and the temperature (T) into the equation for Gibbs free energy change: \(\Delta G^{\circ} = \Delta H_{\mathrm{t}}^{\circ} - T\Delta S^{\circ}\) \(\Delta G^{\circ} = (-320.1~kJ/mol) - (298.15~K)(88.7~J/mol\cdot K)\) First, note that we need to convert the entropy change from J/mol·K to kJ/mol·K to match the units of enthalpy change: \(S^{\circ} = 88.7~J / (mol\cdot K) \times \frac{1~kJ}{1000~J} = 0.0887~kJ / (mol\cdot K)\) Now, substitute the values and calculate \(\Delta G^{\circ}\): \(\Delta G^{\circ} = -320.1 - (298.15)(0.0887) = -320.1 - 26.4 = -346.5~kJ/mol\)
03

Calculate the acid dissociation constant (Ka)

With the obtained value of \(\Delta G^{\circ}\), we can now find the acid dissociation constant (\(K_{a}\)) using the equation: \(\Delta G^{\circ} = -RT\ln K_{\mathrm{a}}\) First, let's rearrange the equation to isolate \(K_{\mathrm{a}}\): \(\ln K_{\mathrm{a}} = -\frac{\Delta G^{\circ}}{RT}\) Next, we can plug in the values for \(\Delta G^{\circ}\), R (which is 8.314 J/(mol·K) or 0.008314 kJ/(mol·K)) and T: \(\ln K_{\mathrm{a}} = -\frac{-346.5~kJ/mol}{(0.008314~kJ/(mol\cdot K))(298.15~K)}\) Now calculate the natural logarithm of the \(K_{\mathrm{a}}\): \(\ln K_{\mathrm{a}} = 14.0\) Finally, we need to take the exponent of the natural logarithm to obtain the \(K_{\mathrm{a}}\): \(K_{\mathrm{a}} = e^{14.0} \approx 1.2 \times 10^6\) Therefore, the acid dissociation constant (\(K_{\mathrm{a}}\)) for HF at 25°C is approximately \(1.2 \times 10^6\).

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Most popular questions from this chapter

Consider the reaction $$ 2 \mathrm{SO}_{2}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{SO}_{3}(g) $$ (a) Calculate \(\Delta G^{\circ}\) at \(25^{\circ} \mathrm{C}\). (b) If the partial pressures of \(\mathrm{SO}_{2}\) and \(\mathrm{SO}_{3}\) are kept at 0.400 atm, what partial pressure should \(\mathrm{O}_{2}\) have so that the reaction just becomes nonspontaneous (i.e., \(\Delta G=\) \(+1.0 \mathrm{~kJ}) ?\)

The overall reaction that occurs when sugar is metabolized is $$ \mathrm{C}_{12} \mathrm{H}_{22} \mathrm{O}_{11}(s)+12 \mathrm{O}_{2}(g) \longrightarrow 12 \mathrm{CO}_{2}(g)+11 \mathrm{H}_{2} \mathrm{O}(l) $$ For this reaction, \(\Delta H^{\circ}\) is \(-5650 \mathrm{~kJ}\) and \(\Delta G^{\circ}\) is \(-5790 \mathrm{~kJ}\) $$ \text { at } 25^{\circ} \mathrm{C} $$ (a) If \(25 \%\) of the free energy change is actually converted to useful work, how many kilojoules of work are obtained when one gram of sugar is metabolized at body temperature, \(37^{\circ} \mathrm{C}\) ? (b) How many grams of sugar would a 120 -lb woman have to eat to get the energy to climb the Jungfrau in the Alps, which is \(4158 \mathrm{~m}\) high? \(\left(w=9.79 \times 10^{-3} \mathrm{mb},\right.\) where \(w=\) work in kilojoules, \(m\) is body mass in kilograms, and \(h\) is height in meters.)

Given the following data for sodium $$ \begin{array}{l} \mathrm{Na}(s): S^{\circ}=51.2 \mathrm{~J} / \mathrm{mol} \cdot \mathrm{K} \\ \mathrm{Na}(g): S^{\circ}=153.6 \mathrm{~J} / \mathrm{mol} \cdot \mathrm{K} \quad \Delta H_{\mathrm{f}}^{\circ}=108.7 \mathrm{~kJ} / \mathrm{mol} \end{array} $$ estimate the temperature at which sodium sublimes at 1 atm. $$ \mathrm{Na}(s) \rightleftharpoons \mathrm{Na}(g) $$

Consider the following reaction at \(25^{\circ} \mathrm{C}\) : $$ \mathrm{Cl}_{2}(g) \rightleftharpoons 2 \mathrm{Cl}(g) \quad K=1.0 \times 10^{-37} $$ (a) Calculate \(\Delta G^{\circ}\) for the reaction at \(25^{\circ} \mathrm{C}\). (b) Calculate \(\Delta G_{\mathrm{f}}^{\circ}\) for \(\mathrm{Cl}(g)\) at \(25^{\circ} \mathrm{C}\).

On the basis of your experience, predict which reactions are spontaneous: (a) \(\mathrm{PbO}_{2}(s) \longrightarrow \mathrm{Pb}(s)+\mathrm{O}_{2}(g)\) (b) \(\mathrm{N}_{2}(l) \longrightarrow \mathrm{N}_{2}(g)\) at \(25^{\circ} \mathrm{C}\) (c) \(\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(s) \longrightarrow \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}(l)\) at \(25^{\circ} \mathrm{C}\) (d) \(\mathrm{Ca}^{2+}(a q)+\mathrm{CO}_{3}^{2-}(a q) \longrightarrow \mathrm{CaCO}_{3}(s)\)

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