pH, Ka, Kb and Percent Ionization

In the chemistry lab there is an aqueous solution of nitric acid, $\mathrm{HNO_3}$, of concentration $0.025\,\mathrm{mol\times L^{-1}}$ at $25\,^\circ\mathrm{C}$. Given that nitric acid behaves as a strong monoprotic acid that dissociates completely in water and that the ionic product of water is $K_\mathrm{w} = 1.0\times 10^{-14}$ at that temperature, assume ideal behavior where $\mathrm{pH} = -\log[\mathrm{H_3O^+}]$. Calculate: a) The concentration of hydronium ions, $[\mathrm{H_3O^+}]$, and the value of the $\mathrm{pH}$ of the solution. b) The concentration of hydroxide ions, $[\mathrm{OH^-}]$, present in the medium. Use the ideal model and neglect the autoprotolysis of water where that approximation is valid.

An aqueous solution is prepared by dissolving $0.171\,\mathrm{g}$ of barium hydroxide, $\mathrm{Ba(OH)_2}$, in distilled water to make an exact volume of $500\,\mathrm{mL}$ at $25\,^\circ\mathrm{C}$. This compound is assumed to be a strong base that dissociates completely according to the process $\mathrm{Ba(OH)_2(s) \rightarrow Ba^{2+}(aq) + 2\,OH^-(aq)}$. Molar mass of $\mathrm{Ba(OH)_2}$: $171.3\,\mathrm{g\times mol^{-1}}$; $K_\mathrm{w} = 1.0\times 10^{-14}$. Under the ideal approximation, determine: a) The molar concentration of $\mathrm{OH^-}$ ions in the resulting solution. b) The $\mathrm{pOH}$ and the $\mathrm{pH}$ of the final solution. Use the ideal model and neglect the autoprotolysis of water where that approximation is valid.

Ammonia, $\mathrm{NH_3}$, acts in aqueous solution as a weak base with a base dissociation constant $K_\mathrm{b} = 1.8\times 10^{-5}$ at $25\,^\circ\mathrm{C}$. Consider the proton transfer equilibrium with water for the species ammonia and for its conjugate acid, the ammonium ion ($\mathrm{NH_4^+}$). The ion-product constant of water is $K_\mathrm{w} = 1.0\times 10^{-14}$ at that temperature. a) Write the acid dissociation reaction of the ammonium ion in water and deduce the mathematical relationship between $K_\mathrm{a}(\mathrm{NH_4^+})$, $K_\mathrm{b}(\mathrm{NH_3})$ and $K_\mathrm{w}$. b) Calculate the numerical value of $K_\mathrm{a}$ for the ammonium ion and justify which of the two species reacts to a greater extent with water at equal initial concentration, by comparing their respective constants. Use the ideal model and neglect the autoionization of water where that approximation is valid.

You have an aqueous solution of methylamine, $\mathrm{CH_3NH_2}$, of concentration $0.050\,\mathrm{mol\times L^{-1}}$ at $25\,^\circ\mathrm{C}$. The basicity constant of methylamine is $K_\mathrm{b} = 4.4\times 10^{-4}$ at that temperature and the ionic product of water is $K_\mathrm{w} = 1.0\times 10^{-14}$. a) Set out the ionization equilibrium in water, express the constant $K_\mathrm{b}$ in terms of the initial concentration $c_0$ and the degree of dissociation $\alpha$, and check quantitatively whether the approximation $1 - \alpha \approx 1$ is applicable using the $5\%$ criterion. b) Calculate the value of the degree of dissociation $\alpha$, the concentration of all species at equilibrium and the $\mathrm{pH}$ of the solution, assuming ideal behavior. Use the ideal model and neglect the autoprotolysis of water where that approximation is valid.

Chloroacetic acid, $\mathrm{CH_2ClCOOH}$, is used in organic synthesis. At $25\,^\circ\mathrm{C}$, an aqueous solution of this acid with a concentration $c_0 = 0.010\,\mathrm{mol\times L^{-1}}$ has an acidity constant $K_\mathrm{a} = 1.4\times 10^{-3}$. a) Write the chemical equation for the ionization equilibrium and calculate the concentration of $[\mathrm{H_3O^+}]$ by solving the full quadratic equation. State explicitly the percentage error in $[\mathrm{H_3O^+}]$, relative to the value from the quadratic solution, that would be made if the dissociated amount were neglected compared with the initial concentration. b) Determine the $\mathrm{pH}$ of the solution and the percentage of acid that remains in molecular, undissociated form at equilibrium. Use the ideal model and neglect the autoprotolysis of water where that approximation is valid.

Two aqueous solutions at $25\,^\circ\mathrm{C}$, labeled A and B, are available in the lab, both of concentration $0.050\,\mathrm{mol\times L^{-1}}$. Solution A contains formic acid, $\mathrm{HCOOH}$ ($K_\mathrm{a} = 1.8\times 10^{-4}$), and solution B contains acetic acid, $\mathrm{CH_3COOH}$ ($K_\mathrm{a} = 1.8\times 10^{-5}$). Consider ideal solutions with $K_\mathrm{w} = 1.0\times 10^{-14}$. a) Calculate the percentage degree of dissociation and the $\mathrm{pH}$ of both solutions, justifying which will conduct electric current better. b) If $0.0050\,\mathrm{mol}$ of solid sodium acetate ($\mathrm{CH_3COONa}$, a strong electrolyte) is added, with no change in volume, to $100\,\mathrm{mL}$ of solution B, calculate the new value of $\mathrm{pH}$ and explain the change in the degree of dissociation using Le Chatelier's principle. To compare conductivity, consider the contribution of the hydronium ion to be predominant and the mobilities of the two anions to be comparable. Use the ideal model and neglect the autoprotolysis of water where that approximation is valid.

In the laboratory, a volumetric flask is prepared with $100\,\mathrm{mL}$ of an aqueous solution of a weak monoprotic acid $\mathrm{HA}$ of concentration $0.10\,\mathrm{mol\times L^{-1}}$, whose acidity constant is $K_\mathrm{a} = 1.8\times 10^{-5}$ at $25\,^\circ\mathrm{C}$. This sample is then transferred in its entirety to another flask and diluted with distilled water to a final volume of $1000\,\mathrm{mL}$. The diagram of the dilution process and the associated parameters are shown below:

. At $25\,^\circ\mathrm{C}$ and assuming an ideal solution with $\mathrm{pH} = -\log[\mathrm{H_3O^+}]$, determine: a) The degree of dissociation, $\alpha_1$, and the $\mathrm{pH}$ of the initial concentrated solution. b) The degree of dissociation, $\alpha_2$, and the $\mathrm{pH}$ of the resulting dilute solution, justifying the effect of dilution on the degree of ionization using Le Chatelier's principle or Ostwald's law. Use the ideal model and neglect the autoprotolysis of water where that approximation is valid.

A laboratory reactor is filled with a mixture of $250\,\mathrm{mL}$ of an aqueous solution of hydrochloric acid, $\mathrm{HCl}$, of concentration $0.060\,\mathrm{mol\times L^{-1}}$ and $150\,\mathrm{mL}$ of an aqueous solution of barium hydroxide, $\mathrm{Ba(OH)_2}$, of concentration $0.040\,\mathrm{mol\times L^{-1}}$ at $25\,^\circ\mathrm{C}$. Assume that the volumes are additive (final volume $400\,\mathrm{mL}$), that both substances behave as strong electrolytes that are fully dissociated, and that $K_\mathrm{w} = 1.0\times 10^{-14}$ at that temperature in an ideal solution. a) Write the net ionic neutralization reaction and determine, with justification, which reagent is in excess, quantifying the moles remaining. b) Calculate the molar concentration of all the ionic species present in the resulting mixture ($\mathrm{H_3O^+}$, $\mathrm{OH^-}$, $\mathrm{Ba^{2+}}$ and $\mathrm{Cl^-}$) and determine the $\mathrm{pH}$ of the final solution. Use the ideal model and neglect the autoprotolysis of water where that approximation is valid.

A pure sample of $1,220\,\mathrm{g}$ of an unknown solid weak monoprotic acid, $\mathrm{HA}$, is dissolved in distilled water to a total volume of $250\,\mathrm{mL}$ at $25\,^\circ\mathrm{C}$. The $\mathrm{pH}$ of the resulting solution is measured experimentally with a calibrated pH meter, giving a value of $3.11$. In a separate total neutralization experiment, it is found that the whole $250\,\mathrm{mL}$ of this solution requires exactly $20.0\,\mathrm{mL}$ of standard solution of $\mathrm{NaOH}$ $0.500\,\mathrm{mol\times L^{-1}}$ to reach the stoichiometric equivalence point. Assuming an ideal solution with $\mathrm{pH} = -\log[\mathrm{H_3O^+}]$, determine: a) The molar mass of the unknown weak monoprotic acid. b) The acid dissociation constant $K_\mathrm{a}$ of the acid and its degree of dissociation $\alpha$ in the prepared solution, and justify whether the classical equilibrium approximation was valid. Use the ideal model and neglect the autoprotolysis of water where that approximation is valid.