The solubility product \( K_{\text{sp}} \) for \( \text{Mg(OH)}_2 \) is given as \( 1.0 \times 10^{-11} \). The dissolution equilibrium for \( \text{Mg(OH)}_2 \) is:
\[ \text{Mg(OH)}_2 \rightleftharpoons \text{Mg}^{2+} + 2\text{OH}^- \] The concentration of \( \text{OH}^- \) ions required to precipitate \( \text{Mg(OH)}_2 \) can be found by solving for \( [\text{OH}^-] \) using the equation: \[ K_{\text{sp}} = [\text{Mg}^{2+}][\text{OH}^-]^2 \] Substitute \( [\text{Mg}^{2+}] = 0.1 \, \text{M} \) and \( K_{\text{sp}} = 1.0 \times 10^{-11} \): \[ 1.0 \times 10^{-11} = (0.1)[\text{OH}^-]^2 \] Solving for \( [\text{OH}^-] \): \[ [\text{OH}^-] = \sqrt{\frac{1.0 \times 10^{-11}}{0.1}} = \sqrt{1.0 \times 10^{-10}} = 1.0 \times 10^{-5} \, \text{M} \] The pOH is
given by:
\[ \text{pOH} = -\log[\text{OH}^-] = -\log(1.0 \times 10^{-5}) = 5 \] Thus, the pH is: \[ \text{pH} = 14 - \text{pOH} = 14 - 5 = 9 \]
At 15 atm pressure, $ \text{NH}_3(g) $ is being heated in a closed container from 27°C to 347°C and as a result, it partially dissociates following the equation: $ 2\text{NH}_3(g) \rightleftharpoons \text{N}_2(g) + 3\text{H}_2(g) $ If the volume of the container remains constant and pressure increases to 50 atm, then calculate the percentage dissociation of $ \text{NH}_3(g) $
If equilibrium constant for the equation $ A_2 + B_2 \rightleftharpoons 2AB \quad \text{is} \, K_p, $ then find the equilibrium constant for the equation $ AB \rightleftharpoons \frac{1}{2} A_2 + \frac{1}{2} B_2. $
Consider the following reaction: $ \text{CO}(g) + \frac{1}{2} \text{O}_2(g) \rightarrow \text{CO}_2(g) $ At 27°C, the standard entropy change of the process becomes -0.094 kJ/mol·K. Moreover, standard free energies for the formation of $ \text{CO}_2(g) $ and $ \text{CO}(g) $ are -394.4 and -137.2 kJ/mol, respectively. Predict the nature of the above chemical reaction.