Problem 70
Question
Consider the titration of \(\mathrm{HF}\left(K_{\mathrm{a}}=6.7 \times 10^{-4}\right)\) with \(\mathrm{NaOH}\). What is the \(\mathrm{pH}\) when a third of the acid has been neutralized?
Step-by-Step Solution
Verified Answer
Answer: The pH of the solution is approximately 3.05 when one-third of the acid has been neutralized.
1Step 1: Determine the Moles of HF and F- after Neutralization
Let's assume that the initial number of moles of HF is x. After one-third of the moles of HF have been neutralized by NaOH, we will have 2x/3 moles of HF and x/3 moles of F-
2Step 2: Setting up the Equation for H+ Concentration
Now, we can set up the equation for the H+ concentration. The acid dissociation constant, Ka, is given by the following expression:
$$
K_a = \frac{[\mathrm{H}^{+}][\mathrm{F}^{-}]}{[\mathrm{HF}]}
$$
We are given the value of Ka for HF, which is \(6.7 \times 10^{-4}\). From step 1, we know the concentrations of HF and F-. Let's substitute these values into the Ka expression to find the concentration of H+:
$$
6.7 \times 10^{-4} = \frac{[\mathrm{H}^{+}]\frac{x}{3}}{\frac{2x}{3}}
$$
3Step 3: Solve for H+ Concentration
Now, we can solve the equation for the H+ concentration.
$$
[\mathrm{H}^{+}] = 6.7 \times 10^{-4} \times \frac{\frac{2x}{3}}{\frac{x}{3}} = \frac{4}{3}(6.7 \times 10^{-4})
$$
After calculating the value, we get:
$$
[\mathrm{H}^{+}] = 8.93 \times 10^{-4} \thinspace \mathrm{M}
$$
4Step 4: Calculate the pH of the Solution
Finally, we can use the H+ concentration to calculate the pH of the solution using the following formula:
$$
\mathrm{pH} = -\log[\mathrm{H}^{+}]
$$
Substituting the H+ concentration, we get:
$$
\mathrm{pH} = -\log(8.93 \times 10^{-4})
$$
After calculating, the pH of the solution is about 3.05 when one-third of the acid has been neutralized.
Key Concepts
Acid-Base EquilibriumpH CalculationAcid Dissociation Constant
Acid-Base Equilibrium
Acid-base equilibrium involves the balance between acid and base species in a solution. In our titration problem, we're dealing with hydrofluoric acid (HF) and sodium hydroxide (NaOH). As NaOH, a strong base, is added to the HF solution, it starts converting HF molecules into their conjugate base, the fluoride ion (
F^-
). This is how the equilibrium shifts:
- HF (acid) reacts with OH⁻ (base from NaOH) to produce F⁻ and water.
- This neutralization causes HF to decrease and F⁻ to increase.
pH Calculation
The pH value represents how acidic or basic a solution is. It's calculated from the concentration of hydrogen ions ([H⁺]) in the solution using the formula: \[\text{pH} = -\log[H^+]\]In the given exercise, after a portion of HF is neutralized by NaOH, we solve for [H⁺] through equilibrium expressions. First, we use the expression for the acid dissociation constant and rearrange to solve for [H⁺]:
- Plug in known concentrations and K_a value into the equation: \[K_a = \frac{[H^+][F^-]}{[HF]}\]
- Resolve it to find [H⁺] using simple algebraic manipulations.
- This ultimately gives [H^+] = 8.93 \times 10^{-4} \thinspace M.
Acid Dissociation Constant
The acid dissociation constant, K_a, is essential for understanding an acid's strength in water. It quantifies how readily an acid donates a proton to form its conjugate base. In our HF titration example, K_a is critical for calculating hydrogen ion concentration:
- K_a indicates how much HF dissociates into H^+ and F^- in solution: \[K_a = \frac{[H^+][F^-]}{[HF]}\]
- A higher K_a means a stronger acid because more of the acid is dissociated.
- Here, HF has a K_a of 6.7 \times 10^{-4}, indicating it's weaker than strong acids like HCl but not negligible.
Other exercises in this chapter
Problem 66
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Four grams of a monoprotic weak acid are dissolved in water to make \(250.0 \mathrm{~mL}\) of solution with a pH of \(2.56\). The solution is divided into two e
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Explain why it is not possible to prepare a buffer with a pH of \(6.50\) by mixing \(\mathrm{NH}_{3}\) and \(\mathrm{NH}_{4} \mathrm{Cl}\).
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