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π Stoichiometry of Weak Acid-Strong Base Titrations: A Detailed Explanation
Weak acid-strong base titrations involve the reaction of a weak acid with a strong base. The pH changes during the titration can be determined using stoichiometry and equilibrium calculations. This guide explains the process step-by-step, focusing on key points in the titration curve.
π― Objectives
- π¬ Understand the reaction between a weak acid and a strong base.
- π Calculate the pH at different stages of the titration (initial, before equivalence point, at equivalence point, after equivalence point).
- π§ͺ Interpret titration curves for weak acid-strong base titrations.
π§° Materials
- π§ͺ A weak acid solution (e.g., acetic acid, $CH_3COOH$).
- π§ A strong base solution (e.g., sodium hydroxide, $NaOH$).
- βοΈ Burette, beakers, and volumetric flasks.
- π‘οΈ pH meter or indicator.
π₯ Warm-up (5 mins)
- β Review the concepts of weak acids and strong bases.
- π€ Briefly discuss equilibrium constants ($K_a$) for weak acids.
- β Remind students of the definition of pH and its calculation.
π§ͺ Main Instruction
The titration of a weak acid with a strong base involves several key stages. Let's use acetic acid ($CH_3COOH$) titrated with sodium hydroxide ($NaOH$) as an example.
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π Initial pH:
Before any base is added, the pH is determined by the dissociation of the weak acid. Use an ICE table to calculate the $[H^+]$ concentration and then the pH.
Example: For 0.1 M $CH_3COOH$ ($K_a = 1.8 \times 10^{-5}$):
$CH_3COOH(aq) \rightleftharpoons H^+(aq) + CH_3COO^-(aq)$
ICE Table:
$CH_3COOH$ $H^+$ $CH_3COO^-$ Initial 0.1 0 0 Change -x +x +x Equilibrium 0.1-x x x $K_a = \frac{[H^+][CH_3COO^-]}{[CH_3COOH]} = \frac{x^2}{0.1-x} = 1.8 \times 10^{-5}$
Assuming x is small, $x = \sqrt{1.8 \times 10^{-6}} = 0.00134$
$pH = -log(0.00134) = 2.87$
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β Before the Equivalence Point:
The solution contains a mixture of the weak acid and its conjugate base. Use the Henderson-Hasselbalch equation to calculate the pH.
$pH = pK_a + log(\frac{[A^-]}{[HA]})$
Where $pK_a = -log(K_a)$, $[A^-]$ is the concentration of the conjugate base ($CH_3COO^-$), and $[HA]$ is the concentration of the weak acid ($CH_3COOH$).
Example: After adding 10 mL of 0.1 M $NaOH$ to 100 mL of 0.1 M $CH_3COOH$, calculate the new moles of $CH_3COOH$ and $CH_3COO^-$ and then use the Henderson-Hasselbalch equation.
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βοΈ At the Equivalence Point:
The weak acid has been completely neutralized, and the solution contains only the conjugate base. The pH is determined by the hydrolysis of the conjugate base.
$CH_3COO^-(aq) + H_2O(l) \rightleftharpoons CH_3COOH(aq) + OH^-(aq)$
Calculate the concentration of $CH_3COO^-$ and use an ICE table with $K_b$ to find $[OH^-]$ and then calculate pOH and pH.
$K_b = \frac{K_w}{K_a}$
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β
After the Equivalence Point:
The solution contains the conjugate base and excess strong base. The pH is determined primarily by the excess strong base.
Calculate the concentration of the excess $OH^-$ and then calculate pOH and pH.
π Assessment
Solve the following problems to assess your understanding:
- β What is the pH of a 0.2 M solution of formic acid ($HCOOH$), $K_a = 1.8 \times 10^{-4}$?
- π§ͺ 25 mL of 0.1 M $NaOH$ is added to 50 mL of 0.1 M $CH_3COOH$. What is the pH of the solution?
- π What is the pH at the equivalence point when 50 mL of 0.1 M $CH_3COOH$ is titrated with 0.1 M $NaOH$?
- β What is the pH after adding 60 mL of 0.1 M $NaOH$ to 50 mL of 0.1 M $CH_3COOH$?
- π€ Sketch the titration curve for a weak acid-strong base titration, labeling the buffer region and equivalence point.
- β Explain why the pH at the equivalence point of a weak acid-strong base titration is greater than 7.
- π‘ How does the $K_a$ of a weak acid affect the shape of the titration curve?
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