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How To Calculate Ph Of Weak Acid Strong Base Titration

Henderson-Hasselbalch Equation:

\[ pH = pK_a + \log\left(\frac{[A^-]}{[HA]}\right) \]

(log K_a)
M
M

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1. What Is The Henderson-Hasselbalch Equation?

The Henderson-Hasselbalch equation is used to calculate the pH of a solution containing a weak acid and its conjugate base during titration. It provides a mathematical relationship between pH, pK_a, and the ratio of conjugate base to weak acid concentrations.

2. How Does The Calculator Work?

The calculator uses the Henderson-Hasselbalch equation:

\[ pH = pK_a + \log\left(\frac{[A^-]}{[HA]}\right) \]

Where:

Explanation: The equation describes the pH of a buffer solution and is particularly useful during the titration of a weak acid with a strong base, especially around the half-equivalence point.

3. Importance Of pH Calculation In Titration

Details: Accurate pH calculation during weak acid-strong base titration is crucial for determining equivalence points, understanding buffer regions, and predicting the shape of titration curves. This information is essential for analytical chemistry and biochemical applications.

4. Using The Calculator

Tips: Enter pK_a value (typically between 0-14), conjugate base concentration in molarity (M), and weak acid concentration in molarity (M). All concentrations must be non-negative, and weak acid concentration must be greater than zero.

5. Frequently Asked Questions (FAQ)

Q1: When is the Henderson-Hasselbalch equation most accurate?
A: The equation is most accurate when the concentrations of weak acid and conjugate base are similar, typically within the buffer region (pH = pK_a ± 1).

Q2: Can this equation be used at the equivalence point?
A: No, at the equivalence point of a weak acid-strong base titration, the solution contains only the conjugate base, and pH should be calculated using hydrolysis of the conjugate base.

Q3: What are typical pK_a values for common weak acids?
A: Acetic acid (4.76), formic acid (3.75), phosphoric acid (2.15, 7.20, 12.32), carbonic acid (6.35, 10.33).

Q4: Are there limitations to this equation?
A: The equation assumes ideal behavior, neglects activity coefficients, and becomes less accurate for very dilute solutions or when the acid is very weak or very strong.

Q5: How does temperature affect the calculation?
A: Temperature affects both pK_a values and the autoprotolysis constant of water (K_w), so pK_a values should be specified at the temperature of interest.

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