๐ Titration Curves & Equivalence Points
๐ What is a Titration Curve?
A titration curve is a graph that shows how the pH of a solution changes when you slowly add one solution (the titrant) to another (the analyte). Usually, the x-axis is the volume of titrant added, and the y-axis is the pH of the mixture.
These curves help us visualize acid-base reactions and identify the equivalence point, where neutralization occurs.
๐งช 4 Regions on Every Titration Curve
- Start: Where the solution contains only acid or only base.
- Buffering Region: pH starts changing more slowly. There's a mix of acid and conjugate base or base and conjugate acid. This forms a buffer.
- Equivalence Point: Number of moles of acid = moles of base. Neutralization is complete!
- Post-Equivalence: Excess titrant dominates and pH spikes up or down.
⚖️ What is the Equivalence Point?
This is the **exact point** where the amount of acid added is exactly enough to neutralize the base — or vice versa. It’s usually right in the middle of the steep vertical rise in the titration curve.
Important: The pH at the equivalence point depends on the strength of acid/base involved:
- Strong acid + strong base → pH = 7
- Weak acid + strong base → pH > 7
- Strong acid + weak base → pH < 7
๐ฏ How to Read a pH Curve
- Starting pH = pH of acid/base alone
- Buffer zone = where pH rises slowly → use Henderson-Hasselbalch here
- Half-Equivalence Point = [HA] = [A⁻] → pH = pKa
- Equivalence point = where neutralization is complete
๐ Worked Example: Molar Mass from Titration
Q: A 0.675 g sample of HA was made into 100 mL solution. 25.0 mL was titrated with 0.100 M NaOH. It took 12.1 mL to reach the equivalence point. What is the molar mass of HA?
Step 1: Write balanced equation
Step 2: Moles of NaOH
Step 3: Moles of HA = moles of NaOH (1:1 ratio)
Step 4: Scale up to full solution
Step 5: Calculate molar mass
✅ Final Answer: 139.5 g/mol
๐จ Common Student Mistakes (And How to Fix Them)
- Wrong indicator? Use one that changes color at the correct pH.
- Adding titrant too fast? Near the endpoint, go drop-by-drop!
- Not swirling the flask? Uneven mixing = pH errors
- Reading burette wrong? Always view from eye-level and read from the bottom of the meniscus.
- Units confusion? You can use mL or L in C₁V₁ = C₂V₂, as long as they’re the same!
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