Titration – Complete Interactive Guide | EverExams

Titration – Complete Interactive Guide

Quantitative analytical technique for determining unknown concentrations through acid-base reactions

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SAFETY FIRST: Always wear appropriate PPE (goggles, gloves, lab coat) when performing titrations

Titration – Quantitative Analytical Technique

Titration is a quantitative analytical technique used to determine the concentration of an unknown solution by reacting it with a solution of known concentration. The principle behind titration involves the gradual addition of a titrant (the known solution) to a sample until a reaction reaches completion, indicated by a change that can be observed (such as a colour change, pH change, or precipitation).

What is Titration?

A laboratory method where a solution of known concentration (titrant) is used to determine the concentration of an unknown solution (analyte). The process involves adding the titrant gradually until the reaction is complete.

Principle

Based on stoichiometry – the exact volume of titrant needed to completely react with the analyte is measured. This volume is used to calculate the concentration of the unknown solution using the formula: M₁V₁ = M₂V₂ for 1:1 reactions.

Types of Titration

  • Acid-base titration (neutralization)
  • Redox titration (oxidation-reduction)
  • Precipitation titration
  • Complexometric titration

Titration Memory Tip

Remember: “Titration finds concentration through controlled reaction.” The key is measuring the exact volume needed for complete reaction.

Formula to remember: M₁V₁ = M₂V₂ (for 1:1 stoichiometry). Always check the mole ratio first!

Key Concepts in Titration

Equivalence Point

Definition: The point at which the amount of titrant added is exactly enough to completely neutralize the analyte (the unknown solution).

Characteristics:

  • Stoichiometrically complete reaction
  • Moles of titrant = moles of analyte (adjusted for stoichiometry)
  • Theoretical point, may not be directly observable
  • pH at equivalence point varies with acid/base strength

End Point

Definition: The point at which a noticeable change occurs (often indicated by a colour change due to an indicator), which is ideally close to the equivalence point.

Characteristics:

  • Experimentally observable
  • Should be as close as possible to equivalence point
  • Determined by indicator colour change
  • Slight difference from equivalence point is “indicator error”

Indicator

Definition: A substance that changes colour at (or near) the equivalence point, used to visually signal the end point of the titration.

Common Indicators:

  • Phenolphthalein: Colourless (acid) to pink (base), pH range 8.2-10.0
  • Methyl orange: Red (acid) to yellow (base), pH range 3.1-4.4
  • Bromothymol blue: Yellow (acid) to blue (base), pH range 6.0-7.6

pH Scale with Indicator Ranges

0 1 2 3 4 5 6 7 8 9 10 11 12 13 14
Methyl Orange (acidic range)
Bromothymol Blue (neutral range)
Phenolphthalein (basic range)

End Point vs Equivalence Point

Key Difference: Equivalence point is theoretical (moles acid = moles base). End point is experimental (when indicator changes colour).

Choosing an indicator: Select one whose colour change range includes the pH at the equivalence point of your specific titration.

Acid-Alkali Titration Types

Strong Acid with Strong Base

Example: HCl titrated with NaOH

Reaction: HCl + NaOH → NaCl + H₂O

Characteristics:

  • Sharp pH change at equivalence point
  • Equivalence point at pH 7
  • Suitable indicators: Phenolphthalein, Bromothymol blue
  • Most straightforward titration type

Indicator Choice:

Any indicator with pH range around 4-10 works well due to sharp pH change

Weak Acid with Strong Base

Example: CH₃COOH titrated with NaOH

Reaction: CH₃COOH + NaOH → CH₃COONa + H₂O

Characteristics:

  • Gradual pH change before equivalence
  • Equivalence point > pH 7 (basic)
  • Suitable indicator: Phenolphthalein (pH 8.2-10.0)
  • Forms buffer solution during titration

Indicator Choice:

Must change in basic range (phenolphthalein)

Strong Acid with Weak Base

Example: HCl titrated with Na₂CO₃ or NaHCO₃

Reaction: 2HCl + Na₂CO₃ → 2NaCl + CO₂ + H₂O

Characteristics:

  • Sharp initial pH drop
  • Equivalence point < pH 7 (acidic)
  • Suitable indicator: Methyl orange (pH 3.1-4.4)
  • CO₂ formation may affect accuracy

Indicator Choice:

Must change in acidic range (methyl orange)

Weak Acid with Weak Base

Example: CH₃COOH titrated with NH₃

Reaction: CH₃COOH + NH₃ → CH₃COONH₄

Characteristics:

  • No sharp pH change at equivalence
  • Difficult to choose suitable indicator
  • Potentiometric titration preferred
  • Equivalence point around pH 7

Indicator Choice:

Often no suitable visual indicator; use pH meter

Titration Type Memory Tip

Remember:

  • Strong-Strong: pH 7, any indicator works
  • Weak-Strong: pH > 7, use phenolphthalein
  • Strong-Weak: pH < 7, use methyl orange
  • Weak-Weak: No sharp change, use pH meter
The conjugate of a weak acid/base determines the pH at equivalence point.

Activity 1: Determining HCl Concentration with NaOH

Objective

Determine the exact strength of a prepared HCl solution using titration with 0.1 M NaOH solution.

Background

Titration is based on neutralization: acid + base → salt + water. The point of complete reaction (equivalence point) is detected using an indicator.

Safety Measures

  • Wear safety goggles, lab coat, and gloves
  • Handle concentrated HCl with extreme care in fume hood
  • Wash immediately if skin contact occurs
  • Neutralize spills with sodium bicarbonate

Theory

Acid-base neutralization: HCl + NaOH → NaCl + H₂O. At equivalence point: moles HCl = moles NaOH. Using M₁V₁ = M₂V₂ (1:1 stoichiometry).

Apparatus

  • Volumetric flask (250 cm³)
  • Burette (50 cm³)
  • Pipette (10 cm³)
  • Conical flask (250 cm³)
  • Graduated pipette (5 cm³)
  • Phenolphthalein indicator

Procedure

Step 1: Preparation of 0.1 M HCl Solution

Conc. HCl is approximately 12 M. Prepare 250 cm³ of 0.1 M HCl using dilution formula:

M₁V₁ = M₂V₂ → 12 × V₁ = 0.1 × 250 → V₁ = 2.08 cm³

Transfer 2.08 cm³ conc. HCl to 250 cm³ volumetric flask. Add distilled water to mark and shake well.

Step 2: Fill Burette

Rinse and fill burette with prepared HCl solution. Ensure no air bubbles in tip.

Step 3: Prepare NaOH Solution

Transfer 10 cm³ of standard 0.1 M NaOH solution to conical flask using pipette.

Step 4: Add Indicator

Add 2-3 drops of phenolphthalein indicator. Solution turns pink (basic).

Step 5: Titration

Slowly add HCl from burette while swirling flask. Continue until pink colour just disappears (colourless or very light pink).

Step 6: Record Volume

Record initial and final burette readings. Calculate volume of HCl used.

Step 7: Repeat

Repeat titration 2-3 times until concordant readings (±0.1 cm³) are obtained.

Observations

Sr. No. Initial Reading (cm³) Final Reading (cm³) Volume of HCl used (cm³)
1 0.0 10.0 10.0
2 10.0 20.0 10.0
3 20.0 30.0 10.0
Mean Volume (V₂): 10.0 cm³

Calculations

Given:

Molarity of NaOH (M₁) = 0.1 M

Volume of NaOH (V₁) = 10 cm³

Volume of HCl (V₂) = 10 cm³ (mean)

Molarity of HCl (M₂) = ?

Reaction: HCl + NaOH → NaCl + H₂O (1:1 mole ratio)


Using formula: M₁V₁/n₁ = M₂V₂/n₂

(0.1 × 10)/1 = (M₂ × 10)/1

1 = M₂ × 10

M₂ = 1/10 = 0.1 M

Result

The exact concentration of HCl solution is 0.1 M.

Post-Lab Discussion

  • The prepared HCl solution concentration matches the theoretical value (0.1 M)
  • Potential sources of error: Parallax error in readings, incomplete mixing, indicator error
  • Improvements: Use digital burette, pH meter for end point, more precise glassware

Short Questions with Answers

1. What is the difference between equivalence point and end point in titration?

Answer: The equivalence point is the theoretical point at which the amount of titrant added is exactly stoichiometrically equivalent to the amount of analyte present. It represents complete reaction. The end point is the experimental point where a detectable change (usually colour change of an indicator) occurs. The end point should ideally coincide with the equivalence point, but there may be a slight difference known as indicator error.

2. Why is phenolphthalein used as an indicator in the titration of a weak acid with a strong base, but not in the titration of a weak base with a strong acid?

Answer: Phenolphthalein changes colour in the pH range of 8.2-10.0 (colourless in acid, pink in base). In weak acid-strong base titrations, the equivalence point occurs at pH > 7 (basic) due to the formation of the conjugate base. Phenolphthalein’s colour change occurs within this basic range. In weak base-strong acid titrations, the equivalence point occurs at pH < 7 (acidic), so phenolphthalein would change colour before the equivalence point, giving inaccurate results. Methyl orange (pH range 3.1-4.4) is more suitable for weak base-strong acid titrations.

3. Calculate the volume of 0.1 M NaOH required to completely neutralize 25 cm³ of 0.2 M HCl.

Answer: Using the formula M₁V₁ = M₂V₂ (for 1:1 stoichiometry of NaOH and HCl):

M₁V₁ (acid) = M₂V₂ (base)

0.2 M × 25 cm³ = 0.1 M × V₂

5 = 0.1 × V₂

V₂ = 5 / 0.1 = 50 cm³

Therefore, 50 cm³ of 0.1 M NaOH is required to neutralize 25 cm³ of 0.2 M HCl.

4. What are concordant readings in titration and why are they important?

Answer: Concordant readings in titration are two or more volume readings that agree within a specified range (usually ±0.1 cm³). They are important because:

  1. They indicate the reliability and precision of the titration
  2. They help minimize random errors
  3. They provide a more accurate average value for calculations
  4. They confirm that the technique is consistent
  5. They validate that the end point is being detected consistently

Typically, at least two concordant readings are required, and the first rough titration is not included in calculating the mean.

5. Explain why the titration of a weak acid with a weak base does not have a sharp pH change at the equivalence point.

Answer: In weak acid-weak base titrations, both the acid and base are only partially dissociated. At the equivalence point, the salt formed (e.g., ammonium acetate from acetic acid and ammonia) undergoes hydrolysis of both cations and anions, resulting in a solution that is nearly neutral. The hydrolysis reactions buffer the pH change, preventing a sharp rise or fall. Since both conjugate acid and conjugate base are present and can react with added H⁺ or OH⁻ ions, the pH changes gradually throughout the titration. This gradual change makes it difficult to identify the exact equivalence point using visual indicators, which is why potentiometric titration (using a pH meter) is preferred for weak acid-weak base titrations.

Daily Life Applications of Titration

Pharmaceutical Industry

Quality control of drugs, determining active ingredient concentrations, testing purity of pharmaceutical products.

Water Treatment

Testing water hardness, chlorine content, pH adjustment, monitoring water quality in treatment plants.

Food & Beverage Industry

Determining acidity of fruit juices, vinegar, wine; testing fat content; quality control in food production.

Chemical Manufacturing

Quality control of raw materials and final products, concentration determination in chemical processes.

Environmental Monitoring

Testing acid rain, monitoring pollution levels, analyzing soil and water samples for contaminants.

Clinical Laboratory

Blood tests, cholesterol measurements, glucose monitoring, analysis of body fluids.

Real-World Connection

Everyday Examples:

  • Vinegar testing: Determining acetic acid concentration
  • Antacid tablets: Measuring acid-neutralizing capacity
  • Swimming pools: Testing and adjusting chlorine and pH levels
  • Winemaking: Measuring acidity for quality control
  • Soil testing: Determining lime requirement for agriculture

Titration Knowledge Quiz

Test your understanding of titration concepts with these 20 multiple choice questions. Select your answer and click submit to check your score.

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