pH = pKa + log([salt]/[acid]) for acidic buffer (weak acid + conjugate base). Buffer resists pH change on small acid/base addition.
-- NCERT Class 11 Chemistry, Ch. 6, p. 42Buffer Solutions
Lesson
A buffer solution resists pH change when small amounts of acid or base are added. This is the property NEET tests — not equilibrium shifts, not Ksp, not Kp/Kc conversion, but the mechanism by which a weak acid–conjugate base (or weak base–conjugate acid) pair absorbs added H⁺ or OH⁻ without significant pH change.
Two types of buffer:
Acidic buffer — weak acid + its salt with a strong base (e.g., CH₃COOH + CH₃COONa). pH < 7.
Basic buffer — weak base + its salt with a strong acid (e.g., NH₄OH + NH₄Cl). pH > 7.
The Henderson-Hasselbalch equation (NCERT Class 11 Chemistry Chapter 7, page 42):
- Acidic buffer: pH = pKₐ + log₁₀([salt]/[acid])
- Basic buffer: pOH = pK_b + log₁₀([salt]/[base])
When [salt] = [acid], the log term vanishes and pH = pKₐ. This is the maximum buffer capacity point — a common NEET conceptual question.
How the buffer works: Add a small amount of strong acid → extra H⁺ reacts with the conjugate base (salt component), converting it to the weak acid. The ratio [salt]/[acid] shifts only slightly, so pH barely changes. Add a small amount of strong base → extra OH⁻ reacts with the weak acid, converting it to the conjugate base. Again, the ratio shifts only slightly.
Buffer capacity is finite. Once the weak acid or conjugate base component is consumed, the buffer fails and pH changes sharply. NEET may ask which buffer has higher capacity — it is the one with higher total concentrations of the acid-salt pair.
Watch-out: A solution of a strong acid + its salt (e.g., HCl + NaCl) is NOT a buffer. The weak-acid/weak-base component is essential. Identifying what qualifies as a buffer is a frequent recall question.
Practice MCQs
Select an option to see the explanation. Wrong answers show why your choice was tempting — and name the exact trap it exploits.
Which of the following pairs constitutes an acidic buffer solution?
Which of the following is a basic buffer?
For an acidic buffer, when [salt] = [acid], what is the pH of the solution?
The pKₐ of a weak acid HA is 4.75. A buffer is prepared with 0.10 M HA and 0.10 M NaA. What is the pH of this buffer?
A buffer is made from 0.20 M CH₃COOH (pKₐ = 4.76) and 0.02 M CH₃COONa. The pH of this buffer is:
When a small amount of HCl is added to a CH₃COOH / CH₃COONa buffer, which species neutralises the added H⁺?
Two acidic buffers are prepared:
The pKₐ of a weak acid HA is 5.00. A buffer is prepared with 0.10 M HA and 1.0 M NaA. The pH of this buffer is:
Quick recall before you leave
Worked Example
- 1
Given
- Weak base: NH₄OH, concentration = 0.20 M - Salt (conjugate acid): NH₄Cl, concentration = 0.20 M - pK_b = 4.74 - Temperature = 25 °C (so pH + pOH = 14)
- 2
Required
pH of the basic buffer.
- 3
Concept
This is a basic buffer (weak base + salt with strong acid). Use the Henderson-Hasselbalch equation for a basic buffer: pOH = pK_b + log₁₀([salt]/[base]). Then convert: pH = 14 − pOH.
- 4
Formula
pOH = pK_b + log₁₀([salt]/[base]) pH = 14 − pOH
- 5
Substitution
pOH = 4.74 + log₁₀(0.20/0.20)
- 6
Calculation
[salt]/[base] = 0.20/0.20 = 1 log₁₀(1) = 0 pOH = 4.74 + 0 = 4.74 Note on exact values: the ratio 1 and its logarithm 0 are exact mathematical values and do not affect significant-figure counting. pH = 14.00 − 4.74 = 9.26
- 7
Final answer
pH = 9.26
- 8
Common trap
The common error is forgetting to convert pOH to pH. A student who stops at pOH = 4.74 and reports it as the pH would give an acidic value for what is clearly a basic buffer — a quick sanity check (basic buffer → pH > 7) catches this.
- 9
Similar NEET-style question
Calculate the pH of a buffer made from 0.50 M NH₄OH (pK_b = 4.74) and 0.05 M NH₄Cl at 25 °C. (Answer: pOH = 4.74 + log(0.05/0.50) = 4.74 − 1 = 3.74; pH = 14 − 3.74 = 10.26.) ---
Before solving, remember these
Formulas
Henderson-Hasselbalch (buffer)
pH of acidic buffer in terms of conjugate base/acid concentrations. For basic buffer: pOH = pKb + log10([salt]/[base]).
| Symbol | Quantity | SI Unit |
|---|---|---|
| pKa | -log Ka | - |
| [salt] | conjugate base conc | mol/L |
| [acid] | weak acid conc | mol/L |
Valid when
- Buffer (weak acid + conjugate base)
- Concentrations not too dilute
- Approximate (assumes negligible dissociation)
Ka, Kb, Kw relationship
Stronger acid → weaker conjugate base, and vice versa. pKa + pKb = 14.
| Symbol | Quantity | SI Unit |
|---|---|---|
| Ka | acid dissociation | - |
| Kb | base dissociation | - |
| Kw | water 10^-14 | - |
Valid when
- Conjugate acid-base pair
- 25°C
Equilibrium constant K_p and K_c
Convert between pressure-based and concentration-based equilibrium constants. T in K; R = 0.0821 L atm/mol/K (when K_p in atm).
| Symbol | Quantity | SI Unit |
|---|---|---|
| K_p | pressure constant | - |
| K_c | concentration constant | - |
| Δn | mole change | - |
Valid when
- Gas-phase equilibrium
- Same temperature
Solubility product
Equilibrium constant for sparingly soluble salt. Q < K_sp: dissolves; Q > K_sp: precipitates.
| Symbol | Quantity | SI Unit |
|---|---|---|
| K_sp | solubility product | - |
Valid when
- Sparingly soluble salt
- Saturated solution
pH and pOH
Logarithmic acidity scale. Pure water at 25°C: pH = 7 = pOH.
| Symbol | Quantity | SI Unit |
|---|---|---|
| [H+] | hydrogen ion conc | mol/L |
| [OH-] | hydroxide conc | mol/L |
Valid when
- Aqueous solution
- Use Kw = 10^-14 at 25°C
Exam Traps & Common Mistakes
These are the exact patterns that cause wrong answers in NEET. Each trap includes when it triggers and how to avoid it.
Category: Overthinking
Student claims catalyst shifts equilibrium toward products. Catalyst speeds up forward AND reverse equally; equilibrium position unchanged.
When it triggers
Question lists catalyst addition among options for shifting equilibrium.
How to avoid
Catalyst lowers activation energy of BOTH forward and reverse reactions equally. Time to reach equilibrium decreases; equilibrium position is unchanged.
Category: Sign Convention
Δn = (mol gas product) - (mol gas reactant). Sign matters; K_p = K_c (RT)^Δn.
When it triggers
Convert K_p ↔ K_c for gas-phase reaction.
How to avoid
Count moles of gas only (ignore solids/liquids). Δn = product - reactant. If Δn = 0, K_p = K_c. If Δn = +1, K_p = K_c × RT.
Category: Similar Terms
For salt M_aX_b: K_sp = [M⁺]^a [X⁻]^b. Student uses [M⁺][X⁻] regardless of stoichiometry.
When it triggers
K_sp problem with non-1:1 salt (e.g. CaF₂, Mg(OH)₂, Ag₂CrO₄).
How to avoid
Write dissolution: M_aX_b → aM + bX. Then K_sp = [M]^a · [X]^b. For CaF₂ ↔ Ca + 2F: K_sp = s · (2s)² = 4s³.
Root cause: concept gap
Correction
Catalyst speeds up forward AND reverse equally. Equilibrium position is unchanged. Time to reach equilibrium decreases.
Root cause: concept gap
Correction
Δn = (moles GAS product) - (moles GAS reactant). Solids and liquids excluded.
Root cause: formula misuse
Correction
For M_aX_b: K_sp = [M]^a · [X]^b. CaF₂: K_sp = s · (2s)² = 4s³.
Root cause: concept gap
Correction
Increase P → shift toward FEWER moles of gas. Decrease P → shift toward MORE moles. Reactions with same number of moles of gas: P doesn't shift equilibrium.
Root cause: concept gap
Correction
Weak acid: only fraction ionises. [H+] ≈ √(Ka · C). For 0.1 M acetic acid (Ka ~10⁻⁵): [H+] ~10⁻³ (pH ~3), not 1 (pH=1).
Past Year Questions
15 questions from NEET 2021, 2022, 2023, 2024, 2025. Answers verified against NTA official keys.
C [A] = [B] = [C] = 2 × 10–3 M. Then, which of the following is correct?
Amongst the given options which of the following molecules/ ion acts as a Lewis acid?
Which complex compound is most stable?
How NEET usually asks this
Recurring question shapes from past papers. Each pattern shows why wrong options look tempting.
Convert between K_p and K_c using K_p = K_c (RT)^Δn. Identify Δn carefully.
Common distractors
wrong delta n sign
Counts moles incorrectly
Predict equilibrium shift on changing concentration, P, T, or adding catalyst.
Common distractors
treats catalyst as shifting
Believes catalyst shifts equilibrium
Compute pH of weak acid/base solution using Ka or Kb. Approximation: [H+] ≈ √(Ka·C).
Common distractors
ignores weak vs strong
Treats weak acid as fully dissociated
Compute solubility from K_sp or vice versa. Apply common-ion effect when relevant.
Common distractors
forgets stoichiometric coefficient power
Uses [M+]^1 [X-]^1 for M(X)_2 salt
Sources
Test yourself on this topic with real past-paper questions:
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