A weak acid HA has degree of dissociation x. Which option gives the correct expression of pH - pKₐ ?

Solution & Explanation

Related Formula

For a weak acid solution:

HA leftharpoons H^+ + A^- Kₐ = [H^+][A^-][HA]
Step 1: Expressing Concentration

Let the initial concentration be a. At equilibrium:

[HA] = a(1-x), [H^+] = ax, [A^-] = ax

Substituting into the equilibrium expression:

Kₐ = ((ax)(x))/(1-x) = [H^+] ((x)/(1-x))
Step 2: Logarithmic Rearrangement

Taking negative logarithms on both sides:

- Kₐ = - [H^+] - ((x)/(1-x)) pKₐ = pH - ((x)/(1-x)) pH - pKₐ = ((x)/(1-x))
Pattern Recognition

Sees: pH - pKₐ for weak acid equilibrium. Shortcut: This is equivalent to the Henderson-Hasselbalch framework: pH = pKₐ + [Salt][Acid] = pKₐ + (x)/(1-x).

Chapter Mix

Class 11 Chemistry: Ionic Equilibrium

Reference Study Guides

More Ionic Equilibrium Previous-Year Questions — Page 2

Q72 jee_main_2026_24_january_morning Precipitation and pH Dependence
Consider two Group IV metal ions X²⁺ and Y²⁺. A solution containing 0.01 M X²⁺ and 0.01 M Y²⁺ is saturated with H₂S. The pH at which the metal sulphide YS will form as a precipitate is ____ (Nearest integer) (Given : Kₛₚ(XS) = 1 × 10⁻²² at 25°C, Kₛₚ(YS) = 4 × 10⁻¹⁶ at 25°C, [H₂S] = 0.1 M in solution, Kₐ₁ × Kₐ₂(H₂S) = 1.0 × 10⁻²¹, 2 = 0.30, 3 = 0.48, 5 = 0.70)
Numerical Answer. Answer: 4 to 4

Solution

Related Formula
For precipitation: [M²⁺][S²⁻] ≥ Kₛₚ [S²⁻] = Kₐ₁ · Kₐ₂ · [H₂S][H^+]²
Core Logic

For precipitation of YS(s): [Y²⁺][S²⁻] ≥ Kₛₚ(YS) [S²⁻] ≥ 4 × 10⁻¹⁶0.01 = 4 × 10⁻¹⁴ M

Since H₂S dissociates in water: H₂S leftharpoons 2H^+ + S²⁻ [S²⁻][H^+]²[H₂S] = Kₐ₁ × Kₐ₂ = 1.0 × 10⁻²¹

Substitute the [S²⁻] threshold: [S²⁻] = 1.0 × 10⁻²¹ × [H₂S][H^+]² ≥ 4 × 10⁻¹⁴

Step 1: Calculate pH

Using [H₂S] = 0.1 M: 10⁻²¹ × 0.1[H^+]² = 4 × 10⁻¹⁴ 10⁻²²[H^+]² = 4 × 10⁻¹⁴ [H^+]² = 10⁻²²4 × 10⁻¹⁴ = (1)/(4) × 10⁻⁸ = 0.25 × 10⁻⁸ = 25 × 10⁻¹⁰ [H^+] = 5 × 10⁻⁵ M

pH = - (5 × 10⁻⁵) = 5 - 5 = 5 - 0.70 = 4.3 Rounding to the nearest integer, pH ≈ 4.

Pattern Recognition

Equating the S²⁻ concentration required for Kₛₚ with the S²⁻ provided by the H₂S equilibrium directly links solubility product to pH.

Chapter Mix

Class 11 Chemistry: Equilibrium Class 12 Chemistry: Qualitative Analysis

Q55 jee_main_2026_24_january_evening Le Chatelier's Principle and Equilibrium Constant
Consider the following gaseous equilibrium in a closed container of volume "V" at T(K). P _ 2 (g) + Q _ 2 (g) leftharpoons 2 PQ (g) 2 moles each of P₂(g) , Q₂(g) and PQ (g) are present at equilibrium. Now one mole each of ' P₂ ' and ' Q₂ ' are added to the equilibrium keeping the temperature at T(K). The number of moles of P₂ , Q₂ and PQ at the new equilibrium, respectively, are -
  • A. 2.67, 2.67, 2.67
  • B. 1.21, 2.24, 1.56
  • C. 1.66, 1.66, 1.66
  • D. 2.56, 1.62, 2.24

Solution

Core Logic
P₂(g) + Q₂(g) leftharpoons 2PQ(g)

Initially at equilibrium (t = teq): 2 mole, 2 mole, 2 mole.

Calculate Keq:

Keq = [PQ]²[P₂][Q₂] = 2²2 · 2 = 1

(Since Δ ng = 0, volume V cancels out in the expression.)

Now 1 mole of each P₂ and Q₂ is added. The reaction will move in the forward direction. t = t'eq : Moles of P₂ = 2 + 1 - x = 3 - x Moles of Q₂ = 2 + 1 - x = 3 - x Moles of PQ = 2 + 2x

Step 1: Solve for x
Kc = 1 = (2 + 2x)²(3 - x)(3 - x)

Taking the square root on both sides:

(2 + 2x)/(3 - x) = 1

2 + 2x = 3 - x

3x = 1 x = (1)/(3)
Step 2: Final Moles

At the new equilibrium: Moles of P₂ = 3 - (1)/(3) = (8)/(3) 2.67 Moles of Q₂ = 3 - (1)/(3) = (8)/(3) 2.67 Moles of PQ = 2 + 2((1)/(3)) = (8)/(3) 2.67

Pattern Recognition

For reactions where Δ ng = 0, concentration can be directly substituted with moles in the Kc expression because the volume terms cancel entirely.

Chapter Mix

Class 11 Chemistry: Equilibrium

Q56 jee_main_2026_28_january_morning Buffer Solutions
Consider a weak base 'B' of pKb = 5.699. 'x' mL of 0.02~M HCl and 'y' mL of 0.02~M weak base 'B' are mixed to make 100~mL of a buffer of pH 9 at 25°C. The values of 'x' and 'y' respectively are: [Given: 2 = 0.3010, 3 = 0.4771, 5 = 0.699]
  • A. x = 11.1, y = 88.9
  • B. x = 42.7, y = 57.3
  • C. x = 14.3, y = 85.7
  • D. x = 85.7, y = 14.3

Solution

Related Formula
pOH = pKb + [ SaltBase]
Step 1: Find Active Moles

Reaction: B + HCl arrow BH^+ + Cl^- Moles of HCl = 0.02x mmol Moles of Base B = 0.02y mmol Since a buffer is formed, Base B is in excess. Moles of Salt formed (BH^+) = 0.02x Moles of Base remaining = 0.02y - 0.02x

Step 2: Apply Henderson-Hasselbalch Equation

Given pH = 9, so pOH = 14 - 9 = 5.

5 = 5.699 + [(0.02x)/(0.02y - 0.02x)] -0.699 = ((x)/(y - x))

We know 5 = 0.699, therefore (1/5) = -0.699.

(x)/(y - x) = (1)/(5) 5x = y - x y = 6x
Step 3: Solve for x and y

Total volume x + y = 100~mL.

x + 6x = 100 7x = 100 x = (100)/(7) ≈ 14.3~mL y = 100 - 14.3 = 85.7~mL
Pattern Recognition

Buffer mixing implies partial neutralization. The ratio of acid volume to base volume defines the logarithmic salt-to-base ratio. Using inverse logs directly maps variables to total volume restrictions.

Chapter Mix

Class 11 Chemistry: Equilibrium

Q75 jee_main_2026_28_january_morning pH of Weak Acids
Consider the dissociation equilibrium of the following weak acid HA leftharpoons H⁺(aq) + A⁻(aq) If the pKₐ of the acid is 4, then the pH of 10~mM HA solution is _____. (Nearest integer) [Given : The degree of dissociation can be neglected with respect to unity]
Numerical Answer. Answer: 3 to 3

Solution

Related Formula
pH = (1)/(2) [pKₐ - C]
Step 1: Identify Parameters

pKₐ = 4

Concentration C = 10~mM = 10 × 10⁻³~M = 10⁻²~M

Step 2: Execute Calculation
pH = (1)/(2) [4 - (10⁻²)] = (1)/(2) [4 - (-2)] = (1)/(2) [6] = 3
Pattern Recognition

For weak monoprotic acids where α ll 1, the pH is always the arithmetic mean of the pKₐ and the negative logarithm of molarity.

Chapter Mix

Class 11 Chemistry: Equilibrium

Q54 jee_main_2026_28_january_evening Le Chatelier Principle And Equilibrium Calculation
Observe the following equilibrium in a 1 L flask. A(g) leftharpoons B(g) At T(K), the equilibrium concentrations of A and B are 0.5 M and 0.375 M respectively. 0.1 moles of A is added into the flask and heated to T(K) to establish the equilibrium again. The new equilibrium concentrations (in M) of A and B are respectively.
  • A. (1) 0.367, 0.275
  • B. (2) 0.53, 0.4
  • C. (3) 0.742, 0.557
  • D. (4) 0.557, 0.418

Solution

Related Formula
Keq = [B]eq[A]eq
Core Logic

Initial equilibrium: A leftharpoons B [A] = 0.5 M, [B] = 0.375 M

Keq = (0.375)/(0.5) = 0.75

Now 0.1 mole of A is added to the 1 L flask. New initial [A] = 0.5 + 0.1 = 0.6 M. Reaction shifts forward: A leftharpoons B Eq: 0.6 - x 0.375 + x

Step 1: Solve for x
Keq = 0.75 = (0.375 + x)/(0.6 - x) 0.75(0.6 - x) = 0.375 + x 0.45 - 0.75x = 0.375 + x

1.75x = 0.075

x = (0.075)/(1.75) = (3)/(70) ≈ 0.043 M
Step 2: Calculate New Concentrations

New concentration of A = 0.6 - 0.043 = 0.557 M New concentration of B = 0.375 + 0.043 = 0.418 M

Pattern Recognition

Le Chatelier addition problems require maintaining Keq constant. Set up ICE table after perturbation, equate to initial Keq.

Chapter Mix

Class 11 Chemistry: Equilibrium

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