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Gibbs energy and equilibrium constant: NEET MCQs with answers

89 questions on this topic of Chemical Thermodynamics (NEET 2027 syllabus). Here are 12; tap one to see its answer and explanation.

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easy

1. The relationship between the equilibrium constant (K) and the standard Gibbs free energy change (ΔᵣG°) is given by ΔᵣG° = -RT ln K. If a reaction has K = 1 at temperature T, the value of ΔᵣG° is:

  1. Greater than 0
  2. Equal to 0
  3. Less than 0
  4. Equal to -RT
Show answer and explanation

Answer: (B) Equal to 0

From the equation ΔᵣG° = -RT ln K, when K = 1, ln(1) = 0. Therefore, ΔᵣG° = -RT(0) = 0.

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2. For a reaction, ΔH = 90 kJ mol⁻¹ and ΔS = 180 J K⁻¹ mol⁻¹. At 250 K, ΔG is:

  1. 45 kJ mol⁻¹
  2. −44910 kJ mol⁻¹
  3. −45 kJ mol⁻¹
  4. 135 kJ mol⁻¹
Show answer and explanation

Answer: (A) 45 kJ mol⁻¹

ΔG = ΔH − TΔS = 90 − 250 × (180/1000) = 45 kJ mol⁻¹ (convert ΔS to kJ).

hard

3. A hypothetical reaction A(g) ⇌ 2B(g) has an equilibrium constant K_p = 0.5 at 300 K. What is the standard Gibbs energy change ΔᵣG° for the reverse reaction: 2B(g) ⇌ A(g) at 300 K? (Take R = 8.314 J K⁻¹ mol⁻¹, ln 2 = 0.693)

  1. +1.73 kJ mol⁻¹
  2. +3.46 kJ mol⁻¹
  3. -1.73 kJ mol⁻¹
  4. -3.46 kJ mol⁻¹
Show answer and explanation

Answer: (C) -1.73 kJ mol⁻¹

For the forward reaction, K_p = 0.5. For the reverse reaction, K_p' = 1/K_p = 1/0.5 = 2. The standard Gibbs free energy change for the reverse reaction is ΔᵣG° = -RT ln(K_p') = -8.314 × 300 × ln(2) = -8.314 × 300 × 0.693 J mol⁻¹ ≈ -1728.5 J mol⁻¹ ≈ -1.73 kJ mol⁻¹.

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4. For a reaction, ΔH = −30 kJ mol⁻¹ and ΔS = −180 J K⁻¹ mol⁻¹. At 250 K, ΔG is:

  1. 15 kJ mol⁻¹
  2. −15 kJ mol⁻¹
  3. −75 kJ mol⁻¹
  4. 44970 kJ mol⁻¹
Show answer and explanation

Answer: (A) 15 kJ mol⁻¹

ΔG = ΔH − TΔS = -30 − 250 × (-180/1000) = 15 kJ mol⁻¹ (convert ΔS to kJ).

easy

5. Which of the following expressions correctly relates the reaction quotient Q, standard Gibbs energy change ΔG°, and the non-standard Gibbs energy change ΔG?

  1. ΔG = ΔG° - RT ln Q
  2. ΔG° = ΔG + RT ln Q
  3. ΔG = ΔG° + RT ln Q
  4. Q = exp(-ΔG / RT)
Show answer and explanation

Answer: (C) ΔG = ΔG° + RT ln Q

The thermodynamic relationship between the actual Gibbs energy change (ΔG) and standard Gibbs energy change (ΔG°) is ΔG = ΔG° + RT ln Q, where Q is the reaction quotient.

hard

6. In a biochemical process at 310 K, the standard Gibbs free energy change is ΔG° = +17.1 kJ mol⁻¹. To drive this process, it is coupled with ATP hydrolysis which has ΔG° = -30.5 kJ mol⁻¹. What is the net standard Gibbs energy change and the approximate equilibrium constant of the coupled reaction? [Given: 2.303 RT at 310 K = 5.93 kJ mol⁻¹]

  1. +47.6 kJ mol⁻¹ and 9.3 × 10⁻⁹
  2. +13.4 kJ mol⁻¹ and 5.5 × 10⁻³
  3. -47.6 kJ mol⁻¹ and 1.1 × 10⁸
  4. -13.4 kJ mol⁻¹ and 1.8 × 10²
Show answer and explanation

Answer: (D) -13.4 kJ mol⁻¹ and 1.8 × 10²

ΔG°_net = +17.1 + (-30.5) = -13.4 kJ mol⁻¹. The equilibrium constant is found using log₁₀ K = -ΔG°_net / (2.303 RT) = -(-13.4) / 5.93 ≈ 2.26. Thus K = 10²·²⁶ ≈ 1.8 × 10².

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7. For a reaction, ΔH = +90 kJ mol⁻¹ and ΔS = +275 J K⁻¹ mol⁻¹. ΔG for the reaction at 550 K is:

  1. 89.73 kJ mol⁻¹
  2. -61.25 kJ mol⁻¹
  3. 241 kJ mol⁻¹
  4. 61.25 kJ mol⁻¹
Show answer and explanation

Answer: (B) -61.25 kJ mol⁻¹

ΔG = ΔH − TΔS = 90 − 550 × (275/1000) = -61.25 kJ mol⁻¹. Convert ΔS to kJ before subtracting.

Quick tip: ΔS is usually in J; ΔH in kJ. Divide ΔS by 1000 first.

NCERT Class 11, Chapter 5

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8. For a reaction, ΔH = −90 kJ mol⁻¹ and ΔS = −120 J K⁻¹ mol⁻¹. At 250 K, ΔG is:

  1. −60 kJ mol⁻¹
  2. 60 kJ mol⁻¹
  3. −120 kJ mol⁻¹
  4. 29910 kJ mol⁻¹
Show answer and explanation

Answer: (A) −60 kJ mol⁻¹

ΔG = ΔH − TΔS = -90 − 250 × (-120/1000) = −60 kJ mol⁻¹ (convert ΔS to kJ).

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9. For a reversible reaction, the standard enthalpy change is positive (ΔᵣH° > 0). If the temperature of the reaction mixture is increased, what will be the effect on ΔᵣG° and the equilibrium constant K?

  1. ΔᵣG° increases and K decreases
  2. ΔᵣG° decreases and K increases
  3. Both ΔᵣG° and K decrease
  4. Both ΔᵣG° and K increase
Show answer and explanation

Answer: (B) ΔᵣG° decreases and K increases

For an endothermic reaction (ΔᵣH° > 0, typically ΔᵣS° > 0 for favorable high-T equilibria), increasing T increases K (van 't Hoff equation: d ln K/dT = ΔH°/RT² > 0). Since K increases, ln K becomes more positive, and ΔᵣG° = -RT ln K becomes more negative (decreases).

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10. For a reaction, ΔH = −40 kJ mol⁻¹ and ΔS = −60 J K⁻¹ mol⁻¹. At 300 K, ΔG is:

  1. 17960 kJ mol⁻¹
  2. −22 kJ mol⁻¹
  3. 22 kJ mol⁻¹
  4. −58 kJ mol⁻¹
Show answer and explanation

Answer: (B) −22 kJ mol⁻¹

ΔG = ΔH − TΔS = -40 − 300 × (-60/1000) = −22 kJ mol⁻¹ (convert ΔS to kJ).

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11. A reaction has ΔH = +60 kJ mol⁻¹ and ΔS = +125 J K⁻¹ mol⁻¹. At 450 K its Gibbs energy change is:

  1. 116 kJ mol⁻¹
  2. -3.75 kJ mol⁻¹
  3. 59.88 kJ mol⁻¹
  4. 3.75 kJ mol⁻¹
Show answer and explanation

Answer: (D) 3.75 kJ mol⁻¹

ΔG = ΔH − TΔS = 60 − 450 × (125/1000) = 3.75 kJ mol⁻¹. Convert ΔS to kJ before subtracting.

Quick tip: ΔS is usually in J; ΔH in kJ. Divide ΔS by 1000 first.

NCERT Class 11, Chapter 5

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12. For a reaction, ΔH = 100 kJ mol⁻¹ and ΔS = 200 J K⁻¹ mol⁻¹. At 250 K, ΔG is:

  1. 50 kJ mol⁻¹
  2. −50 kJ mol⁻¹
  3. 150 kJ mol⁻¹
  4. −49900 kJ mol⁻¹
Show answer and explanation

Answer: (A) 50 kJ mol⁻¹

ΔG = ΔH − TΔS = 100 − 250 × (200/1000) = 50 kJ mol⁻¹ (convert ΔS to kJ).

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