Chemical Thermodynamics — NEET UG practice

86 questions

Practice NEET UG Chemical Thermodynamics questions free — each with a detailed solution, graded instantly. Nothing is saved; log in to track your accuracy and build a streak.

Sample questions with solutions

Q1 · 2026

A protein undergoes reversible thermal denaturation from its initial state N to denatured state D according to NDN \rightleftharpoons D. At 60C60^{\circ}C, the concentrations of both N and D are equal at equilibrium, and the standard enthalpy change of denaturation is 666 kJ mol1666\ \text{kJ mol}^{-1}. The standard entropy change ΔS\Delta S^{\circ} (in kJ K1mol1\text{kJ K}^{-1}mol^{-1}) of the protein upon denaturation at 60C60^{\circ}C is closest to

  • A.

    11.1

  • B.

    2.0

  • C.

    2000.0

  • D.

    333.0

Answer: B
  1. Since the concentrations of N and D are equal at 60C60^{\circ}C, the system is at equilibrium at this temperature, which means the standard Gibbs free energy change is zero.
ΔG=0\Delta G^{\circ} = 0
  1. Using the relation between free energy, enthalpy, and entropy,
ΔG=ΔHTΔS\Delta G^{\circ} = \Delta H^{\circ} - T\Delta S^{\circ}
  1. Since ΔG=0\Delta G^{\circ} = 0, this simplifies to
ΔH=TΔS\Delta H^{\circ} = T\Delta S^{\circ}
  1. Converting the given temperature to Kelvin, T=60+273=333 KT = 60 + 273 = 333\ K, and rearranging for ΔS\Delta S^{\circ},
ΔS=ΔHT=666333\Delta S^{\circ} = \frac{\Delta H^{\circ}}{T} = \frac{666}{333}
  1. Calculating this ratio,
ΔS=2.0 kJ K1mol1\Delta S^{\circ} = 2.0\ \text{kJ K}^{-1}mol^{-1}

Hence, the correct answer is B.

Q2 · 2026

Consider the following reaction :

2A(g)+B(g)2D(g)2A(g) + B(g) \rightarrow 2D(g) ΔU=10 kJ mol1 and ΔS=44 JK1 at 298 K.\Delta U^{\ominus} = -10\ \text{kJ mol}^{-1} \text{ and } \Delta S^{\ominus} = -44\ JK^{-1} \text{ at } 298\ K.

Identify the correct option with ΔG\Delta G^{\ominus} for the reaction and spontaneity of the reaction at 298 K.

(Given : R=8.31 J mol1K1R = 8.31\ J\ mol^{-1}K^{-1})

  • A.

    1.635 kJ mol1-1.635\ \text{kJ mol}^{-1}, spontaneous

  • B.

    0.63568 kJ mol1-0.63568\ \text{kJ mol}^{-1}, spontaneous

  • C.

    +0.63568 kJ mol1+0.63568\ \text{kJ mol}^{-1}, non-spontaneous

  • D.

    +1.635 kJ mol1+1.635\ \text{kJ mol}^{-1}, non-spontaneous

Answer: C
  1. To connect ΔU\Delta U^{\ominus} with ΔH\Delta H^{\ominus}, use the relation between enthalpy change and internal energy change for a reaction involving gases,
ΔH=ΔU+ΔngRT\Delta H^{\ominus} = \Delta U^{\ominus} + \Delta n_g RT
  1. Here Δng\Delta n_g is the change in the number of moles of gas, calculated as moles of gaseous products minus moles of gaseous reactants. For 2A(g)+B(g)2D(g)2A(g)+B(g)\rightarrow 2D(g),
Δng=2(2+1)=1\Delta n_g = 2 - (2+1) = -1
  1. Substituting ΔU=10000 J/mol\Delta U^{\ominus} = -10000\ J/mol, Δng=1\Delta n_g = -1, R=8.31 J mol1K1R = 8.31\ J\ mol^{-1}K^{-1}, and T=298 KT = 298\ K,
ΔH=10000+(1)(8.31)(298)=12476 J/mol12.48 kJ/mol\Delta H^{\ominus} = -10000 + (-1)(8.31)(298) = -12476\ J/mol \approx -12.48\ kJ/mol
  1. To find whether the reaction is spontaneous, use the Gibbs-Helmholtz equation,
ΔG=ΔHTΔS\Delta G^{\ominus} = \Delta H^{\ominus} - T\Delta S^{\ominus}
  1. Substituting ΔH=12.48 kJ/mol\Delta H^{\ominus} = -12.48\ kJ/mol, T=298 KT = 298\ K, and ΔS=0.044 kJ/K\Delta S^{\ominus} = -0.044\ kJ/K,
ΔG=12.48(298)(0.044)=12.48+13.112=+0.632 kJ/mol\Delta G^{\ominus} = -12.48 - (298)(-0.044) = -12.48 + 13.112 = +0.632\ kJ/mol
  1. Since ΔG\Delta G^{\ominus} comes out positive, the reaction is non-spontaneous at 298 K.

Hence, the correct option is C.

Q3 · 2026

At a certain temperature, T(K)T(K), during a process, 500 J is absorbed by the system and work of 200 J is done by the system. Then change in internal energy of the system is :

  • A.

    400 J

  • B.

    300 J

  • C.

    700 J

  • D.

    500 J

Answer: B
  1. The first law of thermodynamics relates the change in internal energy to heat and work as
ΔU=q+w\Delta U = q + w
  1. Since heat is absorbed by the system, qq is taken as positive,
q=+500 Jq = +500\ J
  1. Since work is done by the system (not on it), ww is taken as negative,
w=200 Jw = -200\ J
  1. Substituting these values into the first law equation,
ΔU=500+(200)=300 J\Delta U = 500 + (-200) = 300\ J

Hence, the change in internal energy is 300 J, so the correct option is B.

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