Chemistry Chemical Thermodynamics

Thermodynamics Previous Year Questions (JEE Main 2026)

Solved JEE Main 2026 previous year questions on Chemical Thermodynamics with concise step-by-step solutions covering first law, Hess's law, Gibbs free energy, entropy, heat capacities and isothermal work.

10 min read Updated Jul 2026 #pyq#previous year questions#jee-main-2026

Practice the actual JEE Main 2026 Thermodynamics questions below, each worked out step by step so you can check both the final answer and the method.

Solutions are AI-generated and pending review.

JEE Main 2026 · 4 Apr, Shift 1 Q695278279
Given below are two statements: **Statement I:** For an ideal gas, heat capacity at constant volume is always greater than the heat capacity at constant pressure. **Statement II:** In a constant volume process, no work is produced and all the heat withdrawn goes into the chaotic motion and is reflected by a temperature increase of the ideal gas. In the light of the above statements, choose the correct answer from the options given below.
Solution

For an ideal gas the Mayer relation holds:

$$C_p = C_V + R$$

Since $R > 0$, we always have $C_p > C_V$. So Statement I (claiming $C_V > C_p$) is false.

At constant volume, $w = -p_{ext}\,\Delta V = 0$, so the first law gives:

$$q_V = \Delta U = nC_V\,\Delta T$$

All the heat added raises the internal (chaotic) molecular energy and hence the temperature. Statement II is true.

Answer: D

  1. A Both Statement I and Statement II are true
  2. B Both Statement I and Statement II are false
  3. C Statement I is true but Statement II is false
  4. D Statement I is false but Statement II is true
JEE Main 2026 · 4 Apr, Shift 1
JEE Main 2026 · 6 Apr, Shift 1 Q6952782190
Arrange the following isothermal processes in order of the magnitude of the work $(p\text{-}V)$ involved between states 1 and 2. A. Expansion in single stage $w_A$; B. Expansion in multi stages $w_B$; C. Compression in single stage $w_C$; D. Compression in multi stages $w_D$. Choose the correct option.
Solution

For an isothermal gas moving between the same two states, the work magnitude depends on the external pressure profile.

Expansion (1 → 2, gas pushes out):

  • Single stage against the low final pressure $p_2$: $|w_A| = p_2(V_2 - V_1)$ — smallest expansion work.
  • Multi stage / reversible (external pressure tracks the gas): $|w_B| = nRT\ln\dfrac{V_2}{V_1}$ — larger.

Compression (2 → 1, surroundings push in):

  • Multi stage / reversible: $|w_D| = nRT\ln\dfrac{V_2}{V_1} = |w_B|$ — minimum compression work.
  • Single stage against the high pressure $p_1$: $|w_C| = p_1(V_2 - V_1)$ — maximum.

So the ranking is:

$$|w_C| > |w_B| = |w_D| > |w_A|$$

The single-stage compression is largest and the single-stage expansion is smallest. Among the choices, this matches:

$$|w_C| > |w_D| > |w_B| > |w_A|$$

Answer: C

  1. A $
  2. B w_B
  3. C >
  4. D w_A
  5. E >
  6. F w_C
  7. >
  8. w_D
  9. $
  10. $
  11. w_C
  12. >
  13. w_D
  14. >
  15. w_A
  16. >
  17. w_B
  18. $
  19. $
  20. w_C
  21. >
  22. w_D
  23. >
  24. w_B
  25. >
  26. w_A
  27. $
  28. $
  29. w_B
  30. >
  31. w_A
  32. >
  33. w_D
  34. >
  35. w_C
  36. $
JEE Main 2026 · 6 Apr, Shift 1
JEE Main 2026 · 6 Apr, Shift 1 Q6952782210
Consider the reaction $X \rightleftharpoons Y$ at 300 K. If $\Delta H^\theta$ and K are 28.40 kJ mol$^{-1}$ and $1.8 \times 10^{-7}$ at the same temperature, then the magnitude of $\Delta S^\theta$ for the reaction in J K$^{-1}$ mol$^{-1}$ is ________. (Nearest integer) (Given: R = 8.3 J K$^{-1}$ mol$^{-1}$, ln 10 = 2.3, log 3 = 0.48, log 2 = 0.30)
Solution

First find $\Delta G^\theta$ from the equilibrium constant:

$$\Delta G^\theta = -RT\ln K$$

Evaluate $\ln K = 2.303\log(1.8\times10^{-7})$ using the given logs:

$$\log 1.8 = \log 2 + 2\log 3 - 1 = 0.30 + 0.96 - 1 = 0.26$$$$\log K = 0.26 - 7 = -6.74 \implies \ln K = 2.3 \times (-6.74) = -15.5$$$$\Delta G^\theta = -(8.3)(300)(-15.5) = 38{,}600 \text{ J mol}^{-1}$$

Now use $\Delta G^\theta = \Delta H^\theta - T\Delta S^\theta$:

$$\Delta S^\theta = \frac{\Delta H^\theta - \Delta G^\theta}{T} = \frac{28{,}400 - 38{,}600}{300} = -34 \text{ J K}^{-1}\text{mol}^{-1}$$

Magnitude $= 34$.

Answer: 34

JEE Main 2026 · 6 Apr, Shift 1
JEE Main 2026 · 2 Apr, Shift 1 Q69112154
Consider the following data (values are heat released, so each $\Delta H$ is negative): (i) $2\mathrm{Al}(s) + 6\mathrm{HCl}(aq) \rightarrow \mathrm{Al}_2\mathrm{Cl}_6(aq) + 3\mathrm{H}_2(g) + 1200$ kJ/mol (ii) $\mathrm{H}_2(g) + \mathrm{Cl}_2(g) \rightarrow 2\mathrm{HCl}(g) + 164$ kJ/mol (iii) $\mathrm{HCl}(g) + aq \rightarrow \mathrm{HCl}(aq) + 83$ kJ/mol (iv) $\mathrm{Al}_2\mathrm{Cl}_6(s) + aq \rightarrow \mathrm{Al}_2\mathrm{Cl}_6(aq) + 663$ kJ/mol The enthalpy of formation of anhydrous solid Al$_2$Cl$_6$ is:
Solution

Target reaction:

$$2\mathrm{Al}(s) + 3\mathrm{Cl}_2(g) \rightarrow \mathrm{Al}_2\mathrm{Cl}_6(s)$$

Assign $\Delta H$ values (heat released ⇒ negative):

$$\Delta H_1=-1200,\quad \Delta H_2=-164,\quad \Delta H_3=-83,\quad \Delta H_4=-663 \text{ kJ}$$

Combine: take (i), add $3\times$(ii) to make 6 HCl(g), add $6\times$(iii) to convert HCl(g) → HCl(aq), and reverse (iv) to precipitate the solid. The aqueous $\mathrm{Al}_2\mathrm{Cl}_6(aq)$, $3\mathrm{H}_2$, HCl(g) and HCl(aq) species all cancel, leaving the target:

$$\Delta H_f = \Delta H_1 + 3\Delta H_2 + 6\Delta H_3 - \Delta H_4$$$$\Delta H_f = -1200 + 3(-164) + 6(-83) - (-663)$$$$= -1200 - 492 - 498 + 663 = -1527 \text{ kJ mol}^{-1}$$

Answer: $-1527$ kJ mol$^{-1}$ (D)

  1. A $-648$ kJ mol$^{-1}$
  2. B $-1350$ kJ mol$^{-1}$
  3. C $-2002$ kJ mol$^{-1}$
  4. D $-1527$ kJ mol$^{-1}$
JEE Main 2026 · 2 Apr, Shift 1
JEE Main 2026 · 2 Apr, Shift 1 Q69112175
At the transition temperature T, $A \rightleftharpoons B$ and $\Delta G^0 = 105 - 35\log T$ where A and B are two states of substance X. The transition temperature in °C when pressure is 1 atm is __________. (Nearest integer)
Solution

At the transition temperature the two states are in equilibrium, so $\Delta G^0 = 0$:

$$105 - 35\log T = 0 \implies \log T = 3 \implies T = 10^{3} = 1000 \text{ K}$$

Convert to Celsius:

$$t = 1000 - 273 = 727\ ^\circ\text{C}$$

Answer: 727

JEE Main 2026 · 2 Apr, Shift 1
JEE Main 2026 · 4 Apr, Shift 2 Q695278446
If 3.365 g of ethanol ($l$) is burnt completely in a bomb calorimeter at 298.15 K, the heat produced is 99.472 kJ. The $|\Delta H_f^\ominus|$ of ethanol at 298.15 K is __________ $\times 10^2$ kJ mol$^{-1}$. (Nearest integer) Given: Standard enthalpy for combustion of graphite $= -393.5$ kJ mol$^{-1}$; Standard enthalpy of formation of water(l) $= -285.8$ kJ mol$^{-1}$; Molar masses of C, H, O are 12, 1 and 16 g mol$^{-1}$.
Solution

Molar mass of C$_2$H$_5$OH $= 46$ g mol$^{-1}$, so moles burnt:

$$n = \frac{3.365}{46} = 0.07315 \text{ mol}$$

A bomb calorimeter is a constant-volume system, so the measured heat is $\Delta U_c$:

$$\Delta U_c = \frac{-99.472}{0.07315} = -1359.8 \text{ kJ mol}^{-1}$$

Convert to $\Delta H_c$ for $\mathrm{C_2H_5OH}(l) + 3\mathrm{O_2}(g) \rightarrow 2\mathrm{CO_2}(g) + 3\mathrm{H_2O}(l)$, with $\Delta n_g = 2-3 = -1$:

$$\Delta H_c = \Delta U_c + \Delta n_g RT = -1359.8 + (-1)(8.314\times10^{-3})(298.15) \approx -1362.3 \text{ kJ mol}^{-1}$$

Apply Hess’s law, $\Delta H_c = 2\Delta H_f(\mathrm{CO_2}) + 3\Delta H_f(\mathrm{H_2O}) - \Delta H_f(\text{ethanol})$:

$$\Delta H_f(\text{ethanol}) = 2(-393.5) + 3(-285.8) - (-1362.3) = -282.1 \text{ kJ mol}^{-1}$$$$|\Delta H_f^\ominus| = 282.1 \text{ kJ mol}^{-1} = 2.82\times10^2 \approx 3\times10^2$$

Answer: 3

JEE Main 2026 · 4 Apr, Shift 2
JEE Main 2026 · 2 Apr, Shift 2 Q691121204
Gas 'A' undergoes change from state 'X' to state 'Y'. In this process, the heat absorbed and work done by the gas is 10 J and 18 J respectively. Now gas is brought back to state 'X' by another process during which 6 J of heat is evolved. In the reverse process of 'Y' to 'X':
Solution

Internal energy is a state function. For X → Y (using $\Delta U = q - w_{by}$):

$$\Delta U_{X\to Y} = q - w_{by} = 10 - 18 = -8 \text{ J}$$

For the return Y → X, the change reverses sign:

$$\Delta U_{Y\to X} = +8 \text{ J}, \qquad q = -6 \text{ J (evolved)}$$

Apply the first law again:

$$\Delta U_{Y\to X} = q - w_{by} \implies 8 = -6 - w_{by} \implies w_{by} = -14 \text{ J}$$

A negative $w_{by}$ means 14 J of work is done on the gas by the surroundings.

Answer: D

  1. A 18 J of the work is done by the gas 'A'.
  2. B 2 J of the work is done by the gas 'A'.
  3. C 12 J of the work is done on the gas 'A' by the surrounding.
  4. D 14 J of the work is done on the gas 'A' by the surrounding.
JEE Main 2026 · 2 Apr, Shift 2
JEE Main 2026 · 6 Apr, Shift 2 Q6911211254
Match List - I with List - II. Given $V_1$ and $V_2$ are initial and final volumes respectively. **List - I (Isothermal process):** A. Reversible expansion; B. Free expansion; C. Irreversible Compression; D. Cyclic reversible. **List - II (Expression):** I. $q=0$; II. $q=nRT\ln\dfrac{V_2}{V_1}$; III. $w=-p_{ext}(V_1-V_2)$; IV. $\dfrac{q_{rev}}{T}=0$. Choose the correct answer from the options given below:
Solution
  • A. Reversible isothermal expansion: $\Delta U = 0$, so $q = -w = nRT\ln\dfrac{V_2}{V_1}$ → II.
  • B. Free expansion: $p_{ext}=0 \Rightarrow w=0$; isothermal ideal gas has $\Delta U=0$, so $q=0$ → I.
  • C. Irreversible compression: work against constant external pressure, $w=-p_{ext}(V_2-V_1)=-p_{ext}(V_1-V_2)$ as written → III.
  • D. Cyclic reversible: entropy is a state function, so over a cycle $\displaystyle\oint \dfrac{q_{rev}}{T}=0$ → IV.

So A-II, B-I, C-III, D-IV.

Answer: C

  1. A A-II, B-III, C-I, D-IV
  2. B A-II, B-I, C-IV, D-III
  3. C A-II, B-I, C-III, D-IV
  4. D A-I, B-II, C-III, D-IV
JEE Main 2026 · 6 Apr, Shift 2
JEE Main 2026 · 5 Apr, Shift 2 Q691121504
Consider the following data for the reaction $X_2(g) + Y_2(g) \rightleftharpoons 2XY(g)$ at 600 K. The $\Delta_r G^\circ$ (in kJ mol$^{-1}$) for the reaction is: | Compound | $\Delta_f H^\circ_{600K}$ (kJ mol$^{-1}$) | $S^\circ_{600K}$ (J mol$^{-1}$ K$^{-1}$) | | --- | --- | --- | | XY(g) | 42 | 200 | | X$_2$(g) | 8 | 140 | | Y$_2$(g) | 80 | 250 |
Solution

Enthalpy of reaction:

$$\Delta_r H^\circ = 2(42) - (8 + 80) = 84 - 88 = -4 \text{ kJ mol}^{-1}$$

Entropy of reaction:

$$\Delta_r S^\circ = 2(200) - (140 + 250) = 400 - 390 = 10 \text{ J mol}^{-1}\text{K}^{-1}$$

Gibbs free energy at 600 K:

$$\Delta_r G^\circ = \Delta_r H^\circ - T\Delta_r S^\circ = -4 - 600\times\frac{10}{1000} = -4 - 6 = -10 \text{ kJ mol}^{-1}$$

Answer: $-10$ (B)

  1. A $-21000$
  2. B $-10$
  3. C $-1000$
  4. D $-9.012$
JEE Main 2026 · 5 Apr, Shift 2
JEE Main 2026 · 5 Apr, Shift 2 Q691121505
The correct order of molar heat capacities measured at 298 K and 1 bar is:
Solution

Compare typical molar heat capacities at 298 K:

  • Helium(g) — monatomic ideal gas, $C_{p,m} = \tfrac{5}{2}R \approx 20.8$ J mol$^{-1}$K$^{-1}$ (only translational modes).
  • Copper(s) — solid, $C_{p,m} \approx 24.4$ J mol$^{-1}$K$^{-1}$ (Dulong–Petit, $\approx 3R$).
  • Bromine(l) — a polyatomic liquid with many active vibrational/rotational modes, $C_{p,m} \approx 75.7$ J mol$^{-1}$K$^{-1}$, the highest.

So the order is:

$$\text{Bromine(l)} > \text{Copper(s)} > \text{Helium(g)}$$

Answer: B

  1. A Copper(s) > Bromine(l) > Helium(g)
  2. B Bromine(l) > Copper(s) > Helium(g)
  3. C Helium(g) > Bromine(l) > Copper(s)
  4. D Helium(g) > Bromine(l) = Copper(s)
JEE Main 2026 · 5 Apr, Shift 2
JEE Main 2026 · 8 Apr, Shift 2 Q691121599
Consider the reaction $$2H_2S(g) + 3O_2(g) \rightarrow 2H_2O(l) + 2SO_2(g)$$ The magnitude of enthalpy change for the reaction in kJ mol$^{-1}$ is __________. (Nearest integer) Given: $\Delta_f H^{\ominus}(H_2S) = -20.1$ kJ mol$^{-1}$, $\Delta_f H^{\ominus}(H_2O) = -286.0$ kJ mol$^{-1}$, $\Delta_f H^{\ominus}(SO_2) = -297.0$ kJ mol$^{-1}$.
Solution

Using $\Delta_r H = \sum \Delta_f H_{\text{products}} - \sum \Delta_f H_{\text{reactants}}$, with $\Delta_f H(\mathrm{O_2}) = 0$:

$$\Delta_r H = \big[2(-286.0) + 2(-297.0)\big] - \big[2(-20.1) + 3(0)\big]$$$$= (-572.0 - 594.0) - (-40.2) = -1166.0 + 40.2 = -1125.8 \text{ kJ mol}^{-1}$$

Magnitude $= 1125.8 \approx 1126$.

Answer: 1126

JEE Main 2026 · 8 Apr, Shift 2