For the reaction, N_2O_4 rightleftharpoons 2NO_2, graph is plotted as shown below. Identify correct statements. A. Standard free energy change for the reaction is -5.40text kJ mol^-1. B. As Delta G^ominus in graph is positive, N_2O_4 will not dissociate into NO_2 at all. C. Reverse reaction will go to completion. D. When 1 mole of N_2O_4 changes into equilibrium mixture, value of Delta G = -0.84text kJ mol^-1. E. When 2 mole of NO_2 changes into equilibrium mixture, Delta G for equilibrium mixture is -6.24text kJ mol^-1.
Gibbs Free Energy and Equilibrium diagram for Q69 - JEE Main 2026 Morning
A plot of Gibbs free energy against the fraction of N2O4 dissociated.
Choose the correct answer from the options given below :

Solution & Explanation

### Core Logic Let's analyze the statements based on the given Gibbs free energy (G) vs. extent of reaction plot.
Gibbs Free Energy and Equilibrium diagram for Q69 - JEE Main 2026 Morning
A plot of Gibbs free energy against the fraction of N2O4 dissociated.
A. Standard free energy change (Delta_r G^circ) is the difference between standard free energies of pure products (point B) and pure reactants (point A): Delta_r G^circ = G_B^circ - G_A^circ. Since B is higher than A, Delta_r G^circ is positive, not -5.40text kJ mol^-1. Statement A is false. B. Even if Delta_r G^circ is positive, the minimum of the curve (equilibrium state E) lies between the pure reactant and product states. Therefore, partial dissociation occurs to reach equilibrium. It is false to say it will not dissociate at all. Statement B is false. C. The minimum E is not at fraction = 0 or 1, meaning an equilibrium mixture exists. Reverse reaction does not go to completion. Statement C is false. D. From 1 mole of pure reactant (point A) to the equilibrium mixture (point E), the drop in Gibbs energy is 0.84text kJ mol^-1. Thus Delta G = -0.84text kJ mol^-1 is correct. Statement D is true. E. The difference from pure products (point B, equivalent to 2 moles NO_2) to equilibrium (E) is the entire vertical distance. The drop from B to A is 5.40, and A to E is 0.84. So drop from B to E is - (5.40 + 0.84) = -6.24text kJ mol^-1. Statement E is true. ### Step 1: Final Conclusion Only statements D and E are correct. ### Pattern Recognition The free energy of mixing creates a minimum 'dip' (Equilibrium) below both pure reactants and pure products, preventing either forward or reverse reactions from going absolutely to 100% completion. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Thermodynamics Class 11 Chemistry: Equilibrium

Reference Study Guides

More Thermodynamics Previous-Year Questions — Page 5

Q31 jee_main_2025_24_jan_evening Enthalpy of Neutralization
Which of the following mixing of 1M base and 1M acid leads to the largest increase in temperature?
  • A. \text{30 mL HCl and 30 mL NaOH}
  • B. \text{30 mL } \mathrm{CH_{3}COOH} \text{ and 30 mL NaOH}
  • C. \text{50 mL HCl and 20 mL NaOH}
  • D. \text{45 mL } \mathrm{CH_{3}COOH} \text{ and 25 mL NaOH}

Solution

### Related Formula Q = n_textreacted cdot Delta H_textneutralization Delta T = fracQm cdot c ### Core Logic The temperature rise depends directly on the total heat released (Q) normalized by the total heat capacity of the resulting mixed volume (m cdot c). Let's evaluate the millimoles of mathrmH^+ and mathrmOH^- that react in each mixture: 1. **Option 1:** 30text mL of 1mathrmM mathrmHCl + 30text mL of 1mathrmM mathrmNaOH textReactive millimoles = 30text mmol. Both are strong electrolytes, releasing full neutralization energy (sim -57.3text kJ/mol). Total volume = 60text mL. 2. **Option 2:** 30text mL of 1mathrmM mathrmCH_3COOH + 30text mL of 1mathrmM mathrmNaOH textReactive millimoles = 30text mmol. However, since acetic acid is a weak acid, part of the heat is consumed in its ionization. Thus, less total heat is evolved compared to Option 1. 3. **Option 3:** 50text mL of 1mathrmM mathrmHCl + 20text mL of 1mathrmM mathrmNaOH textLimiting reagent = mathrmNaOH = 20text mmol. Only 20text mmol reacts. Total volume = 70text mL. 4. **Option 4:** 45text mL of 1mathrmM mathrmCH_3COOH + 25text mL of 1mathrmM mathrmNaOH textLimiting reagent = 25text mmol weak neutralization profile. Comparing Option 1 and Option 3, Option 1 releases significantly more heat (30text mmol vs 20text mmol) into a smaller volume (60text mL vs 70text mL), yielding the largest increase in temperature Delta T. ### Pattern Recognition To maximize Delta T, look for the option that maximizes the amount of reacting strong acid and strong base equivalents while keeping the total solution volume as small as possible. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Thermodynamics Class 11 Chemistry: Equilibrium
Q41 jee_main_2025_24_jan_evening Hess's Law of Constant Heat Summation
mathrmS(g) + frac32 O_2(g) ightarrow SO_3(g) + 2xtext kcal mathrmSO2(mathrmg) + frac12mathrmO2(mathrmg) ightarrow mathrmSO3(mathrmg) + ytext kcal The heat of formation of mathrmSO_2(mathrmg) is given by:
  • A. \frac{2x}{y}\mathrm{\ kcal}
  • B. y - 2x\mathrm{\ kcal}
  • C. 2x + y\mathrm{\ kcal}
  • D. x + y\mathrm{\ kcal}

Solution

### Related Formula Using Hess's Law, the enthalpy change of a net reaction can be determined by linearly combining the steps: Delta Htextnet = sum Delta Htextproducts - sum Delta Htextreactants ### Core Logic The heat of formation of mathrmSO_2(g) corresponds to the target thermochemical equation: textTarget: mathrmS(g) + mathrmO2(g) ightarrow mathrmSO2(g) quad Delta H_f = ? Let's write out the given equations along with their enthalpy changes (remembering that exothermic reactions release heat, so Delta H = -Q): 1. mathrmS(g) + frac32mathrmO_2(g) ightarrow mathrmSO_3(g) quad Delta H_1 = -2xtext kcal 2. mathrmSO_2(g) + frac12mathrmO_2(g) ightarrow mathrmSO_3(g) quad Delta H_2 = -ytext kcal To isolate mathrmSO_2(g) on the product side, subtract Equation (2) from Equation (1): left[mathrmS(g) + frac32mathrmO2(g) ight] - left[mathrmSO2(g) + frac12mathrmO2(g) ight] ightarrow mathrmSO3(g) - mathrmSO3(g) mathrmS(g) + mathrmO2(g) ightarrow mathrmSO2(g) Now apply the same operation to the enthalpy values: Delta H_f = Delta H1 - Delta H_2 = -2x - (-y) = y - 2xtext kcal This matches Option (2). ### Pattern Recognition To isolate your target species on the desired side of the equation, use Hess's Law to add or subtract the given elemental equations. Make sure to invert the sign of the enthalpy change if you reverse a reaction. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Thermodynamics
Q33 jee_main_2025_24_jan_morning Spontaneity and Gibbs Energy Change
Let us consider an endothermic reaction which is non-spontaneous at the freezing point of water. However, the reaction is spontaneous at boiling point of water. Choose the correct option.
  • A. Both Delta H and Delta S are (+ve)
  • B. Delta H is (-ve) but Delta S is (+ve)
  • C. Delta H is (+ve) but Delta S is (-ve)
  • D. Both Delta H and Delta S are (-ve)

Solution

### Related Formula Delta G = Delta H - TDelta S ### Core Logic An endothermic profile specifies that Delta H > 0. For the system to become spontaneous (Delta G < 0) specifically when shifting to higher temperatures (T), the temperature-dependent entropic subtraction term (-TDelta S) must outweigh the enthalpic barrier. This transition demands a positive structural entropy step, i.e., Delta S > 0. Hence, both Delta H and Delta S are positive. ### Pattern Recognition Spontaneity driven purely by elevated thermal thresholds mandates matching positive signs for enthalpy and entropy. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Chemical Thermodynamics
Q47 jee_main_2025_24_jan_morning Gibbs Free Energy and Equilibrium Temperature
Standard entropies of mathrmX_2, mathrmY_2 and mathrmXY_5 are 70, 50 and 110 mathrm~J mathrm~K^-1 mathrm~mol^-1 respectively. The temperature in Kelvin at which the reaction frac 12 mathrm X _ 2 + frac 52 mathrm Y _ 2 rightarrow mathrm X Y _ 5 quad Delta mathrm H ^ circ = - 3 5 mathrm k J mathrm m o l ^ - 1 will be at equilibrium is (Nearest integer)
Numerical Answer. Answer: 700 to 700

Solution

### Related Formula Delta S_textrxn^0 = sum S_textproducts^0 - sum S_textreactants^0 quad textand quad T = fracDelta H^0Delta S^0 quad textat equilibrium (Delta G^0 = 0text) ### Core Logic First, calculate the standard entropy change for the reaction system (Delta S_textrxn^0): Delta S_textrxn^0 = S^0(XY_5) - left[ frac12S^0(X_2) + frac52S^0(Y_2) right] Delta S_textrxn^0 = 110 - left[ left(frac12 times 70right) + left(frac52 times 50right) right] = 110 - [35 + 125] Delta S_textrxn^0 = 110 - 160 = -50text J K^-1text mol^-1 At thermodynamic equilibrium, the change in Gibbs free energy drops to zero (Delta G^0 = 0): 0 = Delta H^0 - TDelta S^0 implies T = fracDelta H^0Delta S^0 Convert the enthalpy value into Joules (Delta H^0 = -35 times 10^3text J/mol) and substitute the parameters: T = frac-35000text J mol^-1-50text J K^-1text mol^-1 = 700text Kelvin ### Pattern Recognition Ensure all variables use matching energy units (Joules vs. Kilojoules) before setting up your final division step. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Chemical Thermodynamics
Q33 jee_main_2025_28_jan_evening First Law of Thermodynamics and State Functions
An ideal gas undergoes a cyclic transformation starting from the point A and coming back to the same point by tracing the path mathrmAto mathrmBto mathrmC rightarrow mathrmDrightarrow mathrmA as shown in the three cases below.
Thermodynamic cyclic path diagrams for Q33 - JEE Main 2025
The diagram displays three distinct cyclic paths (Case I, Case II, Case III) on volume vs pressure graphs.
Choose the correct option regarding Delta U:
Thermodynamic cyclic path diagrams for Q33 - JEE Main 2025
The diagram displays three distinct cyclic paths (Case I, Case II, Case III) on volume vs pressure graphs.
Thermodynamic cyclic path diagrams for Q33 - JEE Main 2025
The diagram displays three distinct cyclic paths (Case I, Case II, Case III) on volume vs pressure graphs.
  • A. Delta Utext (Case-III) > Delta Utext (Case-II) > Delta Utext (Case-I)
  • B. Delta Utext (Case-I) > Delta Utext (Case-II) > Delta Utext (Case-III)
  • C. Delta Utext (Case-I) > Delta Utext (Case-III) > Delta Utext (Case-II)
  • D. Delta Utext (Case-I) = Delta Utext (Case-II) = Delta Utext (Case-III)

Solution

### Related Formula For any state function like Internal Energy (U), the cyclic integral over a complete closed loop is identically zero: oint dU = 0 implies Delta U_textcyclic = 0 ### Core Logic Internal energy (U) depends only on the initial and final states of the thermodynamic system, not on the path followed. In all three listed cases, the ideal gas undergoes a complete cyclic path that returns to its original configuration state A. ### Step 1: Final Evaluation Since every transformation begins and ends at point A: Delta U_textCase-I = 0 Delta U_textCase-II = 0 Delta U_textCase-III = 0 Therefore, Delta Utext (Case-I) = Delta Utext (Case-II) = Delta Utext (Case-III). ### Pattern Recognition Do not waste time calculating path areas or values if the question asks for a state function change (Delta U, Delta H, Delta S, Delta G) over a cyclic loop. The answer is instantly zero for all cases! ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 11 Chemistry: Thermodynamics

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