Which of the following properties will change when system containing solution 1 will become solution 2?
Solution state transition grid for Q35 - JEE Main 2025 Morning
The flowchart maps Solution 1 containing 10 mol solute in 10 L water transitioning to Solution 2 containing 1 mol solute in 1 L water.

Solution & Explanation

Core Logic

Let us compute the concentration of both solutions:

Concentration of Solution 1 = 10 mol10 L = 1 mol/L Concentration of Solution 2 = 1 mol1 L = 1 mol/L

Since concentration is identical, both systems share matching compositions. Consequently, all intensive properties (independent of mass/size) like concentration, density, and molar heat capacity remain exactly equal.

Step 1: Identifying the Variable

Gibbs free energy (G) is an extensive property that scales directly with the amount of matter in the system. Because Solution 1 contains a larger total mass and volume than Solution 2, its overall Gibbs free energy value will change.

Pattern Recognition

Shortcut: Look for the only extensive property in the options. Density, concentration, and molar parameters are always intensive. Gibbs free energy (G) scales with total matter quantity.

Chapter Mix

Class 11 Chemistry: Chemical Thermodynamics

More Chemical Thermodynamics Previous-Year Questions — Page 6

Q27 jee_main_2025_04_april_morning Spontaneity and Gibbs Energy
Let us consider a reversible reaction at temperature, T. In this reaction, both Δ H and Δ S were observed to have positive values. If the equilibrium temperature is Tₑ, then the reaction becomes spontaneous at:
  • A. T = Tₑ
  • B. Tₑ > T
  • C. T > Tₑ
  • D. Tₑ = 5T

Solution

Related Formula
Δ G = Δ H - TΔ S
Core Logic

For a reaction to be spontaneous, the change in Gibbs free energy must be negative:

Δ G < 0 Δ H - TΔ S < 0

Given that both Δ H > 0 and Δ S > 0:

Δ H < TΔ S T > (Δ H)/(Δ S)

At the equilibrium temperature Tₑ, Δ G = 0, which gives:

Tₑ = (Δ H)/(Δ S)

Substituting this back into the inequality reveals that the reaction is spontaneous when:

T > Tₑ

Pattern Recognition

When both Δ H and Δ S are positive, the reaction is entropy-driven and becomes spontaneous only at higher temperatures (T > Tₑ).

Chapter Mix

Class 11 Chemistry: Chemical Thermodynamics

Q30 jee_main_2025_04_april_morning Isothermal and Reversible Expansion
One mole of an ideal gas expands isothermally and reversibly from 10~dm³ to 20~dm³ at 300~K. Δ U, q and work done in the process respectively are: Given: R = 8.3 ~J~K⁻¹~mol⁻¹, ln 10 = 2.3, 2 = 0.30, 3 = 0.48
  • A. 0, 21.84~kJ, -1.26~kJ
  • B. 0, -17.18~kJ, 1.718~J
  • C. 0, 21.84~kJ, 21.84~kJ
  • D. 0, 1.718~kJ, -1.718~kJ

Solution

Related Formula
Δ U = n Cv Δ T w = -n R T ln((V₂)/(V₁)) Δ U = q + w
Core Logic

Since the expansion step is strictly isothermal (Δ T = 0):

Δ U = 0

Now compute the work command parameter w:

w = -n R T ln((V₂)/(V₁)) = -1 · 8.3 · 300 · ln((20)/(10)) w = -2490 · ln(2) = -2490 · (2.3 · 2) w = -2490 · (2.3 · 0.30) = -2490 · 0.69 = -1718.1~J = -1.718~kJ

Applying the first law equation constraint:

q = -w = +1.718~kJ

Hence, Δ U = 0, q = 1.718~kJ, w = -1.718~kJ.

Pattern Recognition

Isothermal expansion of an ideal gas ALWAYS yields Δ U = 0. Work is negative (done by system) and heat exchange q matches work magnitude inversely.

Chapter Mix

Class 11 Chemistry: Chemical Thermodynamics

Q28 jee_main_2025_07_april_evening Lattice Enthalpy and Born-Haber Cycle
The hydration energies of K^+ and Cl^- are -x and -y kJ/mol respectively. If lattice energy of KCl is -z kJ/mol, then the heat of solution of KCl is:
  • A. +x - y - z
  • B. x + y + z
  • C. z - (x + y)
  • D. -z - (x + y)

Solution

Related Formula
Δ Hsol = Lattice Energy (L.E.) + Δ Hhyd(Cation) + Δ Hhyd(Anion)
Core Logic

According to Hess's Law, the dissolution process can be mapped as follows:

Lattice Enthalpy and Born-Haber Cycle diagram for Q28 - JEE Main 2025 Evening
Lattice Enthalpy and Born-Haber Cycle diagram for Q28 - JEE Main 2025 Evening

Given parameters:

  • Lattice Energy of KCl breaking into gaseous ions = -(-z) = z kJ/mol (since lattice energy released on formation is given as -z).
  • Hydration energy of K^+ = -x kJ/mol
  • Hydration energy of Cl^- = -y kJ/mol
Step 1: Computation

Substituting the values into the governing formulation:

Δ Hsol = z + (-x) + (-y) Δ Hsol = z - x - y = z - (x + y)
Pattern Recognition

To dissolve an ionic crystal, energy equal to the lattice energy must be supplied (endothermic step, +z), and hydration releases energy (exothermic steps, -x and -y). Net heat of solution is simply the sum of these parts: z - x - y.

Chapter Mix

Class 11 Chemistry: Chemical Thermodynamics Class 11 Chemistry: Chemical Bonding and Molecular Structure

Q33 jee_main_2025_07_april_evening Standard Enthalpy of Formation
The correct statement amongst the following is:
  • A. The term 'standard state' implies that the temperature is 0°C
  • B. The standard state of pure gas is the pure gas at a pressure of 1 and temperature 273 K
  • C. ΔfH298θ is zero for O(g)
  • D. ΔfH500θ is zero for O2(g)

Solution

Related Formula
ΔfHθ = 0 for an element in its reference/most stable standard state
Core Logic
  • Standard state conditions prescribe a pressure of 1. Temperature is not fixed by definition but is explicitly specified (often reference tables use 298.15 K).
  • Oxygen naturally and stably exists as diatomic gas molecules (O₂(g)) at standard thresholds.
  • The enthalpy of formation of an element in its reference elemental state is identically zero at any reference temperature:
ΔfH₅₀₀θ[O2(g)] = 0

Conversely, atomic oxygen gas (O(g)) is not the reference phase, so its formation enthalpy is non-zero.

Step 1: Verification of Options

Statement (4) accurately aligns with thermodynamic core definitions, while statement (1) and (2) mistakenly conflate standard ambient reference states with STP conditions (273.15 K, 1 atm).

Pattern Recognition

Standard state definitions checklist: Pressure = 1. Temperature is variable/assigned independently. Elements in their most stable natural form take ΔfHθ = 0 at all thermal profiles.

Chapter Mix

Class 11 Chemistry: Chemical Thermodynamics

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 = nreacted · Δ Hneutralization Δ T = (Q)/(m · 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 · c). Let's evaluate the millimoles of H^+ and OH^- that react in each mixture:

  • Option 1: 30 mL of 1M HCl + 30 mL of 1M NaOH
  • Reactive millimoles = 30 mmol. Both are strong electrolytes, releasing full neutralization energy (-57.3 kJ/mol). Total volume = 60 mL.

  • Option 2: 30 mL of 1M CH₃COOH + 30 mL of 1M NaOH
  • Reactive millimoles = 30 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.

  • Option 3: 50 mL of 1M HCl + 20 mL of 1M NaOH
  • Limiting reagent = NaOH = 20 mmol. Only 20 mmol reacts. Total volume = 70 mL.

  • Option 4: 45 mL of 1M CH₃COOH + 25 mL of 1M NaOH
  • Limiting reagent = 25 mmol weak neutralization profile.

    Comparing Option 1 and Option 3, Option 1 releases significantly more heat (30 mmol vs 20 mmol) into a smaller volume (60 mL vs 70 mL), yielding the largest increase in temperature Δ T.

Pattern Recognition

To maximize Δ 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.

Chapter Mix

Class 11 Chemistry: Thermodynamics Class 11 Chemistry: Equilibrium

Rankbit System
JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%) | JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%)