Kinetic Theory of Gases: Tricky Questions Solved (3)

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Question

A vessel contains 1 mole1 \text{ mole} of O2\text{O}_2 (molar mass 32 g/mol32 \text{ g/mol}) and 2 moles2 \text{ moles} of H2\text{H}_2 (molar mass 2 g/mol2 \text{ g/mol}) at temperature T=300 KT = 300 \text{ K}. Find (a) the ratio of average kinetic energies per molecule of O2\text{O}_2 to H2\text{H}_2, (b) the ratio of rms speeds of O2\text{O}_2 to H2\text{H}_2, and (c) the total internal energy of the mixture (treat both as diatomic). Take R=8.314 J/mol KR = 8.314 \text{ J/mol K}.

Solution — Step by Step

Average translational KE per molecule is KE=32kBT\langle KE \rangle = \tfrac{3}{2}k_B T. This depends only on temperature, not on mass or molar mass.

So KEO2/KEH2=1\langle KE \rangle_{O_2} / \langle KE \rangle_{H_2} = 1.

vrms=3RTMv_{rms} = \sqrt{\frac{3RT}{M}}

Ratio: vrms,O2/vrms,H2=MH2/MO2=2/32=1/16=1/4v_{rms,O_2}/v_{rms,H_2} = \sqrt{M_{H_2}/M_{O_2}} = \sqrt{2/32} = \sqrt{1/16} = 1/4.

For a diatomic gas (5 degrees of freedom at moderate TT): U=52nRTU = \tfrac{5}{2}nRT per mole.

Utotal=52(nO2+nH2)RT=52(1+2)(8.314)(300)U_{total} = \tfrac{5}{2}(n_{O_2} + n_{H_2})RT = \tfrac{5}{2}(1 + 2)(8.314)(300).

Utotal=52×3×8.314×300=7.5×2494.2=18,706 J1.87×104 JU_{total} = \tfrac{5}{2} \times 3 \times 8.314 \times 300 = 7.5 \times 2494.2 = 18,706 \text{ J} \approx 1.87 \times 10^4 \text{ J}.

Final answers: (a) 1:1\mathbf{1:1}, (b) 1:4\mathbf{1:4}, (c) U1.87×104 JU \approx \mathbf{1.87 \times 10^4 \text{ J}}.

Why This Works

The big idea: temperature is a measure of average KE per molecule. Two gases at the same TT have the same KE per molecule, regardless of mass. But heavier molecules move slower to carry that same KE, so vrms1/Mv_{rms} \propto 1/\sqrt{M}.

For internal energy, we count all degrees of freedom. Diatomic gases have 3 translational + 2 rotational = 5 active modes at room temperature. Vibrational modes “freeze out” below ~1000 K1000 \text{ K}, so we don’t count them here.

Alternative Method

For (b), since 12mvrms2=32kBT\tfrac{1}{2}m v_{rms}^2 = \tfrac{3}{2}k_B T and TT is the same, m1v12=m2v22m_1 v_1^2 = m_2 v_2^2, so v1/v2=m2/m1v_1/v_2 = \sqrt{m_2/m_1}. Same answer, derived from KE equality directly.

Common Mistake

A classic JEE trap: students treat “KE per molecule” and “internal energy per mole” interchangeably. KE per molecule (translational) is 32kBT\tfrac{3}{2}k_B T, same for both gases. But internal energy per mole is f2RT\tfrac{f}{2}RT, where ff depends on the gas (3 for monatomic, 5 for diatomic at room TT). Don’t mix them up.

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