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Chapter 2 · Class 11 Physics

Kinetic Theory — Important Questions

32 questions With answers CBSE format

SUMMARY: The chapter "Kinetic Theory" in Class 11 Physics explores the microscopic behavior of gases and the derivation of macroscopic properties from molecular motion.
KEY TOPICS: ideal gas equation, kinetic theory of gases, degrees of freedom, mean free path, Maxwell-Boltzmann distribution, pressure of an ideal gas, root mean square speed, specific heat capacities of gases, law of equipartition of energy, Avogadro's number.

Q1 1 Mark

The kinetic theory of gases assumes molecules are:

AConnected by springs
BPoint masses with no interaction
CStationary
DTightly packed
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Correct answer: Option 2 — Point masses with no interaction
Q2 1 Mark

The pressure of an ideal gas is proportional to:

AN⟨v⟩
BN⟨v⟩²
CN⟨v²⟩
DN²⟨v⟩²
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Correct answer: Option 3 — N⟨v²⟩
Q3 1 Mark

The average kinetic energy per molecule of an ideal gas at temperature T is:

A(1/2)kT
B(3/2)kT
CkT
D(3/2)RT
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Correct answer: Option 2 — (3/2)kT
Q4 1 Mark

The mean free path of a gas molecule depends on:

ANumber density
BMolecular diameter
CBoth
DNeither
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Correct answer: Option 3 — Both
Q5 1 Mark

For diatomic gases like O₂ the value of γ = C_p/C_v is approximately:

A1.0
B1.4
C1.67
D2.0
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Correct answer: Option 2 — 1.4
Q6 3 Marks

State the postulates of the kinetic theory of gases.

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Postulates: (1) A gas consists of a large number of identical molecules in random motion. (2) The size of molecules is negligible compared to intermolecular distance. (3) No intermolecular forces except during collisions. (4) Collisions between molecules and with container walls are perfectly elastic. (5) Time of collision is negligible compared to time between collisions. (6) Distribution of molecular velocities follows the Maxwell-Boltzmann distribution.
Q7 3 Marks

Define rms speed and write its formula in terms of T.

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Root-mean-square speed v_rms is the square root of the mean of the squared speeds of molecules: v_rms = √⟨v²⟩. From kinetic theory: v_rms = √(3kT/m) = √(3RT/M) where m is molecular mass M is molar mass. At higher T molecules move faster on average; at higher m they move slower (heavy gases like Xe are slower than H₂ at the same T).
Q8 3 Marks

State the law of equipartition of energy.

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Law of equipartition of energy: in thermal equilibrium each quadratic degree of freedom of a gas molecule (translational rotational or vibrational) has an average energy of (1/2)kT per molecule (or (1/2)RT per mole). For an ideal monoatomic gas: 3 translational degrees → U = (3/2)nRT. Diatomic gas at moderate T: 3 trans + 2 rot → U = (5/2)nRT. Predicts γ = 5/3 (mono) and 7/5 (diatomic).
Q9 3 Marks

Calculate the rms speed of oxygen molecules at 300 K. (M(O₂) = 32 × 10⁻³ kg/mol; R = 8.314 J/mol·K)

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v_rms = √(3RT/M) = √((3)(8.314)(300)/(32 × 10⁻³)) = √(7482.6/0.032) = √233830 = 483.6 m/s. So oxygen molecules at room temperature move on average at about 480 m/s — close to the speed of sound in air (~343 m/s). Hydrogen would be much faster: v_rms(H₂)/v_rms(O₂) = √(M(O₂)/M(H₂)) = √(32/2) = 4 ⇒ v_rms(H₂) ≈ 1900 m/s.
Q10 3 Marks

Why are real gases not exactly ideal at high pressure or low temperature?

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Ideal gas assumes (a) molecules are point masses (zero volume) and (b) no intermolecular forces. At high pressure the molecular volume becomes significant compared to container volume — the available volume is less than V. At low temperature molecules move slowly and intermolecular attractive forces become significant — pressure is reduced below ideal. Both effects are corrected in van der Waals equation: (P + a/V²)(V − b) = nRT.
Q11 6 Marks

Derive the relation P = (1/3) ρ ⟨v²⟩ for an ideal gas.

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Consider a gas in a cubic container of side L. Each molecule of mass m moving with velocity component v_x in x-direction strikes the right wall every Δt = 2L/v_x and imparts momentum 2mv_x. Force per molecule on wall = 2mv_x / (2L/v_x) = mv_x²/L. Total force F = (m/L) Σ v_x². Pressure P = F/A = F/L² = (m/L³) Σ v_x² = (m/V) Σ v_x² where V = L³. For a gas with N molecules ⟨v_x²⟩ = (1/N) Σ v_x² = (1/3)⟨v²⟩ by isotropy. So P = N m ⟨v²⟩ / (3V) = (1/3) ρ ⟨v²⟩ where ρ = Nm/V. This is the Maxwell pressure formula.
Q12 6 Marks

Show that the average kinetic energy of a gas molecule is (3/2)kT.

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From P = (1/3)ρ⟨v²⟩ = (Nm/3V)⟨v²⟩ ⇒ PV = (Nm/3)⟨v²⟩. Using ideal gas law PV = NkT (where k = R/N_A is Boltzmann's constant): NkT = (Nm/3)⟨v²⟩ ⇒ ⟨v²⟩ = 3kT/m. Hence (1/2)m⟨v²⟩ = (3/2)kT — the average translational kinetic energy per molecule. This is independent of the type of gas and depends only on temperature. For 1 mole: U = (3/2)RT for monoatomic gas.
Q13 6 Marks

Derive the expression for the molar specific heats C_v and C_p of a monoatomic and a diatomic ideal gas using the equipartition principle.

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Monoatomic gas (3 translational degrees): U = (3/2)nRT ⇒ C_v = (∂U/∂T)/n = (3/2)R. C_p = C_v + R = (5/2)R. γ = C_p/C_v = 5/3 ≈ 1.67. Diatomic gas at moderate T (3 trans + 2 rot = 5 degrees; vibration frozen out): U = (5/2)nRT ⇒ C_v = (5/2)R; C_p = (7/2)R; γ = 7/5 = 1.4. At very high T vibrational modes contribute (2 more: KE + PE of vibration) raising C_v to (7/2)R and γ to 9/7. Polyatomic non-linear gases have 6 degrees → C_v = 3R γ ≈ 1.33.
Q14 6 Marks

A vessel of 1 L contains 1 g of helium at 27°C. Calculate (i) the pressure (ii) the rms speed of the molecules. (R = 8.314 J/mol·K; M(He) = 4 g/mol)

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Moles n = 1/4 = 0.25 mol. (i) Ideal gas: PV = nRT ⇒ P = nRT/V = (0.25)(8.314)(300)/(10⁻³) = 6.236 × 10⁵ Pa = 6.16 atm. (ii) v_rms = √(3RT/M) = √((3)(8.314)(300)/(4 × 10⁻³)) = √(6235.5/0.004) = √(1.559 × 10⁶) = 1248.6 m/s. Helium molecules at room temperature move very fast — about 1.25 km/s.
Q15 6 Marks

Define mean free path and derive the formula for it.

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Mean free path λ is the average distance a gas molecule travels between successive collisions. In time Δt a molecule sweeps a cylindrical volume π d² v_avg Δt (where d is molecular diameter and v_avg is mean speed). Number of collisions = (number density n) × (volume swept) = π d² v_avg n Δt. Mean free path = (distance travelled)/(collisions) = v_avg Δt/(π d² v_avg n Δt) = 1/(π d² n). With more accurate treatment (relative motion of other molecules) λ = 1/(√2 π d² n). For air at STP λ ≈ 70 nm — ~1000 times larger than molecular diameter.
Q16 1 Mark

Assertion (A): Gas molecules are treated as point masses in kinetic theory.

Reason (R): Their size is negligible compared to the intermolecular distances at typical pressures.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q17 1 Mark

Assertion (A): The average translational kinetic energy of a gas molecule is independent of the gas type at a given temperature.

Reason (R): Equipartition gives (3/2)kT per molecule depending only on T.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q18 1 Mark

Assertion (A): Hydrogen molecules move faster on average than oxygen molecules at the same temperature.

Reason (R): v_rms = √(3RT/M); smaller M gives larger v_rms.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q19 1 Mark

Assertion (A): Diatomic gases have higher specific heats than monoatomic gases.

Reason (R): Diatomic molecules have rotational degrees of freedom in addition to translational.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q20 1 Mark

Assertion (A): Real gases deviate from ideal behaviour at high pressure.

Reason (R): Molecular volume becomes significant compared to container volume and intermolecular forces matter.

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Correct answer: Option 1 — Both A and R are true, and R is the correct explanation of A.
Q21 1 Mark

Statement 1: Pressure of a gas is due to molecular collisions with container walls.

Statement 2: Average kinetic energy per molecule depends only on temperature.

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Correct answer: Option 1 — Both statements are true.
Q22 1 Mark

Statement 1: Each translational degree of freedom contributes (1/2)kT to internal energy.

Statement 2: Each rotational degree of freedom of a diatomic molecule also contributes (1/2)kT.

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Correct answer: Option 1 — Both statements are true.
Q23 1 Mark

Statement 1: At a given temperature heavier molecules move slower.

Statement 2: v_rms = √(3RT/M) so v_rms is inversely proportional to √M.

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Correct answer: Option 1 — Both statements are true.
Q24 1 Mark

Statement 1: For an ideal monoatomic gas γ = 5/3.

Statement 2: For an ideal diatomic gas γ = 7/5.

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Correct answer: Option 1 — Both statements are true.
Q25 1 Mark

Statement 1: Mean free path decreases with increasing pressure.

Statement 2: At higher pressure molecular density is higher so collisions occur more frequently.

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Correct answer: Option 1 — Both statements are true.
Q26 3 Marks
At 300 K calculate the rms speed of molecules of (i) hydrogen H₂ (M = 2 g/mol) and (ii) oxygen O₂ (M = 32 g/mol). Compare and explain the difference. R = 8.314 J/mol·K.
  1. The rms speed of H₂ at 300 K is approximately:
    A1.9 km/s
    B3.8 km/s
    C7.6 km/s
    D11.4 km/s
  2. The ratio v_rms(H₂) / v_rms(O₂) at the same T equals:
    A2
    B4
    C8
    D16
  3. Why does Earth's atmosphere have very little hydrogen but plenty of oxygen?
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1. Option 1 — 1.9 km/s
2. Option 2 — 4
3. v_rms = √(3RT/M). For H₂: √((3)(8.314)(300)/(2 × 10⁻³)) = √(3741000) ≈ 1934 m/s ≈ 1.9 km/s. For O₂: √((3)(8.314)(300)/(32 × 10⁻³)) = √(233875) ≈ 484 m/s ≈ 0.48 km/s. Ratio: v_H/v_O = √(M_O/M_H) = √16 = 4. At the same temperature lighter molecules move 4× faster than oxygen.
Q27 3 Marks
A 2 mol of ideal gas occupies 8 L at 300 K. The student wants to compute (i) the pressure (ii) the new pressure if temperature is raised to 600 K at constant volume (iii) the average translational KE per molecule.
  1. The initial pressure equals approximately:
    A2.5 atm
    B5.0 atm
    C6.2 atm
    D10.0 atm
  2. At constant V if T doubles the pressure:
    AHalved
    BDoubled
    CSame
    DTripled
  3. Compute the average kinetic energy at T = 600 K and compare with T = 300 K.
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1. Option 3 — 6.2 atm
2. Option 2 — Doubled
3. Initial: P = nRT/V = (2)(8.314)(300)/(8 × 10⁻³) = 6.235 × 10⁵ Pa = 6.16 atm. At V constant T doubled (300 → 600 K) means P doubles (Gay-Lussac's law): P_new = 12.32 atm. Average translational KE per molecule: (3/2)kT = (1.5)(1.381 × 10⁻²³)(300) = 6.21 × 10⁻²¹ J — independent of gas type only of T.
Q28 3 Marks
For nitrogen molecules at STP (273 K 1 atm) molecular diameter d = 3.7 × 10⁻¹⁰ m. The student wants to compute (i) number density n (ii) mean free path λ.
  1. The number density at STP equals:
    A2.7 × 10²² /m³
    B2.7 × 10²⁴ /m³
    C2.7 × 10²⁵ /m³
    D2.7 × 10²⁷ /m³
  2. The mean free path is approximately:
    A7 nm
    B70 nm
    C700 nm
    D7 μm
  3. Why does the mean free path decrease at higher pressure?
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1. Option 3 — 2.7 × 10²⁵ /m³
2. Option 2 — 70 nm
3. At STP: n = N_A/V_m = 6.022 × 10²³ / 22.4 × 10⁻³ = 2.69 × 10²⁵ /m³. Mean free path: λ = 1/(√2 π d² n) = 1/(1.414 × π × (3.7 × 10⁻¹⁰)² × 2.69 × 10²⁵) = 1/(1.63 × 10⁷) ≈ 6.13 × 10⁻⁸ m ≈ 60 nm. So a nitrogen molecule at STP travels about 60 nm between collisions — about 200× its own diameter.
Q29 3 Marks

Study postulates of kinetic theory of gases:

PostulateDescription
Many particlesA gas consists of a vast number of molecules.
Random motionMolecules move in all directions randomly.
Negligible sizeMolecular size is much less than intermolecular distance.
Elastic collisionsCollisions are perfectly elastic.
No intermolecular forcesExcept during collisions.
Newton's laws applyMechanics of molecules obeys classical mechanics.
  1. Gas molecules are assumed to be:
    ADiffusing
    BRandom
    CStationary
    DAligned
  2. Collisions in an ideal gas are:
    AInelastic
    BElastic
    CBoth
    DNeither
  3. When does an actual gas behave most like an ideal gas?
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1. Option 2 — Random
2. Option 2 — Elastic
3. Kinetic theory's postulates apply to ideal gases. Real gases deviate at high pressure (intermolecular forces matter) and low temperature (molecules move slowly so attractive forces become significant). The success of kinetic theory was deriving macroscopic gas laws (PV = nRT) from molecular-level postulates and predicting useful results like rms speed and average kinetic energy depending only on temperature.
Q30 3 Marks

Study molar specific heats of various gases:

GasTypeC_vC_pγ
He Ne ArMonoatomic(3/2)R(5/2)R5/3 ≈ 1.67
H₂ N₂ O₂Diatomic(5/2)R(7/2)R7/5 = 1.4
H₂O CH₄Polyatomic non-linear3R4R4/3 ≈ 1.33
  1. For a monoatomic ideal gas γ equals:
    A5/3
    B7/5
    C4/3
    D1
  2. For a diatomic gas at moderate T C_v equals:
    A(3/2)R
    B(5/2)R
    C3R
    D4R
  3. Why does γ for diatomic gases approach 9/7 at very high temperature?
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1. Option 1 — 5/3
2. Option 2 — (5/2)R
3. Equipartition assigns (1/2)kT energy to each quadratic degree of freedom. Monoatomic: 3 trans → 3R/2 (×N for N moles). Diatomic at moderate T: 3 trans + 2 rot = 5 → 5R/2 (vibration not yet active). At very high T: vibration adds 2 more degrees → 7R/2. Polyatomic non-linear: 3 trans + 3 rot = 6 → 3R. The values of γ predict the speed of sound: v_s = √(γP/ρ).
Q31 6 Marks

For an ideal monoatomic gas at 300 K and 1 atm, compute (i) the rms speed of helium atoms (M = 4 g/mol), (ii) average translational KE per atom. (R = 8.314 J/mol·K, k_B = 1.38 × 10⁻²³ J/K)

QuantityValue
GasHelium (monoatomic)
M4 g/mol
T300 K
R8.314 J/mol·K
k_B1.38 × 10⁻²³ J/K
Q32 3 Marks

Study the Maxwell-Boltzmann speed distribution at two temperatures and answer:

Kinetic Theory figure
  1. As temperature increases, the speed distribution becomes:
    ASharper and shifted left
    BBroader and shifted right
    CSame as before
    DBecomes a delta function
  2. The relationship between the most probable speed (v_p), average speed (v_avg) and rms speed (v_rms) is:
    Av_p < v_avg < v_rms
    Bv_p > v_avg > v_rms
    Cv_p = v_avg = v_rms
    Dv_p > v_rms > v_avg
  3. Explain how the Maxwell-Boltzmann distribution changes with temperature.
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1. Option 2 — Broader and shifted right
2. Option 1 — v_p < v_avg < v_rms
3. The Maxwell-Boltzmann distribution gives the fraction of molecules with speeds between v and v + dv. At higher temperatures: (i) the most probable speed v_p = √(2kT/m) shifts to higher values; (ii) the curve becomes broader and flatter — more molecules have higher speeds. The total area under each curve equals 1 (all molecules are accounted for). Three characteristic speeds: most probable v_p = √(2kT/m), average v_avg = √(8kT/πm), root-mean-square v_rms = √(3kT/m). They are in the ratio v_p : v_avg : v_rms = 1 : 1.128 : 1.225, so v_p < v_avg < v_rms always.

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