Class 11 Physics Ideal Gas Notes

Unit 2

Heat and Thermodynamics

Class 11 Physics

Chapter 13

Ideal Gas

Class 11 Physics – Ideal Gas Notes PDF

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Chapter Overview

An ideal gas is a theoretical gas whose molecules are treated as point particles with negligible molecular volume and no intermolecular attraction except during collisions. Real gases approach ideal-gas behavior most closely at low pressure and high temperature.

This chapter connects the experimental gas laws with the microscopic kinetic model of matter. The central ideas are the ideal-gas equation, absolute temperature, molecular motion, pressure due to molecular collisions, translational kinetic energy, the Boltzmann constant, root mean square speed, and heat capacities.

Macroscopic View

Describes a gas by measurable quantities such as pressure P, volume V, temperature T, and amount n.

Microscopic View

Explains gas behavior using molecules, molecular mass, random motion, collisions, momentum, and kinetic energy.

1. Gas Laws and the Ideal-Gas Equation

1.1 Boyle’s Law

For a fixed mass of gas at constant temperature, pressure is inversely proportional to volume.

P ∝ 1/V   ⇒   PV = constant   ⇒   P1V1 = P2V2

Diagram 1 — Boyle’s Law: Pressure–Volume Graph

V P V₁ V₂ P₁ P₂ T = constant PV = constant

At constant temperature, increasing volume lowers pressure; the P–V curve is a rectangular hyperbola.

1.2 Charles’s Law

For a fixed mass of gas at constant pressure, volume is directly proportional to its absolute temperature.

V ∝ T   ⇒   V/T = constant   ⇒   V1/T1 = V2/T2

If temperature is measured in degree Celsius and the graph is extrapolated, the volume tends toward zero near −273.15 °C. This defines absolute zero, or 0 K.

Diagram 2 — Charles’s Law and Absolute Zero

t (°C) V −273.15 0 At 0 °C P = constant Absolute zero

Extrapolation of V against Celsius temperature gives zero volume at about −273.15 °C.

1.3 Pressure Law and Equality of Gas Coefficients

At constant volume, the pressure of a fixed mass of gas is directly proportional to absolute temperature:

P ∝ T   ⇒   P/T = constant

For an ideal gas near 0 °C, the volume coefficient at constant pressure and pressure coefficient at constant volume both have the limiting value approximately:

αV = αP ≈ 1/273.15 K−1

Diagram 3 — Pressure–Temperature Graph

t (°C) P −273.15 0 V = constant P → 0 by extrapolation

At constant volume, pressure increases linearly with absolute temperature.

1.4 Combined Gas Equation and Ideal-Gas Equation

Combining Boyle’s law and Charles’s law for a fixed amount of gas gives:

PV/T = constant

For n moles of an ideal gas, the constant becomes nR:

Ideal-gas equation
PV = nRT

Using the number of molecules N instead of moles:

PV = NkBT
SymbolMeaningCommon SI unit / value
PAbsolute pressurepascal (Pa)
VGas volume
nAmount of substancemol
TAbsolute temperaturekelvin (K)
RUniversal gas constant8.314 J mol⁻¹ K⁻¹
NNumber of moleculesdimensionless count
kBBoltzmann constant1.380649 × 10⁻²³ J K⁻¹
Exam tip: Always convert Celsius temperature to kelvin before using the ideal-gas equation: T(K) = t(°C) + 273.15.

2. Molecular Properties of Matter

2.1 Molecules and Intermolecular Forces

Matter is composed of atoms and molecules. Molecules in a real gas have finite size and experience weak attractive or repulsive forces. In the ideal-gas model, these effects are neglected except for the impulsive force during collision.

2.2 Mole and Avogadro Constant

One mole contains exactly 6.02214076 × 10²³ specified particles. This number is the Avogadro constant, NA.

n = N/NA    and    R = NAkB

Diagram 4 — Microscopic Model of a Gas

Random molecular motion in all directions Container wall

Gas pressure is a macroscopic result of enormous numbers of microscopic molecular collisions.

3. Kinetic-Molecular Model of an Ideal Gas

The kinetic theory uses a simplified microscopic model. Its main assumptions are:

  1. A gas contains a very large number of identical molecules in continuous random motion.
  2. The molecular size is negligible compared with the separation between molecules and the container volume.
  3. Molecules obey Newton’s laws of motion.
  4. No intermolecular force acts except during collisions.
  5. Collisions between molecules and with the walls are perfectly elastic.
  6. The duration of a collision is negligible compared with the time between collisions.
  7. Molecular motion is isotropic: no direction is preferred.
Idealization: No real gas satisfies all assumptions perfectly. The model works best for dilute gases, especially at low pressure and sufficiently high temperature.

4. Derivation of Pressure Exerted by an Ideal Gas

Consider a cubical container of side l and volume V = l³. Let one molecule of mass m have velocity components cx, cy, cz.

Diagram 5 — Molecular Collision with a Wall

Before: +cₓ After: −cₓ Wall normal to x-axis l

In an elastic collision with the wall, the x-component reverses while its magnitude is unchanged.

Step 1: Change of Momentum

Before collision, x-momentum is mcx; after collision it is −mcx.

Δpx = (−mcx) − (mcx) = −2mcx

The impulse delivered to the wall has magnitude 2mcx.

Step 2: Time Between Successive Collisions with the Same Wall

The molecule travels a round-trip distance 2l.

Δt = 2l/cx

Step 3: Average Force Due to One Molecule

F = Δp/Δt = (2mcx)/(2l/cx) = mcx2/l

Step 4: Sum Over N Molecules

F = (m/l) Σ cxi2

Since wall area A = l² and V = l³:

P = F/A = (m/V) Σ cxi2

Step 5: Use Isotropy of Molecular Motion

Σcx2 = Σcy2 = Σcz2 = (1/3)Σc2

Therefore, for N molecules:

P = (1/3)(Nm/V) c̄2 = (1/3)ρcrms2

where ρ = Nm/V is gas density and crms = √c̄².

Core derivation to memorize: P = (1/3)ρcrms2. In a long-answer question, clearly state the cube, momentum change, collision time, force, isotropy, and final result.

5. Pressure and Translational Kinetic Energy

Starting from:

P = (1/3)(Nm/V)c̄²

Multiply by volume:

PV = (1/3)Nm c̄² = (2/3)[(1/2)Nm c̄²]

The bracketed term is the total translational kinetic energy K of all molecules.

PV = (2/3)K   ⇒   P = (2/3)(K/V)

Thus, pressure equals two-thirds of the translational kinetic-energy density.

Diagram 6 — Link Between Pressure and Molecular Kinetic Energy

Highertemperature Greater average translational kinetic energy Greaterpressure* *For a fixed number of molecules in a fixed volume P = (2/3)(K/V)

At fixed volume, hotter molecules collide more energetically with the walls and produce greater pressure.

6. Average Translational Kinetic Energy and Boltzmann Constant

For an ideal gas:

PV = NkBT

But from kinetic theory:

PV = (2/3)K

Therefore:

K = (3/2)NkBT

Hence, average translational kinetic energy per molecule is:

K̄ = (3/2)kBT

For one mole:

Kmole = (3/2)RT
Physical meaning: The average translational kinetic energy of an ideal-gas molecule depends only on absolute temperature, not on pressure, volume, or the chemical identity of the gas.

7. Root Mean Square (RMS) Speed

Molecular speeds are not all equal, so kinetic theory uses the root mean square speed:

crms = √(c̄²)

From the pressure equation and ideal-gas equation:

crms = √(3RT/M)

where M is molar mass in kg mol⁻¹. For a single molecule of mass m:

crms = √(3kBT/m)

Dependence on Temperature and Molecular Mass

crms ∝ √T    and    crms ∝ 1/√M
  • At higher temperature, gas molecules have greater RMS speed.
  • At the same temperature, lighter gases have greater RMS speed than heavier gases.

Diagram 7 — RMS Speed: Temperature and Molar Mass

At fixed molar mass T cᵣₘₛ At fixed temperature M cᵣₘₛ cᵣₘₛ ∝ √T cᵣₘₛ ∝ 1/√M

RMS speed rises with √T and falls with √M.

8. Heat Capacities of Gases and Solids

8.1 Heat Capacity and Specific Heat Capacity

Heat capacity is the heat required to raise the temperature of a body by 1 K:

C = Q/ΔT

Specific heat capacity is heat required per unit mass per kelvin:

c = Q/(mΔT)

8.2 Molar Heat Capacities of an Ideal Gas

A gas can be heated at constant volume or at constant pressure, giving two molar heat capacities: CV and CP.

  • At constant volume, no expansion work is done, so supplied heat increases internal energy.
  • At constant pressure, part of the supplied heat increases internal energy and part does expansion work.
  • Therefore, CP > CV.
CP − CV = R

The heat-capacity ratio is:

γ = CP/CV

8.3 Simple Equipartition Results

In the classical model, each independent quadratic degree of freedom contributes (1/2)kBT per molecule to average energy.

Idealized substanceActive degrees of freedomCVCPγ
Monatomic ideal gas3 translational3R/25R/25/3 ≈ 1.67
Diatomic ideal gas (ordinary temperatures, simple model)3 translational + 2 rotational5R/27R/27/5 = 1.40
Classical crystalline solid (Dulong–Petit limit)Lattice vibrationsMolar heat capacity ≈ 3R

Diagram 8 — Constant-Volume vs Constant-Pressure Heating

Rigid container Constant volume Q → internal energy only Movable piston Constant pressure Q → internal energy + expansion work

Because a gas can expand at constant pressure, more heat is needed for the same temperature rise than at constant volume.

9. Formula Summary

ConceptFormulaCondition / Meaning
Boyle’s lawPV = constantFixed mass, constant T
Charles’s lawV/T = constantFixed mass, constant P
Pressure lawP/T = constantFixed mass, constant V
Combined gas equationPV/T = constantFixed amount of gas
Ideal-gas equationPV = nRT = NkBTIdeal gas
Boltzmann relationR = NAkBLinks molar and molecular scales
Pressure from kinetic theoryP = (1/3)ρcrms²Ideal gas
Pressure–energy relationPV = (2/3)KK = total translational KE
Average KE per moleculeK̄ = (3/2)kBTTranslational KE
KE per moleK = (3/2)RTOne mole
RMS speedcrms = √(3RT/M)M in kg mol⁻¹
Mayer’s relationCP − CV = RIdeal gas, molar capacities
Heat-capacity ratioγ = CP/CVIdeal gas

10. Solved Numerical Examples

Example 1 — Ideal-Gas Equation

Question: Find the volume occupied by 2.0 mol of an ideal gas at 300 K and 1.00 × 105 Pa.

V = nRT/P = (2.0)(8.314)(300)/(1.00 × 105) ≈ 4.99 × 10−2

Answer: V ≈ 0.0499 m³ ≈ 49.9 L.

Example 2 — RMS Speed

Question: Estimate the RMS speed of nitrogen gas at 300 K. Take M = 28 × 10−3 kg mol⁻¹.

crms = √(3RT/M) = √[(3)(8.314)(300)/(28 × 10−3)] ≈ 517 m s−1

Answer: crms ≈ 5.17 × 10² m s⁻¹.

Example 3 — Average Molecular Kinetic Energy

Question: Find the average translational kinetic energy of one ideal-gas molecule at 300 K.

K̄ = (3/2)kBT = (3/2)(1.380649 × 10−23)(300) ≈ 6.21 × 10−21 J

Answer: K̄ ≈ 6.21 × 10⁻²¹ J per molecule.

Example 4 — Molecular Speed and Temperature

Question: If the absolute temperature becomes four times as large, by what factor does RMS speed change?

crms ∝ √T   ⇒   c′/c = √(4T/T) = 2

Answer: The RMS speed doubles.

Example 5 — Pressure from Density and RMS Speed

Question: A gas has density 1.20 kg m⁻³ and RMS speed 500 m s⁻¹. Find its pressure.

P = (1/3)ρcrms² = (1/3)(1.20)(500)² = 1.00 × 105 Pa

Answer: P = 1.00 × 10⁵ Pa.

Important Exam Questions

Short-Answer Questions

  1. Define an ideal gas. Under what conditions do real gases approximately behave ideally?
  2. State Boyle’s law and Charles’s law.
  3. What is absolute zero? How is it obtained from a V–t or P–t graph?
  4. Define mole and Avogadro constant.
  5. State the principal assumptions of the kinetic-molecular model of an ideal gas.
  6. Define RMS speed. How does it depend on absolute temperature and molar mass?
  7. Write the relation between gas pressure and translational kinetic-energy density.
  8. What is Boltzmann constant? Write its relation with R and NA.
  9. Why is CP greater than CV for a gas?
  10. State Mayer’s relation for an ideal gas.

Long-Answer Questions

  1. Explain the experimental gas laws and combine them to obtain the ideal-gas equation.
  2. Explain absolute zero with the help of volume–temperature and pressure–temperature graphs.
  3. State and explain the assumptions of kinetic theory of gases.
  4. Derive the expression for pressure exerted by an ideal gas on the walls of a container.
  5. Show that the pressure of an ideal gas is two-thirds of its translational kinetic-energy density.
  6. Derive the average translational kinetic energy per molecule and per mole.
  7. Derive the expression crms = √(3RT/M) and discuss its dependence on T and M.
  8. Explain CV, CP, γ, and the heat capacities of simple gases and solids.

Derivations to Practice

  1. PV = nRT from the gas laws.
  2. P = (1/3)ρcrms² from molecular collisions.
  3. PV = (2/3)K.
  4. K̄ = (3/2)kBT.
  5. crms = √(3RT/M).

Numerical Questions

  1. A gas occupies 2.0 L at 1.2 × 10⁵ Pa. Find its volume at 0.8 × 10⁵ Pa if temperature is constant. Answer: 3.0 L.
  2. A fixed amount of gas occupies 300 cm³ at 300 K. What volume will it occupy at 450 K at constant pressure? Answer: 450 cm³.
  3. Find the pressure of 1.5 mol of an ideal gas occupying 0.030 m³ at 320 K. Answer: ≈ 1.33 × 10⁵ Pa.
  4. Find the average translational kinetic energy per molecule at 400 K. Answer: ≈ 8.28 × 10⁻²¹ J.
  5. Calculate the RMS speed of oxygen at 300 K, taking M = 32 × 10⁻³ kg mol⁻¹. Answer: ≈ 484 m s⁻¹.

Diagram Questions

  1. Draw and label the Boyle’s-law P–V graph.
  2. Draw a V–t graph and indicate absolute zero.
  3. Draw a P–t graph and indicate absolute zero.
  4. Draw a cubical container and show the collision used in the kinetic-theory pressure derivation.
  5. Draw a simple comparison of constant-volume and constant-pressure heating.

One-Minute Revision

  • An ideal gas obeys PV = nRT and is best approximated by real gases at low pressure and high temperature.
  • Boyle’s law: PV = constant at constant T.
  • Charles’s law: V/T = constant at constant P.
  • At constant V, P/T = constant.
  • Absolute zero is 0 K = −273.15 °C.
  • One mole contains NA = 6.02214076 × 10²³ particles.
  • R = NAkB.
  • Kinetic theory assumes random motion, negligible molecular size and perfectly elastic collisions.
  • Pressure from kinetic theory: P = (1/3)ρcrms².
  • Pressure–energy relation: PV = (2/3)K.
  • Average translational KE per molecule = (3/2)kBT.
  • RMS speed: crms = √(3RT/M).
  • RMS speed increases as √T and decreases as 1/√M.
  • For an ideal gas, CP − CV = R and CP > CV.
  • A classical crystalline solid approaches molar heat capacity ≈ 3R at sufficiently high temperature.

Diagram Practice

  1. Redraw the Boyle’s-law rectangular hyperbola and mark two states (P₁,V₁) and (P₂,V₂).
  2. Redraw the V–t graph and extend it to −273.15 °C.
  3. Redraw the P–t graph and extend it to −273.15 °C.
  4. Draw molecules moving randomly inside a container and label the walls and molecular velocity.
  5. Draw the wall-collision diagram and label +cx, −cx, side length l, and the wall normal to the x-axis.
  6. Create a concept map linking temperature → average kinetic energy → collision effect → pressure.
  7. Draw qualitative curves showing crms ∝ √T and crms ∝ 1/√M.
  8. Sketch constant-volume and constant-pressure heating arrangements and state why CP > CV.

Syllabus Coverage Checklist

NEB/CDC Chapter 13 scopeCovered here
13.1 Ideal gas equation; gas laws; pressure/volume coefficients; absolute zeroYes
13.2 Molecular properties of matterYes
13.3 Kinetic-molecular model of an ideal gasYes
13.4 Derivation of pressure exerted by gasYes
13.5 Average translational kinetic energy of gas moleculeYes
13.6 Boltzmann constant and root mean square speedYes
13.7 Heat capacities: gases and solidsYes
Related mathematical problemsYes — solved and practice numericals included

Source handling: The original Nepal eNotes PDF remains embedded above. The typed section follows the verified NEB/CDC syllabus and is designed as a searchable, responsive study companion. Where the PDF viewer does not expose handwritten page text, the typed section is a syllabus-aligned reconstruction and is not claimed to be a word-for-word transcription.

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