Class 11 Chemistry Notes
~9 min readStates of Matter Class 11 Notes
Complete, exam-ready notes on the states of matter: the gas laws, the ideal gas equation and Graham's law, Dalton's law of partial pressures, the kinetic molecular theory, real gases and the van der Waals equation, and the liquid state — written for CBSE, JEE and NEET revision.
What is the ideal gas equation in one line?
PV = nRT connects pressure, volume, amount and temperature of a gas — the combined result of Boyle's, Charles' and Avogadro's laws.
The Three States
- Solids: fixed shape and volume; strong forces; particles vibrate about fixed positions.
- Liquids: fixed volume, no fixed shape; intermediate forces; particles slide past each other.
- Gases: neither fixed shape nor volume; particles far apart in random motion, weak forces between them.
- The state depends on temperature and pressure, and on the balance between kinetic energy and intermolecular forces.
The Gas Laws
Boyle's and Charles' laws
Boyle's law: at constant temperature, volume is inversely proportional to pressure. Charles' law: at constant pressure, volume is proportional to absolute temperature.
Avogadro's law + ideal gas equation
Avogadro's law: equal volumes of gases at the same T and P contain equal numbers of molecules. Combining with Boyle and Charles gives the ideal gas equation. STP: R = 0.0821 L·atm·mol⁻¹·K⁻¹.
Dalton's Law and Graham's Law
Dalton's law of partial pressures
The total pressure of a mixture of non-reacting gases equals the sum of the pressures each gas would exert alone. Partial pressure of a gas = its mole fraction × total pressure.
Graham's law of diffusion
Lighter gases diffuse and effuse faster: the rate of diffusion is inversely proportional to the square root of the molar mass. Hydrogen diffuses faster than oxygen.
Kinetic Molecular Theory
- Gases consist of tiny particles in constant, random, straight-line motion.
- The particles occupy negligible volume compared with the gas volume.
- Collisions are perfectly elastic — no energy is lost.
- There is no attractive or repulsive force between gas particles.
- Average kinetic energy depends only on absolute temperature: KE ∝ T, so at the same T all gases have the same average KE.
Ideal vs Real Gases — van der Waals Equation
Real gases
Real gases deviate from PV = nRT because molecules occupy finite volume (correction b) and attract each other (correction a). The van der Waals equation applies the two corrections. Deviations are largest at high pressure and low temperature.
- Compressibility factor Z = PV/nRT: Z = 1 for ideal; Z < 1 when attraction dominates (moderate pressure); Z > 1 when volume dominates (high pressure).
- Gases approach ideal behaviour at low pressure and high temperature.
- Boyle temperature is where a real gas behaves most ideally.
The Liquid State
- Vapour pressure: the pressure of vapour above a liquid at equilibrium; it rises with temperature and is independent of liquid surface area.
- Boiling occurs when vapour pressure equals external pressure.
- Surface tension: the force along the liquid surface (per unit length) that minimises surface area — water has strong hydrogen bonding and high surface tension.
- Viscosity: internal resistance to flow; liquids with stronger intermolecular forces and lower temperature flow more slowly.
Atmospheric pressure
Solved Examples
Example: A gas occupies 2 L at 300 K and 1 atm. What volume at 600 K and 0.5 atm?
Solution: Use the combined law: V₂ = V₁ × (T₂/T₁) × (P₁/P₂) = 2 × (600/300) × (1/0.5) = 8 L.
Example: Which effuses faster, hydrogen or oxygen, at the same temperature?
Solution: By Graham's law, rate ∝ 1/√M. H₂ (M = 2) has √(32/2) = 4 times the effusion rate of O₂ (M = 32).
NCERT Exercise Questions
From the textbook
Exercises (NCERT Q5.1–Q5.23)
- 5.1) What will be the minimum pressure required to compress 500 dm³ of air at 1 bar to 200 dm³ at 30 °C?
- 5.2) A vessel of 120 mL capacity contains a certain amount of gas at 35 °C and 1.2 bar pressure. The gas is transferred to another vessel of volume 180 mL at 35 °C. What would be its pressure?
- 5.3) Using the equation of state PV = nRT, show that at a given temperature, density of a gas is proportional to the gas pressure P.
- 5.4) At 0 °C, the density of a gaseous oxide at 2 bar is same as that of dinitrogen at 5 bar. What is the molecular mass of the oxide?
- 5.5) Pressure of 1 g of an ideal gas A at 27 °C is found to be 2 bar. When 2 g of another ideal gas B is introduced in the same flask at same temperature, the pressure becomes 3 bar. Find the relationship between their molecular masses.
- 5.6) The drain cleaner, Drainex contains small bits of aluminium which react with caustic soda to produce dihydrogen. What volume of dihydrogen at 20 °C and one bar will be released when 0.15 g of aluminium reacts?
- 5.7) What will be the pressure exerted by a mixture of 3.2 g of methane and 4.4 g of carbon dioxide contained in a 9 dm³ flask at 27 °C?
- 5.8) What will be the pressure of the gas mixture when 0.5 L of H₂ at 0.8 bar and 2.0 L of dioxygen at 0.7 bar are introduced in a 1 L vessel at 27 °C?
- 5.9) Density of a gas is found to be 5.46 g/dm³ at 27 °C and at 2 bar pressure. What will be its density at STP?
- 5.10) 34.05 mL of phosphorus vapour weighs 0.0625 g at 546 °C and 1.0 bar pressure. What is the molar mass of phosphorus?
- 5.11) A student forgot to add the reaction mixture to the round bottomed flask at 27 °C but instead, he/she placed the flask on the flame. After a lapse of time, he realized his mistake, and using a pyrometer, he found the temperature of the flask was 477 °C. What fraction of air would have been expelled out?
- 5.12) Calculate the temperature of 4.0 moles of a gas occupying 5 dm³ at 3.32 bar (R = 0.083 bar dm³ K⁻¹ mol⁻¹).
- 5.13) Calculate the total number of electrons present in 1.4 g of dinitrogen gas.
- 5.14) How much time would it take to distribute one Avogadro number of wheat grains if 10¹⁰ grains are distributed each second?
- 5.15) Calculate the total pressure in a mixture of 8 g of oxygen and 4 g of hydrogen confined in a vessel of 1 dm³ at 27 °C. R = 0.083 bar dm³ K⁻¹ mol⁻¹.
- 5.16) Pay load is defined as the difference between the mass of the displaced air and the mass of the balloon. Calculate the pay load when a balloon of radius 10 m, mass 100 kg is filled with helium at 1.66 bar at 27 °C (Density of air = 1.2 kg m⁻³ and R = 0.083 bar dm³ K⁻¹ mol⁻¹).
- 5.17) Calculate the volume occupied by 8.8 g of CO₂ at 31.1 °C and 1 bar pressure. R = 0.083 bar L K⁻¹ mol⁻¹.
- 5.18) 2.9 g of a gas at 95 °C occupied the same volume as 0.184 g of hydrogen at 17 °C at the same pressure. What is the molar mass of the gas?
- 5.19) A mixture of dihydrogen and dioxygen at one bar pressure contains 20% by weight of dihydrogen. Calculate the partial pressure of dihydrogen.
- 5.20) What would be the SI unit for the quantity PV²T²/n?
- 5.21) In terms of Charles' law explain why −273 °C is the lowest possible temperature.
- 5.22) Critical temperature for CO₂ and CH₄ are 31.1 °C and −81.9 °C respectively. Which of these has stronger intermolecular forces and why?
- 5.23) Explain the physical significance of van der Waals parameters.
Answers at a glance
- 1Q5.1 → Temperature is constant, so P₁V₁ = P₂V₂: P₂ = (1 bar × 500 dm³)/200 dm³ = 2.5 bar.
- 2Q5.2 → At constant temperature, P₂ = P₁V₁/V₂ = (1.2 bar × 120 mL)/180 mL = 0.8 bar.
- 3Q5.3 → n = m/M, so PV = (m/M)RT giving d = m/V = PM/RT; at constant T (and M, R), density d ∝ P.
- 4Q5.4 → Equal density at the same temperature means M₁P₁ = M₂P₂: M₁ × 2 bar = 28 × 5 bar, so M₁ = 70 u.
- 5Q5.5 → nₐ = 1/Mₐ and n_B = 2/M_B. Pressure doubles-add splits: nₐ/(nₐ + n_B) = 2/3 gives nₐ = 2n_B, so 1/Mₐ = 4/M_B and M_B = 4Mₐ.
- 6Q5.6 → 2Al + 2NaOH + 2H₂O → 2NaAlO₂ + 3H₂. Moles Al = 0.15/27 = 5.56 × 10⁻³; H₂ = (3/2)(5.56 × 10⁻³) = 8.33 × 10⁻³ mol. V = nRT/P ≈ 8.33 × 10⁻³ × 0.083 × 293/1 ≈ 0.20 L (≈ 203 mL).
- 7Q5.7 → n(CH₄) = 3.2/16 = 0.2 mol, n(CO₂) = 4.4/44 = 0.1 mol, n_total = 0.3 mol. P = nRT/V = (0.3 × 0.083 × 300)/9 = 0.83 bar.
- 8Q5.8 → p(H₂) = (0.8 × 0.5)/1.0 = 0.40 bar and p(O₂) = (0.7 × 2.0)/1.0 = 1.4 bar; total = 0.40 + 1.4 = 1.8 bar.
- 9Q5.9 → d/P·T is constant, so d₂ = d₁ × (P₂/P₁) × (T₁/T₂) = 5.46 × (1.01325/2) × (300/273) ≈ 3.04 g/dm³.
- 10Q5.10 → M = mRT/PV = (0.0625 × 0.083 × 819.15)/(1.0 × 0.03405) ≈ 124.9 g/mol — phosphorus vapour is P₄ (≈ 124 u).
- 11Q5.11 → V₂/V₁ = T₂/T₁ = 750 K/300 K = 2.5; air expelled = (V₂ − V₁)/V₂ = 1.5/2.5 = 0.6, i.e. 60% of the air.
- 12Q5.12 → T = PV/nR = (3.32 × 5)/(4.0 × 0.083) = 16.6/0.332 = 50 K.
- 13Q5.13 → 0.05 mol N₂ = 3.011 × 10²² molecules; each N₂ has 14 electrons, so total = 14 × 3.011 × 10²² = 4.215 × 10²³ electrons.
- 14Q5.14 → t = 6.022 × 10²³ / 10¹⁰ = 6.022 × 10¹³ s ≈ 1.91 × 10⁶ years.
- 15Q5.15 → n(O₂) = 0.25 mol, n(H₂) = 2 mol, n_total = 2.25 mol. P = (2.25 × 0.083 × 300)/1 ≈ 56.0 bar.
- 16Q5.16 → V = (4/3)π(10)³ = 4186.7 m³; displaced air = 5024.0 kg. Moles He = (1.66 × 4.1867 × 10⁶)/(0.083 × 300) ≈ 2.79 × 10⁵, mass He ≈ 1116 kg. Pay load = 5024 − (100 + 1116) ≈ 3811 kg.
- 17Q5.17 → n(CO₂) = 8.8/44 = 0.2 mol. V = nRT/P = (0.2 × 0.083 × 304.25)/1 ≈ 5.05 L.
- 18Q5.18 → Same P and V means n₁T₁ = n₂T₂: (2.9/M)(368) = (0.184/2)(290) → M = (2.9 × 368)/(0.092 × 290) = 40 g/mol.
- 19Q5.19 → 20 g H₂ = 10 mol and 80 g O₂ = 2.5 mol; mole fraction of H₂ = 10/12.5 = 0.8. p(H₂) = 0.8 × 1 bar = 0.8 bar.
- 20Q5.20 → P in N m⁻², V in m³, T in K, n in mol: unit = (N m⁻²)(m³)²(K)²/mol = N m⁴ K² mol⁻¹ = J m³ K² mol⁻¹.
- 21Q5.21 → By Charles' law, V ∝ T: at −273 °C the volume of the gas becomes zero, i.e. the gas ceases to exist, so no temperature below it is possible.
- 22Q5.22 → CO₂: the higher the critical temperature, the more easily the gas is liquefied, which reflects greater intermolecular forces of attraction.
- 23Q5.23 → 'a' measures the magnitude of the intermolecular attractive forces between gas molecules; 'b' measures the effective size (excluded volume) of the gas molecules.
CBSE Pattern Questions
How CBSE asks this chapter
MCQ Questions
1 Mark Questions
- 1State Boyle's law. (Ans: at constant temperature, the volume of a fixed mass of gas is inversely proportional to its pressure, PV = constant)
- 2State Charles' law. (Ans: at constant pressure, the volume of a fixed mass of gas is directly proportional to its absolute temperature)
- 3Write the ideal gas equation. (Ans: PV = nRT, where R is the universal gas constant)
- 4What is STP? (Ans: standard temperature 273.15 K and pressure 1 bar)
2 Mark Questions
- 1Using PV = nRT, show that at a given temperature the density of a gas is proportional to its pressure. (Ans: d = PM/RT, so at constant T, d ∝ P)
- 2State the postulates of the kinetic molecular theory in brief. (Ans: gas has tiny molecules in constant random motion, negligible volume, collisions perfectly elastic, average KE ∝ absolute temperature)
- 3State Dalton's law of partial pressures and one use. (Ans: total pressure of a mixture of non-reacting gases is the sum of their partial pressures; used to collect gases over water)
- 4Two gases at the same temperature and pressure have equal volumes. What can you say about their mole numbers? (Ans: they contain the same number of moles and molecules — Avogadro's law)
3 Mark Questions
- 1Derive the relationship between molar mass and density of a gas from the ideal gas equation. (Ans: d = PM/RT, hence molar mass M = dRT/P)
- 2Explain the causes of deviation of real gases from ideal behaviour, and state the van der Waals corrections. (Ans: finite molecular volume (b) and intermolecular attractions (a); (P + a/V²)(V − b) = RT)
- 3Calculate the total pressure in a mixture of 8 g of O₂ and 4 g of H₂ in a 1 dm³ vessel at 27 °C. (Ans: n = 2.25 mol, P = nRT/V ≈ 56 bar)
- 4Explain why −273 °C is the absolute zero of temperature using Charles' law. (Ans: volume extrapolates to zero at −273 °C)
5 Mark Questions
- 1State and explain the five gas laws with their mathematical forms, and combine them into the ideal gas equation PV = nRT. State the conditions giving each law from the equation.
- 2Discuss the kinetic molecular theory of gases, derive the expression PV = (1/3)mNu² for the pressure of a gas, and relate it to the kinetic interpretation of temperature.
- 3Explain the deviation of real gases from ideal behaviour with a plot of PV vs P. Explain the two van der Waals corrections and how they improve the equation of state.
PDF: Assignments & Tests
Printable study material
Assignments walk the chapter's topics in order; the tests follow the current CBSE blueprint (MCQ/VSA, 2M, 3M and 5M questions) with answer keys. They will appear here as direct download links.
Quick Revision
Key formulas at a glance
Memorise these equations — direct application numericals and derivations in CBSE & JEE frequently hinge on these.
Ideal gas equation
Combined gas law
Dalton's law
Graham's law
rms speed
van der Waals equation
Compressibility factor
Exam Strategy
How this chapter is asked
High-yield question patterns observed across CBSE boards, JEE Main & Advanced, and NEET.
- Ideal gas: PV = nRT with R = 0.0821 L·atm·mol⁻¹·K⁻¹.
- Graham's law: lighter gas diffuses faster, rate ∝ 1/√M.
- Partial pressure = mole fraction × total pressure (Dalton).
- van der Waals corrections: a = attraction, b = molecule volume.
- Real gases behave ideally at LOW pressure and HIGH temperature.
- Z = 1 ideal; Z < 1 attraction dominates; Z > 1 size dominates.
- Boiling point = temperature at which vapour pressure equals external pressure.
FAQ
Frequently asked questions
What is the ideal gas equation?
PV = nRT, combining Boyle's, Charles' and Avogadro's laws. P is pressure, V volume, n number of moles, T absolute temperature, and R the universal gas constant (0.0821 L·atm·mol⁻¹·K⁻¹).
What is Graham's law of diffusion?
The rate of diffusion or effusion of a gas is inversely proportional to the square root of its molar mass, so hydrogen (M = 2) diffuses four times faster than oxygen (M = 32).
Why do real gases deviate from ideal behaviour?
Real molecules occupy a finite volume and attract each other, which the ideal model ignores. The van der Waals equation adds corrections (a for attraction, b for volume); deviations peak at high pressure and low temperature.
What is vapour pressure?
The pressure of the vapour in equilibrium with its liquid at a given temperature. It increases with temperature and equals atmospheric pressure at the boiling point.
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