Physics / Class XI / Chapter 11 – Thermodynamics / Exercise Solutions
NCERT End‑of‑Chapter Exercise

Complete Worked Solutions for
Thermodynamics – NCERT Exercise

Fully solved answers to the NCERT textbook exercise of Chapter 11, from short reasoning parts to numericals on heat, work, internal energy, entropy and heat engines, written in clear, exam‑oriented steps.[web:27][web:30]

CBSE Board JEE Foundation NEET Foundation Extra Concept Notes
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NCERT Exercise Coverage
First & Second Law
Conceptual Questions Definitions of temperature, heat, thermodynamic system and state variables with precise NCERT terminology.[web:27][web:31]
Numerical Problems Step‑wise calculations using first law of thermodynamics, equation of state \(PV=nRT\) and process‑specific work/heat relations.[web:27][web:36]
Engines & Entropy Qualitative and quantitative parts on Carnot engine, efficiency, refrigerators, entropy and second‑law statements.[web:27][web:33]
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How the Thermodynamics Exercise Solutions Are Organised

Section A – Concepts & Reasoning

Initial questions focus on thermodynamic systems, equilibrium, state variables and processes (isothermal, adiabatic, isochoric, cyclic), explaining each answer using diagrams and precise textbook language so you can mirror them in exams.[web:27][web:31]

Section B – Numericals & Applications

The second part applies the first law of thermodynamics, work from \(P\!-\!V\) graphs, heat engines and efficiency to compute heat exchange, internal‑energy change and work done, with units and sign conventions highlighted at every step.[web:27][web:36]

Entrance Exam Value

Why This NCERT Thermodynamics Exercise Matters for JEE, NEET and Boards

JEE Main / Advanced

Energy & Process Mastery

Thermodynamics usually contributes multiple questions across JEE papers, and NCERT‑style exercise problems on work, heat and cyclic processes form the base for many objective and integer‑type questions.[web:36]

NEET & Medical

Quick Calculations & Concepts

NEET focuses on straightforward calculations and conceptual clarity in topics like heat engines and specific heat, so mastering each NCERT exercise part gives direct scoring opportunities.[web:31][web:36]

Boards & Olympiads

Standard Question Source

Board papers and school tests often adapt directly from the NCERT exercise, and olympiad‑style questions frequently extend these same ideas on entropy, reversibility and engine efficiency.[web:27][web:33]

Ready to Work Through Every NCERT Thermodynamics Question?

Start from Question 1 and move sequentially, or jump straight to numericals using the index — each solution is designed to revise theory and problem‑solving for Chapter 11 in a single focused pass.[web:27][web:31]

Q1. A geyser heats water flowing at the rate of 3.0 litres per minute from 27 °C to 77 °C. If the geyser operates on a gas burner, what is the rate of consumption of the fuel if its heat of combustion is \(4.0 × 10^4\ J/g\) ?

Concept / Theory

When heat is supplied to a substance, its temperature increases. The amount of heat required to raise the temperature of a given mass of a substance is given by the formula:

\[ Q = mc\Delta T \]

Where:

  • Q = Heat energy supplied (Joules)
  • m = Mass of substance (kg)
  • c = Specific heat capacity (J kg⁻¹ °C⁻¹)
  • ΔT = Change in temperature

For water, the specific heat capacity is:

\[ c = 4.2 \times 10^3 \; J\,kg^{-1}°C^{-1} \]

In this problem, the geyser supplies heat to continuously flowing water. The fuel in the gas burner releases heat during combustion. By equating the heat needed by water and the heat released by fuel, we can calculate the fuel consumption rate.


Understanding the Process

Water enters the geyser at a lower temperature and exits at a higher temperature due to heat supplied by burning fuel.


Given Data

  • Flow rate of water = 3 litres/min
  • Initial temperature = 27 °C
  • Final temperature = 77 °C
  • Specific heat of water = \(4.2 × 10^3\ J kg^{-1} °C^{-1}\)
  • Heat of combustion of fuel = \(4.0 × 10^4\ J/g\)

Step 1: Convert Volume Flow Rate to Mass Flow Rate

The density of water is approximately:

\[ 1 \text{ litre of water} \approx 1 \text{ kg} \]

Therefore,

\[ 3 \text{ litres/min} = 3 \text{ kg/min} \]

So, the mass of water heated per minute is:

m = 3 kg/min


Step 2: Calculate Temperature Rise

\[ \Delta T = T_f - T_i \]

\[ \Delta T = 77 - 27 \]

\[ \Delta T = 50^\circ C \]


Step 3: Calculate Heat Required Per Minute

Using the heat formula:

\[ Q = mc\Delta T \]

Substitute the values:

\[ Q = 3 \times 4.2 \times 10^3 \times 50 \]

\[ Q = 6.3 \times 10^5 \; J/min \]

So, the geyser must supply 6.3 × 10⁵ Joules of heat every minute.


Step 4: Calculate Fuel Consumption

Heat released by fuel:

\[ 4.0 \times 10^4 \; J/g \]

Fuel required per minute:

\[ \text{Fuel rate} = \frac{\text{Heat required per minute}}{\text{Heat released per gram}} \]

\[ = \frac{6.3 \times 10^5}{4.0 \times 10^4} \]

\[ = 15.75 \; g/min \]


Final Answer

The rate of fuel consumption of the geyser is:

15.75 g per minute


Key Learning Points
  • Water density ≈ 1 kg per litre
  • Heat required to raise temperature depends on mass, specific heat, and temperature change
  • Fuel consumption is found by comparing heat required vs heat released by fuel

Q2. What amount of heat must be supplied to \(2.0 × 10^{–2}\) kg of nitrogen (at room temperature) to raise its temperature by 45 °C at constant pressure ? (Molecular mass of \(N_2 = 28\); \(R = 8.3\ J\ mol^{-1}\ K^{-1}\).)

Concept / Theory

When heat is supplied to a gas, its temperature increases. The amount of heat required depends on the number of moles of the gas, its molar heat capacity, and the temperature change.

For a gas heated at constant pressure, the heat supplied is given by:

\[ Q = nC_p\Delta T \]

  • Q = Heat supplied (J)
  • n = Number of moles of gas
  • C_p = Molar specific heat capacity at constant pressure
  • ΔT = Change in temperature

For a diatomic gas such as nitrogen (\(N_2\)), the molar heat capacity at constant pressure is:

\[ C_p = \frac{7}{2}R \]

where \(R\) is the universal gas constant.


Understanding the Process

At constant pressure, heat supplied increases the temperature of the gas and allows expansion.


Given Data

  • Mass of nitrogen = \(2.0 × 10^{-2}\) kg
  • Temperature rise = \(45^\circ C\)
  • Molar mass of \(N_2\) = 28 g/mol
  • Gas constant \(R = 8.3\ J mol^{-1}K^{-1}\)

Step 1: Convert Mass to Grams

\[ 2.0 × 10^{-2} \text{ kg} = 0.02 \text{ kg} \]

\[ 0.02 \text{ kg} = 20 \text{ g} \]


Step 2: Calculate Number of Moles

Number of moles is given by:

\[ n = \frac{\text{mass}}{\text{molar mass}} \]

\[ n = \frac{20}{28} \]

\[ n = 0.714\ \text{mol (approximately)} \]


Step 3: Determine Molar Heat Capacity

Since nitrogen is a diatomic gas:

\[ C_p = \frac{7}{2}R \]

\[ C_p = \frac{7}{2} × 8.3 \]


Step 4: Calculate Heat Supplied

Using the formula:

\[ Q = nC_p\Delta T \]

Substitute the values:

\[ Q = \frac{20}{28} × \frac{7}{2} × 8.3 × 45 \]

Simplifying:

\[ Q = \frac{5}{7} × \frac{7}{2} × 8.3 × 45 \]

\[ Q = 933.75\ J \]


Final Answer

The heat required to raise the temperature of nitrogen gas is:

\(Q \approx 9.34 × 10^2\ J\)

≈ 934 Joules


Key Learning Points
  • Heat required for a gas depends on moles, molar heat capacity, and temperature change
  • For diatomic gases: \(C_p = \frac{7}{2}R\)
  • Always convert kg → grams before calculating moles if molar mass is in g/mol
  • At constant pressure, gases can expand while heating

Q3. Explain why
(a) Two bodies at different temperatures T1 and T2 if brought in thermal contact do not necessarily settle to the mean temperature (T1 + T2)/2.
(b) The coolant in a chemical or a nuclear plant should have high specific heat.
(c) Air pressure in a car tyre increases during driving.
(d) The climate of a harbour town is more temperate than that of a town in a desert at the same latitude.

Concept / Theory

When bodies at different temperatures interact, heat flows from the hotter body to the colder body until thermal equilibrium is reached. The amount of heat exchanged depends on the relation:

\[ Q = mc\Delta T \]

  • m = mass of the substance
  • c = specific heat capacity
  • ΔT = change in temperature

Therefore, the final temperature after heat exchange depends not only on the initial temperatures but also on the heat capacities (mc) of the bodies.


(a) Final temperature is not always the average

When two bodies at temperatures \(T_1\) and \(T_2\) are brought in contact, heat flows from the hotter body to the colder body until thermal equilibrium is reached.

However, the final temperature depends on the heat capacity of each body:

Heat capacity = \(mc\)

If the bodies have different masses or different specific heat capacities, they exchange different amounts of heat for the same temperature change.

Thus, the equilibrium temperature lies closer to the temperature of the body with the larger heat capacity.

Therefore, the final temperature is not necessarily the simple average \((T_1 + T_2)/2\).


(b) Coolant should have high specific heat

In chemical and nuclear plants, large amounts of heat are produced during reactions. A coolant is used to absorb this excess heat and prevent overheating.

A substance with high specific heat capacity can absorb a large amount of heat without undergoing a large temperature rise.

Therefore, coolants with high specific heat can:

  • absorb large amounts of heat efficiently
  • maintain stable temperatures
  • prevent damage to equipment

Water is often used as a coolant because it has a very high specific heat capacity.


(c) Air pressure in a tyre increases during driving

While driving, the tyre continuously deforms where it touches the road. This causes:

  • friction with the road
  • repeated compression of air inside the tyre

These processes increase the internal energy of the air inside the tyre, raising its temperature.

According to the gas law:

\[ P \propto T \quad (\text{for nearly constant volume}) \]

Since the tyre volume changes very little, an increase in temperature causes the air pressure to increase.


(d) Harbour towns have a more moderate climate

Harbour towns are located near large water bodies such as seas or oceans. Water has a high specific heat capacity.

Because of this:

  • Water heats up slowly during the day
  • Water cools down slowly at night

This slow heating and cooling moderates the temperature of nearby land areas.

In contrast, desert regions have sand with low specific heat capacity. Sand heats and cools rapidly, causing large temperature variations.

Therefore, harbour towns experience a more moderate (temperate) climate compared to desert towns at the same latitude.


Key Learning Points
  • Final temperature after heat exchange depends on heat capacities, not just temperature.
  • Substances with high specific heat can absorb large amounts of heat.
  • Gas pressure increases with temperature when volume is nearly constant.
  • Water moderates climate due to its high specific heat capacity.

Q4. A cylinder with a movable piston contains 3 moles of hydrogen at standard temperature and pressure. The walls of the cylinder are made of a heat insulator, and the piston is insulated by having a pile of sand on it. By what factor does the pressure of the gas increase if the gas is compressed to half its original volume ?

Concept / Theory

When a gas is compressed or expanded without any heat exchange with the surroundings, the process is called an adiabatic process.

In an adiabatic process, pressure and volume are related by:

\[ PV^{\gamma} = \text{constant} \]

or

\[ P_1 V_1^{\gamma} = P_2 V_2^{\gamma} \]

Where:

  • \(P_1, P_2\) = initial and final pressure
  • \(V_1, V_2\) = initial and final volume
  • \(\gamma = \frac{C_p}{C_v}\) = ratio of specific heats

For a diatomic gas such as hydrogen:

\[ \gamma = \frac{7}{5} = 1.4 \]


Understanding the Process

During adiabatic compression, volume decreases while pressure and temperature increase.


Given Data

  • Gas = Hydrogen (diatomic)
  • Number of moles = 3
  • \(\gamma = 1.4\)
  • Final volume = half of the initial volume

Step 1: Write the Adiabatic Relation

\[ P_1 V_1^{\gamma} = P_2 V_2^{\gamma} \]

Rearranging to find the pressure ratio:

\[ \frac{P_2}{P_1} = \left(\frac{V_1}{V_2}\right)^{\gamma} \]


Step 2: Substitute the Volume Relation

The gas is compressed to half of its original volume:

\[ V_2 = \frac{V_1}{2} \]

Therefore,

\[ \frac{V_1}{V_2} = 2 \]


Step 3: Calculate the Pressure Ratio

Substitute the value of \(\gamma = 1.4\):

\[ \frac{P_2}{P_1} = 2^{1.4} \]

\[ \frac{P_2}{P_1} \approx 2.64 \]


Final Answer

When the gas is compressed to half of its original volume under adiabatic conditions, the pressure increases by a factor of:

≈ 2.64


Key Learning Points
  • An adiabatic process occurs when no heat exchange takes place.
  • Pressure and volume follow the relation \(PV^\gamma = constant\).
  • For diatomic gases like hydrogen: \(\gamma = 1.4\).
  • During adiabatic compression, pressure and temperature increase.

Q5. In changing the state of a gas adiabatically from an equilibrium state A to another equilibrium state B, an amount of work equal to 22.3 J is done on the system. If the gas is taken from state A to B via a process in which the net heat absorbed by the system is 9.35 cal, how much is the net work done by the system in the latter case ? (Take 1 cal = 4.19 J)

Concept / Theory

The relationship between heat, work, and internal energy of a system is given by the First Law of Thermodynamics:

\[ \Delta U = Q - W \]

  • \(\Delta U\) = Change in internal energy of the system
  • \(Q\) = Heat absorbed by the system
  • \(W\) = Work done by the system

Important points:

  • If work is done on the system, then \(W\) becomes negative.
  • In an adiabatic process, no heat is exchanged, so \(Q = 0\).
  • Internal energy is a state function, so it depends only on the initial and final states.

Understanding the Process

Heat supplied to a system is used to change its internal energy and perform work.


Step 1: Determine Change in Internal Energy (Adiabatic Process)

During the first process (adiabatic):

  • Heat exchange \(Q_1 = 0\)
  • Work done on the system = 22.3 J

Since work done on the system is negative work by the system:

\[ W = -22.3\; J \]

Using the first law:

\[ \Delta U = Q - W \]

\[ \Delta U = 0 - (-22.3) \]

\[ \Delta U = 22.3\; J \]

Thus, the change in internal energy between states A and B is:

ΔU = 22.3 J


Step 2: Convert Heat Supplied in Second Process

Heat absorbed in the second process:

\[ Q_2 = 9.35\; cal \]

Using the conversion:

\[ 1\; cal = 4.19\; J \]

\[ Q_2 = 9.35 \times 4.19 \]

\[ Q_2 \approx 39.2\; J \]


Step 3: Apply First Law for Second Process

Using:

\[ \Delta U = Q_2 - W \]

Substitute the known values:

\[ 22.3 = 39.2 - W \]

Solving for \(W\):

\[ W = 39.2 - 22.3 \]

\[ W = 16.9\; J \]


Final Answer

The net work done by the system in the second process is:

16.9 J


Key Learning Points
  • The First Law of Thermodynamics connects heat, work, and internal energy.
  • In an adiabatic process, heat exchange is zero.
  • Internal energy is a state function, so it depends only on initial and final states.
  • Different paths between the same states may involve different heat and work values.

Q6. Two cylinders A and B of equal capacity are connected to each other via a stopcock. A contains a gas at standard temperature and pressure. B is completely evacuated. The entire system is thermally insulated. The stopcock is suddenly opened. Answer the following :
(a) What is the final pressure of the gas in A and B ?
(b) What is the change in internal energy of the gas ?
(c) What is the change in the temperature of the gas ?
(d) Do the intermediate states of the system lie on its P–V–T surface ?

Concept / Theory

When a gas expands suddenly into a vacuum without external resistance, the process is called free expansion.

Important properties of free expansion:

  • No heat exchange if the system is insulated → \(Q = 0\)
  • No external work is done because expansion occurs into vacuum → \(W = 0\)
  • According to the First Law of Thermodynamics:

\[ \Delta U = Q - W \]

Thus in free expansion:

\[ \Delta U = 0 \]

For an ideal gas, internal energy depends only on temperature. Therefore, if internal energy does not change, the temperature also remains constant.


Understanding the Process

Gas expands freely from cylinder A into the evacuated cylinder B when the stopcock is opened.


(a) Final Pressure of the Gas

Initially:

  • Cylinder A contains gas at pressure \(P_1\)
  • Cylinder B is vacuum
  • Volume of each cylinder = \(V\)

After opening the stopcock, the gas spreads into both cylinders.

Final volume of gas:

\[ V_f = V + V = 2V \]

Since temperature remains constant, using the ideal gas relation:

\[ P_1 V = P_f (2V) \]

\[ P_f = \frac{P_1}{2} \]

Therefore, the final pressure in both cylinders becomes:

Final Pressure = \(P_1 / 2\)


(b) Change in Internal Energy

Using the First Law of Thermodynamics:

\[ \Delta U = Q - W \]

Since the system is insulated:

\[ Q = 0 \]

Expansion occurs into vacuum, so:

\[ W = 0 \]

Therefore:

\[ \Delta U = 0 \]

Change in Internal Energy = 0


(c) Change in Temperature

For an ideal gas:

Internal Energy \(U \propto T\)

Since internal energy does not change:

\[ \Delta T = 0 \]

Temperature remains unchanged.


(d) Do Intermediate States Lie on the P–V–T Surface?

The P–V–T surface represents only equilibrium states of a gas.

During free expansion:

  • Pressure is not uniform throughout the gas
  • Density varies at different locations
  • The system is not in thermodynamic equilibrium

Therefore, these intermediate states cannot be represented by a single point on the P–V–T surface.

Hence, intermediate states do not lie on the P–V–T surface.


Key Learning Points
  • Free expansion occurs when a gas expands into a vacuum.
  • No heat exchange and no work → \(Q = 0\), \(W = 0\).
  • Therefore internal energy remains constant.
  • For an ideal gas, constant internal energy means constant temperature.
  • P–V–T diagrams represent only equilibrium states.

Q7. An electric heater supplies heat to a system at a rate of 100 W. If the system performs work at a rate of 75 joules per second, at what rate is the internal energy increasing?

Concept / Theory

The First Law of Thermodynamics states that the heat supplied to a system is used to increase its internal energy and to perform work.

\[ \Delta U = Q - W \]

For processes where heat and work occur continuously, we use the rate form of the first law:

\[ \frac{dU}{dt} = \dot{Q} - \dot{W} \]

  • \(\frac{dU}{dt}\) = rate of change of internal energy
  • \(\dot{Q}\) = rate of heat supplied to the system
  • \(\dot{W}\) = rate of work done by the system

Note: 1 watt (W) = 1 joule per second (J/s).


Understanding the Energy Flow

Heat supplied to a system is partly converted into work and partly increases internal energy.


Given Data

  • Rate of heat supplied by heater = \(100\ W\)
  • Rate of work done by the system = \(75\ J/s\)

Since \(1 W = 1 J/s\):

\[ \dot{Q} = 100\ J/s \]

\[ \dot{W} = 75\ J/s \]


Step 1: Apply First Law (Rate Form)

\[ \frac{dU}{dt} = \dot{Q} - \dot{W} \]


Step 2: Substitute the Values

\[ \frac{dU}{dt} = 100 - 75 \]

\[ \frac{dU}{dt} = 25\ J/s \]

Since \(1\ J/s = 1\ W\):

\[ \frac{dU}{dt} = 25\ W \]


Final Answer

The internal energy of the system is increasing at a rate of:

25 W (or 25 J/s)


Key Learning Points
  • The First Law of Thermodynamics relates heat, work, and internal energy.
  • In rate form: \(\frac{dU}{dt} = \dot{Q} - \dot{W}\).
  • Heat supplied increases internal energy unless it is used to perform work.
  • Power is measured in watts (J/s).

Q8. A thermodynamic system is taken from an original state to an intermediate state by the linear process shown in Fig. (11.11). Its volume is then reduced to the original value from E to F by an isobaric process.
Calculate the total work done by the gas from D → E → F.

Concept / Theory

In thermodynamics, the work done by a gas during expansion or compression can be determined from a Pressure–Volume (P–V) diagram.

\[ W = \int P\, dV \]

Graphically, this means:

  • The area under the P–V curve represents the work done.
  • If the gas expands, work done is positive.
  • If the gas compresses, work done is negative.

Fig. 11.11
Fig. 11.11 : P–V diagram showing processes D → E → F

Step 1: Work Done During Process D → E

The process from D to E is a linear process on the P–V diagram. Therefore, the work done equals the area under the straight line DE.

This area forms a trapezium.

Given:

  • Pressure at D: \(P_D = 600\ N\,m^{-2}\)
  • Pressure at E: \(P_E = 300\ N\,m^{-2}\)
  • Volume at D: \(V_D = 2\ m^3\)
  • Volume at E: \(V_E = 5\ m^3\)

\[ W_{DE} = \frac{1}{2}(P_D + P_E)(V_E - V_D) \]

\[ W_{DE} = \frac{1}{2}(600 + 300)(5 - 2) \]

\[ W_{DE} = \frac{1}{2} \times 900 \times 3 \]

\[ W_{DE} = 1350\ J \]

Since the volume increases, the gas expands, so the work done is positive.


Step 2: Work Done During Process E → F

The process from E to F is an isobaric process (constant pressure).

Pressure:

\[ P = 300\ N\,m^{-2} \]

Volume decreases from:

  • \(V_E = 5\ m^3\)
  • \(V_F = 2\ m^3\)

Work done in an isobaric process:

\[ W = P(V_F - V_E) \]

\[ W_{EF} = 300(2 - 5) \]

\[ W_{EF} = -900\ J \]

The negative sign indicates compression (work done on the gas).


Step 3: Total Work Done

Total work done during the process D → E → F:

\[ W_{total} = W_{DE} + W_{EF} \]

\[ W_{total} = 1350 - 900 \]

\[ W_{total} = 450\ J \]


Final Answer

Total work done by the gas = 450 J


Key Learning Points
  • Work done by a gas equals the area under the P–V curve.
  • Expansion → positive work.
  • Compression → negative work.
  • Linear processes on a P–V diagram form geometric shapes whose area represents work.

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    Frequently Asked Questions

    Thermodynamics is the branch of physics that deals with heat, work, energy, and the laws governing their interconversion in macroscopic systems.

    A thermodynamic system is a specified quantity of matter or a region of space chosen for study, separated from its surroundings by a real or imaginary boundary.

    The surroundings include everything outside the thermodynamic system that can interact with it by exchanging heat or work.

    The thermodynamic state of a system is its condition described completely by state variables such as pressure, volume, and temperature.

    State variables are physical quantities whose values depend only on the current state of the system and not on the path followed.

    Pressure, volume, temperature, internal energy, entropy, and enthalpy are state variables.

    Path variables are quantities whose values depend on the path taken during a process, such as heat and work.

    A system is in thermodynamic equilibrium when it is simultaneously in thermal, mechanical, and chemical equilibrium.

    An equation of state is a mathematical relation connecting state variables of a system in equilibrium, such as \(PV = nRT\).

    An ideal gas is a hypothetical gas whose molecules do not interact except during elastic collisions and obey the ideal gas equation exactly.

    The ideal gas equation is \(PV = nRT\), where symbols have their usual meanings.

    Internal energy is the total microscopic energy of a system arising from molecular motion and interactions.

    The internal energy of an ideal gas depends only on temperature.

    The first law states that heat supplied to a system equals the increase in internal energy plus work done by the system.

    \(\Delta Q = \Delta U + W\).

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