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  3. First Law of Thermodynamics

Thermodynamics · JEE & NEET Physics

First Law of Thermodynamics: notes and previous year questions

Systems and state variables, internal energy, heat and work, Q = ΔU + W with its signs, and the special processes.

First Law of Thermodynamics in short

  • Open systems exchange energy and matter, closed ones energy only, isolated ones neither.
  • Intensive variables (T, P, density) do not depend on the amount; extensive ones (V, U, mass) do.
  • Internal energy is the kinetic plus potential energy of the molecules; for an ideal gas it depends only on T.
  • U is a state function; Q and W depend on the path.

1Systems and surroundings

The system is the part of the universe we study (for example, the gas in a cylinder). Everything else is the surroundings, and the surface between them (walls, piston) is the boundary.

SystemEnergy crosses?Matter crosses?Example
OpenYesYesa pot with no lid, the human body
ClosedYesNogas under a piston, a sealed can
IsolatedNoNoan ideal thermos flask

State variables such as PP, VV, TT and UU describe the state of a system. Intensive ones do not depend on the amount (temperature, pressure, density); extensive ones grow with it (volume, internal energy, mass). Cut a hot block in half: each half keeps the temperature but has half the mass.

2Internal energy

The internal energy UU is the total energy of all the molecules: their kinetic energy (moving and spinning) plus the potential energy of the forces between them. Heat a gas and its molecules move faster: TT and UU both rise.

In an ideal gas the molecules do not pull on each other, so UU depends only on the temperature. For any process of an ideal gas:

ΔU=nCv ΔT\Delta U = nC_v\,\Delta TCᵥ is the molar heat capacity at constant volume.

3Heat and work

There are two ways to change UU: supply heat (energy that flows because of a temperature difference) or do work (push, stir, squeeze). A bicycle pump warms up because pushing the handle does work on the air. Heating one box of gas and stirring an identical box can bring both to exactly the same state; afterwards nobody can tell which way the energy got in.

A gas at pressure PP pushes a piston of area AA with force PAPA. If the piston moves Δx\Delta x, the work done by the gas is PA Δx=P ΔVPA\,\Delta x = P\,\Delta V. If the pressure changes, add small pieces:

W=P ΔVW = P\,\Delta VAt constant pressure.
W=∫V1V2P dVW = \int_{V_1}^{V_2} P\,dVIn general: the area under the P–V curve.
  • Expansion: W>0W > 0 (the gas does work).
  • Compression: W<0W < 0 (work is done on the gas).
  • 1 L=10−3 m31\ \text{L} = 10^{-3}\ \text{m}^3 and 1 atm≈1.01×1051\ \text{atm} \approx 1.01 \times 10^5 Pa.

4The first law

Give a gas 500 J of heat. It lifts a loaded piston, doing 200 J of work, and the other 300 J stays inside as internal energy. This is energy conservation for heat and work:

Q=ΔU+WQ = \Delta U + WQ: heat given to the system; ΔU: rise in internal energy; W: work done by the system.
ΔU=Q−W\Delta U = Q - W
QuantityPositive (+)Negative (−)
Qheat goes into the gasheat comes out
Wgas expands (work by it)gas is compressed (work on it)
ΔUtemperature risestemperature falls

5Special processes

ProcessWhat is fixedFirst law becomes
IsothermalT (ideal gas: ΔU = 0)Q = W
Adiabaticno heat: Q = 0ΔU = −W
IsochoricV: W = 0Q = ΔU
IsobaricPQ=ΔU+PΔV=nCpΔTQ = \Delta U + P\Delta V = nC_p\Delta T

In an adiabatic expansion the work comes out of the gas's own internal energy, so it cools; an adiabatic compression heats it (the bicycle pump). At constant pressure, W=PΔV=nRΔTW = P\Delta V = nR\Delta T for an ideal gas, so Q=nCvΔT+nRΔT=nCpΔTQ = nC_v\Delta T + nR\Delta T = nC_p\Delta T with Cp=Cv+RC_p = C_v + R (Mayer's relation).

Wiso=nRTln⁡V2V1W_{\text{iso}} = nRT\ln\frac{V_2}{V_1}Isothermal work (see Thermodynamic Processes).
Wadia=nR(T1−T2)γ−1W_{\text{adia}} = \frac{nR(T_1 - T_2)}{\gamma - 1}Adiabatic work.

6Cycles and free expansion

In a cyclic process the system returns to its starting state, so ΔU=0\Delta U = 0 and the net heat taken in equals the net work done: the area inside the loop on the P–V graph. A rectangle 3 L wide and 2×1052 \times 10^5 Pa tall gives 600 J. If a gas takes in 800 J and gives out 500 J per cycle, it does 300 J of work.

In a free expansion a gas rushes into a vacuum inside an insulated box. It pushes against nothing (W=0W = 0) and no heat crosses (Q=0Q = 0), so ΔU=0\Delta U = 0: an ideal gas keeps its temperature.

Summary

Key ideas

  • Open systems exchange energy and matter, closed ones energy only, isolated ones neither.
  • Intensive variables (T, P, density) do not depend on the amount; extensive ones (V, U, mass) do.
  • Internal energy is the kinetic plus potential energy of the molecules; for an ideal gas it depends only on T.
  • U is a state function; Q and W depend on the path.
  • Heat and work are both energy in transit; either can raise U.
  • The work done by a gas is the area under its P–V curve; expansion gives positive work.
  • First law: Q = ΔU + W, with Q into the gas and W done by the gas positive.
  • Isothermal: ΔU = 0, Q = W. Adiabatic: Q = 0, ΔU = −W. Isochoric: W = 0, Q = ΔU.
  • Isobaric: Q=nCpΔTQ = nC_p\Delta T, with Cp=Cv+RC_p = C_v + R.
  • Over a full cycle ΔU = 0, so the net heat equals the net work (the area inside the loop).
  • In a free expansion Q = W = ΔU = 0, and an ideal gas keeps its temperature.

Every equation

First law
Q=ΔU+WQ = \Delta U + W
Rearranged
ΔU=Q−W\Delta U = Q - W
Ideal gas
ΔU=nCvΔT\Delta U = nC_v\Delta T
Work (general)
W=∫P dVW = \int P\,dV
Work (constant P)
W=PΔV=nRΔTW = P\Delta V = nR\Delta T
Isothermal
ΔU=0, Q=W\Delta U = 0,\ Q = W
Isothermal work
W=nRTln⁡(V2/V1)W = nRT\ln(V_2/V_1)
Adiabatic
Q=0, ΔU=−WQ = 0,\ \Delta U = -W
Adiabatic work
W=nR(T1−T2)γ−1W = \frac{nR(T_1 - T_2)}{\gamma - 1}
Isochoric
W=0, Q=nCvΔTW = 0,\ Q = nC_v\Delta T
Isobaric
Q=nCpΔTQ = nC_p\Delta T
Mayer's relation
Cp−Cv=RC_p - C_v = R
Cycle
ΔU=0, Qnet=Wnet\Delta U = 0,\ Q_{\text{net}} = W_{\text{net}}
Units
1 L=10−3 m3, 1 cal=4.186 J1\ \text{L} = 10^{-3}\ \text{m}^3,\ 1\ \text{cal} = 4.186\ \text{J}

Previous year questions with solutions

Real JEE and NEET questions on first law of thermodynamics. Try each one before you open the solution.

Q1NEET 2026One correct option

An electric heater supplies heat to a system at a rate of 100 W . If the system performs work at a rate of 75 J/s75\ \mathrm{J/s}, then the rate at which internal energy increases will be:

  1. A75 W
  2. B100 W
  3. C125 W
  4. D25 W
Show answer and solution

Answer: Option D

The first law holds for every second of the process, so it can be written as rates: heat in per second == rise of internal energy per second ++ work done per second.

100=dUdt+75100 = \dfrac{dU}{dt} + 75, so dUdt=25 W\dfrac{dU}{dt} = 25\ \mathrm{W}.

The trap is A, 75 W75\ \mathrm{W}, the rate of doing work, and B, 100 W100\ \mathrm{W}, the whole heating rate — as if no work were done. C, 125 W125\ \mathrm{W}, adds the work to the heat, getting the sign of WW backwards: work done BY the system is energy leaving it.

Q2JEE Main 2026One correct option

Heat is supplied to a diatomic gas at constant pressure. Then the ratio of ΔQ:ΔU:ΔW\Delta Q:\Delta U:\Delta W is ______.

  1. A2 : 3 : 5
  2. B5 : 3 : 2
  3. C2 : 5 : 7
  4. D7 : 5 : 2
Show answer and solution

Answer: Option D

At constant pressure, per mole and per kelvin: ΔQ=CP ΔT\Delta Q = C_{P}\,\Delta T, ΔU=CV ΔT\Delta U = C_{V}\,\Delta T and ΔW=R ΔT\Delta W = R\,\Delta T. For a diatomic gas CV=52RC_{V} = \dfrac{5}{2}R and CP=72RC_{P} = \dfrac{7}{2}R, so

ΔQ:ΔU:ΔW=72:52:1=7:5:2\Delta Q : \Delta U : \Delta W = \dfrac{7}{2} : \dfrac{5}{2} : 1 = 7 : 5 : 2

Check with the first law: 7=5+27 = 5 + 2.

The trap is B, 5:3:25 : 3 : 2, which is the monatomic gas (52:32:1\dfrac{5}{2} : \dfrac{3}{2} : 1). A and C list the same numbers backwards, in the order W:U:QW : U : Q — and neither passes the check that QQ is the sum of the other two.

Q3JEE Main 2026Numerical answer

A diatomic gas (γ=1.4)(\gamma =1.4) does 100 J of work when it is expanded isobarically. Then the heat given to the gas ____\_\_\_\_ J.

Show answer and solution

Answer: 350

At constant pressure W=nR ΔTW = nR\,\Delta T and Q=nCP ΔTQ = nC_{P}\,\Delta T, so QW=CPR\dfrac{Q}{W} = \dfrac{C_{P}}{R}. With γ=1.4=75\gamma = 1.4 = \dfrac{7}{5} the gas is diatomic, CP=72RC_{P} = \dfrac{7}{2}R, and QW=72\dfrac{Q}{W} = \dfrac{7}{2} (the same as γγ−1=1.40.4=3.5\dfrac{\gamma}{\gamma - 1} = \dfrac{1.4}{0.4} = 3.5).

Q=3.5×100=350 JQ = 3.5 \times 100 = 350\ \mathrm{J}: 100 J100\ \mathrm{J} goes into work and 250 J250\ \mathrm{J} into internal energy.

The trap is 250 J250\ \mathrm{J}, which is ΔU\Delta U and forgets the work itself. Another is 140 J140\ \mathrm{J}, γ×100\gamma \times 100, which treats γ\gamma as the ratio of heat to work — that ratio is CPR\dfrac{C_{P}}{R}, not CPCV\dfrac{C_{P}}{C_{V}}.

Practice questions, easy to hard

Three questions from the first law of thermodynamics practice ladder: one easy, one medium, one hard.

Q4One correct option

Two simple processes follow straight from the first law.

Constant volume (isochoric): the gas pushes nothing back, so W=0W = 0 and all the heat goes into internal energy, Q=ΔU=nCV ΔTQ = \Delta U = nC_{V}\,\Delta T.

Constant pressure (isobaric): W=p ΔV=nR ΔTW = p\,\Delta V = nR\,\Delta T (from pV=nRTpV = nRT), and Q=ΔU+W=n(CV+R) ΔT=nCP ΔTQ = \Delta U + W = n(C_{V} + R)\,\Delta T = nC_{P}\,\Delta T. So the fraction of the heat that becomes work is

WQ=RCP=1−1γ\dfrac{W}{Q} = \dfrac{R}{C_{P}} = 1 - \dfrac{1}{\gamma}

and the fraction that becomes internal energy is CVCP=1γ\dfrac{C_{V}}{C_{P}} = \dfrac{1}{\gamma}.

A monatomic ideal gas is given 500 J500\ \mathrm{J} of heat at constant pressure. How much work does it do?

  1. A300 J300\ \mathrm{J}
  2. B500 J500\ \mathrm{J}
  3. C200 J200\ \mathrm{J}
  4. D143 J143\ \mathrm{J}
Show answer and solution

Answer: Option C

For a monatomic gas CV=32RC_{V} = \dfrac{3}{2}R and CP=52RC_{P} = \dfrac{5}{2}R, so WQ=RCP=25\dfrac{W}{Q} = \dfrac{R}{C_{P}} = \dfrac{2}{5} and W=25×500=200 JW = \dfrac{2}{5} \times 500 = 200\ \mathrm{J}. The other 300 J300\ \mathrm{J} raises the internal energy.

The trap is A, 300 J300\ \mathrm{J}, which is ΔU\Delta U, not WW. B, 500 J500\ \mathrm{J}, sends all the heat into work — but the gas warms up as it expands at constant pressure. D, 143 J143\ \mathrm{J}, uses the diatomic fraction 27\dfrac{2}{7}.

Q5Numerical answer

Many processes follow pVx=constantpV^{x} = \text{constant} for some number xx — a polytropic process. x=0x = 0 is constant pressure, x=1x = 1 is isothermal, x=γx = \gamma is adiabatic. Integrating p dVp\,dV gives the work for any x≠1x \neq 1:

W=p1V1−p2V2x−1=nR(T1−T2)x−1W = \dfrac{p_{1}V_{1} - p_{2}V_{2}}{x - 1} = \dfrac{nR(T_{1} - T_{2})}{x - 1}

(With x=γx = \gamma this is the adiabatic formula you already know.)

One mole of an ideal gas is heated so that its pressure stays proportional to its volume, p=kVp = kV — that is, pV−1pV^{-1} constant, x=−1x = -1. Its temperature rises from 300 K300\ \mathrm{K} to 400 K400\ \mathrm{K}. How much work does it do, in joules? Take R=8.3 J mol−1 K−1R = 8.3\ \mathrm{J\,mol^{-1}\,K^{-1}}.

Show answer and solution

Answer: 415 J

W=nR(T1−T2)x−1=8.3×(300−400)−1−1=−830−2=415 JW = \dfrac{nR(T_{1} - T_{2})}{x - 1} = \dfrac{8.3 \times (300 - 400)}{-1 - 1} = \dfrac{-830}{-2} = 415\ \mathrm{J}.

Check by area: p=kVp = kV is a straight line through the origin, and the area under it is k(V22−V12)2=p2V2−p1V12=R ΔT2\dfrac{k(V_{2}^{2} - V_{1}^{2})}{2} = \dfrac{p_{2}V_{2} - p_{1}V_{1}}{2} = \dfrac{R\,\Delta T}{2}.

The trap is reading "pp proportional to VV" as x=+1x = +1: written as pVxpV^{x} constant, p=kVp = kV is pV−1=kpV^{-1} = k, so x=−1x = -1 (and x=+1x = +1 would divide by zero). Another is nR ΔT=830 JnR\,\Delta T = 830\ \mathrm{J}, the constant-pressure answer, twice too big.

Q6One correct option

Take logs of pVx=constantpV^{x} = \text{constant}: log⁡p=−xlog⁡V+constant\log p = -x\log V + \text{constant}. So on a graph of log⁡p\log p against log⁡V\log V, every polytropic process is a straight line, and its slope is −x-x. Reading the slope gives xx, and xx gives the heat capacity C=CV+R1−xC = C_{V} + \dfrac{R}{1 - x}.

On a graph of log⁡p\log p against log⁡V\log V, a process is a straight line of slope −γ-\gamma. Which process is it?

  1. Aisothermal
  2. Bisobaric
  3. Cadiabatic
  4. Disochoric
Show answer and solution

Answer: Option C

Slope −γ-\gamma means x=γx = \gamma: pVγpV^{\gamma} is constant, the adiabatic, with C=0C = 0.

The trap is A, isothermal, which is x=1x = 1 and slope −1-1. B, isobaric, is x=0x = 0, a horizontal line. D, isochoric, keeps log⁡V\log V fixed — a vertical line, with no finite slope at all.