1. Physics
  2. Thermodynamics
  3. Second Law of Thermodynamics

Thermodynamics · JEE & NEET Physics

Second Law of Thermodynamics: notes and previous year questions

The direction of natural processes: Kelvin–Planck and Clausius statements, efficiency and COP, reversibility and Carnot's theorem.

Second Law of Thermodynamics in short

  • The second law gives the direction of natural processes; the first law only counts energy.
  • Kelvin–Planck: no cyclic engine turns all the heat from one reservoir into work.
  • Clausius: no cyclic device moves heat from cold to hot with no other effect.
  • The two statements are equivalent: breaking one lets you break the other.

1What the first law misses

Hot tea cools to room temperature; a bouncing ball stops and warms the floor; a gas spreads through an empty box. The reverse processes would conserve energy, so the first law allows them, yet they never happen by themselves. The second law gives the direction of natural processes.

2The Kelvin–Planck statement

A real engine takes heat QHQ_H from a hot reservoir, does work WW and rejects heat QCQ_C to a cold reservoir. It must reject some heat, so its efficiency is always below 1. A machine that ran a ship on the heat of the ocean alone would be a perpetual motion machine of the second kind.

η=WQH<1\eta = \frac{W}{Q_H} < 1

3The Clausius statement

A refrigerator takes heat QCQ_C from the cold inside and gives QHQ_H to the warmer room, but only by using work WW: that is why fridges and air conditioners need electricity.

4Two sides of one law

Suppose a device R broke Clausius, moving 600 J from cold to hot with no work. Pair it with an ordinary engine E that takes 1000 J from the hot reservoir, does 400 J of work and rejects 600 J. Together: the cold reservoir gains and loses 600 J (no change), and the hot reservoir gives just 400 J, all turned into 400 J of work. That breaks Kelvin–Planck. The argument also works the other way, so the two statements are equivalent.

5Efficiency and COP

Over one cycle ΔU=0\Delta U = 0, so QH=W+QCQ_H = W + Q_C.

η=WQH=1−QCQH\eta = \frac{W}{Q_H} = 1 - \frac{Q_C}{Q_H}Engine: always less than 1.
COPR=QCW\text{COP}_R = \frac{Q_C}{W}Refrigerator: can be much more than 1, since it only moves heat.
COPHP=QHW=COPR+1\text{COP}_{HP} = \frac{Q_H}{W} = \text{COP}_R + 1Heat pump (warming a room).
DeviceGoalMeasureTypical
Heat engineworkη=W/QH\eta = W/Q_H0.3–0.6
Refrigeratorcool the insideQC/WQ_C/W2–5
Heat pumpwarm the insideQH/WQ_H/W3–6

6Reversible or not

A reversible process can be undone leaving no trace anywhere. It must be slow (quasi-static), frictionless, and exchange heat only across tiny temperature differences — like taking sand grains off a piston one at a time. Pulling the pins so a piston jumps is irreversible.

  • Causes of irreversibility: friction, heat flow across a finite temperature difference, free expansion, mixing, electrical resistance, plastic deformation.
  • Every real process is irreversible; reversible processes are the ideal limit.

7Carnot's theorem

ηmax⁡=1−TCTH\eta_{\max} = 1 - \frac{T_C}{T_H}Temperatures in kelvin (derived in the next lesson).

Why. If an engine E (50%) beat a Carnot engine C (40%), run C backwards as a refrigerator using 400 J of E's 500 J to return 1000 J to the hot reservoir. The hot reservoir is unchanged, the cold one gives 100 J, and 100 J of work is left over — all from one reservoir, breaking Kelvin–Planck.

Summary

Key ideas

  • The second law gives the direction of natural processes; the first law only counts energy.
  • Kelvin–Planck: no cyclic engine turns all the heat from one reservoir into work.
  • Clausius: no cyclic device moves heat from cold to hot with no other effect.
  • The two statements are equivalent: breaking one lets you break the other.
  • Engine efficiency η=W/QH=1−QC/QH\eta = W/Q_H = 1 - Q_C/Q_H is always below 1.
  • Refrigerator COP=QC/W\text{COP} = Q_C/W can exceed 1; a heat pump's COP is one more.
  • Reversible processes are slow, frictionless and have tiny temperature differences; real ones are irreversible.
  • Carnot's theorem: no engine beats a reversible one; ηmax⁡=1−TC/TH\eta_{\max} = 1 - T_C/T_H.

Every equation

Energy per cycle
QH=W+QCQ_H = W + Q_C
Efficiency
η=W/QH=1−QC/QH\eta = W/Q_H = 1 - Q_C/Q_H
Refrigerator
COPR=QC/W\text{COP}_R = Q_C/W
Heat pump
COPHP=QH/W=COPR+1\text{COP}_{HP} = Q_H/W = \text{COP}_R + 1
Carnot limit
ηmax⁡=1−TC/TH\eta_{\max} = 1 - T_C/T_H
Carnot refrigerator
COPR=TCTH−TC\text{COP}_R = \frac{T_C}{T_H - T_C}
Carnot heat pump
COPHP=THTH−TC\text{COP}_{HP} = \frac{T_H}{T_H - T_C}
Equal engines in series
T=THTCT = \sqrt{T_HT_C}

Previous year questions with solutions

Real JEE and NEET questions on second 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 second 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.