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NDA Physics · Formula sheet

Heat and Thermodynamics formulas

12 formulas, 2 reference tables and 23 common traps for NDA Physics Heat and Thermodynamics, grouped by subtopic.

Full notes with worked examples

Temperature, Scales, and Thermal Expansion

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Temperature and the three scales

Temperature-scale conversions

C5=F−329=K−273.155F=95C+32K=C+273.15\frac{C}{5} = \frac{F - 32}{9} = \frac{K - 273.15}{5} \qquad F = \frac{9}{5}C + 32 \qquad K = C + 273.15
  • CCtemperature in degrees Celsius
  • FFtemperature in degrees Fahrenheit
  • KKtemperature in kelvin (absolute)

Thermal expansion — linear, areal, and volume coefficients

Expansion coefficients are in the ratio 1 : 2 : 3

ΔL=Lα Δθβ=2αγ=3α=32β\Delta L = L\alpha\,\Delta\theta \qquad \beta = 2\alpha \qquad \gamma = 3\alpha = \tfrac{3}{2}\beta
  • α\alphalinear expansion coefficient
  • β\betaareal (superficial) expansion coefficient
  • γ\gammavolume (cubical) expansion coefficient
  • Δθ\Delta\thetarise in temperature

Consequences of expansion — pendulums and liquid measurement

Pendulum period and apparent expansion

T=2πLgΔTT=12α Δθγreal=γapparent+γvesselT = 2\pi\sqrt{\frac{L}{g}} \qquad \frac{\Delta T}{T} = \frac{1}{2}\alpha\,\Delta\theta \qquad \gamma_{\text{real}} = \gamma_{\text{apparent}} + \gamma_{\text{vessel}}
  • TTtime period of the pendulum
  • LLlength of the pendulum rod
  • γreal\gamma_{\text{real}}true volume expansion of the liquid
  • γapparent\gamma_{\text{apparent}}observed expansion (uncorrected)

Common traps

A temperature CHANGE is the same in K and °C, but a temperature VALUE is not

If the question asks 'increase of 30 K equals how many °C?', the answer is 30°C — because the step size is identical. But '300 K equals how many °C?' is 300−273=27°C300 - 273 = 27°\text{C}, because of the offset. Read whether it asks for a value or a change.

Never write a degree sign with Kelvin

It is '273 K' and '0 K', not '273°K'. The kelvin already IS an absolute scale, so the degree symbol is dropped by convention. An option that writes '°K' is usually the planted wrong one.

Absolute zero is −273°C, not −273 K

Absolute zero is 0 K, equivalently −273.15°C. A distractor that says 'absolute zero is −273 K' confuses the two scales — −273 K is meaningless because the Kelvin scale cannot go below 0.

Set the SCALE VARIABLES equal, not the formula sides

The condition 'two scales read the same number' means F=CF = C (or K=FK = F) — set those equal, THEN use a conversion to get one equation in one unknown. Do not just equate 95C+32\frac{9}{5}C+32 to something; first decide which two readings coincide.

Areal to volume is ×3/2, not ×3

Going linear to volume multiplies by 3. But going AREAL to volume multiplies by only 32\frac{3}{2}, because areal is already 2α2\alpha. Decide which coefficient you were given before scaling.

Heated pendulum slows DOWN — the period goes UP

Students sometimes say 'faster' assuming heat speeds things up. Physically the rod lengthens, the period T=2πL/gT = 2\pi\sqrt{L/g} rises, so the clock ticks slower and LOSES time. The effect is slight, not 'more than double'.

Heat, Specific Heat, Calorimetry, and Heat Transfer

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Specific heat, thermal capacity, and Q = mcΔT

Sensible heat (no phase change)

Q=mc ΔθThermal capacity=mcQ = mc\,\Delta\theta \qquad \text{Thermal capacity} = mc
  • QQheat supplied or removed (J)
  • mmmass (kg)
  • ccspecific heat capacity (J/(kg·°C))
  • Δθ\Delta\thetachange in temperature (°C or K)

Latent heat and the calorimetry mixing balance

Latent heat + the mixing balance

Q=mL∑Qlost=∑QgainedQ = mL \qquad \sum Q_{\text{lost}} = \sum Q_{\text{gained}}
  • LLspecific latent heat (cal/g or J/kg)
  • mmmass undergoing phase change
  • QQheat absorbed/released at constant temperature

When specific heat varies with temperature

Heat for a temperature-dependent specific heat

Q=m∫T1T2 ⁣(C0+αT) dT=m(T2−T1)[C0+12α(T1+T2)]Q = m\int_{T_1}^{T_2}\!\big(C_0 + \alpha T\big)\,dT = m(T_2 - T_1)\left[C_0 + \tfrac{1}{2}\alpha(T_1 + T_2)\right]
  • C0C_0specific heat at T = 0 (a constant)
  • α\alpharate of change of specific heat with temperature
  • T1,T2T_1, T_2initial and final temperatures

The three modes of heat transfer — conduction, convection, radiation

ModeHow it worksMedium / key fact
ConductionHeat passes molecule to molecule; molecules vibrate in place and pass energy to neighbours without moving from their positionsNeeds a material medium; dominant in solids (especially metals)
ConvectionHeated fluid becomes less dense and rises; cooler fluid sinks to replace it, setting up a circulating current that carries heatNeeds a fluid (liquid or gas) that can flow; bulk movement of matter
RadiationHeat travels as electromagnetic (infrared) waves in a straight lineNeeds NO medium; travels at the speed of light — how the Sun heats Earth
NDA 2019 — 'heat waves travel in a straight line with the speed of light' is THERMAL RADIATION (not conduction or convection).
Conduction and convection both require a medium; only radiation crosses vacuum. A thermos flask defeats all three: vacuum gap stops conduction/convection, silvered walls reflect radiation.

Common traps

A body has internal energy, not 'heat'

It is loose to say a hot body 'has a lot of heat'. Strictly, heat is energy IN TRANSIT — once absorbed it becomes the body's internal energy. NDA tests the precise definition: energy transferred due to a temperature difference.

Specific heat is intrinsic; thermal capacity is not

Specific heat capacity does NOT depend on mass or shape — it is the same for 1 g or 1 tonne of the material. Thermal capacity =mc= mc DOES scale with mass. The NDA repeatedly tests this distinction (statements like 'specific heat depends on mass' are false).

Watch the units — kJ vs J, kg vs g

Convert kilojoules to joules and grams to kilograms before plugging in, or the answer is off by a factor of 1000. In Q=mc ΔθQ = mc\,\Delta\theta keep cc in J/(kg·°C) with mm in kg.

Don't forget the latent-heat term while ice is melting

A classic error is treating ice → water as pure Q=mc ΔθQ = mc\,\Delta\theta. The melting itself absorbs mLmL at a flat 0°C with no temperature change. Add a separate mLmL term, or your heat budget is hundreds of calories short.

Keep masses in consistent units across both sides

In these problems one mass is in grams (ice) and the other may be given in kg (water). Convert to grams everywhere (or kg everywhere) before equating heat lost and heat gained.

The factor on α\alpha is one-half, not one

The planted distractor uses [C0+α(T1+T2)][C_0 + \alpha(T_1 + T_2)] (no one-half). The integral of αT\alpha T gives α2T2\tfrac{\alpha}{2}T^2, so after factoring you get 12α(T1+T2)\tfrac{1}{2}\alpha(T_1 + T_2) — the half is essential.

Only radiation crosses a vacuum

Conduction and convection BOTH need matter — conduction needs contact, convection needs a flowing fluid. Radiation alone needs no medium, which is why the Sun's heat reaches us through the vacuum of space. Any 'heat travels at the speed of light' clue means radiation.

A thermos REFLECTS radiation — it does not absorb it

The silvered walls are there to reflect infrared back, not to soak it up. An option saying the inner wall radiates and the outer absorbs is the planted wrong statement on 'which is NOT correct' questions.

Phase Change, Boiling, Evaporation, and Cooling

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Latent heat of fusion and vaporization

Latent heat

Q=mLQ = mL
  • QQheat absorbed or released at constant temperature
  • mmmass changing phase
  • LLspecific latent heat (fusion or vaporization)

Boiling point depends on pressure

Boiling condition

Pvapour=PatmosphericP_{\text{vapour}} = P_{\text{atmospheric}}
  • PvapourP_{\text{vapour}}saturated vapour pressure of the liquid
  • PatmosphericP_{\text{atmospheric}}external (atmospheric) pressure

Newton's law of cooling

−dθdt∝(θ−θ0)-\frac{d\theta}{dt} \propto (\theta - \theta_0)
  • θ\thetatemperature of the body
  • θ0\theta_0temperature of the surroundings
  • dθdt\frac{d\theta}{dt}rate of change of temperature with time

Common traps

Latent heat is absorbed at CONSTANT temperature

The defining phrase the NDA hunts for is 'without changing the temperature'. During a phase change the thermometer reading is flat while heat is still flowing — the heat breaks molecular bonds instead of warming the substance.

Boiling is vapour pressure = atmospheric, not 'less than'

Distractors offer 'vapour pressure becomes less than' or 'greater than' atmospheric. Boiling is the exact EQUALITY: the liquid's vapour pressure rises to meet the external pressure. Pick the 'equal to' option.

Evaporation happens at ALL temperatures; boiling does not

A common confusion is that a liquid only evaporates when heated. Evaporation occurs at any temperature (wet clothes dry in the shade). Boiling is the one that needs the specific boiling-point temperature.

Newton's law does NOT apply to phase changes or furnace heat

The law needs the body's temperature to actually be changing and the temperature difference to be small. Melting ice and boiling water hold a constant temperature; a furnace-hot rod has a huge difference dominated by radiation. Only gentle convective cooling qualifies.

Gas Laws and the Laws of Thermodynamics

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The ideal gas law

Ideal gas law and the combined gas law

PV=nRTP1V1T1=P2V2T2PV = nRT \qquad \frac{P_1 V_1}{T_1} = \frac{P_2 V_2}{T_2}
  • PPpressure
  • VVvolume
  • nnnumber of moles (or molecules)
  • RRuniversal gas constant
  • TTabsolute temperature (K)

First law of thermodynamics

ΔU=Q−W\Delta U = Q - W
  • ΔU\Delta Uchange in internal energy
  • QQheat supplied to the system
  • WWwork done BY the system

Named processes — isothermal, adiabatic, isochoric, isobaric

Identify a process by substituting PV = nRT

P=kT  ⇒  V=nRk=const  ⇒  isochoric,  C=CVP = kT \;\Rightarrow\; V = \frac{nR}{k} = \text{const} \;\Rightarrow\; \text{isochoric},\; C = C_V
  • kkthe constant in the given process equation
  • CVC_Vmolar heat capacity at constant volume
  • CPC_Pmolar heat capacity at constant pressure

The second law and a process summary table

Process / lawWhat is held / statedKey consequence
IsothermalTemperature constantΔU=0\Delta U = 0; PV=constPV = \text{const}; all heat becomes work
AdiabaticNo heat exchanged (Q = 0)Insulated; temperature still changes (compression heats the gas)
IsochoricVolume constant (W = 0)ΔU=Q\Delta U = Q; molar heat capacity CVC_V; P∝TP \propto T
IsobaricPressure constantMolar heat capacity CPC_P (and CP>CVC_P > C_V); V∝TV \propto T
Second lawHeat won't flow cold → hot unaidedExternal work needed to move heat uphill (refrigerator); sets the direction of natural processes
NDA 2017 — 'heat cannot flow by itself from a lower to a higher temperature' is the SECOND law of thermodynamics.
The first law is energy bookkeeping (ΔU = Q − W); the second law sets the one-way direction of heat flow.

Common traps

Temperature in the gas law is ALWAYS in kelvin

Using Celsius in PV=nRTPV = nRT or in P∝TP \propto T gives wrong ratios. Convert to kelvin first. 'Pressure doubles when temperature doubles' is only true on the absolute scale.

Internal energy of an ideal gas depends only on temperature

In an ISOTHERMAL process (constant T) the internal energy does not change at all (ΔU=0\Delta U = 0), so any heat absorbed is entirely converted to work. Don't assume absorbing heat always raises internal energy.

Don't guess the process — substitute PV = nRT

A process given as P=kTP = kT or PV2=constPV^2 = \text{const} is not one of the four standard names on sight. Substitute the ideal gas law to see which variable is actually constant, then read off the heat capacity or T-V relation.

Adiabatic means no HEAT exchange, not no temperature change

An adiabatic process has Q=0Q = 0 but the temperature usually DOES change (an adiabatic compression heats a gas). 'No heat exchange' is the definition; 'constant temperature' is isothermal — a different process.

First law = energy; second law = direction

The first law (ΔU = Q − W) is conservation of energy and is direction-blind. The second law adds the arrow: heat flows hot → cold spontaneously, never the reverse without work. Statements about 'cannot flow by itself' point to the SECOND law.

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