The quasi-static idealisation
Before any process can be drawn as a curve, it must be quasi-static. Suppose the weight on a movable piston is suddenly lifted. The piston accelerates outward and, for an instant, the gas passes through non-equilibrium states that have no well-defined single pressure or temperature. A non-equilibrium state cannot be plotted as one point on a P-V diagram, so a sudden change cannot be drawn as a continuous curve at all.
NCERT therefore introduces the quasi-static process: an idealised, infinitely slow change in which the system remains in thermal and mechanical equilibrium with its surroundings at every stage. At each instant the system's pressure differs from the external pressure only infinitesimally, and the same holds for temperature. Only such a process traces a continuous, well-defined path that can be integrated for work. Every formula in this article assumes the process is quasi-static — this is the silent assumption NCERT states it will keep "from now on... except when stated otherwise."
The first law as a sorting engine
The whole subject of processes is one equation read four ways. The first law of thermodynamics states
$$\Delta Q = \Delta U + \Delta W, \qquad \Delta W = P\,\Delta V .$$Here $\Delta Q$ is heat supplied to the system, $\Delta U$ the change in internal energy (a state variable, depending only on temperature for an ideal gas), and $\Delta W$ the work done by the system. Each special process fixes one quantity, and that constraint kills one term in the equation. Read the table below as the spine of everything that follows.
| Process | Held fixed | Term that vanishes | First law reduces to |
|---|---|---|---|
| Isothermal | Temperature $T$ | $\Delta U = 0$ | $\Delta Q = \Delta W$ |
| Adiabatic | Heat $\Delta Q = 0$ (insulated) | $\Delta Q = 0$ | $\Delta U = -\Delta W$ |
| Isochoric | Volume $V$ | $\Delta W = 0$ | $\Delta Q = \Delta U$ |
| Isobaric | Pressure $P$ | none | $\Delta Q = \Delta U + P\,\Delta V$ |
Notice the symmetry: isothermal and adiabatic kill different terms ($\Delta U$ versus $\Delta Q$) yet are constantly confused; isochoric and isobaric are the constant-volume and constant-pressure twins that pair with $C_v$ and $C_p$ respectively. We now take each in turn, then assemble the master grid.
Isothermal process
An isothermal process holds the temperature fixed throughout — for example, a gas expanding slowly in a metallic cylinder immersed in a large constant-temperature reservoir, whose heat capacity is so large that the heat it exchanges does not alter its own temperature. With $T$ constant, the ideal gas equation gives
$$PV = \text{constant} \qquad (\text{Boyle's Law}),$$so pressure varies inversely with volume. To find the work, sum $\Delta W = P\,\Delta V$ over the path, substituting $P = \mu RT / V$ and taking the constants out of the integral:
$$W = \int_{V_1}^{V_2} P\,dV = \mu RT \int_{V_1}^{V_2}\frac{dV}{V} = \mu RT \,\ln\!\frac{V_2}{V_1} = 2.303\,\mu RT \,\log_{10}\!\frac{V_2}{V_1}.$$Because the internal energy of an ideal gas depends only on temperature, $\Delta U = 0$, and the first law gives the defining result $\Delta Q = \Delta W$: the heat absorbed is spent entirely on work. For $V_2 > V_1$ (expansion) $W > 0$ — the gas absorbs heat and does work; for $V_2 < V_1$ (compression) $W < 0$ — work is done on the gas and heat is released.
Adiabatic process
An adiabatic process is the opposite bargain: the system is thermally insulated from its surroundings so that no heat is exchanged, $\Delta Q = 0$. The first law then reads $\Delta U = -\Delta W$. When the gas expands and does positive work, that work is paid for out of internal energy, so the gas cools; when work is done on the gas, its internal energy and temperature rise. The governing relations, quoted by NCERT without proof, are
$$PV^{\gamma} = \text{constant}, \qquad TV^{\gamma-1} = \text{constant}, \qquad \gamma = \frac{C_p}{C_v}.$$For a change from $(P_1, V_1, T_1)$ to $(P_2, V_2, T_2)$ this gives $P_1 V_1^{\gamma} = P_2 V_2^{\gamma}$. The work done is obtained by integrating $\int P\,dV$ with $P = (\text{const})V^{-\gamma}$:
$$W = \frac{P_1 V_1 - P_2 V_2}{\gamma - 1} = \frac{\mu R\,(T_1 - T_2)}{\gamma - 1}.$$Consistency check: if the gas does work ($W > 0$) then $T_2 < T_1$ — the gas cools, exactly as the first law demands; if work is done on the gas ($W < 0$) then $T_2 > T_1$.
Isochoric process
An isochoric (isovolumetric) process holds the volume constant — heating a gas sealed in a rigid vessel is the standard example. Since $\Delta V = 0$, the work term vanishes outright:
$$\Delta W = P\,\Delta V = 0.$$The first law then collapses to $\Delta Q = \Delta U$. Every joule of heat supplied goes into raising the internal energy and hence the temperature; none escapes as work. The temperature change for a given heat input is set by the molar specific heat at constant volume:
$$\Delta Q = \Delta U = \mu C_v\,\Delta T.$$On a P-V diagram this is a vertical line — and a vertical line encloses no area, the geometric statement that no work is done.
Isobaric process
An isobaric process holds the pressure constant — boiling water in an open vessel at atmospheric pressure is the textbook case. No term vanishes, so this is the one process where the full first law stays in play. With $P$ constant the work is simply
$$W = P\,(V_2 - V_1) = P\,\Delta V = \mu R\,(T_2 - T_1) = \mu R\,\Delta T,$$using $PV = \mu RT$ for the last step. The heat supplied splits between raising the internal energy and doing this work, and the temperature change is governed by the molar specific heat at constant pressure:
$$\Delta Q = \mu C_p\,\Delta T.$$This is why $C_p > C_v$: at constant pressure the gas must be fed extra heat to cover the work $\mu R\,\Delta T$ that it does in expanding, on top of the $\mu C_v\,\Delta T$ that goes into internal energy — the origin of the relation $C_p - C_v = R$.
Every reduction above starts from one equation. If $\Delta Q$, $\Delta U$ and $\Delta W$ feel slippery, lock them down in the first law of thermodynamics first.
The master comparison table
The four processes form a perfect parallel structure. Memorise this single grid — condition, the first-law reduction, the work expression, and the shape of the P-V curve — and the bulk of NEET thermodynamics is mechanical recall.
| Process | Defining condition | First-law form | Work done $W$ | P-V curve |
|---|---|---|---|---|
| Isothermal | $T$ const; $PV=$ const | $\Delta U=0,\ \Delta Q=\Delta W$ | $\mu RT\ln\!\dfrac{V_2}{V_1}=2.303\,\mu RT\log\!\dfrac{V_2}{V_1}$ | Rectangular hyperbola |
| Adiabatic | $\Delta Q=0$; $PV^{\gamma}=$ const | $\Delta U=-\Delta W$ | $\dfrac{P_1V_1-P_2V_2}{\gamma-1}=\dfrac{\mu R(T_1-T_2)}{\gamma-1}$ | Steeper hyperbola (slope $\times\gamma$) |
| Isochoric | $V$ const; $\dfrac{P}{T}=$ const | $\Delta Q=\Delta U=\mu C_v\Delta T$ | $W=0$ | Vertical line |
| Isobaric | $P$ const; $\dfrac{V}{T}=$ const | $\Delta Q=\mu C_p\Delta T=\Delta U+P\Delta V$ | $P\Delta V=\mu R\Delta T$ | Horizontal line |
Isothermal vs adiabatic slope
The most heavily tested single fact in this subtopic is which curve is steeper. Differentiate each constraint at a common point. For the isothermal $PV = \text{const}$,
$$P\,dV + V\,dP = 0 \;\Rightarrow\; \left(\frac{dP}{dV}\right)_{\text{iso}} = -\frac{P}{V}.$$For the adiabatic $PV^{\gamma} = \text{const}$,
$$V^{\gamma}\,dP + \gamma P V^{\gamma-1}\,dV = 0 \;\Rightarrow\; \left(\frac{dP}{dV}\right)_{\text{adi}} = -\gamma\,\frac{P}{V}.$$Both slopes are negative, but the adiabatic slope is larger in magnitude by exactly the factor $\gamma = C_p/C_v > 1$. The adiabatic curve is steeper than the isothermal by the factor $\gamma$. Physically, an adiabatic compression also heats the gas, so its pressure climbs faster than in an isothermal compression where the extra heat is bled off to the reservoir.
A direct corollary, asked in NEET 2016: compressing a gas to the same final volume takes more work adiabatically than isothermally. The steeper adiabatic curve sits above the isothermal one during compression, so the area under it — the work — is larger.
Cyclic process and loop area
A cyclic process returns the system to its initial state after a sequence of steps. Since internal energy is a state variable depending only on the state, the net change over a complete cycle is zero:
$$\Delta U_{\text{cycle}} = 0 \;\Rightarrow\; \Delta Q_{\text{net}} = W_{\text{net}}.$$All the heat absorbed over the cycle emerges as net work. Geometrically, that net work equals the area enclosed by the closed loop on the P-V diagram: positive for a clockwise loop (the gas does net work, as in a heat engine) and negative for an anticlockwise loop (net work is done on the gas, as in a refrigerator). The straight-segment legs of a rectangular loop are simply isobaric (horizontal) and isochoric (vertical) processes back to back.
Four processes in one breath
- Isothermal: $T$ fixed, $PV=$ const, $\Delta U=0$, so $\Delta Q=\Delta W=\mu RT\ln(V_2/V_1)=2.303\,\mu RT\log(V_2/V_1)$.
- Adiabatic: $\Delta Q=0$, $PV^{\gamma}=$ const and $TV^{\gamma-1}=$ const, $\Delta U=-\Delta W$, $W=(P_1V_1-P_2V_2)/(\gamma-1)=\mu R(T_1-T_2)/(\gamma-1)$.
- Isochoric: $V$ fixed, $W=0$, so $\Delta Q=\Delta U=\mu C_v\Delta T$; vertical P-V line.
- Isobaric: $P$ fixed, $W=P\Delta V=\mu R\Delta T$, $\Delta Q=\mu C_p\Delta T$; horizontal P-V line.
- Slopes: isothermal $-P/V$, adiabatic $-\gamma P/V$; the adiabatic is steeper by $\gamma$, so adiabatic compression takes more work.
- Cyclic: $\Delta U=0$ over a loop, net $W=$ enclosed area; clockwise positive, anticlockwise negative.
- Two zeros to never swap: isothermal is $\Delta U=0$; adiabatic is $\Delta Q=0$.