Prove Cp - Cv = R for ideal gas

easy CBSE JEE-MAIN NEET 3 min read

Question

Prove that for an ideal gas, CpCv=RC_p - C_v = R, where CpC_p is the molar heat capacity at constant pressure, CvC_v is the molar heat capacity at constant volume, and RR is the universal gas constant.

Solution — Step by Step

The first law: ΔQ=ΔU+PΔV\Delta Q = \Delta U + P\Delta V (heat added = increase in internal energy + work done by gas).

For 1 mole of ideal gas:

  • At constant volume: Qv=CvΔTQ_v = C_v \Delta T (all heat goes to increasing internal energy, since ΔV=0\Delta V = 0 means no work done)
  • At constant pressure: Qp=CpΔTQ_p = C_p \Delta T

At constant volume, ΔU=Qv=CvΔT\Delta U = Q_v = C_v \Delta T (since ΔW=PΔV=0\Delta W = P\Delta V = 0).

Since internal energy of an ideal gas depends only on temperature (not volume or pressure), this same ΔU=CvΔT\Delta U = C_v \Delta T applies to any process for an ideal gas — including the constant pressure process.

At constant pressure:

CpΔT=ΔU+PΔV=CvΔT+PΔVC_p \Delta T = \Delta U + P\Delta V = C_v \Delta T + P\Delta V

So: CpΔTCvΔT=PΔVC_p \Delta T - C_v \Delta T = P\Delta V

(CpCv)ΔT=PΔV(C_p - C_v)\Delta T = P\Delta V

For 1 mole of ideal gas: PV=RTPV = RT.

At constant pressure: PΔV=RΔTP\Delta V = R\Delta T.

Substituting:

(CpCv)ΔT=RΔT(C_p - C_v)\Delta T = R\Delta T

Dividing both sides by ΔT\Delta T (assuming ΔT0\Delta T \neq 0):

CpCv=R\boxed{C_p - C_v = R}

Why This Works

The difference between CpC_p and CvC_v arises because at constant pressure, the gas must expand as it’s heated. This expansion requires the gas to do work against the external pressure (W=PΔVW = P\Delta V). At constant volume, no such work is needed — all the heat goes into increasing the internal energy.

The work done per mole per degree of temperature rise at constant pressure is exactly RR (from the ideal gas law). So CpC_p is always RR greater than CvC_v — it takes more heat to raise the temperature by 1 K at constant pressure than at constant volume.

Alternative Method

Using enthalpy: At constant pressure, Qp=ΔHQ_p = \Delta H (heat at constant pressure equals enthalpy change). So Cp=(H/T)pC_p = (\partial H/\partial T)_p and Cv=(U/T)vC_v = (\partial U/\partial T)_v. Since H=U+PV=U+RTH = U + PV = U + RT (for 1 mole ideal gas), Cp=Cv+RC_p = C_v + R.

Typical values: for a monoatomic ideal gas (He, Ne, Ar), Cv=32RC_v = \frac{3}{2}R and Cp=52RC_p = \frac{5}{2}R. For diatomic gases (N₂, O₂, H₂) at room temperature, Cv=52RC_v = \frac{5}{2}R and Cp=72RC_p = \frac{7}{2}R. The ratio γ=Cp/Cv\gamma = C_p/C_v is 5/3 for monoatomic and 7/5 for diatomic. These are frequently asked in JEE.

Common Mistake

Students sometimes write ΔU=CpΔT\Delta U = C_p \Delta T for the constant pressure process (using CpC_p instead of CvC_v). This is wrong. The internal energy change is ALWAYS ΔU=nCvΔT\Delta U = nC_v\Delta T for an ideal gas — regardless of whether the process is at constant pressure, constant volume, or neither. CvC_v characterises how internal energy changes with temperature for an ideal gas; CpC_p only appears in expressions for heat added at constant pressure.

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