For a canonical ensemble, and . The kinetic and factorial factors do not depend on , so differentiating only the volume-dependent terms gives
Thus the equation of state is
The excluded-volume correction raises pressure relative to the same gas without that correction; the attractive mean-field term lowers it. No Stirling formula is required for this derivative.
Differentiate the Euler relation for a single-component simple compressible system:
The thermodynamic fundamental relation for the same system is . Subtraction gives
Dividing by , with and , proves the Gibbs-Duhem equation
The underlying Euler relation assumes extensive bulk thermodynamics and no additional work coordinates. The result says that the intensive quantities are constrained; the chemical potential cannot be varied independently of temperature and pressure within one homogeneous phase.
Let denote the fluctuating microscopic energy and its mean, at fixed . In a canonical ensemble with ,
Since , this gives
Here denotes an energy fluctuation about the mean, as in the question. The relation is not restricted to ideal gases when the Hamiltonian operator has no explicit temperature dependence. Alternatively, the stated equilibrium free-energy curvature gives a Gaussian energy weight proportional to , with the same variance.
For the relative energy fluctuation of a monatomic ideal gas, and , hence
Taking room conditions as approximately K and Pa, with m, gives
The mean energy is about J and its standard deviation about J. The tiny relative fluctuation explains why macroscopic equilibrium internal energy behaves as a sharply defined thermodynamic quantity. The estimate uses a thermal reservoir, not a particle reservoir; allowing itself to fluctuate changes the relevant fluctuation problem.

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