On Molecule Symmetry, Latent Heat, and Entropy

20 March 2025, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

This paper suggested correlating the entropy with the geometric symmetry of the molecular orbits instead of the atomic mass distribution in a molecule. Employing the NIST thermodynamic parameters of substances at saturation, linear regressions of exothermic heat over T give ε_exo=B-(3+2A)/2 RT. B is the molar heat of liquefication, which equals the latent heat (∆H_v^Φ) at the boiling point. A reflects the molecule's symmetry; the more symmetric the molecular orbits, the smaller A. For example, the symmetry of inert gas atoms gives the operation number n = 1 in the theoretical frame of the geometric symmetry of atomic mass distribution. However, three p orbits give n = 7; correspondingly, A values of Ne, Ar, Kr, and Xe are 2.5518, 2.9104, 2.9140, and 2.9178. Similarly, a tetrahedron of C sp3 gives n = 8, CH4: A=2.9519. Hence, assuming that (3+2A)/2 R is the lost entropy, (n-2A)/2 R may be regarded as the residual in liquid. According to the above suggestion, CO is more symmetric than CO2. Moreover, the similarity in A between ethylene and ethane, propylene and propane, etc., implies that the C-C π bond should be rotatable rather than rigid. Helium-4 superfluid finds an increase in entropy as T decreases from 3.5 to 0.8 K. Clausius-Clapeyron equation was derived from ε_exo.

Keywords

Molecule Symmetry
Latent Heat
Heat Transfer
Superfluid
Phase Transition
Thermodynamics
Entropy

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