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Evaporation Heats of Compounds

As mentioned above, the evaporation heat can be calculated as the difference between the sublimation heat and the melting heat. A survey of direct measurements of AH from 1910 to 2010 is available [85] extracts from it are presented in Table 9.7, together with data from the reference book [45] and papers [86]. A comparison with Table 9.6 reveals that AHy are close to AH for various substances. [Pg.406]

Evaporation heats of organic compounds are additive properties, i.e. can be expressed through the sum of increments corresponding to individual atoms, chemical bonds and/or radicals. Thus, Korolev et al. [87] derived the formula AHy (kJ/mol) = A//vx-l-A//vch [85], where AT/yx and AHvch are the increments of [Pg.406]

Vaporization enthalpy appears to be a linear function of the number of carbon atoms not only for alkanes or nitriles but also for alkyl-azides. The dependence of vaporization enthalpy (in kJ/mol) on the number of carbon atoms (Nc = 4-10) for mono-azides CH3—(CH2)n N3 obeys the equation AH —16.6-1-5.8 Nc. The dependence of vaporization enthalpy on the number of carbon atoms for di-azides N3 (CH2)n—N3 with n = (3 to 6) is described by the equation A Wv = 33.3-1-6.6 Vc [89]. [Pg.408]

Class Group a Class Group a Class Group a [Pg.409]


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