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Acetic acid compressibility factor

FIGURE 1.3-3 Compressibility factor Z for acetic acid vapor at 40°C, Circles are data curve is computed from chemical theory, assuming dimerization, with K = 380. [Pg.21]

For acetic acid and HF, where tetramers or hexamers are regarded, the equation must be solved numerically, which is, however, pretty easy, as 0 < zi < 1. Having calculated zi, the compressibility factor z can be determined as the ratio between the number of associates and the number of molecules in the vapor phase ... [Pg.575]

In the intramolecular reactions studied by Bruice and Koshland and their co-workers, proximity effects (reduction in kinetic order and elimination of unfavourable ground state conformations) and orientation effects might give rate accelerations of 10 -10 . Hence, these effects can by themselves account for the enhancements seen in most intramolecular reactions. However, a factor of 10 -10 is less than the rate acceleration calculated for many enzyme reactions and certain intramolecular reactions, for example, hydrolysis of benzalde-hyde disalicyl acetal (3 X 10 ) (Anderson and Fife, 1973) and the lactonization reaction of[l] (10 ) where a trimethyl lock has been built into the system. If hydrolysis of tetramethylsuccinanilic acid (Higuchi et al., 1966) represents a steric compression effect (10 rate acceleration), then proximity, orientation, and steric compression... [Pg.18]


See other pages where Acetic acid compressibility factor is mentioned: [Pg.188]    [Pg.141]    [Pg.188]    [Pg.392]    [Pg.21]    [Pg.21]    [Pg.490]    [Pg.289]    [Pg.21]    [Pg.1110]    [Pg.1110]    [Pg.1110]    [Pg.265]   
See also in sourсe #XX -- [ Pg.20 ]

See also in sourсe #XX -- [ Pg.20 ]

See also in sourсe #XX -- [ Pg.20 ]




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