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Phosgene physical constants

The cyclic analogs of chloroformamidines are virtually unknown. Suzuki mentioned the synthesis of 2-chloroimidazolidine but reported no physical constants. The cyclic chloroformamidinium chloride XXV can be obtained from l,3-dimethylimidazolidine-2-one (XXVI) and carbonyl chloride, but this reaction is considerably slower than the phosgenation of the tetrasubstituted linear urea C ). [Pg.199]

The mechanism of the formation of phosgene according to the reaction, CO (A) + C12(B) =4 C0C12(C), is to be checked with given data at 30.6 C (Potter Baron, CEP 47 473, 1951). Six Langmuir-Hinshelwood equations and a power law model are examined. The rate equations are analyzed in linearized forms. Those that have negative constants are not physically realistic. [Pg.675]


See other pages where Phosgene physical constants is mentioned: [Pg.279]    [Pg.279]    [Pg.531]   
See also in sourсe #XX -- [ Pg.536 ]




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