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Benzene derivatives physical properties

In general, pyridazine can be compared with pyridine. It is completely miscible with water and alcohols, as the lone electron pairs on nitrogen atoms are involved in formation of hydrogen bonds with hydroxylic solvents, benzene and ether. Pyridazine is insoluble in ligroin and cyclohexane. The solubility of pyridazine derivatives containing OH, SH and NH2 groups decreases, while alkyl groups increase the solubility. Table 1 lists some physical properties of pyridazine. [Pg.3]

The separation of substituted benzene derivatives on a reversed-phase C-18 column has been examined [78]. The correlations between the logarithm of the capacity factor and several descriptors for the molecular size and shape and the physical properties of a solute were determined. The results indicated that hydrophobicity is the dominant factor to control the retention of substituted benzenes. Their retention in reversed-phase HPLC can be predicted with the help of the equations derived by multicombination of the parameters. [Pg.537]

Borazine is isoelectronic with benzene, as B=N is with C=C, (Fig. 16.21). in physical properties, borazine is indeed a close analogue of benzene. The similarity of the physical properties of the alkyl-substituted derivatives of benzene and borazine is ever more remarkable. For example, the ratio of the absolute boiling points of the substituted borazines to those of similarly substituted benzene is constant. This similarity in physical properties led to a labeling of borazine as "inorganic benzene." This is a misnomer because tbe chemical properties of borazine and benzene are quite different Both compounds have aromatic rr clouds of electron density with potential for delocalization over all of the ring atoms. Due to the difference m electronegativity between boron and nitrogen, the cloud in borazine is "lumpy" because more electron... [Pg.918]

This section is concerned with the quantitative correlation of reaction rates and equilibria of organic reactions with the structure of the reactants. We will restrict the discussion to benzene derivatives. The focus is on a remarkably simple treatment developed by L. P. Hammett in 1935, which has been tremendously influential. Hammett s correlation covers chemical reactivity, spectroscopy and other physical properties, and even the biological activity of drugs. Virtually all quantitative treatments of reactivity of organic compounds in solution start with the kinds of correlations that are discussed in this section. [Pg.1329]

Halogenation. Halogenation of the asphaltenes—by addition of the halogen to a solution of the asphaltenes in refluxing carbon tetrachloride —occurs readily to afford the corresponding halo derivatives (10). The physical properties of the halogenated materials are markedly different from those of the parent asphaltenes. For example, the unreacted asphaltenes are dark brown, amorphous, and readily soluble in benzene, nitrobenzene, and carbon tetrachloride, but the products are black, shiny, and only sparingly soluble, if at all, in these solvents. [Pg.151]

Physical Properties of Benzene and Its Derivatives 742 16-15 Spectroscopy of Aromatic Compounds 743 EssentialTerms 746 Study Problems 748... [Pg.16]

Depending on the substitution pattern of the monomers, different kinds of cross-linking can be anticipated, which can lead to small oligomers, but also to rings, chains, or polydimensional networks [1]. This applies to standard benzene derivatives, as well as to condensed arenes with more sophisticated molecular structures. These products are interesting in their own right owing to their physical and opto-physical properties, but also as precursors for refractory materials prepared in pyrolysis or plasma processes [1]. [Pg.4]

The quasi racemate method proved very useful for the steric correlation of these compounds with the corresponding benzene derivatives,as geometrically the differences between these groups are so small that the limits of isomorphic exchar eability are not often exceeded/ This confirms the view that the largest similarity between the thiophenes and benzenes is related to such physical properties as shape, size, and molecular weight, which, for instance, are reflected in the melting and boiling points. [Pg.147]


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See also in sourсe #XX -- [ Pg.742 ]

See also in sourсe #XX -- [ Pg.734 , Pg.735 ]




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