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Hydrocarbon functional groups arenes

Hydrocarbons contain only hydrogen and carbon. The hydrocarbon functional groups include alkanes, alkenes, alkynes, and arenes (aromatic compounds). Simple hydrocarbons have few medicinal applications, but are the feedstock of the petrochemical industry to produce plastics, dyes, solvents, detergents, and adhesives (to name just a few). Therefore, hydrocarbons are essential to the medical field. Additionally, all hydrocarbons are flammable and, therefore, find application as fuels. For example, gasoline is a mixture of hydrocarbons. [Pg.282]

You first should decide what type of compound it is. The decision usually is straightforward for hydrocarbons, which will fall in one or the other of the categories alkanes, alkenes, alkynes, arenes, cycloalkanes, and so on. But when the compound has more than one functional group it is not always obvious which is the parent function. For example, Compound 1 could be named as an alkene (because of the double-bond function) or as an alcohol (because of the OH function) ... [Pg.186]

It is convenient to consider the indifferent or neutral oxygen derivatives of the hydrocarbons - (a) aldehydes and ketones, (b) esters and anhydrides, (c) alcohols and ethers - together. All of these, with the exception of the water-soluble members of low molecular weight, are soluble only in concentrated sulphuric acid, as are alkenes and readily sulphonated arenes. The above classes of compounds must be tested for in the order in which they are listed, otherwise erroneous conclusions may be drawn from the reactions for the functional group about to be described. [Pg.1218]

The structures and abbreviations used for designating the calix[4]arenes are shown in (5). These calix[4]arenes, have both a wide (upper) and a narrow (lower) rim that can be chemically modified to produce complexants that are selective for particular metal ions. In the simple calixarene framework the wide rim has hydrocarbon functionalities, and the narrow rim phenolic groups. Calixarenes are conformationally mobile, and the extreme structures for the calix[4]arenes have been termed the cone, partial cone, 1,3-alternate, and 1,2-alternate conformations (6). Because of the conical geometry of the calix[4]arene structure, the cavity size of the wide rim is larger than that of the narrow rim. [Pg.485]


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See also in sourсe #XX -- [ Pg.290 ]




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