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Aromatic compounds derivatives

Toluene A basic aromatic compound derived from petroleum. It is the most common hydrocarbon purchased for use in increasing octane. Toluene is also used to produce phenol and TNT. [Pg.28]

The discrepancy between physicochemical and reactivity criteria for aromaticity was known long ago. Yet the data procured by the studies of compounds like 186 or 189 shed a new light on this problem. The observed deviation from planarity did not cause any substantial changes in the spectral parameters of these compounds. Thus they still should be considered aromatic from the point of view of physical chemists. At the same time, this distortion of geometry so dramatically affected their reactivity pattern that, in accordance with this criterion, cyclophanes 186 or 189 should best be referred to as non-aromatic compounds, derivatives of 1,3,5-cyclohexatriene. ... [Pg.376]

Each of these groups of substances may be sub-divided into four series The first three of these comprise the aliphatic compounds derived from methane (series I), ethane (series II) and propane (series III). The fourth series comprises the aromatic compounds derived from benzene and its homologues. [Pg.32]

Another species in this genus. Cinnamon camphora, is the source of camphor. This tree is native to Southeast Asia. Camphor is an aromatic compound derived from the bark and wood of the camphor tree and is used as a... [Pg.75]

Aromatic compounds derived from six, seven and eight or more acetate units are also found as metabolites of these fungi. These metabolites include a series of anthraquinone pigments, which are discussed later in Chapter 7. [Pg.61]

With the exception of isochorismic acid the above mentioned acids are aromatic compounds, derived from benzoic acid by an additional hydroxy or amino group in o- or p-position. [Pg.264]

Quaternary aromatic compounds derived from 2-methyl-2-phenylbutyric add... [Pg.60]

Saturated or alicyclic ring systems actually are of equal if not greater importance in biochemistry than aromatic compounds derived from benzene, which dominate... [Pg.1]

The secondary metabolites of Medusozoa are broadly similar to those of the Hexacorallia (Anthozoa), that is, there are only small amounts of terpenes, few nitrogen derivatives and, in Tridentata (Hydrozoa), atypical sulfur-containing derivatives. Among the categories of metabolites that could be considered characteristic of the class Hydrozoa are aromatic compounds derived from anthracene and the bioluminescent substances formd in some jellyfish, such as aequorin (see Chapter 4). [Pg.1356]

The composition of coal tar varies with the carbonization method but consists, largely, of mononuclear and polynuclear aromatic compounds and their derivatives. Coke oven tars are relatively low in aliphatic and phenolic content while low-temperature tars have much higher contents of both. [Pg.103]

Hammen equation A correlation between the structure and reactivity in the side chain derivatives of aromatic compounds. Its derivation follows from many comparisons between rate constants for various reactions and the equilibrium constants for other reactions, or other functions of molecules which can be measured (e g. the i.r. carbonyl group stretching frequency). For example the dissociation constants of a series of para substituted (O2N —, MeO —, Cl —, etc.) benzoic acids correlate with the rate constant k for the alkaline hydrolysis of para substituted benzyl chlorides. If log Kq is plotted against log k, the data fall on a straight line. Similar results are obtained for meta substituted derivatives but not for orthosubstituted derivatives. [Pg.199]

In practice superheated steam is generally employed for substances with a low vapour pressure (< 5-1 mm.) at 100°. Thus in the recovery of the products of nitration or aromatic compounds, the ortho derivative e.g., o-nitrophenol) can be removed by ordinary steam distillation the... [Pg.16]

Table 111,42 deals with a number of aliphatic halogen compounds together with their crystalline derivatives. Some aromatic compounds, which simulate the properties of aliphatic haUdes in some respects, are included. [Pg.292]

COMPOUNDS DERIVED FROM AROMATIC SULPHONIC ACIDS... [Pg.820]

In addition to inorganic radicals, which profoundly modify the properties of a paraflSn hydrocarbon residue, there is a whole series of organic groupings which are distinguished by exceptional reactivity, for example, the ethylene and acetylene groupings, and the phenyl and naphthyl radicals. Thus the characterisation of unsaturated hydrocarbons and their derivatives, e.g., the aromatic compounds, becomes possible. [Pg.1026]

Thallation of aromatic compounds with thallium tris(trifluoroacetate) proceeds more easily than mercuration. Transmetallation of organothallium compounds with Pd(II) is used for synthetic purposes. The reaction of alkenes with arylthallium compounds in the presence of Pd(Il) salt gives styrene derivatives (433). The reaction can be made catalytic by use of CuCl7[393,394], The aryla-tion of methyl vinyl ketone was carried out with the arylthallium compound 434[395]. The /9-alkoxythallium compound 435, obtained by oxythallation of styrene, is converted into acetophenone by the treatment with PdCh[396]. [Pg.83]

As is broadly true for aromatic compounds, the a- or benzylic position of alkyl substituents exhibits special reactivity. This includes susceptibility to radical reactions, because of the. stabilization provided the radical intermediates. In indole derivatives, the reactivity of a-substituents towards nucleophilic substitution is greatly enhanced by participation of the indole nitrogen. This effect is strongest at C3, but is also present at C2 and to some extent in the carbocyclic ring. The effect is enhanced by N-deprotonation. [Pg.3]

All compounds that contain a benzene ring are aromatic and substituted derivatives of benzene make up the largest class of aromatic compounds Many such compounds are named by attaching the name of the substituent as a prefix to benzene... [Pg.432]

Cyclic compounds that contain at least one atom other than carbon within their ring are called heterocyclic compounds, and those that possess aromatic stability are called het erocyclic aromatic compounds Some representative heterocyclic aromatic compounds are pyridine pyrrole furan and thiophene The structures and the lUPAC numbering system used m naming their derivatives are shown In their stability and chemical behav lor all these compounds resemble benzene more than they resemble alkenes... [Pg.460]

Many aromatic compounds are simply substituted derivatives of benzene and are named accordingly Many others have names based on some other parent aromatic compound... [Pg.464]

Halides derived from certain heterocyclic aromatic compounds are often quite reac tive toward nucleophiles 2 Chloropyridme for example reacts with sodium methoxide some 230 million times faster than chlorobenzene at 50°C... [Pg.981]

Monocyclic Aromatic Compounds. Except for six retained names, all monocyclic substituted aromatic hydrocarbons are named systematically as derivatives of benzene. Moreover, if the substituent introduced into a compound with a retained trivial name is identical with one already present in that compound, the compound is named as a derivative of benzene. These names are retained ... [Pg.5]

Diketones and tetraketones derived from aromatic compounds by conversion of two or four SCH groups into keto groups, with any necessary rearrangement of double bonds to a quinonoid structure, are named by adding the suffix -quinone and any necessary affixes. [Pg.33]

FLUORINECOMPOUNDS,ORGANIC - FLUORINATED AROMATIC COMPOUNDS] (Volll) -malonate derivative TALONIC ACID AND DERIVATIVES] (Vol 15)... [Pg.698]


See other pages where Aromatic compounds derivatives is mentioned: [Pg.99]    [Pg.172]    [Pg.522]    [Pg.176]    [Pg.87]    [Pg.319]    [Pg.642]    [Pg.80]    [Pg.528]    [Pg.91]    [Pg.296]    [Pg.258]    [Pg.99]    [Pg.172]    [Pg.522]    [Pg.176]    [Pg.87]    [Pg.319]    [Pg.642]    [Pg.80]    [Pg.528]    [Pg.91]    [Pg.296]    [Pg.258]    [Pg.28]    [Pg.42]    [Pg.99]    [Pg.181]    [Pg.254]    [Pg.321]    [Pg.387]    [Pg.108]    [Pg.27]    [Pg.101]    [Pg.545]   


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