Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nomenclature difficulties with

It is often the case that chemists involved or familiar with ethylene oxide (oxiran) chemistry refer to these cyclic oligomers as EO-4, EO-6 and EO-7 respectively. Such designations are informal if not colloquial but, like any name, are useful if they correctly convey an idea. The difficulty with these informalities, indeed with the crown nomenclature system is that it cannot adequately deal with complicated structures or even isomers of simple ones. [Pg.3]

A selection of carboxylic ester hydrolases (EC 3.1.1) of major or more-modest significance in xenobiotic metabolism is given in Table 2.5. The recommendations of the Enzyme Nomenclature Committee on the classification of esterases cannot be considered completely satisfactory, but, even after decades of debate, a more satisfactory classification system remains to be proposed [56] [57], The main difficulties with esterase classification have been summarized as follows [58],... [Pg.43]

A remarkable reaction of the phospho group is its transfer onto carbon in the biosynthesis of the C—P bond (Fig. 6). Incidentally, this leads to a difficulty with nomenclature, because the group -P03H2, which is known to chemists as phosphono, is called phospho only when on a heteroatom (64), so the transfer changes its name Despite much ealier guessing from labeling patterns that phosphoenolpyruvate was the source of the C—P bond, it was only in 1988 (65, 66) that the enzyme responsible was isolated. The difficulty proved to be that the equilibrium favors phosphoenolpyruvate by about 2000-fold (67), so that assays only detected the enzyme in the direction contrary to biosynthesis evidently the biosynthesis takes place because subsequent reac-... [Pg.204]

Polygalaceae), Virginia (Aristolochia serpentaria, Aristolochiaceae) and white snakeroot (Eupatorium rugosum, Asteraceae). In the United States, a list of standardized common names called Herbs of Commerce (American Herbal Products Association, 1992) was adopted by the FDA as the only permitted source for common names on product labeling. Products that contain plants not listed in Herbs of Commerce are required to use the correct Latin name of the plant on the label. In addition to difficulties with nomenclature, problems have arisen because of the difficulty in determining exactly which plants are present in a finished product. Capsules that contain more than one plant and/or a dried crude extract make identification of the plant(s) by traditional means such as microscopy virtually impossible (Betz et al., 1995). Determination of the identity of a misidentified plant then becomes a matter of looking for specific toxic chemical constituents, which is usually a needle in a haystack approach unless symptoms are characteristic of a particular compound. Good quality assurance of raw material obviates the need for this detective work. [Pg.371]

But her instincts had been correct Mendeleev was worth the effort. He continued at the University of St. Petersburg, writing a dissertation that won him a traveling fellowship. While in Europe on this fellowship, he, like Lothar Meyer, attended the Karlsruhe Conference, the first international chemical conference, which was held to resolve difficulties with definitions of atoms, atomic weights, and nomenclature. The conference was not particularly productive, but on the way out the door, Mendeleev was handed a pamphlet by Cannizzaro, explaining the hypothesis of Avogadro. He read it, and it made sense. [Pg.259]

Hydroxy-substituted azo compounds frequently exhibit tautomerism which can lead to difficulties with nomenclature and CAS registration (see note in Introduction). [Pg.1391]

This polymer has one of the simplest molecular structures ([CH2CH2— ] ) and is at present the largest toimage plastic material, having first been produced commercially in 1939 for use in electrical insulation. There is a difficulty over the nomenclature of this polymer. The lUPAC recommended name for the monomer is ethene, rather than the older ethylene. Hence the lUPAC name for the polymer is poly (ethene). However, this name is almost never used by chemists working with the material throughout this book, therefore, this polymer will be referred to by its more widespread name, poly(ethylene). [Pg.6]

Although symbols are not a part of nomenclature, the two are closely related, and the former have played an extremely important role in chemistry. Because of the difficulty of establishing priority of discovery for most of the elements of atomic number above 100, and because of the need to refer to hypothetical elements with higher atomic numbers, IUPAC has developed interim systematic symbols and names for such elements. [Pg.1088]

The 191 problems in this book cover most of the area of stereochemistry, including nomenclature, stereogenic elements (centers, axes, planes) and their descriptors, symmetry, inorganic stereochemistry, determination of enantiomer excess, conformation of acyclic and cyclic compounds, and more. The answers, in addition to providing solutions to the problems, frequently include additional explanations of the underlying principles. The problems are ordered more or less in order of increasing difficulty. (I had a hard time with some of the problems toward the end myself )... [Pg.204]

Because one of the motivations in creating the proposed nomenclature system was predicated on its interface with the computer, there is no need for a word-stem, such as the suffix "-nodane" created in nodal nomenclature. If one wishes to make the system more user-friendly, especially for the student user, such a word-stem could easily be included however, a problem with such an inclusion is that it encourages the inclusion of other functionalities so that eventually several of the difficulties that the system has eliminated will be reintroduced. [Pg.40]

It is appropriate too to clarify some nomenclature and aspects of many-body theory. Indeed here (and what seems often to be the usage elsewhere) "many-body" is applied to a theory if it is applicable in practice to infinite systems. That is, if a theory s computational "difficulty scales with the number N of electrons as N°, it is to be a many-body theory only if a=0, at least for some standard sorts of systems, say with translational symmetry. Since it is often said that the number of 2-electron integrals... [Pg.407]


See other pages where Nomenclature difficulties with is mentioned: [Pg.11]    [Pg.304]    [Pg.518]    [Pg.57]    [Pg.11]    [Pg.145]    [Pg.2]    [Pg.73]    [Pg.650]    [Pg.1211]    [Pg.116]    [Pg.118]    [Pg.520]    [Pg.24]    [Pg.4]    [Pg.269]    [Pg.4]    [Pg.63]    [Pg.26]    [Pg.403]    [Pg.158]    [Pg.1]    [Pg.216]    [Pg.116]    [Pg.144]    [Pg.1089]    [Pg.32]    [Pg.87]    [Pg.398]    [Pg.3]    [Pg.54]    [Pg.117]    [Pg.272]    [Pg.326]    [Pg.1328]   
See also in sourсe #XX -- [ Pg.145 ]




SEARCH



Nomenclature Difficulties

© 2024 chempedia.info