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Interchange, nomenclature

Having wide and increasing quantity of RP HPLC sorbents in disposal the main question in RP HPLC is their interchangeability. Column chai acteristics that ai e usually described by their manufacturers are not full enough for the analytic to choose a suitable column for the specified resolutions or he ought to choose other similar column used before. In fact, nomenclature of reversed-phase stationai y phases is too unsophisticated and is a source of confusion in their application. [Pg.131]

This reaction converts ribulose-5-P to another ketose, namely, xylulose-5-P. This reaction also proceeds by an enediol intermediate, but involves an inversion at C-3 (Figure 23.31). In the reaction, an acidic proton located a- to a carbonyl carbon is removed to generate the enediolate, but the proton is added back to the same carbon from the opposite side. Note the distinction in nomenclature here. Interchange of groups on a single carbon is an epimerization, and interchange of groups between carbons is referred to as an isomerization. [Pg.765]

Before discussing column preparation procedures a few comments on nomenclature are in order. Open tubular columns are also widely known as capillary columns. The characteristic feature of these columns is their openness, which provides an unrestricted gas path through the column. Thus open tubular colximn rather than capillary column is a more apt description. However, both descriptions appear frequently in the literature and can be emsidered interchangeable. The type of columns discussed so far are also known as wall-coated open tubular columns (WCOT). Here the liquid phase is deposited directly onto the column wall without the inclusion of any additive that might be considered as... [Pg.590]

FIGURE 1.1 Chemical and stereochemical nature of amino acids. Substituents in (a) and (b) are on opposite sides of the plane N-Ca-C, the bold bond being above the plane. Interchange of any two substituents in (a) changes the configuration. For the Cahn-Ingold-Prelog system of nomenclature, the order of preference NH2 > COOH > R2 relative to H is anticlockwise in (a) = (S) and clockwise in (c) = (R). [Pg.1]

For a field of scientific and engineering endeavor, polymers have one of the more sloppy sets of nomenclature. Ask six people in the business to give you definitions of resins and plastics, and you ll get at least six different answers. Almost everyone will tell you that they re both polymers, and that s right. Some will tell you they re interchangeable. Strictly spealdng, they re wrong. [Pg.320]

In recent years luminescence nomenclature has become confusing within the literature and in practice. Luminescence involves both phosphorescence and fluorescence phenomena. While luminescence is the appropriate term when the specific photochemical mechanism is unknown, fluorescence is far more prevalent in practice. Moreover, the acronym LIE has historically inferred laser -induced fluorescence however, in recent years it has evolved to the more general term light -induced fluorescence due to the various light sources found within laboratory and real-time instruments. Within this chapter fluorescence and LIE are interchangeable terms. [Pg.338]

The synthesis of a typical p-blocker starts with the mono-alkylation of catechol to give the ether (19-1). Application of the standard side chain budding sequence leads to the nonselective (3-blocker oxprenolol (19-2) [16] (the olol ending is approved USAN nomenclature for (3-blockers). Atenolol (19-5) is one of the most widely used (3i selective agents. The requisite phenol (19-4) can be obtained by ester interchange of methyl 4-hydroxyphenylacetate (19-3) with ammonia. Elaboration of the thus obtained intermediate (19-4) via the customary scheme then affords atenolol (19-5) [17]. [Pg.55]

The nomenclature of the family of compounds to be discussed below has for long been the cause of much confusion. The systematic name for a six-membered ring containing one sulfur atom is thiin, but Chemical Abstracts uses the name thiopyran, while many earlier publications have used the replacement nomenclature thiapyran (which is strictly inaccurate as thia implies replacement of carbon, rather than oxygen, by sulfur). Throughout this chapter the terms thiopyran and thiin will be used interchangeably, while thiadecalin nomenclature will be found convenient for the perhydrobenzothiopyran systems. [Pg.885]

There are two competing and equivalent nomenclature systems encountered in the chemical literature. The description of data in terms of ways is derived from the statistical literature. Here a way is constituted by each independent, nontrivial factor that is manipulated with the data collection system. To continue with the example of excitation-emission matrix fluorescence spectra, the three-way data is constructed by manipulating the excitation-way, emission-way, and the sample-way for multiple samples. Implicit in this definition is a fully blocked experimental design where the collected data forms a cube with no missing values. Equivalently, hyphenated data is often referred to in terms of orders as derived from the mathematical literature. In tensor notation, a scalar is a zeroth-order tensor, a vector is first order, a matrix is second order, a cube is third order, etc. Hence, the collection of excitation-emission data discussed previously would form a third-order tensor. However, it should be mentioned that the way-based and order-based nomenclature are not directly interchangeable. By convention, order notation is based on the structure of the data collected from each sample. Analysis of collected excitation-emission fluorescence, forming a second-order tensor of data per sample, is referred to as second-order analysis, as compared with the three-way analysis just described. In this chapter, the way-based notation will be arbitrarily adopted to be consistent with previous work. [Pg.478]

At the Federal level, controlled substances are listed within a system of five schedules in the Controlled Substances Act. These Schedules are described in Table 1.2. Schedule I contains the most strongly controlled substances, while Schedule V includes the most moderately controlled. Those drugs contained in Schedules II to V may be prescribed, while those in Schedule I may not. The data in the table illustrate a point which requires to be addressed, particularly at cross-border (International, State or County) levels, that is, one of nomenclature. In the United Kingdom, heroin is taken to mean the mixture of products resulting from the synthesis of diamorphine from morphine. Both compounds are listed separately in UK legislation, although heroin is not. However, in the United States, heroin can sometimes be taken to mean diamorphine and the two are sometimes used interchangeably. [Pg.5]

In this reference the names of the angles ip and are interchanged from the usage adopted here. To avoid confusion I stick to the same nomenclature throughout the book. [Pg.69]

The lUPAC-IUB Commission on Biochemical Nomenclature (13) recommends that the term vitamin B 2 used as the generic descriptor for aU corrinoids exhibiting qualitatively the biological activity of cyanocobalamin. However, because of its commercial importance, cyanocobalamin is used interchangeably with vitamin B 2 herein. [Pg.110]

In the first part of this section the elucidation of the mechanism will be presented, while the second part will be devoted to a discussion of the effect of cations on the viscoelastic properties. Both of these topics are grouped together because, as will be shown below, the relaxation mechanism of all the polymers discussed here is perfectly normal, i.e., simple molecular flow, [or the a mechanism according to the nomenclature of Ferry (27, 28, 29) and Hoff 37a), and the materials can thus be called chemically inactive. Finally, the work on viscoelasticity of bulk organic polyelectrol5des will be mentioned. The next section will be devoted to a discussion of the viscoelastic properties of materials in which, in addition to the a mechanism, bond interchange (the x mechanism) is also encoimtered, the chemical (hence x) activity being due to catalysis by transition metal ions. [Pg.83]

Regarding nomenclature, the terms indicators and metrics are both commonly used, often interchangeably, in referring to measurement of sustainability. [Pg.199]


See other pages where Interchange, nomenclature is mentioned: [Pg.94]    [Pg.227]    [Pg.94]    [Pg.227]    [Pg.146]    [Pg.324]    [Pg.259]    [Pg.46]    [Pg.486]    [Pg.10]    [Pg.273]    [Pg.250]    [Pg.205]    [Pg.188]    [Pg.19]    [Pg.324]    [Pg.123]    [Pg.338]    [Pg.486]    [Pg.316]    [Pg.283]    [Pg.309]    [Pg.161]    [Pg.162]    [Pg.22]    [Pg.144]    [Pg.89]    [Pg.259]    [Pg.109]    [Pg.142]    [Pg.46]    [Pg.253]    [Pg.447]    [Pg.1766]    [Pg.384]    [Pg.10]   
See also in sourсe #XX -- [ Pg.227 ]




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