Reference classes

Type of soil/reference Class of soil Average Scatter... 

The equation for the diffusion coefficient in a gaseous state, Dc, is the starting point for the derivation of an equation for diffusion coefficients in an amorphous solid state (S). The homologous series of n-alkanes is used as a reference class of chemical compounds which asymptotically reach an unlimited molecular chain in the form of poly methylene. The diffusion coefficient, DSji, is derived theoretically for a member of the series with j carbon atoms at infinite dilution in a matrix of a n-alkane with i carbon atoms in the molecule. In addition, the diffusion in polymethylene, which is considered as the reference structure for all polymers is also derived theoretically. 

The corresponding diffusion coefficient in the liquid state (L), DLderived from Ds.ji and Dc. Starting from the reference class of n-alkanes, diffusion coefficients can be estimated for any solute and matrix with corresponding specific values for the critical temperature and critical pressure of the matrix and the critical molar volume of the solute. 

Table 4.3 Summary of quantitative SAR characteristics of 16 reference classes. ...

SARI scores for 16 sets of active compounds used as reference classes for SARI calculations. The table is adapted from. The SARI scoring range of approximately 0.4-0.6 is considered intermediate and indicates the presence of heterogeneous SARs. 

These controls represent the reference class of today s hot runner control systems, depending on the accuracy, functionality, ease of use, and adaptability. All control functions can be easily adapted to the Windows-like user interface. Fault analysis and diagnosis of the hot runner system are possible as well as master-slave configurations and loading of drawings or photos into the user-friendly touch-screen display for intuitive adjustment of the nozzles and hot runner block control areas. 

Nylon A class of synthetic fibres and plastics, polyamides. Manufactured by condensation polymerization of ct, oj-aminomonocarboxylic acids or of aliphatic diamines with aliphatic dicarboxylic acids. Also rormed specifically, e.g. from caprolactam. The different Nylons are identified by reference to the carbon numbers of the diacid and diamine (e.g. Nylon 66 is from hexamethylene diamine and adipic acid). Thermoplastic materials with high m.p., insolubility, toughness, impact resistance, low friction. Used in monofilaments, textiles, cables, insulation and in packing materials. U.S. production 1983 11 megatonnes. 

The base of this estimation is the signal to noise ratio. The lowest signal to noise ratio S/N which is necessary as a minimum to discern a signal from noise is S/N = 2 1 (4). Referring to the limiting values for the granularity Oj, of the film system classes the smallest density difference AD of an defect which would just be visible should be at least two times greater than On. 

The film density is chosen to be D-D = 2.0 as the values for Oj, G and G/Oj, in EN 584-1 refer to this density. For the value of the gradient G the condition given by the value G/op of the standard has to be considered, that means the value of the gradient has mostly to be greater than the minimum gradient of the film system class. 

An important class of molecule often described as clusters may better be referred to as micro-particles. This class includes metal, semiconductor and carbon clusters. Particularly interesting are the carbon clusters, C. ... 

Electrochemical methods may be classified into two broad classes, namely potentiometric metiiods and voltannnetric methods. The fonner involves the measurement of the potential of a working electrode iimnersed in a solution containing a redox species of interest with respect to a reference electrode. These are equilibrium experiments involving no current flow and provide themiodynamic infomiation only. The potential of the working electrode responds in a Nemstian maimer to the activity of the redox species, whilst that of the reference electrode remains constant. In contrast, m voltannnetric methods the system is perturbed... 

At potentials positive to the bulk metal deposition, a metal monolayer-or in some cases a bilayer-of one metal can be electrodeposited on another metal surface this phenomenon is referred to as underiDotential deposition (upd) in the literature. Many investigations of several different metal adsorbate/substrate systems have been published to date. In general, two different classes of surface stmetures can be classified (a) simple superstmetures with small packing densities and (b) close-packed (bulklike) or even compressed stmetures, which are observed for deposition of the heavy metal ions Tl, Hg and Pb on Ag, Au, Cu or Pt (see, e.g., [63, 64, 65, 66, 62, 68, 69 and 70]). In case (a), the metal adsorbate is very often stabilized by coadsorbed anions typical representatives of this type are Cu/Au (111) (e.g. [44, 45, 21, 22 and 25]) or Cu/Pt(l 11) (e.g. [46, 74, 75, and 26 ]) It has to be mentioned that the two dimensional ordering of the Cu adatoms is significantly affected by the presence of coadsorbed anions, for example, for the upd of Cu on Au(l 11), the onset of underiDotential deposition shifts to more positive potentials from 80"to Br and CE [72]. 

Another way to overcome the step-size restriction fc < is to use multiple-time-stepping methods [4] or implicit methods [17, 18, 12, 3). In this paper, we examine the latter possibility. But for large molecular systems, fully implieit methods are very expensive. For that reason, we foeus on the general class of scmi-implicit methods depicted in Fig. 1 [12]. In this scheme. Step 3 of the nth time step ean be combined with Step 1 of the (n - - l)st time step. This then is a staggered two-step splitting method. We refer to [12] for further justification. 

Location of the compound within a class (or homologous series) of compounds. Reference to the literature or to tables of the physical properties of the class (or classes) of organic compounds to which the substance has been assigned, will generally locate a number of compounds which boil or melt within 6° of the value observed for the unknown. If other physical properties e.g., refractive index and density for a hquid) are available, these will assist in deciding whether the unknown is identical with one of the known compounds. In general, however, it is more convenient in practice to prepare one, but preferably two, crystalhne derivatives of the substance. 

The production of both an alcohol and the sodium salt of an acid might easily be confused with the hydrolysis products of an ester (in the above instance benzyl benzoate). Such an error would soon be discovered (e.g., by reference to the b.p. and other physical properties), but it would lead to an unnecessary expenditure of time and energy. The above example, however, emphasises the importance of conducting the class reactions of neutral oxygen-containing compounds in the proper order, viz., (1) aldehydes and ketones, (2) esters and anhydrides, (3) alcohols, and (4) ethers. 

The methods of preparation of some of the more important derivatives of a number of classes of organic compounds are described in the various Sections dealing with their reactions and characterisation. These Sections conclude with tables incorporating the melting points and boiling points of the compounds themselves, and also the melting points of selected derivatives. For convenience, the references to the various tables are collected below. 

The bibliography for this chapter is perhaps the most difficult to write. The majority of references in this entire book pertain to organic molecules. The organic references listed here are just a few of the review references pertaining specifically to organic chemistry. This list is incomplete, but attempts to include recent reviews, which will reference earlier work. The listing for other classes of molecules are more complete. 

In this chapter some important synthetic reactions specific to each class of compounds are described. Only small parts of certain total syntheses will be discussed. With the given references, however, the interested reader will easily locate the complete descriptions of the syntheses. I. Fleming s (1973) book is recommended as a guide through some ingenious classic total syntheses. 

Cumulated dienes are those m which one carbon atom is common to two carbon-carbon double bonds The simplest cumulated diene is 1 2 propadiene also called allene and compounds of this class are generally referred to as allenes... 

The task of relating carbohydrate configurations to names requires either a world class memory or an easily recalled mnemonic A mnemonic that serves us well here was pop ularized by the husband-wife team of Lours F Fieser and Mary Fieser of Harvard Uni versity m their 1956 textbook Organic Chemistry As with many mnemonics it s not clear who actually invented it and references to this particular one appeared m the chem ical education literature before publication of the Fiesers text The mnemonic has two features (1) a system for setting down all the stereoisomeric d aldohexoses m a logical order and (2) a way to assign the correct name to each one... 

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