Be Selective

In this Dictionary 1 have aimed to provide an explanation of the terms used in the various branches of chemistry, together with brief accounts of important substances and chemical operations. The Dictionary is intended for use in schools, colleges and universities from the first study of chemistry up to about second year at university or college. We have necessarily had to be selective rather than comprehensive but most chemicals met with at this level should be included. 

Solvent power characterizes the miscibility of solute and solvent. This concept covers two types of uses dissolving a solid or reducing the viscosity of a liquid. The solvent power should be as high as possible. However, a solvent used as an extractant should also be selective, i.e., extract certain substances preferentially from the feed being treated. 

The type of rig which will be selected depends upon a number of parameters, in particular ... 

If we consider a well trajectory from surface to total depth (TD) it is sensible to look at the shallow section and the intermediate and reservoir intervals separately. The shallow section, usually referred to as top hole consists of rather unconsolidated sediments, hence the formation strength is low and drilling parameters and equipment have to be selected accordingly. 

This rather low recovery factor may be boosted by implementing secondary recovery techniques, particularly water Injection, or gas injection, with the aim of maintaining reservoir pressure and prolonging both plateau and decline periods. The decision to implement these techniques (only one of which would be selected) Is both technical and economic. Technical considerations would be the external supply of gas, and the... 

The radiation and temperature dependent mechanical properties of viscoelastic materials (modulus and loss) are of great interest throughout the plastics, polymer, and rubber from initial design to routine production. There are a number of laboratory research instruments are available to determine these properties. All these hardness tests conducted on polymeric materials involve the penetration of the sample under consideration by loaded spheres or other geometric shapes [1]. Most of these tests are to some extent arbitrary because the penetration of an indenter into viscoelastic material increases with time. For example, standard durometer test (the "Shore A") is widely used to measure the static "hardness" or resistance to indentation. However, it does not measure basic material properties, and its results depend on the specimen geometry (it is difficult to make available the identity of the initial position of the devices on cylinder or spherical surfaces while measuring) and test conditions, and some arbitrary time must be selected to compare different materials. 

Let the orthonomial fruictions > be selected eigenfruictions of the corresponding single-... 

XPS is also often perfonned employing syncln-otron radiation as the excitation source [59]. This technique is sometimes called soft x-ray photoelectron spectroscopy (SXPS) to distinguish it from laboratory XPS. The use of syncluotron radiation has two major advantages (1) a much higher spectral resolution can be achieved and (2) the photon energy of the excitation can be adjusted which, in turn, allows for a particular electron kinetic energy to be selected. 

A covalent bond (or particular nomial mode) in the van der Waals molecule (e.g. the I2 bond in l2-He) can be selectively excited, and what is usually observed experimentally is that the unimolecular dissociation rate constant is orders of magnitude smaller than the RRKM prediction. This is thought to result from weak coupling between the excited high-frequency intramolecular mode and the low-frequency van der Waals intemiolecular modes [83]. This coupling may be highly mode specific. Exciting the two different HE stretch modes in the (HF)2 dimer with one quantum results in lifetimes which differ by a factor of 24 [84]. Other van der Waals molecules studied include (NO)2 [85], NO-HF [ ], and (C2i J )2 [87]. 

First, it is possible to excite a chromophore corresponding to the active site, and detennine which modes interact with it. Second, by using UV excitation, the amino acids with phenyl rings (tryptophan and tyrosine, and a small contribution from phenylalanine) can be selectively excited [4], The frequency shifts in the resonance Raman spectrum associated with them provide infomiation on their enviromnent. 

In odier words, ions with a particular mass-to-charge ratio, m/z, can be selectively passed tlirough the magnetic sector by appropriate choice of a value of V and B (though nonnally V is held constant and only B is varied). 

As with the quadmpole ion trap, ions with a particular m/z ratio can be selected and stored in tlie FT-ICR cell by the resonant ejection of all other ions. Once isolated, the ions can be stored for variable periods of time (even hours) and allowed to react with neutral reagents that are introduced into the trapping cell. In this maimer, the products of bi-molecular reactions can be monitored and, if done as a fiinction of trapping time, it is possible to derive rate constants for the reactions [47]. Collision-induced dissociation can also be perfomied in the FT-ICR cell by tlie isolation and subsequent excitation of the cyclotron frequency of the ions. The extra translational kinetic energy of the ion packet results in energetic collisions between the ions and background... 

The saturation coverage during chemisorption on a clean transition-metal surface is controlled by the fonnation of a chemical bond at a specific site [5] and not necessarily by the area of the molecule. In addition, in this case, the heat of chemisorption of the first monolayer is substantially higher than for the second and subsequent layers where adsorption is via weaker van der Waals interactions. Chemisorption is often usefLil for measuring the area of a specific component of a multi-component surface, for example, the area of small metal particles adsorbed onto a high-surface-area support [6], but not for measuring the total area of the sample. Surface areas measured using this method are specific to the molecule that chemisorbs on the surface. Carbon monoxide titration is therefore often used to define the number of sites available on a supported metal catalyst. In order to measure the total surface area, adsorbates must be selected that interact relatively weakly with the substrate so that the area occupied by each adsorbent is dominated by intennolecular interactions and the area occupied by each molecule is approximately defined by van der Waals radii. This... 

One or more interesting hits can be selected by clicking the small white box next to the structure. The resulting list of literature can be analyzed or refined (Figure 5-14). 

The connection table of the query object (similarity probe) is processed to obtain the set of atom pairs, and then the database file is scanned to evaluate the similarity between the query and each of the database structures. The maximum number of structures that the program will select is specified, as well as the minimum similarity score that a database compoimd must show to be selected. Within these limits, the program will select from the database the structures that are most similar (with the highest similarity value) to the query and will create an output file of compoimd numbers and similarity values, sorted by decreasing similarity, for the selected compounds. 

Heats of reaction Heats of reaction can be obtained as differences between the beats of formation of the products and those of the starting materials of a reaction. In EROS, heats of reaction arc calculated on the basis of an additivity scheme as presented in Section 7.1. With such an evaluation, reactions under thermodynamic control can be selected preferentially (Figure 10.3-10). 

Tine force field was then used to predict the results for fhe addition of the E and Z isomers c Ihe enol boronate of butanone (R = Me) to ethanol (R = Me). The relevant transitio. Iructures are shown in Figure 11.34. A Boltzmann distribution, calculated at the ten perature of the reaction (—78°C), predicted that the Z isomer would show almost complel syn selectivity syn anti = 99 1) and that the E isomer would be selective for the an product anti syn = 86 14). These results were in good agreement with the experunenti... 

The analogous procedure for a multivariate problem is to obtain many experimental equations like Eqs. (3-55) and to extract the best slopes from them by regression. Optimal solution for n unknowns requires that the slope vector be obtained from p equations, where p is larger than n, preferably much larger. When there are more than the minimum number of equations from which the slope vector is to be extracted, we say that the equation set is an overdetermined set. Clearly, n equations can be selected from among the p available equations, but this is precisely what we do not wish to do because we must subjectively discard some of the experimental data that may have been gained at considerable expense in time and money. 

To bore a cork, a borer should be selected which gives a hole only very shghtly smaller than that desired. The cork borer is moistened with water or alcohol or best with glycerine it is convenient to keep a small bottle (ca. 25 ml. capacity) containing glycerine. Fig. 

Crystallised sodium sulphide NajS,9HjO is very deliquescent, and only a sample which has been kept in a tightly-stoppered bottle should be used crystals as dry as possible should be selected. Altemativelj, an equivalent amount of analysed fused sodium sulphide may be employed this dis.solves somewhat more slowly in alcohol. 

The derivative selected in any particular instance should be one which clearly singles out one compound from among all the possibilities and thus enables an unequivocal choice to be made. The melting points of the derivatives to be compared should differ by at least 5-10°. Whenever possible, a derivative should be selected which has a neutralisation equivalent as well as a melting point (e.g., an aryloxyacetic acid derivative of a phenol. Section IV,114,4, or a hydrogen S nitrophthalate of an alcohol. Section 111,25,5). 

MesSi- and iPrsSi groups can be selectively removed in the presence of TBS or TBDPS groups. 

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