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A scheme

The R, S convention is a scheme which has largely superseded the D, i. system to denote configuration about a chiral centre in a molecule. The convention allows unequivocal designation of the absolute configuration in a description of the positions in space of ligands attached to a chiral centre, in relation to an agreed standard of chirality like a right-hand helix. [Pg.288]

In such cases the development scheme for the original reserves may have to be modified to make processing capacity available for the new hydrocarbons. The economics of such a scheme can be affected negatively if substantial engineering modifications have to made to meet new safety legislation. For more background to ERD refer to Section 3. [Pg.364]

Figure A3.13.15 shows a scheme for such a Pauli equation treatment of energy transfer m highly excited ethane, e.g. equation (A3.13.75), fomied at energies above both tln-esholds for dissociation in chemical activation ... Figure A3.13.15 shows a scheme for such a Pauli equation treatment of energy transfer m highly excited ethane, e.g. equation (A3.13.75), fomied at energies above both tln-esholds for dissociation in chemical activation ...
We consider a finite space, which contains the NA sample and is in contact with a bath of water or water vapor. That allows one to maintain the r.h. in the experimental space at a constant level and change it when necessary. Such a scheme corresponds to the real experiments with wet NA samples. A NA molecule is simulated by a sequence of units of the same type. Thus, in the present study, we consider the case of a homogeneous NA or the case where averaging over the unit type is possible. Every unit can be found in the one of three conformational states unordered. A- or B- conformations. The units can reversibly change their conformational state. A unit corresponds to a nucleotide of a real NA. We assume that the NA strands do not diverge during conformational transitions in the wet NA samples [18]. The conformational transitions are considered as cooperative processes that are caused by the unfavorable appearance of an interface between the distinct conformations. [Pg.118]

These equations reduce to a 3 x 3 matrix Ricatti equation in this case. In the appendix of [20], the efficient iterative solution of this nonlinear system is considered, as is the specialization of the method for linear and planar molecules. In the special case of linear molecules, the SHAKE-based method reduces to a scheme previously suggested by Fincham[14]. [Pg.356]

Approximating the nonlinear force f(y) over a time step by a suitable constant vector leads to a scheme whose origins for scalar equations can be traced back to [10] ... [Pg.422]

There is, however, another type of learning inductive learning. From a series of observations inferences are made to predict new observations. In order to be able to do this, the observations have to be put into a scheme that allows one to order them, and to recognize the features these observations have in common and the essential features that are different. On the basis of these observations a model of the principles that govern these observations must be built such a model then allows one to make predictions by analogy. [Pg.7]

In the mid 1970s, Ugi and co-workers developed a scheme based on treating reactions by means of matrices - reaction (R-) matrices [16, 17]. The representation of chemical structures by bond and electron (BE-) matrices was presented in Section 2.4. BE-matrices can be constructed not only for single molecules but also for ensembles of them, such as the starting materials of a reaction, e.g., formaldehyde (methanal) and hydrocyanic add as shown with the B E-matrix, B, in Figure 3-12. Figure 3-12 also shows the BE-matrix, E, of the reaction product, the cyanohydrin of formaldehyde. [Pg.185]

The two reaction schemes of Figures 3-13 and 3-15 encompass a large proportion of all organic reactions. However, these reactions do not involve a change in the number of bonds at the atoms participating in them. Therefore, when oxidation and reduction reactions that also change the valency of an atom ate to be considered, an additional reaction scheme must be introduced in which free electron pairs are involved. Figure 3-16 shows such a scheme and some specific reaction types. [Pg.191]

Furthermore, such a scheme cannot distinguish between the values for isomeric hydrocarbons because these compounds have the same number and type of bonds. [Pg.323]

To summarize, such a scheme seems to be sirffident for the estimation of Cp° and S°, but does not give sufficiently accurate values for the heat of formation, AHf. [Pg.323]

After the definition of a reaction type, a scheme for the evaluation of the given reaction type can follow in the reaction rule. An entire hierarchy of evaluations can be implemented, from no evaluation at all to a full-fledged estimation of reaction kinetics [12 ... [Pg.551]

The eigenfunctions of the zeroth-order Hamiltonian are written with energies. ground-state wavefunction is thus with energy Eg° To devise a scheme by Lch it is possible to gradually improve the eigenfunctions and eigenvalues of we write the true Hamiltonian as follows ... [Pg.134]

Combinatorial chemistry has significantly increased the nurnjjers of molecules that can be synthesised in a modern chemical laboratory. The classic approach to combinatorial synthesis involves the use of a solid support (e.g. polystyrene beads) together with a scheme called split-mix. Solid-phase chemistry is particularly appealing because it permits excess reagent to be used, so ensuring that the reaction proceeds to completion. The excess... [Pg.727]

The zeroth-order rates of nitration depend on a process, the heterolysis of nitric acid, which, whatever its details, must generate ions from neutral molecules. Such a process will be accelerated by an increase in the polarity of the medium such as would be produced by an increase in the concentration of nitric acid. In the case of nitration in carbon tetrachloride, where the concentration of nitric acid used was very much smaller than in the other solvents (table 3.1), the zeroth-order rate of nitration depended on the concentrationof nitric acid approximately to the fifth power. It is argued therefore that five molecules of nitric acid are associated with a pre-equilibrium step or are present in the transition state. Since nitric acid is evidently not much associated in carbon tetrachloride a scheme for nitronium ion formation might be as follows ... [Pg.38]

Davies and Warren" found that when 1,4-dimethylnaphthalene was treated with nitric acid in acetic anhydride, and the mixture was quenched after 34 hr, a pale yellow solid with an ultraviolet spectrum similar to that of a-nitro-naphthalene was produced. However, if the mixture was allowed to stand for 5 days, the product was i-methyl-4 nitromethylnaphthalene, in agreement with earlier findings. Davies and Warren suggested that the intermediate was 1,4-dimethyl-5 nitronaphthalene, which underwent acid catalysed rearrangement to the final product. Robinson pointed out that this is improbable, and suggested an alternative structure (iv) for the intermediate, together with a scheme for its formation from an adduct (ill) (analogous to l above) and its subsequent decomposition to the observed product. [Pg.222]

Melting of a quaternary salt with an arylformamidine (method A. Scheme 32). [Pg.48]

Of all the methods described for the synthesis of thiazole compounds, the most efficient involves the condensation of equimolar parts of thiourea (103) and a-haloketones or aldehydes to yield the corresponding 2-aminothiazoles (104a) or their 2-imino-A-4-thiazoline tautomers (104b) with no by-products (Method A, Scheme 46). [Pg.213]

Descnbe a scheme for carrying out the following synthesis (In the synthesis reported in the literature four separate operations were required )... [Pg.1022]

Proof. A scheme of reasoning is the same as that used in the previous subsection, and our attention now focuses on the details related to the nonsmoothness of the boundary. [Pg.338]

Another way to classify high performance fibers and high technology textile materials or products is by types of appHcations. A scheme of 10 main categories has been adopted (Table 4) and is similar to several classification schemes previously reported (28). [Pg.71]

A commercial-scale SNG plant, the Great Plains Plant in North Dakota, was actually built and operated for several years using a scheme based on coal. However, upon termination of the government subsidy, the plant s owner, ANR Inc., found it uneconomical to continue plant operation and shut down the plant in the late 1980s. [Pg.399]

An effective NDE program rehes heavily on periodic certification of the competence of its personnel (13,14). Certification programs designate levels of competence for all levels of personnel. Level I technicians are able to carry out instmctions in an NDE Level III supervisors are qualified to evaluate the needs of the test and devise a scheme that assures the desired level of quaUty or safety. [Pg.123]

The overall objective of research under way as of ca 1997 is to develop a system of sale by description for fine and medium wools whereby the buyer is presented only with measured data on the principal characteristics of the raw wool, as well as an assessment of the less important characteristics by an independent skilled appraiser (8). A scheme for assessing the risk of the presence of colored fiber content in greasy wool has been proposed which depends on production parameters and on the age and sex of the sheep (5). Instmmentation and computer algorithms for the measurement of style and handle... [Pg.339]


See other pages where A scheme is mentioned: [Pg.207]    [Pg.346]    [Pg.678]    [Pg.2253]    [Pg.2344]    [Pg.256]    [Pg.365]    [Pg.422]    [Pg.206]    [Pg.319]    [Pg.372]    [Pg.454]    [Pg.77]    [Pg.6]    [Pg.194]    [Pg.335]    [Pg.7]    [Pg.206]    [Pg.189]    [Pg.427]    [Pg.61]    [Pg.204]    [Pg.256]    [Pg.117]    [Pg.443]    [Pg.128]    [Pg.457]   
See also in sourсe #XX -- [ Pg.18 , Pg.396 , Pg.430 , Pg.439 ]




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A Cost Comparison of VLSI Integration Schemes

A Recursive Scheme for Gross Error Identification and Estimation

A Scheme That Works

A Separation and Purification Scheme

A priori schemes

A realizable finite-volume scheme for bivariate velocity moments

A scheme for classifying agricultural systems

A slightly more complex scheme

Coenzyme A biosynthesis of, scheme

Control Scheme for a Distillation Column

Development of a reaction scheme

Difference schemes as operator equations General formulations

Emergence of a common certification scheme

Hilbert scheme of points on a surface

Hilbert scheme on the cotangent bundle of a Riemann surface

Hybridization a scheme for linear species

Hybridization a scheme for tetrahedral and related species

Hybridization a scheme for trigonal planar species

Invariant Averages for Schemes Using the A, B and O Splitting

Outline of a Laser Isotope Separation Scheme

Outline of a decoupled scheme for the differential constitutive models

Powers of a scheme

Quasi-Coherent Sheaves Over a Diagram of Schemes

Scheme 24. Alcoholysis of diisopropylsilane using Rh2(OAc)4 as catalyst

Scheme 35. Reaction of le with 2-phenylethanol using Mn(CO)5Br as catalyst

Scheme for a Unimolecular Reaction Isomerization

Scheme of a gel chromatograph

Selective Reflection in a Pump-Probe Scheme

Sheaves over a Diagram of S-Schemes

Square of a scheme

Stability of a. difference scheme

The AOM as a Parameterisation Scheme

Truth Within a Conceptual Scheme

Using steady-state methods in a multi-loop control scheme

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