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Rule form, production

On Level 1 in Figure 2, the most abstract test plan is represented by a single component which is always the Test-Plan-of-Sample. The Test-Plan-of-Sample has tens of different templates in production rule form. In this case, as the sample is some kind of water sample and the purpose is the ordinary waste water analysis, the Waste-Water-Task-Set-Rule shown in Figure 4 is applied. [Pg.205]

The Rules are written in what is known in the computer science lingo as the "Production Rule Form" [Davis King, 1975]. [Pg.165]

As mentioned before, the production rule forms of the transforms in SYNCHEM meant that a separate learning program had to be created. In fact, Gelemter and co-workers created two, one to learn by inductive generalization (ISOLDE), and the other to learn by deduction (TRISTAN). ... [Pg.56]

Base-promoted E2 elimination involves simultaneous loss of and X from neighboring carbons. Applying this rule to 2-methylcyclohexyl tosylate suggests that two different products might form, but the actual situation is more complicated. One tosylate isomer gives only one of the two possible alkenes, while the other gives both. [Pg.100]

This finite set of production rules completely specifies the infinite set Oi, which thus forms a regular language. [Pg.299]

The addition of hydrogen halides to simple alkenes, in the absence of peroxides, takes place by an electrophilic mechanism, and the orientation is in accord with Markovnikov s rule. " When peroxides are added, the addition of HBr occurs by a free-radical mechanism and the orientation is anti-Markovnikov (p. 985). It must be emphasized that this is true only for HBr. Free-radical addition of HF and HI has never been observed, even in the presence of peroxides, and of HCl only rarely. In the rare cases where free-radieal addition of HCl was noted, the orientation was still Markovnikov, presumably beeause the more stable product was formed. Free-radical addition of HF, HI, and HCl is energetically unfavorable (see the discussions on pp. 900, 910). It has often been found that anti-Markovnikov addition of HBr takes place even when peroxides have not been added. This happens because the substrate alkenes absorb oxygen from the air, forming small amounts of peroxides... [Pg.991]

One of the simplest and most powerful ways to manipulate information in the knowledge base is through rule-based reasoning, which relies on production rules. A production rule links two or more items of information in a structure of the form ... [Pg.214]

The action in a production rule may take various forms it might be an instruction to the user to bring about some event ... [Pg.217]

The set of rules that comprise a CS is sometimes referred to as a production system, as they have the form of production rules. [Pg.272]

The decision-making engine in the CS is the set of classifier condition-action rules therefore, the key to a successful application is a well-constructed set of rules. If the control problem is straightforward, the necessary classifiers could, in principle, be created by hand, but there is rarely much point in doing this. A single classifier is equivalent to a production rule, the same structures that form the basis of most expert systems if a set of classifiers that could adequately control the environment could be created by hand, it would probably be as easy to create an equivalent expert system (ES). As an ES is able to explain its actions but a CS is not, in these circumstances, an ES would be preferable. [Pg.279]

Ruasse et al, 1978) is totally regioselective and shows X-dependent chemoselectivity. This is partly in agreement with the kinetic data, which indicate no primary carbocation but rather a competition between the benzylic carbocation and the bromonium ion, depending on X. According to the data of Table 6, bridged intermediates would lead to more dibromide than open ions do. From these results and from those on gem-, cis- or frans-disubstituted alkenes, empirical rules have been inferred for chemoselectivity (i) more solvent-incorporated product is formed from open than from bridged ions (ii) methanol competes with bromide ions more efficiently than acetic acid. [Pg.237]

Since 0(2) is abelian, all its irreducible representations must be onedimensional. To identify these irreducible representations, the product rule (20) is used, noting that the only numbers (lxl matrices) that satisfy the rule are of the form... [Pg.89]

The rules relating to which products are formed in these reactions are given in Section 8.3. [Pg.127]

Skell s hypothesis proved to be extremely useful in carbene chemistry even though it was frequently opposed. The principal significance of these rules is represented in the scheme below. The singlet reaction occurs in a concerted step, the cis-addition product being formed in a stereospeciiic manner. In the triplet addition, which is a two-step reaction, rotation is thought to be faster than intersystem crossing (spin inversion) and ring closure, i.e., which would... [Pg.112]

For the determination of energy factored parameters, full isotopic substitution is bound to be useless. This is because, in the energy factored approximation, such substitution is predicted to multiply each frequency by a factor of [fij/j, ), where fx is the reduced mass mcfnol[nic+ o] of carbon monoxide, independent of the values of the parameters concerned. However, a great deal of information can be obtained from the spectra of partially substituted species, for which the Teller-Redlich product rule takes the particularly simple form... [Pg.14]

The tool preparation station receives its orders, initially originated by the CAD data processing system, via the FMS network and technically specified by the CAM system in the form of a production rule base. Order data arriving at the tool preparation station include the following ... [Pg.169]

Thus, as predicted by the orbital symmetry rules, this thermal suprafacial [1,3] sigmatropic reaction took place with complete inversion at C-7. Similar results have been obtained in a number of other cases.426 However, similar studies of the pyrolysis of the parent hydrocarbon of 103, labeled with D at C-6 and C-7, showed that while most of the product was formed with inversion at C-7, a significant fraction (11 to 29%) was formed with retention.427 Other cases of lack of complete inversion are also known.428 A diradical mechanism has been invoked to explain such cases.429 There is strong evidence for a radical mechanism for some [1,3] sigmatropic rearrangements.430 Photochemical suprafacial [1,3] migrations of carbon have been shown to proceed with retention, as predicted.431... [Pg.1127]

Kharasch s earliest studies in this area were carried out in collaboration with graduate student Frank R. Mayo. Mayo performed over 400 experiments in which allyl bromide (3-bromo-1-propene) was treated with hydrogen bromide under a variety of conditions, and determined the distribution of the "normal" and "abnormal" products formed during the reaction. What two products were formed Which is the product of addition in accordance with Markovnikov s rule Which one corresponds to addition opposite to the rule ... [Pg.250]

A further point of interest is the reaction regiochemistry. For the reaction in Scheme 2 we might consider two possible vinylcyclopropane products. Thus the intermediate cyclo-propyldicarbinyl diradical might open in two ways. However, only one product is formed. In Scheme 3 this is shown more definitively where the two modes of unzipping the cyclopropyl dicarbinyl diradical are depicted. A general rule is that the less stabilized diradical center utilizes its odd-electron density to open the three-membered ring. This leads onwards to the more stabilized Diradical II 3. [Pg.324]

The reaction of aryl and hetaryl halides with the nitrile-stabilized carbanions (RC -CN) leads to derivatives of the type ArCH(R)CN. Sometimes, however, dimeric products of the type ArCH(R)CH(R)Ar are formed (Moon et al. 1983). As observed, 1-naphthyl, 2-pyridyl, and 2-quinolyl halides give the nitrile-substituted products, while phenyl halides, as a rule, form dimers. The reason consists of the manner of a surplus electron localization in the anion radical that arises upon replacing halogen with the nitrile-containing carban-ion. If the resultant anion radical contains an unpaired electron within LUMO covering mainly the aromatic ring, such an anion radical is stable, with no inclination to split up. It is oxidized by the initial substrate and gives the final product in the neutral form, Scheme 1-7 ... [Pg.17]

Starting from this rotated set complex orbitals and (t)3 multiplet operators may be constructed in a way which is entirely analogous to the treatment of Sect. 2. Hence the multiplets in Table 2 can be used equally well for trigonal complexes, keeping in mind that the axis of quantization is now the z axis. This implies that the subduction rules for real components in Eq. 15 have to be replaced by the appropriate S03 j. O j D3 subduction rules. In order to obtain the real forms of the (t2)3 basis functions the resulting expressions have to be multiplied once again by the pseudoscalar quantity of A2 symmetry. The appropriate product rules have been given by Ballhausen [59], For the individual orbital functions one obtains ... [Pg.55]


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See also in sourсe #XX -- [ Pg.165 ]




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