Domain extrapolation hypothesis

By the methods of Tasks B to D, minimalll and nonMinimalll are mutually exclusive over the domain of the induction parameter within (r). If the correct domain extrapolation hypothesis is taken by the method of Task D, then minimal/l and nonMinimal/l are also mutually exclusive over the entire intended domain of the induction parameter. ... 

This proof hinges on the fact that the correct domain extrapolation hypothesis must be taken by the method of Task D. We assume that such is the case. Of course, a reasonable implementation of this synthesis mechanism would include some interaction with the specifier so as to maximize the confidence that everything goes right. 

What are the structural forms Task D of Step 2 non-deterministically selects some domain extrapolation hypothesis and extracts the corresponding predefined forms from a typed database. 

Taschner and coworkers proposed a similar model based on two other fla-voenzymes the human and E. coli glutathione reductase. The FAD binding domain of glutathione reductase and p-hydroxybenzoate hydroxylase have been shown to resemble each other closely via comparison of their respective X-ray crystal structures. Extrapolating this information to CHMO leads to the proposal that the hydroperoxide is attached to the re-face of the isoalloxazine ring and that the ketone substrates approach the hydroperoxide from the direction of the dimethylbenzene moiety[97). Further stereochemical and stereoelectronic considerations lead to a hypothesis explaining the observed stereoselectivities. 

Interpretation of microthermometric data (see above) shows the fundamental importance of isochores. Well-determined experimental isochores Linfortunately exist only for a limited nijimber of systems (H2O, H2O + NaCl, CO2, CHl, see p.212), and, except for H2O, they cover but a very small part of the possible geological P-T conditions. Large extrapolations are therefore needed, based to a first approximation on the hypothesis that isochores are straight lines. This approximation is certainly valid for most one component systems in the supercritical domain. For CO2 especially, extremely large extrapolations of experimental data (Fig. k,l) are compatible with P-T estimates derived independently from the study of solid phases (Fig. U.2) (see also Armstrong,... 

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