Reproducibility table

You will easily reproduce Table 14.1 if you have access to an ab initio package. 

At last we are ready to return to the periodic table. At last we are able to begin answering those who are wondering why about the special properties of the electron populations in Table 15-1. Let us reproduce Table 15-1 together with the numbers of orbitals of the hydrogen atom. The suggestion of a connection is irresistible, as seen in Table 15-II. 

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This procedure, which is based entirely on commercially available reagents, is very easy to reproduce. Table 6.12 shows different aryl- and alkyl-substituted enones that can be epoxidised with high asymmetric induction with the in situ formed (/ )-BINOL-zinc-catalyst in diethyl ether, with cumene hydroperoxide as the terminal oxidant. 

As the other comparisons between slopes are significant (p<0.05), the P parameter may help to differentiate one process from another if the optimization experimental conditions are kept constant. There was no significant difference between trials in all the processes, indicating that dissolution values (in terms of P) can be reproduced (Table 7). 

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Initial experiments in which 1-gram samples of silica were heated at 200°C under vacuum, slurried with 30 ml toluene, and treated with an excess of Zr(7r-allyl)4 or CH3MgI showed good agreement between the two reagents and good experimental reproducibility (Table I). 

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The batches of povidone and of copovidone mentioned in the section Reproducibility were tested in parallel with this HPLC method and the Ph.Eur. methods for 2-pyrrolidone and N-vinylpyrrolidone. Table 40 illustrates the resultsobtained with the Ph.Eur. methods. The results are comparable with the results mentioned under Reproducibility (Tables 35 to 37) (Table 41,42). 

The trials shown in Table 128 were done with the same batch 1696/10 used in the trials of reproducibility (Table 127). 

Table 24 indicates one possibility for differentiating the various types of glycoside linkages with conventional mass spectra. The relative intensities appear to be highly sensitive to these glycosidic linkages. However, it is difficult to perform any distinction without ambiguity as a result of mass spectrum reproducibility (Table 24). The measurement of their IKE spectra represents an alternative, since they indicate much more spectacular differences (Fig. 82).

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Streamlined with the incorporation of the SH model into the commercially available MacroModcl modeling package [lO]. Both models have been used extensively to model a large cross-section of intramolecular homolytic addition reactions. Not only can regio- and stereochemical trends be modeled accurately, but the rate-altering effects of substitution are also well reproduced (Table 2). Some calculated transition structures are displayed in Fig, 1,... 

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On-line SFE-SFC-FID is also suited to quantitative analysis of dialkyltin additives in rigid PVC and is able to replace other tedious and time-consuming procedures. The results are highly reproducible. Table 7.14 of ref. [3a] shows other quantitative analyses of polymer additives by means of SFF-SFC. 

I am very grateful to Dr. C. Auerbach, Dr. B. M. Cattanach, and Dr. A. G. Searle, who carefully reviewed the manuscript. I am indebted to Dr. G. Gerber for helpful discussion and for revising the English text. I also thank the editors and authors for permission to reproduce Tables 4, 5, 6, and 8. 

As the working electrode in a spectroelectrochemical experiment, an OTE needs to have both wide optical and potential windows , a sufficiently low resistance for good electrode potential control, good stability and surface reproducibility. Table 1 summarizes the optical and resistance data of some OTEs which are typically thin conducting films on substrate surfaces or minigrids (electroformed mesh). 

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