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V compares EtS- and EtO- and shows similar features. The kEiS kEi0 ratios are relatively low for the vinyl fluorides . The operation of steric effects is shown by the kEtS k f-Bus ratios of 20 in spite of the expected higher basicity of t-BuS-. A combina-

V compares observed temperature rises for each of the cases with the maximum allowable value calculated from Equation .

V compares the degradation of total 2,4-D and 2,4,5-T were still present.

V compares the k.. and kolI rate constants for Nien,

V compares the Sierra waters with some waters from other felsic rocks. The fundamental similarities are clearly apparent as well as the minor variations that show the imprint of the details of rock mineralogy and small additions of constituents from various other sources.

V compares the two laboratory investigations in terms of eye irritation. Here significant differences are observed. Toluene yields the highest eye-irritation reactivity in the Battelle chamber and the lowest in the SRI chamber. For MIBK and diacetone alcohol, both laboratories agree. The other rankings are not significant since the eye-irritation responses are so close to those obtained for air.

V Comparison Between the Experimental J Values Given in Table P

V COMPARISON OF H20 AND H2 TPSR RESULTS AFTER EXPOSURE OF G-56H TO ETHANE

V Comparison of Lipoprotein Sizes Deduced Using Different Technique

V Comparison of Observed and Calculated Absorptivities for Several Proteins

V Comparison of Overall and Response Dispersion portions of Amount Ranges for Dataset B

V Comparison of pH-Dependent Binding Enthalpies for Three Aminoglycosides with an RNA A-Site

V Comparison of Rotatory Dispersion with Hydrogen-Deuterium Exchange for Partial Helical Content in Copolymers of i.-Glutamic Add and i,-Lysine

V Comparison of the -OSOjF Dimensions WITH Those of SOaF in KSOaF and NH.SOaF

V Comparison of the Various Surface Treatments

V compiles the ZIE product isomer ratios of reactions from Table I for which such information has been reported. With 0.5-2 cross-linked polystyrene supptxis, the isomer ratios are similar to those obtained from Wittig reactions in solution. The exceptions appear to be the reactions on more highly cross-linked supports shown in Table IV. There is a clear trend toward greater E selectivity as the degree of cross-linking of the polymer increases. This probably should be explained as an environmental effect, but comparison with solvent effects on stereochemistry of Wittig reactions in the literature reveals no tendency for aromatic solvents, structurally similar to polystyrene, to increase E selectivity.

V Complexes Tp M Derived erom Dicarbonyls

V Composite Bonding with BTDA-3,3 -DABP Polyimide

V Composition of dietetic soy product

V Composition of Sugar Solutions as Determined by Nuclear Magnetic Resonance Measurements

V Compounds Containing Uronic Acids Uronic Acid Plus Simple Monosaccharide

V Conditions of Preparation, and Results, for Selected Polymers 1

V confirms this result for argon and iodine up to very high temperatures. This result is, of course,

V Conformalioda EqiuHliria rfTri- X cetyl- and Tri-O-benioyl D-ribopyranose Derivatives as a Fnnctioa of the AnonMiic Gronp

V Conformational Equilibria of Aldopentopyranose Derivatives in Acetone-d Solution at 31



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