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VI Q-values and taste of individual 1-amino acids

VI Radii and Electronic Configuration of Some High- and Low-Spin Transition Metal Caiion

VI Radii of Puromycin-Generated Particles Calculated from Sedimentation Coefficients and

VI Rate Constants for the Acid Pathway

VI Rates of Oxidative Respiration and Non-Oxidative Fermentation by Yeasts Growing Aerobically in 3 D-Glucose

VI Ratio of Metal Bound Flakes Grits

VI recapitulates the relative response of Synthoil and SRC to hydrotreating in terms of percentage conversion of heptane insolubles, as reported in Table II. Conversion of heptane insolubles was substantially greater in the case of SRC. While the Synthoil was processed at a higher space velocity, the throughput rate of Synthoil feed heptane insolubles was only half that of the SRC feed heptane insolubles. Temperature in the Synthoil run was 5 -10 C lower than in the SRC run.

VI Reduced Specific Viscosity for Emulsifier- and Electrolyte-Free Latex A-2

VI Reductive Ozonolysis op C2Q-PFA from Liver after Administration op 16-Cl -AIX-cis-A8.11.14.Cjg.3

VI Redundancy In the Bitter Almond Pattern

VI Refinery JP-5 Stability Properties

VI Refractive Index Increments of Low Conversion Copolymer

VI Relation, between Degrees Brix and the Specific Gravity at 17 5 C.

VI Relations between Amino Acid Pairs When Comparing the Complete Structure of the a- and 0-Chain of Hemoglobin

VI Relationship between Hydrilla explant position and new shoot production

VI Relative Amplitude of Burst Phase Measured by Time-Resolved Far-UV CD Spectroscopy for Various Globular Proteins a

VI Relative Contributions by Parts of the Disaccharide Gal2 to Its Overall Binding Energy with Protein J539

VI Relative Feb Cent Distbibution of Radioactivitt Among Ubinabt Metabolites of C -Nicotinic Acid and C -Nicotinamidb 12 to 24 Hb Afteb Injection

VI Relative Retention Data for Cholesterol, Ergocalciferol, Cholecalciferol, and Their Derivatives on SE52 Modified X 60

VI reports eamples of cyanation .

VI Residual Activity of Purified, Jack-bean a-D-Mannosidase27 after Incubation for 3 Hours at 37 at Various pH Values

VI resulted from the work of Elovich, Zhabrova, Margolis, and Roginskii upon the extensive oxidation of hydrocarbons.

VI reveals a marked difference in the character of the chemical bond in beryllium and magnesium azides from the rest of group IIA, and the chemical properties and methods of preparation differ accordingly. Beryllium and magnesium azides are moisture sensitive the former decomposes hydrolytically to Be2, and the latter forms basic azides. Hence, they are made in water-free media such as Hquid ammonia, anhydrous hydrazine, or organic solvents. They deflagrate only weakly when ignited with a flame and are not sensitive to mechanical shock. The other IIA azides can be made in aqueous media, in which they are soluble some form hydrates in the soHd state, and they have the property of explosion. BeryUium azide is the only member of the group which is polymeric.

VI reveals the expected couplings for the 2,3-1- and -fused systems containing one substituent in the pyridine ring and shows that unambiguous location of such a substituent should be possible.

VI Risk Assessment CGA-72662



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