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X Neutral-Anionic Imidazole Interactions

X Ni Mo Ratio. Precursor Formula Catalyst Formula 6

X Nitrides and Carbides with the Sodium Chloride Structure

X NMR chemical shifts for the labeled cyclopropyl carbon atom

X NMR SCSs for 3-aniiino-2-nitrobenzothiophenes 75 and 2-aniiino-3-nitrobenzothiophenes 76 in CDCis

X NMR SCSs for 3-anilino-2-nitrobenzothiophenes 75 and 2-anilino-3-nitrobenzothiophenes 76 in DMSO-de

X Nuclease Digestion Buffer

X Nucleophile Y Products

X Occurrence of quinolines in fungi, bacteria, and marine organisms I

X Oil and Protein Content of the Edible Portion of Fish

X Optical Rotatory Properties of Fibrous Proteins

X Optical yield of the asymmetric hydrogenation of CH2 CXY at room temperature

X outlines the effect of changes in the monomer concentration on reaction parameters.

X outlines the results of a number of polymerizations of allyl methacrylate carried out using Procedure 6-3. The reduced viscosities of the isolated polymers are given in Table X. In several cases the reduced viscosities are given for polymer samples taken as the preparation proceeded but before the gel point had been reached.

X Oxidation of Sugar Solutions at 0 C. with Bromine Water in the Presence of Barium

X parameter values in the relation y KN

X Particle Diameters of Latex A-2

X Peptic Hydrolysis of Bonds Formed by the Aromatic Amino Acids in Human a- and -Chains

X Peptides Containing t-UNPAysine from DNP-insulin Sanger 1949b

X Periodate Balance after S-hr Oxidation

X Phenomena Modeled by Percolation Theory

X Photochemical Reactions of Esterified Carbohydrates with Hexamethylphosphoric Triamide

X Pkoperties and Characteristics of Synthetic Trienoic Acids

X present results obtained for the overage coordination number for the lattices considered. Thus, for the inhomogeneous lattices considered this product can be much different from the value 2 which has been obtained for the infinite uniform square lattice .

X presents for both the feedstock and reactor-sample 1 the moles of azaanthracenes plus azaphenanthrenes and their variously hydrogenated analogs. These values were calculated from the weight percents in Tables VII and VIII for the C-13 homologs in the -7 series as follows. Since GC MS of the feedstock bases did not identify partially hydrogenated azaphenanthrenes or azaanthracenes, the weight percents of C13Hl



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