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Reaction alkali

Friberg, L., Kylin, B., and Nystrom, A. Toxicities of trichloroethylene and tetrachloroethylene and Fujiwara s p3n idine-alkali reaction. Acta Pharmacol. Toxicol, 9 303-312,1953. [Pg.1658]

Both the acid and alkali reactions are brisk and vigorous. Reaction with water, however, is very slow ... [Pg.105]

Macphee, D. E. Glasser, F. P. 1996. A modelling approach to the prediction of pore fluid alkalinity in concrete. In Shayan, A. (ed) Alkali Reaction in Concrete. Blackie and Sons, Glasgow, 792-In Giere, R. Stille, P. (eds) Energy, Waste, and the Environment a Geochemical Perspective. Geological Society, London, Special Publications, 236, 796. [Pg.222]

Van Helmont, the most prominent of the seventeenth-century iatro-chemists, made the acid-alkali reaction the chemical model for a theory of animal digestion. One of his pupils, Sylvius by name, carried this idea into a total system by claiming that all bodily functions were acid-alkali reactions, and that all body fluids were either acidic or alkaline. This theory... [Pg.76]

Fiber-Reactive Dyes. These dyes can enter intu chemical reaction with the fiber and form a covalent bond to become an integral part of the liber polymer. They therefote have exceptional wetfastness. Their main use is oil eellulosie fibers where they are applied neutral and then chemical reaction is initialed by the addition of alkali. Reaction with the cellulose can be by either nucleophilic substitution, using, for example, dyes containing activated halogen substituents, or by addition to the double bond in. for example, vinyl sulfone. -SCfCH=CH2, groups. [Pg.519]

TNB+Acetone and Alkali, reaction gave a blk solid complex which is expl(Ref 12). Similar compds, prepd by one of the authors(BTF) during WWII, from TNT, acet and aw KOH were found... [Pg.49]

The reaction should be compared with the simultaneous oxidation and reduction of aromatic aldehydes under the influence of concentrated caustic alkali (Reaction LXIII.). [Pg.264]

There are various processes for synthesizing hydroxyapatite in aqua phase, such as hydrolyzation [223], acid-alkali reaction [224], hydrothermal process [225], coprecipitation [226], sol-gel synthesis [227], aerosol pyrolysis [228], and micro emulsion synthesis [229], etc. [Pg.318]

Oxazoles give acylamino ketones 232 by acid-catalyzed ring scission, although they are somewhat more stable than furans. The oxazole ring is also moderately stable to alkali reaction with hydroxide ions is facilitated by electron-withdrawing substituents and fused benzene rings. [Pg.513]

Friedman, M. (1978). Wheat gluten-alkali reactions. In "Proceedings of the 10th National Conference on Wheat Utilization Research", U. S. Department of Agriculture, Science and Education Administration, Western Regional Research Center, Berkeley, California 94710, ARM-W-4, pp. 81-100. [Pg.238]

Lemery s defense of the five principles and his corpuscular account of the acid-alkali reactions (quoted above) raise the possibility that he was aware of Boyle s critique of chemists principles and of the acid-alkali theory. As a leading Protestant apothecary employed in the royal household, Lemery should have been acquainted with other Protestant chemists in Paris. He returned to Paris in 1672, soon after Du Clos s critique of Boyle caused a stir within the Academy. He also knew Wilhelm Homberg, who had worked briefly in Boyle s laboratory. " It seems quite likely that Lemery incorporated Boyle s critique of chemical principles into the French didactic tradition, creating a unique blend of chemical philosophy. His limited yet flexible use of the corpuscular imagery illustrates well the fluidity of French didactic discourse in accommodating the current philosophical fashion. [Pg.58]

The sulfonamides are distinguishable because the derivative from a primary amine has an acidic hydrogen, which renders the product soluble in alkali (reaction 1) whereas the sulfonamide from a secondary amine is insoluble (reaction 2). Tertiary amines lack the necessary acidic hydrogen for formation of benzenesulfonyl derivatives. [Pg.374]

Three structurally isomeric forms have been established for the six-carbon saccharinic acids. In the order of their discovery, these are the sac-charinic or 2-C -methylpentonic acids, the isosaccharinic or 3-deoxy-2-C -(hydroxymethyl)-pentonic acids, and the metasaccharinic or 3-deoxy-hexonic acids. Although none of these six-carbon, deoxyaldonic acids has been crystallized, six are known in the form of crystalline lactones (saccharins). All the possible metasaccharinic acids of less than six-carbon content have been obtained, in the form of crystalline derivatives, by the sugar-alkali reaction. Only one example of a branched-chain deoxyaldonic acid (the racemic, five-carbon isosaccharinic acid) of other than six-carbon content has been so obtained. The formation of saccharinic acids containing more than six carbon atoms remains to be explored. [Pg.37]

Only the racemic form of this acid is obtained from the sugar-alkali reaction. As in the formation of lactic acid, a non-asymmetric enediol is an intermediate in its production (see Section III), and hence the racemate is the sole representative of the four-carbon metasaccharinic acid class. [Pg.38]

This recently discovered, racemic acid of the five-carbon aeries is only the third example of an isosaccharinic acid to be identified as a product of the sugar-alkali reaction. The other examples are the a- and /3-D-isosac-charinic acids of the six-carbon aeries (see pages 48 and 52). [Pg.40]

These four acids comprise all the possible five-carbon metasaccharinic acids and all were obtained by Nef, in the form of crystalline derivatives, from the pentose-alkali reaction. [Pg.41]


See other pages where Reaction alkali is mentioned: [Pg.41]    [Pg.17]    [Pg.579]    [Pg.580]    [Pg.800]    [Pg.197]    [Pg.590]    [Pg.323]    [Pg.439]    [Pg.490]    [Pg.55]    [Pg.53]    [Pg.59]    [Pg.75]    [Pg.78]    [Pg.78]    [Pg.104]    [Pg.111]    [Pg.145]    [Pg.394]    [Pg.395]    [Pg.362]    [Pg.393]    [Pg.36]    [Pg.37]    [Pg.37]    [Pg.38]    [Pg.39]    [Pg.41]   
See also in sourсe #XX -- [ Pg.244 ]




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1.3.5- Trinitrobenzene reactions with alkalis

3, 5-diamino reaction with alkalis

Acids reaction with alkalis

Addition reaction, alkali metal polyhydrogen

Aggregates alkali silica reaction

Alkali Barbier reaction

Alkali Silica Reaction (ASR)

Alkali aggregate reaction

Alkali concentration reactions

Alkali dimers, reactions

Alkali dolomite reaction

Alkali fusion side reactions

Alkali hydrolytic reactions

Alkali hydroxides, reactions

Alkali hydroxides, reactions aqueous solutions

Alkali metal alkoxides reactions

Alkali metal alkoxides, reactions with

Alkali metal atoms direct reactions

Alkali metal dimers, reactions

Alkali metal peroxides reactions with

Alkali metal phenoxides reactions

Alkali metal phosphides, reactions

Alkali metal reaction with aromatics

Alkali metal reaction with water

Alkali metal-water, or alcohol Balz-Schieman reactions

Alkali metals important reactions

Alkali metals reactions

Alkali metals reactions with

Alkali metals reactions with alcohols

Alkali metals selected reactions

Alkali pulping lignin reactions

Alkali reaction with halogen molecules

Alkali salt reactions

Alkali silicate reaction

Alkali silicate reaction chemistry

Alkali vibrationally excited from reactions

Alkali, reactions alkaline

Alkali, reactions alkaline battery

Alkali-carbonate reaction

Alkali-carbonate rock reaction

Alkali-metal plus halide reactions

Alkali-silica reaction

Alkali-silica/silicate reaction

Alkalies, reaction with osazones

Alkalis reaction with

Anthracene reaction with alkali metal

Benzyl chloride alkali reaction

Bromine reaction + alkali atoms

Carbon reaction + alkali atoms

Cations alkali metal reactions

Cellulosates, alkali metal acetic anhydride reaction

Cements alkali silica reaction

Chemistry of alkali-silica reaction

Chlor-alkali process anode reaction

Chlorine, reaction with alkali metals

Chlorine, reaction with hydrogen alkali metals

Chloroform reaction + alkali atoms

Chromones reaction with alkali

Cobalt reaction with alkali metals

Concrete alkali silica reaction

Corrosion, alkali-silica reaction

Fast Chemical Reactions in a Single-phase Reaction Mixture (Neutralisation of Acid and Alkali Media)

Glucopyranoside, 2-acetamido-3,4,6-triO - acetyl - 2 - deoxy -a-D - glucopyranosyl 2,3,4,6-tetra-Oacetyl reaction with alkali

Graphite reaction with alkali metals

Halides, reaction with alkali metals

Halogen compounds, reaction with alkali metals

Halogens, reaction with alkali metals

Hydroxy halides, alkylation reaction, with alkali

Iodine bromide, reaction+alkali metals

Iodine reaction+alkali metals

Methyl reaction + alkali atoms

Oxygen alkali metal reactions with

Pore solution alkali silica reaction

Potassium chloride, reaction + alkali

Potassium chloride, reaction + alkali atoms

Pozzolanic alkali silica reaction

Preparation reaction with alkalis

Prevention alkali silica reaction

Protein alkali reactions

Pyridone reaction with alkali

Reaction CLXXI.—Action of Alkali Sulphides and Hydrosulphides on Nitro Compounds

Reaction XXXII.—Action of Alkalis on certain a-di-ketones

Reaction of Alcohol with Alkali Metals

Reaction of syringyl alcohol with alkali

Reaction with Halogens, Acids, and Alkalis

Reaction with alkali fluondes

Reactions of Carbohydrates with Strong Alkali

Reactions of alkali atoms

Reactions of alkali dimers

Reactions of alkali halides

Reactions of p-Butyrolactone with Alkali Metal Supramolecular Complexes

Reactions of the Alkali and Alkaline Earth Metals

Reactions with Alkali and Alkaline Earth Metals

Reactions with Other Alkali Metals

Reactions with Silanes and Alkali Aluminiumhydrides

Reactions with acids and alkalis

Regeneration reaction, alkali metal

Salt reactions, alkali halide

Silicon reaction with alkali glycolates

Silicon tetrachloride, reaction + alkali

Substitution reaction, alkali metal

Sugars reactions with alkali

Sulphonyl chloride, reaction + alkali

Syringyl alcohol with alkali, reaction

Water/alkali reactions

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