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SODIUM COMPOUND

Sodium halides, Sodium nitrate, Sodium nitrite. Sodium sulfates. Sodium sulfides. [Pg.175]

Kirk-Othmer Encyclopedia of Chemical Technology (4th Edition) [Pg.175]

The kinetics of the reactions of sulphur dioxide with sodium and with potassium have been investigated at 383—493 and 298—403 K, respectively. The only product identified from the former reaction was sodium sulphide, Na2S. A diflEusion-controlled process was indicated. The reaction with potassium appeared to be simpler since only potassium dithionate was formed  [Pg.29]

A mechanism based on adsorption-reaction is in general agreement with the observed kinetics. New solid-state syntheses of crystalline selenates M2Se04 (M = K, Rb, and Cs) and antimonates, MSbOa (M = K or Rb), M3Sb04 (M = K, Rb, and Cs) involve treatment of the powdered superoxides, MO2, with Se02 and Sb203, respectively. These ternary oxides have been characterized by their X-ray diffraction patterns. [Pg.29]

The crystal structures of the high-temperature modifications of -sodium antimony sulphide and /3-sodium antimony selenide, determined by X-ray methods, are isotypic and possess a fee lattice of the NaCl type with a statistical distribution of (Na + Sb) atoms in the Na positions and of S (or Se) atoms in the Cr positions. Crystal data are space group Fm3m for each, a = 5.7748, 5.965 A d(expt.) = 3.54, 4.68 d(calc.) = 3.60, 4.73 Z = 2, 2 for /8-NaSbS2 and -NaSbSe2, respectively. The low-temperature modifications o -NaSbS2 and a-NaSbSe2 are not isostructural and exhibit lower symmetry. Atoms of Na and Sb in [Pg.29]

Jarzembowski, F. Cassaretto, H. Posvic, and C. E. Moore, Analyt. Chim. Acta, 1974, 73, 409. S. Weiss and H. Krommer, Angew. Chem., 1974, 86, 590. [Pg.29]

172 p Touzain, H. F. Avedi, and J. Besson, Bull. Soc. chim. France, 1974, 421. [Pg.29]

Gmelin s Handbook of Inorganic Chemistry, System No. 21, Index Volume on Sodium, has been published.220 [Pg.46]

Prochazka and M. Nedved, Coll. Czech. Chem. Comm., 1973, 38, 2845. [Pg.46]

The reaction of the catalyst with sodium occurs first, and the catalyst is regenerated by the action of hydrogen and sodium hydride is produced.222 [Pg.47]

Norbert, and D. Cachau-Herreillat, Compt. rend., 1973, 276, C, 677. [Pg.49]

NaOH and gives virtually no hydrogen in the gas phase. The rate of the reaction is given by  [Pg.50]

The anion PgO has a nearly eclipsed configuration. Two of the four Na+ ions are co-ordinated to five O atoms while the remainder are co-ordinated to six O atoms. The structure contains chains of cations with four nearly collinear Na+ per cell parallel to the c-axis. These are surrounded by six anions. Adjacent anions along the c-axis are separated by a pair of Na+ ions.  [Pg.52]


C7H9N402- M.p. 337 C, an alkaloid obtained from cacao seeds or prepared synthetically. Constitutionally it is similar to caffeine, and is also a weak base. It is usually administered as the sodium compound combined with either sodium ethanoate or sodium salicylate, and is employed almost entirely as a diuretic. Physiologically theobromine resembles caffeine, but its effect on the central nervous system is less, while its action on the kidneys, is more pronounced. [Pg.392]

Sodium and potassium hydroxides. The use of these efficient reagents is generally confined to the drying of amines (soda lime, barium oxide and quicklime may also be employed) potassium hydroxide is somewhat superior to the sodium compound. Much of the water may be first removed by shaking with a concentrated solution of the alkali hydroxide. They react with many organic compounds (e.g., acids, phenols, esters and amides) in the presence of water, and are also soluble in certain organic liquids so that their use as desiccants is very limited... [Pg.142]

Sodium compounds are important to the paper, glass, soap, textile, petroleum, chemical, and metal industries. Soap is generally a sodium salt of certain fatty acids. The importance of common salt to animal nutrition has been recognized since prehistoric times. [Pg.28]


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2- nitropropane, sodium compounds

Action of Metals other than Sodium on Halogen Compounds

Allylic compounds Sodium borohydride

Aromatic compounds sodium dodecyl sulfate

Boron Compounds Borane-Dimethyl sulfide-Sodium

Boron Compounds Borane-Sodium borohydride

Carbonyl compounds by sodium borohydride

Carbonyl compounds condensations, sodium hydride

Carbonyl compounds reaction with sodium borohydrid

Carbonyl compounds reaction with sodium borohydride

Carbonyl compounds reduction by sodium borohydride

Carbonyl compounds sodium cyanoborohydride

Compounds by sodium

Compounds sodium chloride

Hydrated sodium compounds

Hydrated sodium compounds intercalation

Hydroxy carbonyl compounds Sodium borohydride

Inorganic compounds sodium thiosulfate

Iron compounds Sodium bicarbonate

Lithium sodium compounds, organo

Methylene compounds deprotonations, sodium hydride

Na NMR Spectra of Sodium Compounds

Nitrobenzene, preparation sodium compounds

Organolithium, -sodium and -magnesium Compounds

Organometallic compounds reduction with sodium

Phosphate compounds, sodium

Reduction of aromatic compounds to dihydroaromatics by sodium and ammonia

Selenium compounds sodium hydride

Silver compounds Sodium complexes

Silver compounds Sodium hypochlorite

Silver compounds Sodium ions

Silver compounds Sodium salts

Silver compounds Sodium thiosulfate

Soaps sodium compounds

Sodium acetylide compounds

Sodium alkyl sulphates compounds)

Sodium amalgam unsaturated carbonyl compounds

Sodium ammonium compound

Sodium and its compounds

Sodium arsenate nitro compounds

Sodium bicarbonate Lithium compounds

Sodium bis aluminum hydride carbonyl compounds

Sodium bisulfite, addition compounds

Sodium bisulfite, reaction with carbonyl compounds

Sodium borohydride carbonyl compound reduction

Sodium borohydride carbonyl compounds

Sodium borohydride compounds

Sodium borohydride nitro compounds

Sodium borohydride unsaturated carbonyl compounds

Sodium borohydride with metal compounds

Sodium borohydride, reaction with compounds

Sodium borohydride, reduction of carbonyl compounds

Sodium carbonyl compound reduction

Sodium carbonyl compounds

Sodium chloride Lithium compounds

Sodium chloride, addition compound

Sodium compounds azide

Sodium compounds boron fluoride

Sodium compounds bromate

Sodium compounds hydride

Sodium compounds hypochlorite

Sodium compounds nucleophilic trapping

Sodium compounds perborate

Sodium compounds percarbonate

Sodium compounds tungstate

Sodium compounds with oxygen

Sodium compounds, organo

Sodium compounds, organo reactions with

Sodium compounds, organo sulfide

Sodium cyanoborohydride benzylic compounds

Sodium cyanoborohydride unsaturated carbonyl compounds

Sodium cyanodithioformate, compound

Sodium cyclopentadienyl compound

Sodium dithionite compounds

Sodium fusion, pure organic compounds

Sodium hydrosulfite nitroso compounds

Sodium in glycerin of thymol, compound

Sodium lactate injection, compound

Sodium mixture, compound

Sodium mouth-wash, compound

Sodium nitrogen compounds

Sodium organometallic compounds

Sodium periodate synthesis of carbonyl compounds

Sodium salicylate Lithium compounds

Sodium sulfide nitro compounds

Sodium thiosulfate sulfur compounds

Sodium trimethoxyborohydride unsaturated carbonyl compounds

Sodium unsaturated carbonyl compounds

Sodium wash, compound

Sodium zirconium silicate compounds

Sodium, cyclopentadienyl-, compound with

Sodium, cyclopentadienyl-, compound with 1,2-dimethoxyethane

Sodium, cyclopentadienyl-, compound with l,2-dimethoxyethane

Sodium-graphite compounds

Sodium-vanadium oxide compounds

Some old potassium and sodium compounds

Sulfur compounds sodium hydride

Tritiated compounds Sodium borohydride

Tungsten Compounds Sodium tungstate

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