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Silicon disulfide tetrachloride

Without carbon, the basis for life would be impossible. While it has been thought that silicon might take the place of carbon in forming a host of similar compounds, it is now not possible to form stable compounds with very long chains of silicon atoms. The atmosphere of Mars contains 96.2% CO2. Some of the most important compounds of carbon are carbon dioxide (CO2), carbon monoxide (CO), carbon disulfide (CS2), chloroform (CHCb), carbon tetrachloride (CCk), methane (CHr), ethylene (C2H4), acetylene (C2H2), benzene (CeHe), acetic acid (CHsCOOH), and their derivatives. [Pg.16]

D.5 Write the formula of (a) titanium dioxide (b) silicon tetrachloride (c) carbon disulfide (d) sulfur tetrafluoride ... [Pg.61]

FIGURE 3 2 Solvent extraction efficiencies (EF) as functions of dielectric constants (D), solubility parameters (6), and polarity parameters (P and E -). Solvents studied silicon tetrachloride, carbon disulfide, n pentane. Freon 113, cyclopentane, n-hexane, carbon tetradiloride, diethylether, cyclohexane, isooctane, benzene (reference, EF 100), toluene, trichloroethylene, diethylamine, chloroform, triethylamine, methylene, chloride, tetra-hydrofuran, l,4 dioxane, pyridine, 2 propanol, acetone, ethanol, methanol, dimethyl sulfoxide, and water. Reprinted with permission from Grosjean. ... [Pg.47]

Silicon tetrachloride is reported not to react with carbon disulfide solutions of terpy this is rather surprising in view of the facile reactions observed with the lower members of the group (37,470). A number of... [Pg.77]

DisiUcon hexabromide, hexabromodisUane, forms well-crystallized white plates or prisms (m.p. 95°, b.p. 265°). It is soluble in a variety of organic solvents, such as carbon tetrachloride, chloroform, carbon disulfide, and benzene, as well as in silicon tetrachloride or tetrabi omide. It is rapidly hydrolyzed by the moisture of the air, forming insoluble "silicooxalic acid, (H2Si204)x and with solutions of ammonia or of strong bases it forms sihcic acid or silicates, with liberation of hydrogen. [Pg.101]

Carbonothioic acid, 0-(6-chloro-3-phenyl-4-pyridazinyl) S-octyl ester. See Pyridate, Carbonothioic dichloride. See Thiophosgene Carbon oxide. See Carbon monoxide Carbon oxide sulfide. See Carbonyl sulfide Carbon oxychloride. See Phosgene Carbon oxysulfide. See Carbonyl sulfide Carbon silicide. See Silicon carbide Carbon sulfide. See Carbon disulfide Carbon tet. See Carbon tetrachloride Carbon tetraboride. See Boron carbide Carbon tetrabromide CAS 558-13-4 EINECS/ELINCS 209-189-6 UN 2516... [Pg.768]

Calcination of limestone Decomposition of magnesium hydroxide Production of carbon disulfide Chlorination of rutile to titanium tetrachloride Gasification of carbon Decomposition of ammonium chloride Decompositions of ammonium sulfate Mond process for nickel production Oxidation of silicon tetrachloride to silicon dioxide... [Pg.326]


See other pages where Silicon disulfide tetrachloride is mentioned: [Pg.201]    [Pg.332]    [Pg.285]    [Pg.67]    [Pg.413]    [Pg.658]    [Pg.650]    [Pg.53]    [Pg.437]    [Pg.496]    [Pg.90]    [Pg.638]    [Pg.732]    [Pg.696]    [Pg.730]    [Pg.650]   
See also in sourсe #XX -- [ Pg.310 ]




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