Nonmetal alcohols

Chlorine Ammonia, acetylene, alcohols, alkanes, benzene, butadiene, carbon disulflde, dibutyl phthalate, ethers, fluorine, glycerol, hydrocarbons, hydrogen, sodium carbide, flnely divided metals, metal acetylides and carbides, nitrogen compounds, nonmetals, nonmetal hydrides, phosphorus compounds, polychlorobi-phenyl, silicones, steel, sulfldes, synthetic rubber, turpentine... 

Numerous fluorinated and perfluorinated alkyl hypochlorites have been synthesized and characterized, eg, CF OCl [22082-78-6] C2F OCl [22675-67-8] /-C F OCl [22675-68-9] and /-C F OCl [22082-78-6]. These nonmetal oxychlorine compounds are much more thermally stable than the corresponding parent compounds and can be prepared by reaction of GIF with the appropriate carbonyl compound or alcohol. 

In many ways, TiCl4 behaves as a covalent compound of a nonmetal. It is a strong Lewis acid that forms complexes with many types of Lewis bases, and it hydrolyzes in water. It also reacts with alcohols to yield compounds having the formula Ti(OR)4. However, it is the behavior of TiCl4 (reacting with [A1(C2H5)3]2) as a catalyst in the Ziegler-Natta polymerization of ethylene that is the most important use of the compound (see Chapter 22). 

Nitropropane Nitrosyl fluoride Nitrosyl perchlorate Nitrourea Nitrous acid Nitryl chloride Oxalic acid See under Nitromethane chlorosulfonic acid, oleum Haloalkenes, metals, nonmetals Acetones, amines, diethyl ether, metal salts, organic materials Mercury(II) and silver salts Phosphine, phosphorus trichloride, silver nitrate, semicarbazone Ammonia, sulfur trioxide, tin(IV) bromide and iodide Furfuryl alcohol, silver, mercury, sodium chlorate, sodium chlorite, sodium hypochlorite... 

Derivatives of nonmetals and alcohols with very low acidity (pK=15-19). These are esters of inorganic acids, characterized by low melting and boiling points, solubility in alcohols and nonpolar solvents, and sensitivity even to the traces of water. They are usually monomeric or weakly aggregated. The representatives of this group areB(OR)3, P(OR)3 and Se(OR)4. 

Ammonia, alkylamines, and other proton acceptor species can react with boric acid in aqueous or alcoholic solutions to form a wide range of crystalline nomnetal borate salts. Borate salts of aprotic nomnetal cations, such as quaternary ammonium cations, have also been characterized. The ammonium borates are significant commercial products, and the recognition that both protic and aprotic nonmetal cations can stabilize unusual borate anions has led to increased interest in the study of this area. 

Adam, W., Mitchell, C. M., Saha-Moeller, C. R. Regio- and Diastereoselective Catalytic Epoxidation of Acyclic Ailylic Alcohols with Methyltrioxorhenium A Mechanistic Comparison with Metal (Peroxy and Peroxo Complexes) and Nonmetal (Peracids and Dioxirane) Oxidants. J. Org. Chem. 1999, 64, 3699-3707. 

CHLOROCHROMIC ANHYDRIDE (14977-61-8) A powerful oxidizer. Violent reaction with water, producing hydrochloric and chromic acids, and chlorine gas. Potentially violent and explosive reaction with reducing agents, acetone, alcohols, calcium sulfide, combustible materials, gaseous or liquid ammonia, ethers, nonmetal halides, fuels, nonmetal hydrides, fluorine, organic matter, organic solvents, phosphorus, phosphorus trichloride, sodium azide, elemental sulfur, sulfur monochloride, turpentine, urea. Decomposes slowly in light. 

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