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Alcohol aniline

Acetylene, fulminic acid (produced in ethanol - nitric acid mixtures), ammonia Acetic acid, acetone, alcohol, aniline, chromic acid, hydrocyanic acid, hydrogen sulphide, flammable liquids, flammable gases, or nitratable substances, paper, cardboard or rags Inorganic bases, amines Silver, mercury... [Pg.233]

The same technique was applied to a mixture of polyethylene terephthalate and acrylic acid (34). The polymerizations were followed by looking at the acid number of the product the parameters studied were time, temperature, and monomer content see Fig.9a,b,c. The hydrophilicity, the solubility of the copolymer in benzyl alcohol, aniline, and a mixture of phenol and CHQ3 were increased by graft copolymerization. [Pg.20]

Maman, A., Compt. rend., 198, 1324 (1934). Nitrobenzene, Benzyl alcohol, Aniline-Hexanes. [Pg.237]

Bipropellant. A rocket proplnt consisting of two unmixed chemicals(usually liquid) fed into the combustion chamber separately. One of the chemicals is a fuel(such as alcohol, aniline, hydrazine, etc), while the other is an oxidizeif such as liq O, nitric acid, hydrogen peroxide or nitrogen tetr-oxide). The energy released on combustion of fuel operates a propulsive rocket unit Refs l)warren( 1958), 13-14 2)Rocket Encycl (1959), 43-4... [Pg.126]

Copper acetylpropionylmethane (10 2 grams, i.e. 1 mol.) is slowly added with shaking to 7 8 grams of selenium tetrachloride suspended in 56 c.c. of anhydrous chloroform. After 30 minutes the mixture is filtered, the solvent removed from the filtrate by a current of air, and the residue triturated with absolute alcohol. A 24 5 per cent, yield of selenium acetylpropionylmethane is isolated as a yellow crystalline powder. It separates from absolute alcohol as pale yellow, glistening plates, M.pt. 137° C., is only faintly acid to litmus, and dissolves to a yellow solution in aqueous sodium hydroxide, decomposition gradually setting in with precipitation of selenium. The compound is practically insoluble in water or ether. It yields selenium when warmed with alcoholic aniline, and becomes superficially coated with red selenium on exposure to light. [Pg.103]

E1 Chlorzoxazone, isoniazid, acetaminophen, halothane, enflurane, methoxyflurane Dimethylnitrosamine, benzene, halogenated alkanes (eg, CCLj) acylonitrile, alcohols, aniline, styrene, vinyl chloride Chlorzoxazone (6-OH), [p-nitrophenol]... [Pg.118]

Show how you would use extractions with a separatory funnel to separate a mixture of the following compounds benzoic acid, phenol, benzyl alcohol, aniline. [Pg.975]

The thermal decomposition of salts of fluorinated acids gives tw o different types of products. depending on the reaction conditions and the type of cation. When the decarboxylation of alkali and alkaline earth metal salts is carried out in the presence of proton donors, such as water, alcohol, aniline, pyridine or other basic solvents, the product of the reaction is a fluorocarbon hydride. This is a general procedure for the preparation of 1 /Z-perfluoroalkanes. ... [Pg.699]

It is noted that the magnitude of the contact contribution varies considerably between the and resonances. In order to obtain structural information on the lanthanide complexes at least six Gj values are, in general, required (three polar coordinates to fix the position of the lanthanide ion relative to the molecule, two additional angles to define the main magnetic axis orientation, and one signed value for the proportionality constant). The six nuclei used to provide these Gj values need not necessarily be protons. In a later paper Reilley et al. (388) discuss certain refinements of their method and apply it to a wide variety of LSR complexes including those of water, pyridines, alcohols, anilines, aliphatic amines, and ketones. The contact contributions of the C shifts of Ln(DPA)3 and Ln(MDPA)3 complexes are found to be important even for carbons five bonds removed from the lanthanide ion. (390)... [Pg.70]

The crj stalline chloride was obtained in 30 per cent, yield by Reitzen-stein and Stamm, the acetate and sodium chloride solution being boiled for thirty minutes. The plates, which were recrystallised from benzene, melted at 240° C. When treated with sodium thiosulphate, p-amino-phenylmercuric thiosulphate is formed, and from the amori hous form Pesci isolated a crystalline product by the action of alcoholic aniline hydrochloride. It crystallised in fine, colourless needles, decomposing above 150° C. [Pg.115]

TheAy rocA/orifi c, C2oHi7N3(C6H.,)3HC1, is the technical product obtained first in the fractional precipitation of the blue melt with hydrochloric acid. In this state it forms brilliant green crystals, insoluble in water and sparingly soluble in hot alcohol. Aniline dissolves it somewhat more easily. The alcoholic solution has a pure blue colour. Some of this product is used as spirit-blue, but by far the greater quantity is used for the manufacture of soluble blues. Triphenylrosaniline salts dissolve in sulphuric acid with a brown colour. [Pg.126]

Ammonium Nitrate Ammonium Persulfate Ammonium Sulfate Amyi Acetate Amyl Alcohol Aniline... [Pg.763]

Properties Gas or liquid. Ignites in contact with alcohol, aniline, and ether. [Pg.573]

Unstable (transient) foams, which have a life time of seconds, are generally produced using mild surfactants, for example short-chain alcohols, aniline, phenol, pine oil, and short-chain undissociated fatty acids. Most of these compounds are sparingly soluble and may produce a low degree of elasticity. [Pg.328]

Ru(Tp)(PPh3)(MeCN)2]PFg has been employed as catalyst to produce l-iodo-2-naphthol in DMF and 2-iodobenzo[d]oxepin in benzene from l-(2/-iodoethynylphenyl)-2-propyloxirane. The solvent-dependent chemoselectivity has been ascribed to a solution equilibrium between ruthenium-Tt-iodoalkyne and ruthenium-2-iodovinylidene intermediates.66 The same ruthenium phosphine complex has been efficiently employed as catalyst in the nucleophilic addition of water, alcohols, aniline, acetylacetone, pyrroles, and dimethyl malonate to unfunctionalized enediynes that yielded functionalized benzene products in good yields (Fig. 8.6).67 [Ru(Tp)-(PPh3)(MeCN)2]PFg has been also found very active in catalytic benzannulation of l-phenyl-2-ethynylbenzenes in dichloroethane to afford phenanthrene.68... [Pg.451]


See other pages where Alcohol aniline is mentioned: [Pg.279]    [Pg.55]    [Pg.307]    [Pg.115]    [Pg.58]    [Pg.263]    [Pg.272]    [Pg.280]    [Pg.372]    [Pg.566]    [Pg.246]    [Pg.464]    [Pg.436]    [Pg.71]    [Pg.353]    [Pg.114]    [Pg.116]    [Pg.409]    [Pg.592]    [Pg.873]    [Pg.874]    [Pg.877]    [Pg.956]    [Pg.963]    [Pg.1077]    [Pg.1085]   
See also in sourсe #XX -- [ Pg.200 , Pg.201 ]




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Aniline, formation Benzyl alcohol

Hydroxylation of Aniline by Alcohols

Methyl, alcohol anilines

Microsomal p-Hydroxylation of Anilines by Alcohols

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