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Reactions with acid and alkali

Heat of crystallization and heat of evaporation Heat of combustion and heat of formation Heat of nitration Chemical properties Reactions with acids and alkalis Reaction with inorganic substances Effect of heat Effect of light... [Pg.689]

Properties. Put a small amount of boron into a crucible. Put the latter into a hot crucible furnace. What happens Write the equation of the reaction. How does boron react with acids and alkalies ... [Pg.176]

Stearyl Alcohol Reduction of ethyl stearate in the presence of lithium aluminum hydride yields stearyl alcohol, which contains not less than 90% of 1-octadecanol. It is available as flakes or granules which are white in color and possesses a characteristic odor. It is insoluble in water and melts at 55-60 °C. Stearyl alcohol has stiffening, viscosity-enhancing, and emollient properties and hence is used in the preparation of hydrophobic ointments and creams. Its weak emulsifying properties help in improving the water-holding capacity of ointments. Hypersensitivity reactions are sometimes observed due to the presence of some minor impurities. Stearyl alcohol preparations are compatible with acids and alkalis and are preserved in well-closed containers in a cool and dry place [6]. [Pg.275]

TABLE 1.25. Reaction of Tungsten Metal with Acids and Alkalis... [Pg.47]

Fig. 21 Reactions of the perfluorophosphonic monomer with acid and alkali... Fig. 21 Reactions of the perfluorophosphonic monomer with acid and alkali...
Therefore, the neutralisation reaction of acidic and alkali media is a fast chemical process which should be carried out in the new type of reactors, i.e., low energy- and resource-efficient tubular turbulent reactors of cylinder or diffuser-confusor design, which provides the jet mode of reaction mixture flow, quasi-isometric conditions in the reaction zone, complete conversion of reactants, and so on. Industrial wastewaters with an acid content of up to 30 wt% can be neutralised in a tubular turbulent reactor by a 10% or 20% aqueous solution of alkali, without any additional external heat removal. [Pg.219]

Reactions with acids and alkahs SUght with acids more pronounced with alkalis Not attacked by HCl or dilute aqueous NaOH reacts vigorously with molten NaOH Not dissolved by HCl or H2SO4 or dUute NaOH dissolved by concentrated NaOH... [Pg.131]

These water-insoluble acid-resistant complex iron cyanides are widely used as pigments and hence their detection, if need be in the presence of other materials, is of technical significance. The rapid test given here is based on the finding that Prussian Blue (I) and TurnbulFs Blue (II) yield dicyanogen when subjected to thermal decomposition. This volatile product responds to the reaction with oxine and alkali cyanide described on page 356. The partial reactions underlying the thermal production of (CN)2 are ... [Pg.564]

Ethyl trimethylsilylacetate (1) is reactive to nucleophiles and readily undergoes desilylation reactions with acid or alkali, ethanol, and bromine (eq 1). ... [Pg.297]

Unfortunately the addition of large amounts of alkali oxides to silica leads to a reduction of the chemical durability of the resulting glass. Although commercial alkali alkaline earth silicate glasses are used as bottles and other containers for liquids, these glasses are compared with silica glass rather susceptible to dissolution in water and chemical reactions with acids and alkaline lyes. [Pg.33]

Prepared by the dehydration of benzamide. Hydrolysed by dilute acids and alkalis to benzoic acid. Good solvent. benzopheDone,C]3HioO,PhC(0)Ph. Colourless rhombic prisms, m.p. 49 C, b.p. 306°C. Characteristic smell. It is prepared by the action of benzoyl chloride upon benzene in the presence of aluminium chloride (Friedel-Crafts reaction) or by the oxidation of di-phenylmethane. It is much used in perfumery. Forms a kelyl with sodium. [Pg.57]

A further improvement is embodied in the Klndler variation of the Willgerodt reaction this consists in heating the ketone with approximately equal amounts of sulphur and a dry amine instead of aqueous ammonium polysulphide. The principal product is a thioamide, and hydrolysis with acid or alkali affords the carboxylic acid, usually in good yield. [Pg.923]

Esterification. The esterification of rosin provides important commercial products for the adhesive industry. Rosin esters are formed by the reaction of rosins with alcohols at elevated temperatures. Because the carboxyl group of the resin acids is hindered by attachment to a tertiary carbon, esterification with an alcohol can only be accomplished at elevated temperatures. This hindrance is in turn responsible for the high resistance of the resin acid ester linkage to cleavage by water, acid and alkali. [Pg.602]

Lewis acid (fluoride-ion acceptor) behaviour is exemplified by reactions with NOF and MF to give [N0]+[C1F2] and M+[C1F2] respectively (M = alkali metal or NH4). Lewis base (fluoride ion donor) activity includes reactions with BF3 and ASF5 ... [Pg.826]


See other pages where Reactions with acid and alkali is mentioned: [Pg.300]    [Pg.132]    [Pg.83]    [Pg.23]    [Pg.300]    [Pg.132]    [Pg.83]    [Pg.23]    [Pg.184]    [Pg.348]    [Pg.78]    [Pg.401]    [Pg.149]    [Pg.388]    [Pg.348]    [Pg.508]    [Pg.328]    [Pg.412]    [Pg.413]    [Pg.648]    [Pg.290]    [Pg.693]    [Pg.868]    [Pg.35]    [Pg.183]    [Pg.72]    [Pg.292]    [Pg.300]    [Pg.387]    [Pg.141]    [Pg.436]    [Pg.256]    [Pg.26]    [Pg.208]    [Pg.80]    [Pg.421]   
See also in sourсe #XX -- [ Pg.46 ]




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