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Sulphuric acid properties

COT is prepared by the polymerization of ethyne at moderate temperature and pressure in the presence of nickel salts. The molecule is non-planar and behaves as a typical cyclic olefin, having no aromatic properties. It may be catalytically hydrogenated to cyclo-octene, but with Zn and dil. sulphuric acid gives 1,3,6-cyclooclairiene. It reacts with maleic anhydride to give an adduct, m.p. 166 C, derived from the isomeric structure bicyclo-4,2,0-octa-2,4,7-triene(I) ... [Pg.122]

Lead dioxide is slightly soluble in concentrated nitric acid and concentrated sulphuric acid, and it dissolves in fused alkalis. It therefore has amphoteric properties, although these are not well characteri.sed since it is relatively inert. [Pg.194]

Hence the strength of the acid goes up as sulphur trioxide is dissolved in it. The acidity of pure and fuming sulphuric acids is not so apparent as in ordinary aqueous acids because it is masked by the oxidising and other properties moreover, the conductivity... [Pg.302]

The presence of chloric(I) acid makes the properties of chlorine water different from those of gaseous chlorine, just as aqueous sulphur dioxide is very different from the gas. Chloric(I) acid is a strong oxidising agent, and in acid solution will even oxidise sulphur to sulphuric acid however, the concentration of free chloric(I) acid in chlorine water is often low and oxidation reactions are not always complete. Nevertheless when chlorine bleaches moist litmus, it is the chloric(I) acid which is formed that produces the bleaching. The reaction of chlorine gas with aqueous bromide or iodide ions which causes displacement of bromine or iodine (see below) may also involve the reaction... [Pg.323]

The most widely used cleansing agent is the chromic acid cleaning mixture. It is essentially a mixture of chromic acid (CrOj) and concentrated sulphuric acid, and possesses powerful oxidising and solvent properties. Two methods of preparation are available —... [Pg.53]

Chakactkrisation of Unsaturatkd Aliphatic Hydrocarbons Unlike the saturated hydrocarbons, unsaturated aliphatic hydrocarbons are soluble in concentrated sulphuric acid and exhibit characteristic reactions with dUute potassium permanganate solution and with bromine. Nevertheless, no satisfactory derivatives have yet been developed for these hydrocarbons, and their characterisation must therefore be based upon a determination of their physical properties (boiling point, density and refractive index). The physical properties of a number of selected unsaturated hydrocarbons are collected in Table 111,11. [Pg.241]

It is marketed as a 35-40 per cent, solution in water (formalin). The rpactions of formaldehyde are partly typical of aldehydes and partly peculiar to itself. By evaporating an aqueous solution paraformaldehyde or paraform (CHjO), an amorphous white solid is produced it is insoluble in most solvents. When formaldehyde is distilled from a 60 per cent, solution containing 2 per cent, of sulphuric acid, it pol5unerises to a crystalline trimeride, trioxane, which can be extracted with methylene chloride this is crystalline (m.p. 62°, b.p. 115°), readily soluble in water, alcohol and ether, and devoid of aldehydic properties ... [Pg.319]

Nitriles and simple amides differ in physical properties the former are liquids or low-melting Solids, whilst the latter are generally solids. If the amide is a solid and insoluble in water, it may be readily prepared from the nitrile by dissolving in concentrated sulphuric acid and pouring the solution into water ... [Pg.1075]

Hydrolysis of a nitrile to an acid. Reflux 1 g. of the nitrile with 6 ml. of 30-40 per cent, sodium hydroxide solution until ammonia ceases to be evolved (2-3 hours). Dilute with 5 ml. of water and add, with coohng, 7 ml. of 50 per cent, sulphuric acid. Isolate the acid by ether extraction, and examine its solubility and other properties. [Pg.1077]

Separations based upon differences in the chemical properties of the components. Thus a mixture of toluene and anihne may be separated by extraction with dilute hydrochloric acid the aniline passes into the aqueous layer in the form of the salt, anihne hydrochloride, and may be recovered by neutralisation. Similarly, a mixture of phenol and toluene may be separated by treatment with dilute sodium hydroxide. The above examples are, of comse, simple apphcations of the fact that the various components fah into different solubihty groups (compare Section XI,5). Another example is the separation of a mixture of di-n-butyl ether and chlorobenzene concentrated sulphuric acid dissolves only the w-butyl other and it may be recovered from solution by dilution with water. With some classes of compounds, e.g., unsaturated compounds, concentrated sulphuric acid leads to polymerisation, sulphona-tion, etc., so that the original component cannot be recovered unchanged this solvent, therefore, possesses hmited apphcation. Phenols may be separated from acids (for example, o-cresol from benzoic acid) by a dilute solution of sodium bicarbonate the weakly acidic phenols (and also enols) are not converted into salts by this reagent and may be removed by ether extraction or by other means the acids pass into solution as the sodium salts and may be recovered after acidification. Aldehydes, e.g., benzaldehyde, may be separated from liquid hydrocarbons and other neutral, water-insoluble hquid compounds by shaking with a solution of sodium bisulphite the aldehyde forms a sohd bisulphite compound, which may be filtered off and decomposed with dilute acid or with sodium bicarbonate solution in order to recover the aldehyde. [Pg.1091]

Hughes, Ingold and Reed discussed the relative merits of the and e3 schemes as mechanisms for nitration by considering the properties of acetic acid, nitromethane, nitric acid and sulphuric acid as media for the reaction. The facts have already been discussed ( 2.2.3, 2.2.4, 2.3.2, 2.4.2, 2.4.3, 3-2). [Pg.108]

In the cases of 4-hydroxyquinoline and 4-methoxyquinoline the predominance of 6-nitration supports the evidence presented above that nitration in sulphuric acid proceeds via the cations. For both these compounds reaction via the neutral molecules would be expected to occur to a considerable extent at C(j) as a result of the directing properties of the hydroxyl and methoxyl groups. [Pg.215]

The properties of the polyurethane moulding compositions are also very similar to nylon 66. The greatest difference in properties is in water absorption, the 6,4-polyurethane absorbing only about of that of nylon 66 under comparable conditions. This results in better dimensional stability and a good retention of electrical insulation properties in conditions of high humidity. Resistance to sulphuric acid is somewhat bettter than with nylon 66 but both types of polymer are dissolved by phenols and formic acid. [Pg.784]

Properties.—Colourless liquid possessing a sweet smell, b. p. 60—62° sp.gr. 1-498 at 15° very slightly soluble in water non-inflammable. As chloroform slowly decomposes in presence of air and sunlight into phosgene, it is usual to add a little alcohol to the commcicial product, which arrests the change. Pure chloroform is neutral to litmus, has no action on silver nitrate solution and does not discolour concentrated sulphuric acid when shaken with it for an hour or left for a day. [Pg.71]

Although the odour of the pseudo-ionone does not appear to render it of great importance for its direct use in perfumery, it is capable of serving as raw material lor the production of perfumes, the pseudo-ionone being converted by the action of dilute acids into an isomeric ketone, which I term lonone, and which has most valuable properties for perfumery purposes. This conversion may be effected, for example, by heating for several hours in an oil-bath 20 parts of pseudo-ionone with 100 parts of water, 2-5 parts of sulphuric acid, and 100 parts of glycerine, to the boiling-point of the mixture. [Pg.219]

Chemical deposition Simple immersion deposits of copper may be obtained on iron and steel in a solution containing, for example, 15 g/1 of copper sulphate and 8 g/1 sulphuric acid, and on zinc-base alloy in a solution containing copper sulphate 300 g/1, tartaric acid 50 g/1 and ammonium hydroxide 30ml/l . Such deposits are thin and porous and are mainly plated for their colour, e.g. for identification, or for their lubricating properties, e.g. in wire drawing. [Pg.519]

Table 98) correlated with the Hammett acidity function H0 rather than with log [ROH]/[R+]377. However, subsequent spectroscopic analysis and colligative property measurements showed that anils are present in strong sulphuric acid entirely as the monoprotonated species and since reaction is not instantaneous, it must be occurring on some other species, assumed to be diprotonated. For this to be true a plot of log rate versus the acidity function H+ would have to be linear the values of H+ were not known in this medium but were considered to parallel... [Pg.161]

Toluene is continuously nitrated to mononitrotoluene in a cast-iron vessel, 1 m diameter, fitted with a propeller agitator 0.3 m diameter rotating at 2.5 Hz. The temperature is maintained at 310 K by circulating 0.5 kg/s cooling water through a stainless steel coil 25 mm o.d. and 22 mm i.d. wound in the form of a helix, 0.80 m in diameter. The conditions are such that the reacting material may be considered to have the same physical properties as 75 per cent sulphuric acid. If the mean water temperatute is 290 K, what is the overall coefficient of heat transfer ... [Pg.498]


See other pages where Sulphuric acid properties is mentioned: [Pg.18]    [Pg.110]    [Pg.231]    [Pg.330]    [Pg.2777]    [Pg.230]    [Pg.302]    [Pg.145]    [Pg.43]    [Pg.53]    [Pg.178]    [Pg.1067]    [Pg.1]    [Pg.123]    [Pg.220]    [Pg.272]    [Pg.520]    [Pg.274]    [Pg.219]    [Pg.236]    [Pg.139]    [Pg.628]    [Pg.721]    [Pg.612]    [Pg.893]    [Pg.112]    [Pg.243]    [Pg.255]    [Pg.118]    [Pg.314]   
See also in sourсe #XX -- [ Pg.300 , Pg.301 ]

See also in sourсe #XX -- [ Pg.300 , Pg.301 ]




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Sulphur properties

Sulphuric acid

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