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Dilute-acid

Hydrolysed by dilute acids and alkalis to aniline. It chlorinates more slowly than aniline to o-and p-chloroacetanilides. [Pg.10]

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]

CoAsS, are also used as sources. The ore is roasted and Co is precipitated as the hydroxide and then reduced to Co with carbon (hep below 417 - C, cep to m.p.). The metal is silvery white and readily polished. It dissolves in dilute acids and is slowly oxidized in air. Adsorbs hydrogen strongly. The main use of cobalt is in alloys. Cobalt compounds are used in paints and varnishes, catalysts. Cobalt is an essential element in the diet. World production 1976 32 000 tonnes metal. [Pg.104]

They are stable compounds and are not decomposed by dilute acids or alkalis. They are frequently employed in synthetic organic chemistry for protecting the carbonyl group. [Pg.254]

Prepared by stirring phthalimide with cold concentrated ammonia solution. Hydrolysed to phlhalic acid with dilute acids. Dehydration with ethanoic anhydride gives first n-cyano-benzamide and then phthalonitrile. [Pg.311]

Colourless needles m.p. 14rC, b.p. 290"C. Slowly hydrolysed to phthalic acid by dilute acids and alkalis. [Pg.313]

CfiHsNjOs. Red needles m.p. 168-169°C. Soluble in dilute acids and alkalis. Prepared by reduction of picric acid with sodium hydrogen sulphide, ft is used for the preparation of azodyes, which can be after-chromed by treatment with metallic salts owing to the presence of a hydroxyl group ortho to the amino-group. [Pg.313]

Trichloroethylene is not attacked by dilute acids or alkalis, but when heated with sodium hydroxide under pressure it yields sodium gly-collate. In the presence of light and oxygen dichloroethanoyl chloride is formed, which can react with any moisture present to give small amounts of highly corrosive HCl. Numerous stabilizers have been patented. [Pg.404]

One of the most readily observed reactions in chemistry is the familiar production of bubbles of a colourless gas when certain metals (for example, iron, zinc) react with dilute acids. Cavendish investigated these reactions rather more than 200 years ago, and found the gas evolved to be the same in each case the gas, later named hydrogen, was much lighter than air and when burned in air produced water. [Pg.111]

Dilute acids have no effect on any form of carbon, and diamond is resistant to attack by concentrated acids at room temperature, but is oxidised by both concentrated sulphuric and concentrated nitric acid at about 500 K, when an additional oxidising agent is present. Carbon dioxide is produced and the acids are reduced to gaseous oxides ... [Pg.168]

Silicon, like carbon, is unaffected by dilute acids. Powdered silicon dissolves incompletely in concentrated nitric acid to give insoluble silicon dioxide, SiOj ... [Pg.169]

It is amphoteric it gives tin(II) salts with dilute acids and hydroxo stannates(II) with alkalis, for example ... [Pg.192]

If a dilute acid is added to this solution, a white gelatinous precipitate of the hydrated tin(IV) oxide is obtained. It was once thought that this was an acid and several formulae were suggested. However, it now seems likely that all these are different forms of the hydrated oxide, the differences arising from differences in particle size and degree of hydration. When some varieties of the hydrated tin(IV) oxide dissolve in hydrochloric acid, this is really a breaking up of the particles to form a colloidal solution—a phenomenon known as peptisation. [Pg.193]

Metals which do liberate hydrogen from dilute acids, for example zinc, magnesium, can react with nitric acid to give dinitrogen oxide, for example ... [Pg.241]

Concentrated sulphuric acid displaces more volatile acids from their salts, for example hydrogen chloride from chlorides (see above) and nitric acid from nitrates. The dilute acid is a good conductor of electricity. It behaves as a strong dibasic acid ... [Pg.301]

Hydrochloric acid is a strong monobasic acid, dissolving metals to form salt and evolving hydrogen. The reaction may be slow if the chloride formed is insoluble (for example lead and silver are attacked very slowly). The rate of attack on a metal also depends on concentration thus aluminium is attacked most rapidly by 9 M hydrochloric acid, while with other metals such as zinc or iron, more dilute acid is best. [Pg.331]

Electrolysis of hydrochloric acid yields hydrogen at the cathode and oxygen at the anode from the dilute acid, but chlorine at the anode (of carbon) from the concentrated acid. Electrolysis of the concentrated acid is used on the large scale to recover chlorine. [Pg.331]

The metal looks like iron it exists in four allotropic modifications, stable over various temperature ranges. Although not easily attacked by air. it is slowly attacked by water and dissolves readily in dilute acids to give manganese(II) salts. The stable form of the metal at ordinary temperatures is hard and brittle—hence man ganese is only of value in alloys, for example in steels (ferroalloys) and with aluminium, copper and nickel. [Pg.384]

Manganese(IV) oxide is a dark-brown solid, insoluble in water and dilute acids. Its catalytic decomposition of potassium chlor-ate(V) and hydrogen peroxide has already been mentioned. It dissolves slowly in alkalis to form manganates(lW), but the constitution of these is uncertain. It dissolves in ice-cold concentrated hydrochloric acid forming the complex octahedral hexachloromangan-ate(IV) ion ... [Pg.387]

Iron combines with most non-metals on heating, and forms the oxides Fe203 and (mainly) Fej04 when heated in air above 430 K. Steam above 8(X) K produces the oxide Fe304 and hydrogen. Iron dissolves in most dilute acids, giving iron(II) solutions, i.e. [Pg.392]

Cobalt is a bluish silvery metal, exhibits ferromagnetism, and can exist in more than one crystal form it is used in alloys for special purposes. Chemically it is somewhat similar to iron when heated in air it gives the oxides C03O4 and CoO, but it is less readily attacked by dilute acids. With halogens, the cobalt(II) halides are formed, except that with fluorine the (III) fluoride, C0F3, is obtained. [Pg.401]


See other pages where Dilute-acid is mentioned: [Pg.38]    [Pg.55]    [Pg.61]    [Pg.104]    [Pg.119]    [Pg.119]    [Pg.139]    [Pg.164]    [Pg.188]    [Pg.196]    [Pg.211]    [Pg.223]    [Pg.254]    [Pg.260]    [Pg.294]    [Pg.297]    [Pg.301]    [Pg.314]    [Pg.318]    [Pg.328]    [Pg.376]    [Pg.389]    [Pg.396]    [Pg.398]    [Pg.423]    [Pg.432]    [Pg.174]    [Pg.180]    [Pg.241]    [Pg.331]   
See also in sourсe #XX -- [ Pg.172 ]

See also in sourсe #XX -- [ Pg.344 ]

See also in sourсe #XX -- [ Pg.8 ]




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