Iridium tetrachloride, IrC1 41 is obtained by dissolving the finely divided metal in aqua regia; by dissolving the hydroxide in hydrochloric acid; and by digesting the hydrated sesquichloride with nitric acid.
It is an indigo-blue powder, soluble in hydrochloric acid, but insoluble in dilute nitric and sulphuric acids.
It decomposes steam at a red heat, and slowly dissolves in dilute hydrochloric and sulphuric acids, but more readily in nitric acid.
The dithionates are all soluble in water and when boiled with hydrochloric acid decompose with evolution of sulphur dioxide and formation of a sulphate.
Soc., 1856, 7, p. 11) by the direct union of sulphur trioxide with hydrochloric acid gas, may also be obtained by distilling concentrated sulphuric acid with phosphorus oxychloride: 2H 2 SO 4 +POC1 3 =2SO 2 C1.
It dissolves easily in water, forming the hydrated chloride, CoC12.6H20, which may also be prepared by dissolving the hydroxide or carbonate in hydrochloric acid.
Podophyllin is a resinous powder obtained by precipitating an alcoholic tincture of the rhizome by means of water acidulated with hydrochloric acid.
Concentrated hydrochloric acid converts it into oxamide.
It may be prepared by boiling a-dichlorpropionic acid with silver oxide; by the hydrolysis of acetyl cyanide with hydrochloric acid (J.
Sodium amalgam or zinc and hydrochloric acid reduce it to lactic acid, whilst hydriodic acid gives propionic acid.
They form compounds with hydrochloric acid when this gas is passed into their ethereal solution; these compounds, however, are very unstable, being readily decomposed by water.
After the vigorous reaction has ceased and all the sodium has been used up, the mass is thrown into dilute hydrochloric acid, when the soluble sodium salts go into solution, and the insoluble boron remains as a brown powder, which may by filtered off and dried.
The dark product obtained is washed with water, hydrochloric acid and hydrofluoric acid, and finally calcined again with the oxide or with borax, being protected from air during the operation by a layer of charcoal.
Boron hydride has probably never been isolated in the pure condition; on heating boron trioxide with magnesium filings, a magnesium boride Mg 3 B 2 is obtained, and if this be decomposed with dilute hydrochloric acid a very evil-smelling gas, consisting of a mixture of hydrogen and boron hydride, is obtained.
It is a colourless fuming liquid boiling at 17-18° C., and is readily decomposed by water with formation of boric and hydrochloric acids.
After fusion, the melt is well washed with dilute hydrochloric acid and then with water, the nitride remaining as a white powder.
When heated with concentrated hydrochloric acid the amino group is replaced by the hydroxyl group and the phenolic eurhodols are produced.
It is formed by reducing diortho-dinitrodiphenyl with sodium amalgam and methyl alcohol, or by heating diphenylene-ortho-dihydrazine with hydrochloric acid to 150° C. It crystallizes in needles which melt at 156° C. Potassium permanganate oxidizes it to pyridazine tetracarboxylic acid.
A curious property is to be observed when a crystal of pharmacosiderite is placed in a solution of ammonia - in a few minutes the green colour changes throughout the whole crystal to red; on placing the red crystal in dilute hydrochloric acid the green colour is restored.
It can be purified by solution in hydrochloric acid and subsequent precipitation by metallic zinc.
Molybdenum sesquioxide, Mo 2 O 3, a black mass insoluble in acids, is formed by heating the corresponding hydroxide in vacuo, or by digesting the trioxide with zinc and hydrochloric acid.
It forms quadratic prisms, having a violet reflex and insoluble in boiling hydrochloric acid.
Several hydrated forms of the oxide are known, and a colloidal variety may be obtained by the dialysis of a strong hydrochloric acid solution of sodium molybdate.
The molybdates may be recognized by the fact that they give a white precipitate on the addition of hydrochloric or nitric acids to their solutions, and that with reducing agents (zinc and sulphuric acid) they give generally a blue coloration which turns to a green and finally to a brown colour.
Meta-aminophenol is prepared by reducing metanitrophenol, or by heating resorcin with ammonium chloride and ammonia to 200° C. Dimethyl-meta-aminophenol is prepared by heating meta-aminophenol with methyl alcohol and hydrochloric acid in an autoclave; by sulphonation of dimethylaniline, the sulphonic acid formed being finally fused with potash; or by nitrating dimethylaniline, in the presence of sulphuric acid at 0° C. In the latter case a mixture of nitro-compounds is obtained which can be separated by the addition of sodium carbonate.
It can also be obtained by passing sulphuretted hydrogen through a solution of the dioxide in hydrochloric acid.
The mixed solution of poiysulphides and thiosulphate of calcium thus produced is clarified, diluted largely, and then mixed with enough of pure dilute hydrochloric acid to produce a feebly alkaline mixture when sulphur is precipitated.
Rend., 1891, 112, p. 866) is obtained by mixing a solution of sodium hyposulphite with double its volume of hydrochloric acid, filtering and extracting with chloroform; the extract yielding the variety on evaporation.
Sulphur dioxide and hydrochloric acid, and accelerated by others, e.g.
To obtain pure sulphuretted hydrogen the method generally adopted consists in decomposing precipitated antimony sulphide with concentrated hydrochloric acid.
By the action of dilute hydrochloric acid on metallic polysulphides, an oily product is obtained which C. L.
Water decomposes it violently with formation of hydrochloric and sulphurous acids.
It is frequently used as an "antichlor," since in presence of water it has the power of converting chlorine into hydrochloric acid: SO 2 + C12 + 2H 2 0 = 2HC1 + H 2 SO 4.
Water decomposes it into hydrochloric and sulphurous acids.
OH =S02C12+ H 2 SO It is a colourless fuming liquid which boils at 69° C. and which is readily decomposed by water into sulphuric and hydrochloric acids.
The following table gives the heats of neutralization of the commoner strong monobasic acids with soda: - Hydrochloric acid Hydrobromic acid Hydriodic acid Nitric acid Chloric acid Bromic acid Within the error of experiment these numbers are identical.
In the Glatz process the lye is treated with a little milk of lime, the liquid then neutralized with hydrochloric acid, and the liquid filtered.
The mass is then covered with two-thirds of its weight of alcohol, and saturated with hydrochloric acid gas.
Thus by heating spirits of salt he obtained "marine acid air" (hydrochloric acid gas), and he was able to collect it because he happened to use mercury, instead of water, in his pneumatic trough.
Heating spirits of hartshorn, he was able to collect "alkaline air" (gaseous ammonia), again because he was using mercury in his pneumatic trough; then, trying what would happen if he passed electric sparks through the gas, he decomposed it into nitrogen and hydrogen, and "having a notion" that mixed with hydrochloric acid gas it would produce a "neutral air," perhaps much the same as common air, he synthesized sal ammoniac. Dephlogisticated air (oxygen) he prepared in August 1774 by heating red oxide of mercury with a burning-glass, and he found that in it a candle burnt with a remarkably vigorous flame and mice lived well.
Glycerin when treated with hydrochloric acid gives propenyl dichlorhydrin, which may be oxidized to s-dichloracetone.
Potassium cyanide reacts with this acid to form the corresponding dinitrile, which is converted by hydrochloric acid into citric acid.
At Paris and Leiden, are quite dissimilar from the Latin works attributed to Geber, and show few if any traces of the positive chemical knowledge, as of nitric acid (aqua dissolutiva or fortis) or of the mixture of nitric and hydrochloric acids known as aqua regis or regia, that appears in the latter.
Ruthenium in bulk resembles platinum in its general appearance, and has been obtained crystalline by heating an alloy of ruthenium and tin in a current of hydrochloric acid gas.
The peroxide, Ru04, is formed when a solution of potassium ruthenate is decomposed by chlorine, or by oxidizing ruthenium compounds with potassium chlorate and hydrochloric acid, or with potassium permanganate and sulphuric acid.
Ruthenium sulphides are obtained when the metal is warmed with pyrites and some borax, and the fused mass treated with hydrochloric acid first in the cold and then hot.
It is a colourless, oily, fuming liquid which is decomposed by water into sulphuric and hydrochloric acids.
It is a black amorphous powder soluble in concentrated sulphuric and hydrochloric acids, and when in the moist state readily oxidizes on exposure.
It is a brown-black powder soluble in hydrochloric acid, chlorine being simultaneously liberated.