Permanganate Sentence Examples

On oxidation with potassium permanganate it is converted into acetyl urea, together with other products.

Carbon bisulphide slowly oxidizes on exposure to air, but by the action of potassium permanganate or chromic acid it is readily oxidized to carbon dioxide and sulphuric acid.

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.

Klaproth in 1799, is obtained when pure carbon (graphite or charcoal) is oxidized by alkaline permanganate, or when carbon forms the positive pole in an electrolytic cell (Ber., 1883, 16, p. 1209).

From these results Baeyer concluded that Claus' formula with three para-linkings cannot possibly be correct, for the Q2.5 dihydroterephthalic acid undoubtedly has two ethylene linkages, since it readily takes up two or four atoms of bromine, and is oxidized in warm aqueous solution by alkaline potassium permanganate.

Where a solution is likely to change in composition on keeping, such as potassium permanganate, iodine, sodium hydrate, &c., it is necessary to check or re-standardize it periodically.

Sulphur and phosphorus can sometimes be estimated by Messinger's method, in which the oxidation is effected by potassium permanganate and caustic alkali, or by potassium bichromate and hydrochloric acid.

In acid solution, potassium permanganate oxidizes it to nitric acid, but in alkaline solution only to nitrous acid.

It oxidizes a manganese salt (free from chlorine) in the presence of nitric acid to a permanganate; this is a very delicate test for manganese.

The usual test for solutions of aconitine consists in slight acidulation with acetic acid and addition of potassium permanganate, which causes the formation of a red crystalline precipitate.

Potassium permanganate in acid solution oxidizes it to carbon dioxide and water; the manganese sulphate formed has a catalytic accelerating effect on the decomposition.

Since it does not form an addition product with bromine, reduction must have taken place in one of the nuclei only, and on account of the aromatic character of the compound it must be in that nucleus which does not contain the amino group. This tetrahydro compound yields adipic acid, (CH 2) 4 (CO 2 H) 2, when oxidized by potassium permanganate.

Chemical methods of sterilization have also been suggested, depending on the use of iodine, chlorine, bromine, ozone, potassium permanganate, copper sulphate or chloride and ()their substances.

It is an unsaturated compound, and on oxidation with potassium permanganate gives succinic acid.

Sodium in amyl alcohol solution reduces it to hydroecgonidine C9H15N02, while moderate oxidation by potassium permanganate converts it into norecgonine.

Potash fusion converts it into acetic acid; nitric acid oxidizes it to acetic and oxalic acids; chromic acid mixture to acetaldehyde and acetic acid, and potassium permanganate to a0-dioxybutyric acid.

Potassium permanganate oxidizes it to fry-dioxybutyric acid.

Dilute nitric acid oxidizes it to acetic and oxalic acids, while potassium permanganate oxidizes it to acetone, carbon dioxide and oxalic acid.

Alkaline potassium permanganate oxidizes it to phenyl-glyoxyl-ortho-carboxylic acid, H02C C6H4 CO.

Potassium permanganate, in the presence of dilute sulphuric acid, is rapidly reduced by hydrogen peroxide, oxygen being given off, 2KM7,04+ 3H2S04+5H202= K2S04+2MnS04+8H20+502.

Potassium permanganate oxidizes it to f3-oxyisovaleric acid (CH 3) 2 C(OH) CH2.002H, whilst nitric acid gives, among other products, dinitropropane, (CH3)2C(N02)2.

Potassium bichromate and sulphuric acid oxidize it to carbon dioxide and acetic acid, while alkaline potassium permanganate oxidizes it to carbon dioxide.

Alkaline potassium permanganate oxidizes it to a-oxyisobutyric acid, (CH 3) 2.

The precipitate is dissolved in boiling water, decolorized by potassium permanganate and decomposed by barium carbonate.

Acid potassium permanganate oxidizes it to carbon dioxide and nitrogen.

This acid is also formed by decomposing barium or lead permanganate with dilute sulphuric acid.

Sodium Permanganate, NaMn0 4.3H 2 O (?), may be prepared in a similar manner, or by precipitating the silver salt with sodium chloride.

Barium Permanganate, BaMn 2 0 8, crystallizes in almost black needles, and is formed by passing carbon dioxide through water containing suspended barium manganate.

Chem., 1898, p. 845) or by potassium permanganate (E.

The manganese dioxide may be replaced by various other substances, such as red lead, lead dioxide, potassium bichromate, and potassium permanganate.

Potassium permanganate, in acid solution, oxidizes it to carbon dioxide and water.

Two salts are in common use for this purpose, potassium permanganate and potassium bichromate.

The end of the reaction when potassium permanganate is employed is known by the change in colour .of the solution.

As the solution of potassium permanganate, which is deep red in colour, is dropped into the colourless iron solution, it is quickly decolorized while the iron solution gradually assumes a yellowish tinge, the first drop of the permanganate solution in excess giving it a pink tint.

The solution is then ready for titration with the standard permanganate solution.

The permanganate or bichromate solution is standardized by dissolving o.

Goldschmiedt (Monats., 1883-1889), who determined its constitution (formula I., below) by a study of its oxidation products, showing that papaveraldine, which it gives with potassium permanganate, is a tetramethoxybenzoylisoquinoline.

Potassium permanganate decomposes morphine by oxidation, the action being facilitated by the addition of a small quantity of mineral acid to the solution.

Pictet (Ber., 1897, 30, p. 2117) obtained it by oxidizing nicotine methyl hydroxide with potassium permanganate.

Chromic acid oxidizes it to acetic acid and carbon dioxide; potassium permanganate oxidizes it to pyruvic acid; nitric acid to oxalic acid, and a mixture of manganese dioxide and sulphuric acid to acetaldehyde and carbon dioxide.

The solution is stable to oxidizing agents such as dilute hydrogen peroxide and chlorine, but is oxidized by potassium permanganate to phosphoric acid; it does not reduce salts of the heavy metals.

The stomach may be washed out with warm water and then with a 2% solution of permanganate of potash, an enema of the same solution being given.

Oxidation by potassium permanganate gives phthalic acid; whilst chromic acid gives carbon dioxide and water.

The alkaloid is a strong base and is very readily oxidized; chromic acid converts it into normal butyric acid and ammonia; hydrogen peroxide gives aminopropylvalerylaldehyde, NH 2 CH(C 3 11 7) (CH2)3 CHO, whilst the benzoyl derivative is oxidized by potassium permanganate to benzoyl-a-aminovaleric acid, C 6 H 5 CO NH CH(C 3 H 7) (CH 2)3 COOH.

Potassium permanganate oxidizes it to acetylanthranilic acid, [[Hooc(') C 6 H 4 (2)Nh Coch]] 31 while chromic acid oxidizes it to quinaldic acid (quinoline-a-carboxylic acid).

Alkaline potassium permanganate oxidizes it to pyridine tricarboxylic acid (236).

By oxidation with alkaline potassium permanganate it yields phthalic acid and cinchomeronic acid.

It is stable to cold potassium permanganate.

Riiber (Ber., 1902, 35, p. 2411; 1904, 37, P. 22 74), by oxidizing diphenyl-2.4-cyclo-butane-bismethylene malonic acid (fron cinnamic aldehyde and malonic acid in the presence of quinoline) with potassium permanganate.

Alkaline potassium permanganate oxidizes it to adipic acid.

When reduced in alcoholic solution by means of sodium amalgam it yields methyl granatoline, 08H130H NCH3; this substance, on oxidation with cold potassium permanganate, is converted into granatoline, C 8 H, 5 NO, which on distillation over zinc dust yields pyridine.

By gentle oxidation with potassium permanganate it may be converted into glycerin.

Potassium permanganate in neutral solution oxidizes it to nitrobenzene, in alkaline solution to azobenzene, ammonia and oxalic acid, in acid solution to aniline black.

They may also be prepared by oxidizing chromium salts (in alkaline solution) with hydrogen peroxide, chlorine, bleaching powder, potassium permanganate and manganese dioxide.

The methods of bleaching by oxygen include all those which aim at the bleaching by exposure to the air and to sunlight (as in the case of artists' linseed-oil), or where oxygen or ozone is introduced in the form of gas or is evolved by chemicals, as manganese dioxide, potassium bichromate or potassium permanganate and sulphuric acid..

The pharmacological action of hydrogen peroxide (H202), potassium permanganate, powdered charcoal and some other oxidizing agents depends on the readiness with which they give up oxygen.

I gave the shank a quick wipe down with potassium permanganate solution to make the patterns stand out.

You might like to try growing sugar crystals, copper sulfate crystals, sodium silicate crystals, potassium permanganate crystals or iodine crystals.

Internally the permanganate is a valuable antidote in opium poisoning.

Chem., 1866, 9 8, p. 340); by the action of chlorine on steam at a bright red heat; by the decomposition of hydrogen peroxide by bleaching powder, manganese dioxide, potassium ferricyanide in alkaline solution, or potassium permanganate in acid solution; by heating barium peroxide with an aqueous solution of potassium ferricyanide (G.

Its methyl derivatives yield the corresponding carboxylic acids when oxidized by potassium permanganate.

In the first group, we have to notice the titration of a cyanide with silver nitrate, when a milkiness shows how far the reaction has gone; the titration of iron with permanganate, when the faint pink colour shows that all the iron is oxidized.

On oxidation with potassium permanganate it gives homovanillin, vanillin, &c.; with chromic acid in acetic acid solution it is converted into carbon dioxide and acetic acid, whilst nitric acid oxidizes it to oxalic acid.

The permanganate of potash is an irritant if used pure.

After protracted experimenting Sir Thomas Wardle was able in 1873 to show a series of tussurs well dyed in all the darker shades of colour, but the lighter and bright blues, pinks, scarlets, &c., he could not produce, Subsequently Tessie du Motay found that the fawn colour of natural tussur could be discharged by solution of permanganate of potash, but the oxidizing action was so rapid and violent that it destroyed the fibre itself.