The ordinary ammonium molybdate, used as a test reagent for phosphates, is a salt of composition (NH4)10M012041; it has been examined physicochemically by J.
Acetoacetic ester is a most important synthetic reagent, having been used in the production of pyridines, quinolines, pyrazolones, furfurane, pyrrols, uric acid, and many complex acids and ketones.
It is a most important synthetic reagent; with sodium or sodium ethylate it forms sodio-malonic ester, which reacts readily with alkyl halides, forming alkyl malonic esters, which are again capable of forming sodium derivatives, that by further treatment with alkyl halides yield the di-alkyl malonic esters.
Potash soap with the same reagent undergoes double decomposition - a proportion being changed into a soda soap with the formation of potassium chloride.
In quantitative analysis the methods can be subdivided into: (a) gravimetric, in which the constituent is precipitated either as a definite insoluble compound by the addition of certain reagents, or electrolytically, by the passage of an electric current; (b) volumetric, in which the volume of a reagent of a known strength which produces a certain definite reaction is measured; (c) colorimetric, in which the solution has a particular tint, which can be compared with solutions of known strengths.
(a) Gravimetric. - This method is made up of four operations: (I) a weighed quantity of the substance is dissolved in a suitable solvent; (2) a particular reagent is added which precipitates the substance it is desired to estimate; (3) the precipitate is filtered, washed and dried; (4) the filter paper containing the precipitate is weighed either as a tared filter, or incinerated and ignited either in air or in any other gas, and then weighed.
These may be divided into two groups: (I) those in which a change in appearance of the reacting mixture occurs; (2) those in which it is necessary to use an indicator which, by its change in appearance, shows that an excess of one reagent is present.
The colourproducing reagent is added and the tints compared.
The reagents in common use are: Millon's reagent, a solution of mercuric nitrate containing nitrous acid, this gives a violet-red coloration; nitric acid, which gives a yellow colour, turning to gold when treated with ammonia (xanthoproteic reaction); fuming sulphuric acid, which gives violet solutions; and caustic potash and copper sulphate, which, on warming, gives a red to violet coloration (biuret reaction).
Various hydrates have been described, but they cannot be formed by precipitating a uranyl salt with an alkali, this reagent giving rise to salts termed uranates.
Solutions of uranyl salts (nitrate, &c.) behave to reagents as follows: sulphuretted hydrogen produces green uranous salt with precipitation of sulphur; sulphide of ammonium in neutral solutions gives a black precipitate of UO 2 S, which settles slowly and, while being washed in the filter, breaks up partially into hydrated UO 2 an sulphur; ammonia gives a yellow precipitate of uranate of ammonia, characteristically soluble in hot carbonate of ammonia solution; prussiate of potash gives a brown precipitate which in appearance is not unlike the precipitate produced by the same reagent in cupric salts.
Stannous salt solutions yield a brown precipitate of SnS with sulphuretted hydrogen, which is insoluble in cold dilute acids and in real sulphide of ammonium, (NH 4) 2 S; but the yellow, or the colourless reagent on addition of sulphur, dissolves the precipitate as SnS 2 salt.
Soc., 1904, 20, p. 15) has used silicon halides with the Grignard reagent: C2H,MgBr(+SiC14)-C2HiSiC13(-1-MgBrPh)--> Ph C 2 H 1.
All other metals, including palladium, are dissolved as nitrates, the oxidizing part of the reagent being generally reduced to oxides of nitrogen.
And then further oxidizing this with Fenton's reagent, i.e.
The German regulations are apparently based on a keen appreciation of the fact that while one particular denaturizing agent may have little or no effect on one industry, yet it would be quite fatal to the success of another; there is consequently a great choice of denaturizing agents, and in certain cases it is sufficient to mix the alcohol with a reagent necessary for the purpose in hand, or even with a certain amount of the final product, it being only necessary to satisfy the state that the spirit is not available as a beverage.
3, p. 319.) Ammonia finds a wide application in organic chemistry as a synthetic reagent; it reacts with alkyl iodides to form amines, with esters to form acid amides, with halogen fatty acids to form amino-acids; while it also combines with isocyanic esters to form alkyl ureas and with the mustard oils to form alkyl thioureas.
Bamberger), and by the action of the Grignard reagent on quinones (Bamberger).
It crystallizes in dark red prisms which are readily soluble in water; it is a valuable reagent for the detection of sulphur, this element when in the form of an alkaline sulphide giving a characteristic purple blue coloration with the nitroprusside.
The excess of reagent is removed by evaporation and a small quantity of a ferric salt added, when a deep red colour is produced.
In preparing the Grignard reagent the commencement of the reaction is accelerated by a trace of iodine.
The products formed by the action of the Grignard reagent with the various types of organic compounds are usually thrown out of solution in the form of crystalline precipitates or as thick oils, and are then decomposed by ice-cold dilute sulphuric or acetic acids, the magnesium being removed as a basic halide salt.
On passing a current of dry carbon dioxide over the reagent,- the gas is absorbed and the resulting compound, when decomposed by dilute acids, yields an organic acid, and similarly with carbon oxysulphide a thio-acid is obtained: RMgX-R CO 2 MgX?R CO 2 H; COS-CS(OMgX) R--R Csoh.
This solution is frequently used as a test reagent for the detection of aldehydes, giving, in most cases, a red coloration on the addition of a small quantity of the aldehyde.
On treatment with the Grignard reagent, in absolute ether solution, they yield addition products which are decomposed by water with production of tertiary alcohols (V.
With the Grignard reagent, they form addition compounds which on the addition of water yield tertiary alcohols, except in the case of ethyl formate, where a secondary alcohol is obtained.
Both the oxide and hydroxide dissolve in ammonia to form a beautiful azure-blue solution (Schweizer's reagent), which dissolves cellulose, or perhaps, holds it in suspension as water does starch; accordingly, the solution rapidly perforates paper or calico.
It is necessary in the first place, after the ore is in solution, to reduce all the iron to the ferrous condition; then the carefully standardized solution of the oxidizing reagent is added until all the iron is in the ferric state, the volume of the standard solution used being the measure of the iron contained in the ore.
A component is absorbed by a suitable reagent and the diminution in volume noted, or it is absorbed in water and the amount determined by titration with a standard solution.
Derivatives of the type R 2 N OH result in the action of the Grignard reagent on amyl nitrite.