Insoluble silver salt

This reaction may be adapted as a delicate test for arsenic in the following manner. The test is applicable only in the absence of chromates, hexacyano-ferrate(II) and (III) ions, which also give coloured silver salts insoluble in acetic acid. 

If the arsenic is present in the form of arsenious acid, arsenite, sulfide, alkali sulfoarsenite, or sulfoarsenate, it should be converted into arsenate by treatment with ammonia and hydrogen peroxide. The test is only specific in the absence of chromates and ferricyanides which also give colored silver salts, insoluble in acetic acid. 

To obtain the free acid, the ester is hydrolysed by ethanolic potash to the dipotassium salt, which is converted into the insoluble silver salt. A hot aqueous... 

Reaction with alcoholic silver nitrate. To carry out the test, treat 2 ml. of a 2 per cent, solution of silver nitrate in alcohol with 1 or 2 drops (or 0 05 g.) of the compound. If no appreciable precipitate appears at the laboratory temperature, heat on a boiling water bath for several minutes. Some organic acids give insoluble silver salts, hence it is advisable to add 1 drop of dilute (5 per cent.) nitric acid at the conclusion of the test most silver salts of organic acids are soluble in nitric acid. 

Silver All silver salts are insoluble. Exceptions AgNOg and AgC104 AgC2H302 and ... 

If a mixture of an insoluble silver salt and Ag2S is used to make the membrane, then the membrane potential also responds to the concentration of the anion of the added silver salt. Thus, pellets made from a mixture of Ag2S and AgCl can serve as a Ck ion-selective electrode, with a cell potential of... 

Organic Acid Salts. Slightly soluble or insoluble silver salts are precipitated when mono- and dicarboxylic aliphatic acids or their anions are... 

Cyanide Complexes. Insoluble silver cyanide, AgCN, is readily dissolved in an excess of alkah cyanide. The predominant silver species present in such solutions is Ag(CN) 2) with some Ag(CN) 3 and Ag(CN) 4. Virtually all silver salts, including the insoluble silver sulfide, dissolve in the presence of excess cyanide because the dissociation constant for the Ag(CN) 2 complex is only 4 x 10 (see Cyanides). 

Some products are precipitated from the fermentation broth. The insoluble calcium salts of some organic acids precipitate and are col-lec ted, and adding sulfuric acid regenerates the acid while forming gypsum (calcium sulfate) that constitutes a disposal problem. An early process for recovering the antibiotic cycloserine added silver nitrate to the fermentation broth to precipitate an insoluble silver salt. This process was soon obsolete because of poor economics and because the silver salt, when diy, exploded easily. 

Certain problems, for example, the differentiation between the (is)-diazohydroxide (7.3) and the nitrosoamine (7.4), were quite insoluble in Hantzsch s day because of the lack of appropriate methods. The observation that the sodium salt of the anti-diazoate reacts with methyl iodide to yield the TV-derivative (A-methylnitrosoamine), whereas the silver salt gives the O-ether (diazo ether) was often taken to support the presence of constitutional isomerism, but Hantzsch, quite rightly, disagreed. 

Anions (e.g., halides) that form insoluble silver salts can be measured at a rotating silver disk electrode. In this, the deposition and stripping steps involve the reaction... 

It is widely recognized that the solvent in which any chemical reaction takes place is not merely a passive medium in which relevant molecules perform the solvent itself makes an essential contribution to the reaction. The character of the solvent will determine which chemical species are soluble enough to enter solution and hence to react, and which species are insoluble, and thus precipitate out of solution, thereby being prevented from undergoing further chemical change. In the case of water, as will be seen, polar and ionic species are the ones that most readily dissolve. But even so, mere polarity or ionic character is not sufficient to ensure solubility. Solubility depends on a number of subtle energetic factors, and the possible interactions between water and silver chloride, for example, do not fulfil the requirements despite the ionic nature of the silver salt. Hence silver chloride is almost completely insoluble in water. 

What mass of each of the following silver salts would be required to react completely with a solution containing 3.55g of chloride ion to form (insoluble) silver chloride (a) AgNO,. (b) Ag S04, and (c) AgC,H,0,. 

There is an extensive chemistry associated with coordination compounds containing azide ions as a ligands. Like CN-, the azide ion is a pseudohalide ion, which means that it forms an insoluble silver salt, exists as the acid H-X, X-X is volatile, and it can combine with other pseudohalogens to give X-X. Although other pseudohalogens such as (CN)2 result from the oxidation of the CN- ion,... 

Silver occurs naturally in several oxidation states, the most common being elemental silver (Ag°) and the monovalent ion (Ag+). Soluble silver salts are, in general, more toxic than insoluble salts. In natural waters, the soluble monovalent species is the form of environmental concern. Sorption is the dominant process that controls silver partitioning in water and its movements in soils and sediments. As discussed later, silver enters the animal body through inhalation, ingestion, mucous membranes, and broken skin. The interspecies differences in the ability of animals to accumulate, retain, and eliminate silver are large. Almost all of the total silver intake is usually... 

The Koenigs-Knorr method in the presence of an insoluble silver salt proceeds mainly with inversion of configuration. Silver silicate and silver-silicate-aluminate have often been used as the heterogeneous catalyst. This procedure has been traditionally used for the synthesis of p-mannosidcs and has been recently reviewed.35 However, it only works well with very reactive halides and sufficiently reactive alcohol components. 

As shown in the introduction, the DNM anion can be regarded as a resonance stabilized, nonlinear planar pseudohalide, which forms an insoluble, highly explosive brownish silver salt upon addition of silver nitrate to an aqueous solution of 7. The DNM anion is related to the linear fulminate ion (CNO ) and can formally be regarded as the addition product of NO to fulminic acid (HCNO). Starting from CH4, NO containing nonlinear pseudohalides can be derived by successive substitution of H by NO, e.g. H3C(NO)/H2C(NO), H2C(N0)2/HC(N0)2 and HC(NO)3/C(NO)3, whereas the linear pseudohalide CNO is formally formed by replacing three H atoms by one NO unit and deprotonation. 

Application may be found for ionic liquids of resonance-stabilized methanides which can easily be prepared from the alkali salts. The first synthetic step includes the formation of the nearly insoluble silver salts in water (AgX, X = methanide). Since the silver salts dissolve in 2N aqueous NH3, adding ethyl(methyl)imidazolium bromide (EMHBr") results in the formation of a water-soluble ethyl(methyl)imidazolium methanide (EMHX") which can be separated from the AgBr precipitate by filtration. ... 

Bare Ag electrodes. It is noteworthy that the recently studied electrode processes of organic compounds at pc-Ag electrodes involve mainly biochemically important species. For example, Zeng et al. [278] have investigated the voltammetric behavior of 2-mercaptopyrimidine (MPD) and have found that at appropriate potentials, MPD adsorbs on and interacts with the electrode to form an insoluble silver salt at the surface. The first of two cathodic... 

Silver is a white, ductile metal occurring naturally in its pure form and in ores (USEPA 1980). Silver has the highest electrical and thermal conductivity of all metals. Some silver compounds are extremely photosensitive and are stable in air and water, except for tarnishing readily when exposed to sulfur compounds (Heyl et al. 1973). Metallic silver is insoluble in water, but many silver salts, such as silver nitrate, are soluble in water to more than 1220 g/L (Table 7.3). In natural environments, silver occurs primarily in the form of the sulfide or is intimately associated with other metal sulfides, especially fhose of lead, copper, iron, and gold, which are all essentially insoluble (USEPA 1980 USPHS 1990). Silver readily forms compounds with antimony, arsenic, selenium, and tellurium (Smith and Carson 1977). Silver has two stable isotopes ( ° Ag and ° Ag) and 20 radioisotopes none of the radioisotopes of silver occurs naturally, and the radioisotope with the longest physical half-life (253 days) is "° Ag. Several compounds of silver are potential explosion hazards silver oxalate decomposes explosively when heated silver acetylide (Ag2C2) is sensitive to detonation on contact and silver azide (AgN3) detonates spontaneously under certain conditions (Smith and Carson 1977). 

Complexes 123-131 were obtained by the direct reaction of the corresponding triazine and different silver salts according to Eq. (13). These products are sparingly soluble in acetone and insoluble in other conventional organic solvents. 

Tellurium(IV) sulfato complexes of composition 2(2Te02 S03),MHS04-2H20 have been reported,46 from which the anhydrous compounds were obtained by calcination. Carboxylic acids have also been found to form anionic complexes with tellurium(IV) and polonium(IV). For example, the silver salts of the citrato- and tartrato-tellurates(IV) have been described47 as insoluble in water but soluble in nitric acid. 

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