Strong acids soluble salts

The reduction of hydroperoxides by triphenylphosphine in ethanol is second order. Unsuccessful attempts to inhibit the reaction by the use of free-radical traps suggest a non-radical mechanism. The reaction is catalysed by strong acids. Soluble salts of molybdenum or vanadium are 10 —10 times more effective catalysts than H+. 

Oxazines can form salts with strong acids. The salts vary with regard to their solubility and stability. Some of the hydrochlorides are hydrolyzed by water. Some less common salts are known e.g., dichromates and ferrocyanates, " chloroplatinates and chloroaurates. Sometimes the picrates can also be used to identify the 1,3-oxazine derivatives. " In some instances a special procedure is required to form the picrates, as the heterocyclic ring can open under the action of picric acid. " ... 

Amines can be considered derivatives of ammonia, NH3, in which one or more of the hydrogen atoms is replaced by an organic group, such as an alkyl group. The example in Table 15-1 is a primary amine (one H replaced) replacement of two H atoms is a secondary amine replacement of all three results in a tertiary amine. Amines are somewhat soluble in water in which, like ammonia, they take up a proton leaving the solution basic. They dissolve readily in strong acid forming salts similar to ammonium salts. 

Negative substituents enhance the acidic properties of phenols, an effect opposite to that produced with aromatic amines. o and p-Chloro-phenols are considerably stronger acids than phenol itself, and o- and p-nitrophenols are still stronger. Trinitrophenol, picric acid, is a strong acid whose salts are neutral and not decomposed by carbonic acid or by ammonium salts. These salts of picric acid can be salted out of neutral solutions by sodium or potassium chloride. With negatively substituted phenols, it may be possible to separate the phenolate from solutions which are neutral or weakly alkaline to litmus. In doubtful cases, just as with the amines, the precipitated material must be studied to determine whether it is the free phenol or one of its salts. The color of the precipitate gives an indication in the case of the nitrophenols, since the free phenols have only a weak yellow color, whereas the alkali salts are deep yellow. Solubility tests with indififerent solvents may be used in the case of uncolored compounds. Only the free phenol can be separated from acidic solutions. 

Of the solvents reviewed, pyridine is the most reactive chemically and the most costly. It is a relatively strong base (pK 5.25) and reacts quickly with all strong acids. The salts of these acids, particularly pyridine sulphate and chloride, are much more water soluble than pyridine itself and are stable up to 100 C. They thus provide a means of extracting pyridine from solvents that are not water miscible, e.g. hydrocarbons and chlorinated hydrocarbons, since the salts can be transferred to an aqueous phase for subsequent springing and recovery of pyridine from water. The formation of pyridine salts can also be used to remove pyridine from an aqueous solution which includes close-boiling solvents, e.g. isobutanol. In these cases, after the salt has been formed, it will remain in aqueous solution while the other solvents are stripped off by distillation or steam stripping. 

The sulphonic acids are strongly acidic compounds, very soluble in water and readily give water-soluble metallic salts. 

Even though they are weaker bases arylammes like alkylammes can be com pletely protonated by strong acids Aniline is extracted from an ether solution into 1 M hydrochloric acid by being completely converted to a water soluble amlimum salt under these conditions... 

Solid Compounds. The tripositive actinide ions resemble tripositive lanthanide ions in their precipitation reactions (13,14,17,20,22). Tetrapositive actinide ions are similar in this respect to Ce . Thus the duorides and oxalates are insoluble in acid solution, and the nitrates, sulfates, perchlorates, and sulfides are all soluble. The tetrapositive actinide ions form insoluble iodates and various substituted arsenates even in rather strongly acid solution. The MO2 actinide ions can be precipitated as the potassium salt from strong carbonate solutions. In solutions containing a high concentration of sodium and acetate ions, the actinide ions form the insoluble crystalline salt NaM02(02CCH2)3. The hydroxides of all four ionic types are insoluble ... 

In general, the reactions of the perfluoro acids are similar to those of the hydrocarbon acids. Salts are formed with the ease expected of strong acids. The metal salts are all water soluble and much more soluble in organic solvents than the salts of the corresponding hydrocarbon acids. Esterification takes place readily with primary and secondary alcohols. Acid anhydrides can be prepared by distillation of the acids from phosphoms pentoxide. The amides are readily prepared by the ammonolysis of the acid haUdes, anhydrides, or esters and can be dehydrated to the corresponding nitriles (31). 

AH of the [Fe(CN)3] salts maybe considered salts of ferrocyanic acid or tetrahydrogen hexakiscyanoferrate [1712647-5], H4[Fe(CN)3], a strongly acidic, air-sensitive compound. It is soluble in water and alcohol but is insoluble in ether. It can be prepared by precipitation of an etherate by adding ether to a solution of [Fe(CN)3] that was acidified with concentrated sulfuric acid. Removal of the ether of solvation affords a white powder which is stable when dry but slowly turns blue in moist air because of Pmssian Blue formation. 

Heat-reactive resins are more compatible than oil-soluble resins with other polar-coating resins, such as amino, epoxy, and poly(vinyl butyral). They are used in interior-can and dmm linings, metal primers, and pipe coatings. The coatings have excellent resistance to solvents, acids, and salts. They can be used over a wide range of temperatures, up to 370°C for short periods of dry heat, and continuously at 150°C. Strong alkaUes should be avoided. 

In laboratory preparations, sulfuric acid and hydrochloric acid have classically been used as esterification catalysts. However, formation of alkyl chlorides or dehydration, isomerization, or polymerization side reactions may result. Sulfonic acids, such as benzenesulfonic acid, toluenesulfonic acid, or methanesulfonic acid, are widely used in plant operations because of their less corrosive nature. Phosphoric acid is sometimes employed, but it leads to rather slow reactions. Soluble or supported metal salts minimize side reactions but usually require higher temperatures than strong acids. 

Ammonium chloroplatinate often can be used to advantage in place of chloroplatim c acid in the preparation of Adams catalyst. A mixture of 3 g. of ammonium chloroplatinate and 30 g. of sodium nitrate in a casserole or Pyrex beaker is heated gently at first until the rapid evolution of gas slackens and then more strongly until a temperature of 500° is reached. This operation requires about fifteen minutes and there is no spattering. The temperature is held at 500-520° for one-half hour and the mixture is then allowed to cool. The platinum oxide catalyst, collected in the usual way by extracting the soluble salts with water, weighs 1.5 g. and it is comparable in appearance and in activity to the material prepared from chloroplatinic acid. 

Salts are obtained by direct neutralization of the acid with appropriate oxides, hydroxides, or carbonates. Sulfamic acid is a diy, non-volatile, non-hygroscopic, colourless, white, crystalline solid of considerable stability. It melts at 205°, begins to decompose at 210°, and at 260° rapidly gives a mixture of SO2, SO3, N2, H2O, etc. It is a strong acid (dissociation constant 1.01 x 10 at 25° solubility 25gper 100g H2O) and, because of its physical form and stability, is a convenient standard for acidimetry. Over 50000 tonnes are manufactured annually and its principal applications are in formulations for metal cleaners, scale removers, detergents and stabilizers for chlorine in aqueous solution. 

For sparingly soluble salts of a strong acid the effect of the addition of an acid will be similar to that of any other indifferent electrolyte but if the sparingly soluble salt MA is the salt of a weak acid HA, then acids will, in general, have a solvent effect upon it. If hydrochloric acid is added to an aqueous suspension of such a salt, the following equilibrium will be established ... 

With the salts of certain weak acids, such as carbonic, sulphurous, and nitrous acids, an additional factor contributing to the increased solubility is the actual disappearance of the acid from solution either spontaneously, or on gentle warming. An explanation is thus provided for the well-known solubility of the sparingly soluble sulphites, carbonates, oxalates, phosphates(V), arsenites(III), arsenates(V), cyanides (with the exception of silver cyanide, which is actually a salt of the strong acid H[Ag(CN)2]), fluorides, acetates, and salts of other organic acids in strong acids. 

In strongly acid solution the reaction proceeds from left to right, but is reversed in almost neutral solution. Oxidation also proceeds quantitatively in a slightly acid medium in the presence of a zinc salt. The very sparingly soluble potassium zinc hexacyanoferrate(II) is formed, and the hexacyanoferrate(II) ions are removed from the sphere of action ... 

Transformation of bromocriptine free base 2 into water soluble salt -mesylate, is the only way to obtain a suitable therapeutical form. Crystallization of mesylate using alcohol as a solvent in the presence of excess of strong acid, e.g. methanesulphonic acid can induce formation of 12 -0-alkyl-derivative 2. Until now this derivatisation of ergot molecule has been practically unknown. In continuation we developed the preparative method for obtaining these compounds, (using tetrafluoroboric acid as a catalyst) (ref. 20). 

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