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Salt decomposition

Strong acid + carbonate or hydrogen carbonate Unstable product + decomposition Double-replacement -E decomposition Salt + H2O -E CO2 Salt -E H2O -E CO2 H+ + CO32-H+ -E HCO3- H2O + CO2 H2O + CO2... [Pg.261]

Ammonium salt -E hydroxide base NH4OH -E decomposition Double-replacement -E decomposition Salt -E NH3 -E H2O NH4+ + OH- H2O -E NHj... [Pg.261]

When, as in the case of LiH, they can be melted without decomposition, salt-like hydrides conduct electricity. On electrolysis, the melts yield hydrogen at the positive electrode. They all react with water, giving hydrogen and an alkaline solution ... [Pg.51]

On acetylation it gives acetanilide. Nitrated with some decomposition to a mixture of 2-and 4-nitroanilines. It is basic and gives water-soluble salts with mineral acids. Heating aniline sulphate at 190 C gives sulphanilic add. When heated with alkyl chlorides or aliphatic alcohols mono- and di-alkyl derivatives are obtained, e.g. dimethylaniline. Treatment with trichloroethylene gives phenylglycine. With glycerol and sulphuric acid (Skraup s reaction) quinoline is obtained, while quinaldine can be prepared by the reaction between aniline, paraldehyde and hydrochloric acid. [Pg.35]

Decomposition of its internal salt (a zwitter-ion) provides a convenient source of benzyne for organic synthesis. [Pg.36]

The diazoamino-compounds are usually yellow in colour, and do not dissolve in acid they can usually be isolated and crystallized without decomposition. When treated with HNO2 two molecules of diazonium salt are formed. Form an azo compound when warmed with an amine and its hydrochloride, e.g. [Pg.133]

Figure C2.12.2. Fonnation of Br0nsted acid sites in zeolites. Aqueous exchange of cation M witli an ammonium salt yields tlie ammonium fonn of tlie zeolite. Upon tliennal decomposition ammonia is released and tire proton remains as charge-balancing species. Direct ion-exchange of M witli acidic solutions is feasible for high-silica zeolites. Figure C2.12.2. Fonnation of Br0nsted acid sites in zeolites. Aqueous exchange of cation M witli an ammonium salt yields tlie ammonium fonn of tlie zeolite. Upon tliennal decomposition ammonia is released and tire proton remains as charge-balancing species. Direct ion-exchange of M witli acidic solutions is feasible for high-silica zeolites.
In a substance such as a salt hydrate (for example BaCl2.2H20) water can be determined by heating until it is all driven off. Provided that only water is evolved on heating, the difference in weight gives the water content. If water is mixed with other decomposition... [Pg.275]

Tellurium trioxide, TeOa, is an orange yellow powder made by thermal decomposition of telluric(VI) acid Te(OH)g. It is a strong oxidising agent which will, like H2Se04, oxidise hydrogen chloride to chlorine. It dissolves in hot water to give telluric(VI) acid. This is a weak acid and quite different from sulphuric and selenic acids. Two series of salts are known. [Pg.305]

Identification of Amines. Picric acid combines with many amines to give crystalline picrates, of general formula B,(NO )aCeHjOH, where B is a molecule of a monacidic base. These picrates have usually sharp melting- or decomposition-points, and serve to characterise the amines concerned. They may be formed either by (a) direct union of the acid and the base in a suitable solvent, or (6) by the interaction of sodium picrate and a salt of the amine in aqueous solution. [Pg.174]

When an aqueous solution of a diazonium salt is added to an alkaline solution of a phenol, coupling occurs with formation of an azo-compound (p. 188). If ho vc cr the ntiueous solution of the diazonium salt, t. . ., />-bromohenzene diazonium chloride, is mixed with an excess of an aromatic hydrocarbon, and aqueous sodium hydroxide then added to the vigorously stirred mixture, the diazotate which is formed, e.g., BrC,H N OH, dissolves in the hydrocarbon and there undergoes decomposition with the formation of nitrogen and two free radicals. The aryl free radical then reacts with the hydrocarbon to give a... [Pg.201]

Dissolve 13 g. of sodium in 30 ml. of absolute ethanol in a 250 ml. flask carrying a reflux condenser, then add 10 g. (9 5 ml.) of redistilled ethyl malonate, and place the flask on a boiling water-bath. Without delay, add a solution of 5 3 g. of thiourea in a minimum of boiling absolute ethanol (about 100 ml.). The sodium salt of thiobarbituric acid rapidly begins to separate. Fit the water-condenser with a calcium chloride guard-tube (Fig. 61, p. 105), and boil the mixture on the water-bath for 1 hour. Cool the mixture, filter off the sodium salt at the pump and wash it with a small quantity of cold acetone. Dissolve the salt in warm water and liberate the acid by the addition of 30 ml. of concentrated hydrochloric acid diluted with 30 ml. of water. Cool the mixture, filter off the thiobarbituric acid, and recrystallise it from hot water. Colourless crystals, m.p. 245 with decomposition (immersed at 230°). Yield, 3 5 -4 0 g. [Pg.307]

Equip a 1-litre three-necked flask with a powerful mechanical stirrer, a separatory funnel with stem extending to the bottom of the flask, and a thermometer. Cool the flask in a mixture of ice and salt. Place a solution of 95 g. of A.R. sodium nitrite in 375 ml. of water in the flask and stir. When the temperature has fallen to 0° (or slightly below) introduce slowly from the separatory funnel a mixture of 25 ml. of water, 62 5 g. (34 ml.) of concentrated sulphuric acid and 110 g. (135 ml.) of n-amyl alcohol, which has previously been cooled to 0°. The rate of addition must be controlled so that the temperature is maintained at 1° the addition takes 45-60 minutes. AUow the mixture to stand for 1 5 hours and then filter from the precipitated sodium sulphate (1). Separate the upper yellow n-amyl nitrite layer, wash it with a solution containing 1 g. of sodium bicarbonate and 12 5 g. of sodium chloride in 50 ml. of water, and dry it with 5-7 g. of anhydrous magnesium sulphate. The resulting crude n-amyl nitrite (107 g.) is satisfactory for many purposes (2). Upon distillation, it passes over largely at 104° with negligible decomposition. The b.p. under reduced pressure is 29°/40 mm. [Pg.306]

The latter upon decomposition with dilute hydrochloric acid yields laevo sec.-octyl hydrogen phthalate the crystalline brucine salt, when similarly treated, affords the dextro sec.-octyl hydrogen phthalate. These are reerystallised and separately hydrolysed with sodium hydroxide solution to yield pure I- and d-sec.-octyl alcohols ... [Pg.506]

The filtrates from the decomposition of the brucine salts with dilute hydrochloride acid should be carefully preserved. The brucine Is recovered by the addition of an excess of dilute ammonia solution (1 4) if the solution becomes turbid before all the ammonia solution is added, introduce a little alcohol until the solution becomes clear. After several hours in an open beaker, filter oft the brucine, wash it well with cold water and dry it in the air. [Pg.507]

Gattermann (1890) found that the preparation of the cuprous halide may be avoided by making use of the fact that finely-divided copper (e.g., freshly-precipitated or reduced by hydrogen or copper bronze) acts catal3d.ically in the decomposition of solutions of diazonium salts, for example ... [Pg.593]

If the reaction becomes too vigorous, it may be necessary to cool the flask by covering it with a damp cloth. Normally the decomposition proceeds smoothly under the intermittent heating. If the salt is damp, the reaction may proceed more vigorously and unless the flask is cooled, it may pass beyond control. [Pg.611]

Difluorodiphenyl. Bis-diazotise a solution of 46 g. of benzidine (Section IV,88) in 150 ml. of concentrated hydrochloric acid and 150 ml. of water by means of a solution of 35 g. of sodium nitrite in 60 ml. of water add about 200 g. of crushed ice during the process (compare p-Fbtorotoluene above). Filter the solution and add it to a filtered solution of 85 g. of sodium borofluoride in 150 ml. of water. Stir for several minutes, collect the precipitated bis-diazonium borofluoride by suction filtration, wash with 5 ml. of ice-cold water, and dry at 90-100°. Place the dry salt in a flask fitted with an air condenser, immerse the flask in an oil bath, and slowly raise the temperature to 150° (Fume Cupboard ). When decomposition of the salt is complete, steam distil the mixture collect the 4 4 difluoro-diphenyl which passes over and recrystallise it from ethanol. The yield is 21 g., m.p. 92-93°. [Pg.612]

Nitronium salts are colourless, crystalline and very hygroscopic nitronium perchlorate and sulphate are unstable and liable to spontaneous decomposition, whereas nitronium tetrafluoroborate and other complex fluoro-salts are relatively stable. [Pg.61]

The hammer and the surface on which the lithium is flattened should be free from rust traces of iron salts may cause rapid decomposition of the alkyllithium. [Pg.12]

Decomposition of diazonium salts obtained from 2-aminothiazole (4) (29, 34. 35) could be an interesting reaction to introduce O in A-4-thiazoline-2-one. Acidic hydrolvsis of ethers (36. 37). oxidative hydrolysis... [Pg.375]

DiaminoseIenazole was obtained by the action of selenourea on chloracetonitrile (15). Its salts are fairly unstable and decompose to give metallic selenium. All attempts to obtain the free base or 2,4-dihydroxyselenazole from 2,4-diaminoseIenazole hydrochloride were unsuccessful and led to decomposition of the heterocycle. [Pg.224]

The (thermal) decomposition of thiazol-2-yldiazonium salts in a variety of solvents at 0 C in presence of alkali generates thiazol-2-yl radicals (413). The same radicals result from the photolysis in the same solvents of 2-iodothiazole (414). Their electrophilic character is shown by their ability to attack preferentially positions of high rr-electron density of aromatic substrates in which they are generated (Fig. 1-21). The major... [Pg.111]

Some 2-halogeno-5-nitrothiazoles and 2-nitro-5-halogenothiazoles are known. 2-Halogeno-5-nitrothiazoles can be prepared by a Sandmeyer reaction from 2-amino-5-nitrothiazole (1, 85), while 2-nitro-5-halo-genothiazoles can be analogously prepared by decomposition of dia-zonium salts arising from 2-amino-5-halogenothiazoles in presence of nitrite anion (82, 84). [Pg.578]

Triiodoacetic acid [594-68-3] (I CCOOH), mol wt 437.74, C2HO2I3, mp 150°C (decomposition), is soluble in water, ethyl alcohol, and ethyl ether. It has been prepared by heating iodic acid and malonic acid in boiling water (63). Solutions of triiodoacetic acid are unstable as evidenced by the formation of iodine. Triiodoacetic acid decomposes when heated above room temperature to give iodine, iodoform, and carbon dioxide. The sodium and lead salts have been prepared. [Pg.90]


See other pages where Salt decomposition is mentioned: [Pg.434]    [Pg.177]    [Pg.434]    [Pg.177]    [Pg.211]    [Pg.257]    [Pg.351]    [Pg.385]    [Pg.428]    [Pg.223]    [Pg.389]    [Pg.513]    [Pg.592]    [Pg.601]    [Pg.602]    [Pg.603]    [Pg.610]    [Pg.610]    [Pg.611]    [Pg.618]    [Pg.735]    [Pg.813]    [Pg.955]    [Pg.970]    [Pg.201]    [Pg.75]   
See also in sourсe #XX -- [ Pg.698 ]




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Alkyl diazonium salts decomposition

Ammonium phosphate salts, decomposition

Ammonium salt decompositions

Ammonium salt decompositions sublimation

Ammonium salts thermal decomposition

Ammonium salts with oxidizing anions decompositions

Ammonium salts, decompositions, nitrate

Ammonium salts, decompositions, nitrate formation

Ammonium salts, decompositions, proton

Ammonium salts, decompositions, proton transfer

Chloride salt, decomposition potential

Copper salts, decompositions

Decomposition of diazonium salts

Decomposition, diazonium salt to phenol

Decomposition, quaternary ammonium salts

Decompositions, oxyacid metal salts

Decompositions, oxyhalide salts

Diaryliodonium salts thermal decomposition

Diazonium salts decomposition mechanism

Diazonium salts, decomposition

Imidazolium salts decomposition product

Imidazolium salts, thermal decomposition

Metal salts, decomposition

Nitrate salts, thermal decomposition

Salt marshes decomposition

Sulfonium salts decomposition

The Electrolytic Decomposition of Molten Salts

Zinc salt, thermal decomposition

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