Cupric sulfate, reaction with

Let it be desired to determine how much crystallized cuprie sulfate can be obtained from 100 parts of sulfuric acid of 92 strength. As cupric sulfate crystallizes with live molecules of water of crystallization the reaction occurs according to the-equation ... 

Patio [Spanish, a courtyard] A medieval process for extracting silver from argentite, Ag2S. The ore was mixed with salt, mercury, and roasted pyrites, which contains cupric sulfate. This mixture was crashed by stones dragged by mules walking on the paved floor of a courtyard. The overall reactions are ... 

Polymerizations were carried out in a jacketed, 1-gal, stirred, pressure tank reactor. Typical reactions were run by adding water, alcohol, or chain transfer agent, phosphate buffer, and persulfate to the reactor. The reactor was pressurized with CTFE monomer. Sulfite solution was fed at a rate to maintain reaction. Copper and iron ions were used at times as catalysts by adding cupric sulfate or ferrous sulfate.3 The product was filtered, washed with 90 10 water methanol followed with deionized water. The product was dried at 110°C. 

The BCA method is simpler than the Lowry method and relies on the same redox reaction. The target protein is treated with alkaline cupric sulfate in the presence of tartrate, which results in the reduction of the cupric ion to cuprous by the protein. The cuprous ion is then treated with bicichoninic acid (BCA) and two... 

It has been found that the cupric sulfate-mediated aminolysis of 3-bromo[ N]isoquinoline with ethanolic ammonia (130°C, 7 days reaction time) yields a mixture of 13 and 14, ratio 75 25 (74RTC198). It shows that also with the weaker nucleophile ammonia a part of 3-bromoisoquinoline can undergone a ring-opening, ring-closure process. 

Electroless Deposition of Copper. The basic ideas of the mixed-potential theory were tested by Paunovic (10) for the case of electroless copper deposition from a cupric sulfate solution containing ethylenediaminetetraacetic acid (EDTA) as a complexing agent and formaldehyde (HCHO) as the reducing agent (Red). The test involved a comparison between direct experimental values for and the rate of deposition with those derived theoretically from the current-potential curves for partial reactions on the basis of the mixed-potential theory. 

The action of an active intermediate oxidation product would explain another feature of the reaction. The reduction of silver ions by hydrazine is extremely sensitive to the presence of small amounts of copper. For example, a solution containing a mixture of silver nitrate, sodium sulfite and hydrazine which normally showed no sign of reduced silver for several minutes underwent almost immediate reaction when merely stirred with a clean copper rod. In the presence of gum arabic as stabilizer, streamers of colloidal silver passed out from the copper surface. Similarly, the addition of small amounts of cupric sulfate to a hydrazine solution eliminated the induction period of the reaction with silver chloride. 

Nitrobenzo[6]thiophene may be prepared by reaction of the 3,4-dinitro compound with alcoholic ammonium sulfide422-538 other workers have claimed that this method yields only traces of the desired product.84 It may also be prepared by deamination of 5-amino-4-nitrobenzo[6]thiophene,162,422 or by decomposition of 4-benzo[6]-thiophene diazonium cobaltinitrite with aqueous sodium nitrite in the presence of cuprous oxide and cupric sulfate.84 7-Nitrobenzo[6]-thiophene may be obtained by the latter method (15% yield) from the corresponding amine.84... 

C 2-Bromo-4-methylbenzaldehyde A 3-1. three-necked flask is equipped with an efficient stirrer, a dropping funnel (Note 2), and a thermometer. The aqueous 10% formaldoxime prepared in step A is placed in the flask, and to it are added 6 5 g (0.026 mole) of hydrated cupric sulfate, 1.0 g. (0 0079 mole) of sodium sulfite, and a solution of 160 g of hydrated sodium acetate in 180 ml. of water The solution is maintained at 10-15° by means of a cold-water bath and stirred vigorously. The neutral diazonium salt solution prepared in step B is slowly introduced below the surface of the formaldoxime solution (Notes 3 and 4). After the addition of the diazonium salt solution is complete, the stirring is continued for an additional hour and then the mixture is treated with 230 ml. of concentrated hydrochloric acid. The stirrer and the dropping funnel are replaced by stoppers, and the mixture is gently heated under reflux for 2 hours The flask is set up for steam distillation, and the reaction product is steam-distilled. The distillate is saturated with sodium chloride, extracted with three 150-ml portions of ether, and the ethereal extracts are washed successively with three 20-ml portions of a saturated sodium chloride solution, three 20-ml. portions of an aqueous 10% sodium bicarbonate solution, and again with three 20-ml portions of a saturated sodium chloride solution. 

Cu(C2H303)2 (aq.). de Forcrand3 measured the heat of reaction of aqueous cupric sulfate with aqueous lead glycollate. 

Small Quantities (White Phosphorus). Wear nitrile rubber gloves, laboratory coat, and eye protection. Work in the fume hood. Five g (0.16 mol) of white phosphorus are cut under water into 5mm pellets. The pellets are added to 800 mL (0.8 mol) of 1 M cupric sulfate (127.7 g or 199.7 g of CuS04 or CuS04-5H20, respectively, dissolved in 800 mL of water) solution in a 2-L beaker. The mixture is allowed to stand for about a week with occasional stirring. The phosphorus grad-ually disappears, and a fine black precipitate of copper and copper phosphide is formed. The reaction is complete when no waxy white phosphorus is observed when one of the pellets is cut under water. The precipitate is separated, and while still wet, transferred to 500 mL of laundry bleach (5% sodium hypochlorite), and then stirred for about 1 hour to ensure complete decomposition of copper phosphide. The solids are separated and packaged for disposal. The aqueous solution is washed into the drain.33... 

In this section, consideration will be given to the actual processes of acetal- or ketal-formation and not to the more indirect methods by which acetals and ketals of the polyhydric alcohols may be synthesized from compounds (e.g. derivatives of the monosaccharides) containing preformed alkylidene or arylidene groupings. The condensation of a carbonyl compound with a glycol is facilitated by acidic catalysts, and, since the reaction is reversible, by dehydration. The catalysts most frequently employed are concentrated sulfuric, hydrochloric and hydro-bromic acids, gaseous hydrogen chloride, zinc chloride and cupric sulfate others are phosphorus pentoxide, sulfosalicylic acid, and anhydrous sodium sulfate. The formation of benzylidene compounds is promoted less efficiently by phosphorus pentoxide than by either concentrated sulfuric acid or concentrated hydrochloric acid 1" the reaction is assisted by chloro- and nitro-substituents on the aromatic nucleus, but hindered by methyl- and methoxy-groups.18... 

The nitrite ion behaves as a nitrogen nucleophile with vinyliodonium ions. Thus, admixture of the vinyliodonium tetrafluoroborates shown in equations 188 and 189 with sodium nitrite results in the production of nitroalkenes119,125,126. Cupric sulfate is apparently necessary for the success of the latter reaction, although its role has not been clarified. The (cyclohexenyl)iodonium salt also reacts with sodium thiophenoxide to give the corresponding vinyl phenyl sulfide125,126. 

Aromatic tertiary amines and phenolic compounds undergo nuclear nitro sation, as illustrated by the synthesis of p>nitrosodimethyl aniline (89%)i nitrosophenol (80%), and l-nitroso-2-naphthol (99%) In the reaction of a-naphthol, an isomeric mixture of the nitrosonaphthols is obtained. The nitrosation of phenols with nitrous acid usually produces p nitroso compounds however, o-nitiosophenols can be prepared by nitrosating phenols in the presence of cupric sulfate. ... 

Concluding these reactions with halopyridines, 3-bromopyridine (99), which is readily available by bromination of pyridine at 2I5°C (36CBI534), is converted by ammonia at the relatively low temperature of I40°C in the presence of cupric sulfate to 3-aminopyridine (100) (36CBI534,... 

The rates of reactions with different precatalysts also pointed to Cu(I) species. The initial rate of the reaction initiated with Cul was larger than that of the reaction catalyzed by cupric sulfate. However, a steady state of reactions catalyzed by CuCl was rapidly established (<3 min), and at this steady state, the rate was almost the same as that when cupric sulfate was used. The identity of the steady-state rates was probably observed because cuprous chloride was converted to cupric species, and the reaction took the same course as when the cupric salt was added. 

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