Solute and acetone

A reactor was charged with 1,10-diaminodecane (20 mmol) dissolved in 170 ml of /V, /V - d i m e t h I fo rm amide containing pyromellitic anhydride (20 mmol) and the mixture stirred at ambient temperature for 60 hours. It was then precipitated in 4 liters of acetone/hydrochloric acid, 1 4, respectively, and collected. The solid was washed with aqueous hydrochloric acid solution and acetone and then heated and dried in vacuum at 60°C for 36 hours and 7.65 g of product isolated as a white powder. 

Tungsten(VI) tetrabromide oxide is a dark-brown crystalline compound, which is obtained in the form of needles or flakes. It is extremely sensitive to atmospheric moisture, decomposes rapidly in water, which leaves a gray-green precipitate, and is completely dissolved in solutions of ammonia or sodium hydroxide, which form clear, colorless solutions. It is slightly soluble in concentrated hydrochloric acid, dioxane (yellow solution), 2-methoxyethanol (colorless solution), and acetone (green solution). It has a melting point of 322°C., as determined by D.T.A. 

From the area of polymer dielectrics, a sample is presented here using a commercially available and (from many microelectronic applications) well-known high-temperature polyimide. The deposition and the subsequent curing process have been described in Section 18.2.3, resulting in a 190 nm thick insulating film that showed a good chemical resistance towards diluted developer solution and acetone, so that the cathode-sputtered Au drain and source contacts can be structured as described in Section 18.2.1. The 30 nm thick pentacene layer is thermally evaporated at a deposition rate of about 0.1 nm/s and a process pressure of 1 x 10 mbar. 

Technical grade KHFg (100 g.) is dissolved in 250 ml. of water contained in a polyethylene beaker. The KgSiFg and the undissolved KHFg are filtered off after several hours of standing the clear solution is placed in an ice-cold water bath and 40 g. of boric acid is added with stirring. Rapid dissolution occurs. Small crystals separate from the solution within an hour. They are suction-filtered on a fritted glass filter, washed with a small amount of ice-cold water and with 95% methanol solution and acetone. The salt is then dried at 120°C. 

Stray light measurements are made using a sharp cutoff filter. Examples of these filter materials include saturated solutions of such compounds as potassium ferromanganate or lithium carbonate. Other solutions exhibiting abrupt cutoff wavelengths include KBr, KCl, Nal, NaN03 solutions, and acetone. Refer to ASTM E 169-87, Practice for General Techniques of Ultraviolet-Visible Quantitative Analysis. ... 

Acetic acid is the main constituent in vinegar solutions and acetone is a solvent often used in nail polish remover ... 

This different solubility behavior of certain solutes as mentioned before, especially in the presence of an excess of CO2, was also described by other authors by a different approach. The different solvation phenomena in C02-expanded organic solutions characterized by Sala et al. [40] describes the differing interaction of CO2-expanded ethanol and C02-expanded acetone solutions with functional groups of certain solutes. The dipole-dipole interaction between the carbonyl group of a solute and acetone molecules are more effectively disrupted by a CO2 content increase than the H-bond interactions between the carbonyl group and ethanol... 

Like bromine, iodine is soluble in organic solvents, for example chloroform, which can be used to extract it from an aqueous solution. The iodine imparts a characteristic purple colour to the organic layer this is used as a test for iodine (p. 349). NB Brown solutions are formed when iodine dissolves in ether, alcohol, and acetone. In chloroform and benzene a purple solution is formed, whilst a violet solution is produced in carbon disulphide and some hydrocarbons. These colours arise due to charge transfer (p. 60) to and from the iodine and the solvent organic molecules. 

Place 0 5 ml. of acetone, 20 ml. of 10% aqueous potassium iodide solution and 8 ml. of 10% aqueous sodium hydroxide solution in a 50 ml. conical flask, and then add 20 ml. of a freshly prepared molar solution of sodium hypochlorite. Well mix the contents of the flask, when the yellow iodoform will begin to separate almost immediately allow the mixture to stand at room temperature for 10 minutes, and then filter at the pump, wash with cold w ater, and drain thoroughly. Yield of Crude material, 1 4 g. Recrystallise the crude iodoform from methylated spirit. For this purpose, place the crude material in a 50 ml. round-bottomed flask fitted with a reflux water-condenser, add a small quantity of methylated spirit, and heat to boiling on a water-bath then add more methylated spirit cautiously down the condenser until all the iodoform has dissolved. Filter the hot solution through a fluted filter-paper directly into a small beaker or conical flask, and then cool in ice-water. The iodoform rapidly crystallises. Filter at the pump, drain thoroughly and dry. 

Prepare a solution of 12 5 g. of hydroxylamine hydrochloride in 20 ml. of water contained in a too ml. conical flask. Dissolve 7 g. of powdered sodium hydroxide in 20 ml. of water, cool the solution in ice-water, and then add it to that of the hydroxylamine hydrochloride. Place a thermometer in the mixed solution, and chill the flask in ice-water until the temperature of the solution is between 5 and 10 . Now add 12 ml. (9 5 gO of dry acetone (preferably from a burette to ensure... 

To a few drops of formalin solution add a few drops of dinitro-phenylhydrazine reagent A (p. 263) a yellow precipitate is produced in the cold. Acetaldehyde and acetone give orange-coloured precipitates. Dissolve water-insoluble compounds e.g-y benzaldehyde, salicylalde-hyde, acetophenone and benzophenone) in a small volume of methanol before adding reagent B. With benzophenone the precipitate forms slowly. 

Iodoform reaction. To 0 5 ml. of acetone add 3 ml. of 10% KI solution and 10 ml. of freshly prepared sodium hypochlorite solution and mix well. A pale yellow precipitate of iodofonn is rapidly formed without heating. Acetophenone similarly gives iodoform, but the mixture must be shaken vigorously on account of the limited solubility of acetophenone in water. Benzophenone does not give iodoform. 

Make a concentrated solution of anthracene in hot acetone. To about 2 ml. of this solution add a cold concentrated acetone solution of picric acid drop by drop, and note the formation of a red coloration which becomes deeper on further addition of the acid. If excess of picric acid is added, however, the solution becomes paler in colour, and this is to be avoided if possible. Boil to ensure that both components are in solution and then transfer to a small porcelain basin or watch-glass ruby-red crystals of anthracene picrate separate out on cooling. The product, however, is often contaminated with an excess of either anthracene or of picric acid, which appear as yellowish crystals. 

Picric acid is usually stored damp for safety, and acetone is therefore a better solvent than benzene or this test the solutions musi be almost saturated, however. 

Suspend 0 25 g. of 2 4-dinitrophenylhydrazine in 5 ml. of methanol and add 0-4 0-5 ml. of concentrated sulphuric acid cautiously. FUter the warm solution and add a solution of 0 1-0-2 g. of the carbonyl compound in a small volume of methanol or of ether. If no sohd separate within 10 minutes, dUute the solution carefuUy with 2N sulphuric acid. CoUect the solid by suction filtration and wash it with a little methanol. RecrystaUise the derivative from alcohol, dUute alcohol, alcohol with ethyl acetate or chloroform or acetone, acetic acid, dioxan, nitromethane, nitrobenzene or xylene. 

The acetone test reagent consists of a 0 1 per cent, solution of 2 4-dinitro-phenylhydrazine and is prepared as follows Dissolve 0-25 g. of 2 4-dinitrophenyl-hydrazine in 60 ml. of water and 42 ml. of concentrated hydrochloric acid by warming on a water bath cool the clear yellow solution and dilute to 250 ml. with water. The acetone test is considered negative when 5 ml. of the reagent and 4-5 drops of the distillate give no cloudiness or precipitate of acetone 2 4-dinitro-phenylhydrazone within 30 seconds. After a negative test is obtained, it is stron y recommended that the mixture in the flask be refluxed for 5-10 minutes with complete condensation and then to collect a few drops of distillate for another test. If no acetone is now detected, the reduction is complete. 

Either pure aqueous or aqueous/solvent solutions work. It is entirely up to the preference of the chemist as to which one they use. Just to make one feel more secure, there is a little test one can do with the bisulfite solution to see if they got it right. Just put a little of that ketone known as acetone into the saturated solution and watch the crystals grow. Isn t it nice how chemistry works ... 

To a solution of ethylnagnesium bromide in 350 ml of THF, prepared from 0.5 mol of ethyl bromide (see Chapter 11, Exp. 6) was added in 10 min at 10°C 0.47 mol of 1-hexyne (Exp. 62) and at 0°C 0.47 mol of trimethylsilylacetylene (Exp. 31) or a solution of 0.60 mol of propyne in 70 ml of THF (cooled below -20°C). With trimethyl si lylacetylene an exothermic reaction started almost immediately, so that efficient cooling in a bath of dry-ice and acetone was necessary in order to keep the temperature between 10 and 15°C. When the exothermic reaction had subsided, the mixture was warmed to 20°C and was kept at that temperature for 1 h. With 1-hexyne the cooling bath was removed directly after the addition and the temperature was allowed to rise to 40-45°C and was maintained at that level for 1 h. 

A solution of methylmagnesium bromide in 150 ml of diethyl ether, prepared from 0.5 mol of methyl bromide (see Chapter II, Exp. 5) was subsequently added in 20 min with cooling at about 20°C. After the addition the mixture was warmed for 2 h under reflux (the thermometer and gas outlet were replaced with a reflux condenser), a black slurry being formed on the bottom of the flask. The mixture was cooled in a bath of dry-ice and acetone and a solution of 30 g of ammonium chlori.de in 200 ml of water was added with vigorous stirring. The organic layer and four ethereal extracts were combined, dried over potassium carbonate and subsequently concentrated in a water-pump vacuum. Careful distillation of the residue through a 40-cm... 

In the flask were placed 0.20 mol of the acetylenic alcohol, 0.24 mol of tosyl chloride and 350 ml of diethyl ether. The mixture was stirred at room temperature, until the solid had passed into solution and then cooled at -5 to -10 c in a bath of dry-ice and acetone. Machine-powdered KOH (130 g) was added with vigorous stirring, initially in relatively small portions [oa. 5 g), at intervals of 2 min. The reaction was strongly exothermic at first, and efficient cooling was necessary in order to maintain the temperature of the reaction mixture between -5 and O C... 

Phenyl-3-oxopropanoic acid (25 mmol) and EtjN (87.5 mmol) were dissolved in THF (150 ml) and cooled to —40°C. Ethyl chloroformate (27.5 mmol) was added dropwise to this solution and then the reaction mixture was stirred for 30 min at —20°C. Di-n-hexylamine (27.5 mmol) was added to the suspension and it was stirred at room temperature for an additional hour. The reaction mixture was diluted with water (100 ml) and extracted with ether (400 ml). The extract was washed with aq. 5% HCl (100 ml) and brine (2 X 100 ml) and dried over NajSO. The crude amide was obtained by removal of the solvent in vacuo and phenylhydrazine (25 mmol) was added. The mixture was heated to 100°C for 30 min. The residue was held in vacuo to remove the water formed and then powdered ZnCl2 (125 mmol) was added. The mixture was heated at 170"C with manual stirring for 5 min. The cooled residue was dissolved in acetone (100 ml) and diluted with ether (500 ml). Water (100 ml) was added. The organic layer was separated and washed successively with 5% aq. HCl (100 ml) and brine (2 x 100 ml) and dried over NajSO. The solvent was removed in vacuo, and the residue was recrystallized from EtOAc-hexane. The yield was 79%. 

Ethyl bis-(2,4-dinitrophenyl) acetate (indicator) the stock solution is prepared by saturating a solution containing equal volumes of alcohol and acetone with the indicator pH range colorless 7.4-9.1 deep blue. This compound is available commercially. The preparation of this compound is described by Fehnel and Amstutz, Ind. Eng. Chem., Anal. Ed. 16 53 (1944), and by von Richter, Ber. 21 2470 (1888), who recommended it for the titration of orange- and red-colored solutions or dark oils in which the endpoint of phenol-phthalein is not easily visible. The indicator is an orange solid which after crystallization from benzene gives pale yellow crystals melting at 150-153.5°C, uncorrected. 

The Biazzi continuous process is also used. The reactants are continuously fed to a series of nitrators at 15—20°C followed by separation of the PETN, water washing, solution in acetone at 50°C, neutralization with gaseous ammonia, and precipitation by dilution with water. The overall yield is more than 95%. The acetone and the spent acid are readily recovered. 

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