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Ferric chloride, solubility

Ferric Chloride Soluble No Low Not Applicable Low Moderate Minimal... [Pg.356]

Salicin is a colourless crystalline substance, soluble in water. It does not reduce Fehling s solution nor does it give a coloration with ferric chloride. On hydrolysis with emulsin, glucose and salicyl alcohol are produced the former reduces Fehling s solution and the latter gives a violet coloration with ferric chloride. [Pg.517]

Cool the remainder of the filtrate and extract three times with ether, using 20 - 30 ml. for each extraction. Dry the combined ethereal extracts over powdered anhydrous sodium sulphate. Filter into a small flask and distil off the ether on a water-bath. Pour the residual oil into a small dish or beaker crystallisation takes place almost immediately. The salicyl alcohol so obtained is almost pure, but it may, if so desired, be recrystallised from a small quantity of benzene. It is a colourless crystalline solid, m.p. 86 , readily soluble in water it gives a violet coloration with ferric chloride. [Pg.517]

The alkylidene dimethone (dimedone) (I) upon boiling with glacial acetic acid, acetic anhydride, hydrochloric acid and other reagents frequently loses water and passes into a substituted octahydroxanthene or the anhydride (II), which often serves as another derivative. The derivatives (I) are soluble in dilute alkali and the resulting solutions give colourations with ferric chloride solution on the other hand, the anhydrides (II) are insoluble in dilute alkali and hence can easily be distinguished from the alkylidene dimedones (I). [Pg.333]

P Keto esters (t.g., ethyl ocetoacetate) are soluble in solutions of caustic alkalis but not in sodium carbonate solution. They give colours with freshly prepared ferric chloride solution a little alcohol should be added to bring the ester into solution. Sodium ethoxide solution reacts to yield sodio compounds, which usually crystallise out in the cold. Phenylhydrazine yields pyrazolones. They are hydrolysed by boiling sulphuric acid to the Corresponding ketones, which can be identified as usual (Section 111,74). [Pg.392]

Although lead chloride is moderately soluble in the acid, lead is also used occasionaUy in hydrochloric acid service. Addition of 6—25% Sb increases the corrosion resistance. AH and ferric chloride accelerate the corrosion. Durichlor (14.5% Si, 3% Mo, 82% Fe), a sUica-based aUoy, shows exceUent resistance to hot hydrochloric acid in the absence of ferric chloride. [Pg.446]

Cadmium Hydroxide. Cd(OH)2 [21041-95-2] is best prepared by addition of cadmium nitrate solution to a boiling solution of sodium or potassium hydroxide. The crystals adopt the layered stmcture of Cdl2 there is contact between hydroxide ions of adjacent layers. Cd(OH)2 can be dehydrated to the oxide by gende heating to 200°C it absorbs CO2 from the air forming the basic carbonate. It is soluble ia dilute acids and solutions of ammonium ions, ferric chloride, alkah haUdes, cyanides, and thiocyanates forming complex ions. [Pg.395]

Tuduranine, CjgHjgOgN. This member of the aporphine group (p. 306) is the most recent addition to Sinomenium alkaloids and was isolated by Goto from the mother liquors of sinomenine. It is crystalline, has m.p. 125° (with softening at 105°), and yields a sparingly soluble hydrochloride, m.p. 286° (dec.), [a] f — 148° (dilute MeOH), is freely soluble in alkali, and gives feeble ferric chloride and diazo-colour reactions and a fuchsin-red colour with formaldehyde and sulphuric acid. It behaves as a secondary base and yields a diacetyl derivative, m.p. 170°, [a] / — 321-71° (MeOH), which does not form a methiodide, but can be hydrolysed to A -acetyl-tuduranine, m.p. 277°, — 395-24°, and this can be methylated to... [Pg.273]

Muricinine, CijHj g02N(0Me)2. Isolated as the perchlorate, m.p. 206-8°. The base does not contain a dioxymethylene group, is soluble in alkalis and gives a green colour with ferric chloride. ... [Pg.319]

Obermayer s reagent chem A 0.4% solution of ferric chloride in concentrated hydrochloric acid used to test for indican in urine, with a pale-blue or deep-violet color indicating positive. o-b3r,mT-3rz re,a- 3nt n-octadecane orgchem CigHjg Colorless liquid boiling at 318°C soluble in alcohol, acetone, ether, and petroleum, insoluble in water used as a solvent and chemical intermediate. en, ak-t3 de,kan ... [Pg.267]

Alum dosages between 200 and 500 mg/1 were not significantly different. Table II also Illustrates that sedimentation Is effective In lowering the concentration of the pesticides to the solubility limit. Metrlbuzln Is soluble In water to a concentration of about 1200 mg/1 and the sedimentation step reduced the concentration from 2000 and 3000 mg/1 to about 1000 mg/1. At lower concentrations sedimentation was not effective. Other coagulants and flocculant aids such as hydroxide and ferric chloride, were tested but alum with an anionic polymer (Watcon 1255) was the most effective. [Pg.155]

Iron was one of the first metals employed for the reduction of organic compounds over 130 years ago. It is used in the form of filings. Best results are obtained with 80 mesh grain [765]. Although some reductions are carried out in dilute or concentrated acetic acid the majority are performed in water in the presence of small amounts of hydrochloric acid, acetic acid or salts such as ferric chloride, sodium chloride (as little as 1.5-3%) [765], ferrous sulfate [766] and others. Under these conditions iron is converted to iron oxide, Fe304. Methanol or ethanol are used to increase the solubility of the organic material in the aqueous medium [766] (Procedure 34, p. 213). [Pg.29]

Whole-body isotope retention experiments were performed (via the method described above in the Smith experiment and with confirmed corrections for isotope decay rates), using extrinsically labeled ferric chloride hexahydrate and Ca from CCM (i.e., [ FeJFeCla and [" Ca] CaCl2) to determine the bioavailability of these minerals at an Fe Ca ratio of 1 167 mol/mol. CCM solubility was also assessed via a filtration method. [Pg.311]

One milliliter of a 0.05 % w/v solution of benzoic acid is added to a 0.5 mL solution of ferric chloride, and a dull yellow precipitate is produced that is soluble in ether. [Pg.30]

It has long been recognized that ferric iron is a moderately strong acid. As early as 1896, Goodwin (5) concluded from conductometric measurements that simple dilution of ferric chloride solutions led to the formation of FeOH2+. The insolubility of ferric hydroxide has of course been appreciated even longer. The best current estimate of the solubility product constant for Fe OH)s at 25° (in 3 M NaC104) is (d). [Pg.118]

If the ratio be unity, the concentrations of the solute in each solvent will be the same if the ratio be far removed from unity, a correspondingly large proportion of the solute will be found in the one solvent which can be utilized to extract the Soln. from the other solvent. E.g. ether will remove ferric chloride from its aq. soln., and since many other chlorides are almost insoluble in ether, the process is utilized in analysis for the separation of iron from the other elements the solubility of cobalt thiocyanate in ether is utilized for the separation of cobalt perchromic acid is similarly separated from its aq. soln. by ether molten zinc extracts silver and gold from molten lead the extraction of organic compounds from aq. soln. by shaking out with ether or other solvent is much used in organic laboratories. [Pg.75]

Hydroxy-l,2,4-thiadiazoles possess phenolic character they give red to purple colors with ferric chloride, and fail to afford ketonic derivatives.130,178 They resist the action of hot alkaline sodium plumbite.130 The 3-alkoxy homologs are neither alkali soluble nor give colors with ferric chloride.130... [Pg.163]


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See also in sourсe #XX -- [ Pg.313 ]




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