Orange colour

Hence the orange colour of a dichromate is converted to the green colour of the hydrated chromium(III) ion, Cr ", and sulphur is precipitated when hydrogen sulphide is passed through an acid solution.)... 

The chromates of the alkali metals and of magnesium and calcium are soluble in water the other chromates are insoluble. The chromate ion is yellow, but some insoluble chromates are red (for example silver chromate, Ag2Cr04). Chromates are often isomorph-ous with sulphates, which suggests that the chromate ion, CrO has a tetrahedral structure similar to that of the sulphate ion, SO4 Chromates may be prepared by oxidising chromium(III) salts the oxidation can be carried out by fusion with sodium peroxide, or by adding sodium peroxide to a solution of the chromium(IIl) salt. The use of sodium peroxide ensures an alkaline solution otherwise, under acid conditions, the chromate ion is converted into the orange-coloured dichromate ion ... 

To obtain the free acid, dissolve the potassium salt in 50 ml. of cold water, filter the solution if a small undissolved residue remains, and then boil the clear solution gently whilst dilute sulphuric acid is added until the separation of the acid is complete. Cool the solution and filter off the pale orange-coloured crystals of the benzilic acid wash the crystals on the filter with some hot distilled water, drain well, and then dry in a desiccator. Yield of crude acid, 4 g. Recrystallise from benzene (about 50 ml.) to which a small quantity of animal charcoal has been added, filtering the boiling solution through a preheated funnel fitted w ith a fluted filter-paper, as the benzilic acid readily crystallises as the solution cools alternatively, recrystallise from much hot water. The benzilic acid is obtained as colourless crystals, m.p. 150°. 

This is a test for the >C = 0 group. Most aldehydes and ketones readily condense with this reagent giving yello v- or orange-coloured precipitates. 

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. 

Coloured salts loith alkalis. Dissolve a few crystals of o-nitro-phenol in a few ml. of 10% NaOH solution. An orange-coloured solution is produced, and becomes almost colourless on the addition of acids. Alkali restores the orange coloration, and so the solution exhibits the properties of an indicator. 

Dissolve 0-2 g. of fructose in 10 ml. of water, add 0-6 g. of cw-methyl-phenylhydrazine and sufficient rectified spirit to give a clear solution. Since the fructose may not be quite pure, warm the mixture slightly, allow to stand, preferably overnight, so that any insoluble hydrazones may separate if present, remove them by filtration. Add 4 ml. of 50 per cent, acetic acid to the filtrate it will become yellow in colour. Heat the solution on a water bath for 5-10 minutes, and allow to stand in the dark until crystalUsation is complete it may be necessary to scratch the walls of the vessel to induce crystalUsation. Filter the crystals and wash with water, followed by a little ether. RecrystaUise the orange-coloured methylphenylosazone from benzene m.p. 152°. 

Free cydohexene from peroxides by treating it with a saturated solution of sodium bisulphite, separate, dry and distil collect the fraction, b.p. 81-83°. Mix 8 -2 g. of cycZohexene with 55 ml. of the reagent, add a solution of 15 mg. of osmium tetroxide in anhydrous butyl alcohol and cool the mixture to 0°. Allow to stand overnight, by which time the initial orange colouration will have disappeared. Remove the solvent and unused cydohexene by distillation at atmospheric pressure and fractionate the residue under reduced pressure. Collect the fraction of b.p. 120-140°/15 mm. this solidifies almost immediately. Recrystallise from ethyl acetate The yield of pure cis-l 2 cydohexanediol, m.p. 96°, is 5 0 g. 

Eosin (Tetrabromofluorescein). Place 16 5 g. of powdered fluorescein and 80 ml. of rectified (or methylated) spirit in a 250 ml. flask. Support a small dropping funnel, containing 36 g. (12 ml.) of bromine, above the flask make sure that the stopcock of the funnel is well lubricated before charging the latter with bromine. Add the bromine diopwise during about 20 minutes. When half the bromine has been introduced, and the fluorescein has been converted into dibromofluor-escein, all the solid material disappears temporarily since the dibromo derivative is soluble in alcohol with further addition of bromine the tetrabromofluorescein (sparingly soluble in alcohol) separates out. Allow the reaction mixture to stand for 2 hours, filter ofiF the eosin at the pump, wash it with alcohol, and dry at 100°. The yield of eosin (orange-coloured powder) is 25 g. 

A. Carry out the following preliminary test. Dissolve a drop or a few small crystals of the compound in 1 ml. of rectified spirit (95 per cent, ethanol) and add 1 ml. of iV hydrochloric acid. Note the colour produced when 1 drop of 5 per cent, ferric chloride solution is added to the solution. If a pronounced violet, blue, red or orange colour is produced, the hydrox amic acid test described below is not applicable and should not be used. 

Start the heat and wait. It will take about 20 minutes to get going and there usually isn t much to see. The flask will be a nice orange colour from the bromine and it won t change much until just before the end. Make sure the water Is running, everything is secure and leave for three hours - have a sleep or something to eat maybe. 

Friedlander synthesis, 2, 445 Acridine-1,8-diones, hexahydro-synthesis, 2, 482 Acridine Orange colour and constitution, 1, 346 nucleic acid stain, 1, 179... 

Strychnicine. This alkaloid, isolated from nux-vomica leaves grown in. lava, forms needles, m.p. 240° dec.), and is characterised by the following colour reaction. When sodium hydroxide solution is added drop by drop to a solution of a salt of the alkaloid in water, the precipitate formed dissolves on addition of more alkali, forming an orange-coloured liquid which develops a violet colour on addition of hydrochloric acid. Strychnicine is scarcely poisonous, but is said to produce tetanus in frogs. 

This leaction is lesorted to for the reason that naphthalene forms only the n-nitro-compound with niti icacid. The method, similar to that used for prepaiing aniline from nitiobenzene, cannot, therefore, be employed for the production of /3-n.tphtliyl-.amine. u-Naphthol is mainly used foi the manufacture of yellow and orange colours (Martins and naphthol yellow) by the action of nitric acid, and are similai m constitution to picric acid (see Prep. 107). 

Nitro-pJienols and Nitro-acids dissolve in ctiustic alkahs as a rule with a deep yellow or orange colour. On reduction with st. innous chloride or zinc dust, as described above, they yield the amino-derivatives. In the case of the amino-phenol, the solution is made alkaline with caustic soda, satuiated with CO.j, salt added and extracted w ith ether. In the case of the amino-acid, the method used is that desciibed under Prep. 91 (p. 201). 

Sulfur forms two main series of oxohalides, the thionyl dihalides OS X2 and the sulfuryl dihalides 02S X2. In addition, various other oxofluorides and peroxofluorides are known (p. 688). Thionyl fluorides and chlorides are colourless volatile liquids (Table 15.14) OSBt2 is rather less volatile and is orange-coloured. 

Treatment of cycloheptatriene complexes of the type [M(tj -C7H8)(CO)3] (M = Cr, Mo, W) with Ph3C" "BF4 results in hydride abstraction to give orange-coloured tj -cycloheptatrienyl (or tropy-lium) complexes ... 

One of the most sensitive methods for estimating titanium (or, conversely, for estimating H2O2) is to measure the intensity of the orange colour produced when H2O2 is added to acidic solutions of titanium(IV). The colour is due > to the peroxo complex, [Ti(02)(0H)(H20)jt]", though alkaline solutions are needed before crystalline solids such as M3[Ti(02)Fs] or M2[Ti(02)(S04)2]... 

Ta, tetranuclear, orange coloured derivatives Li4[Nb4S2(SPh),2] > and [Nb4S2(SPh) -(PMe2R)4] (R = Me, have been shown to... 

As an alternative, a reversible indicator may be employed, either (a) 1-naphthoflavone (0.5% solution in ethanol, which gives an orange-coloured solution at the end-point), or (b) p-ethoxychrysoidine (0.1% aqueous solution, colour change pink to pale yellow). Under these conditions, the measured 25 mL portion of the arsenic solution is treated with 10 mL of 10 per cent potassium bromide solution, 6 mL of concentrated hydrochloric acid, 10 mL of water and either 0.5 mL of indicator (a) or two drops of indicator (b). 

The filtrate should possess a yellow or orange colour, indicating the presence of excess of precipitant. If a turbidity appears, a portion should be heated if the turbidity disappears, it may be assumed to be due to excess of reagent crystallising out, and is harmless. Otherwise, more reagent should be added, and the solution filtered again. 

The non-penicillin wastewater from a pharmaceutical company was collected and used in the batch aeration wastewater treatment experiment. The pharmaceutical wastewater had a clear orange colour, strong odour, contained toxic chemicals and had a COD value in the range of 3000-30,000 mg per litre. The pH of the wastewater was neutralised and monitored for each experimental ran, as the bacteria would have a higher rate of propagation at neutral pH. 

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