I Hydrogen peroxide

Other oxidizing agents that have been successfully employed are sulfur monochloride,10,11 thionyl chloride,12 sulfuryl chloride,12 phosphorus pentachloride,13 ammonium persulfate,1 i hydrogen peroxide,15... 

Results are shown in the last two columns of Table I. Hydrogen peroxide yield and its mole ratio to propylene were markedly larger with Reactor VII than with Reactor VI. Thus, the decomposition of the hydrogen peroxide formed is remarkably suppressed in Reactor VII. Yields of ethylene, carbon dioxide, and formaldehyde were larger in Reactor VI than VII, but yields of hydrogen peroxide and methanol were low. 

Which of the following acids would be most suitable for preparing a buffer of pH 3.10 (i) hydrogen peroxide (ii) propanoic acid (iii) cyanoacetic acid (iv) 4-aminobenzenesulfonic acid ... 

Peroxides i Hydrogen peroxide 94,736 Bleaching agent, pharmaceuticals... 

Figure 5.1 Hydroxyl radical production via Fenton s treatment, UV/hydrogen peroxide and ozone I hydrogen peroxide.

Chromate, (i) Hydrogen peroxide test (IV.33, 4). (ii) Lead acetate solution test (IV.33,3). (iii) Action of hydrogen sulphide or sulphur dioxide (IV.33, 5,6). 

Problem 4.5 (a) Which of the following compounds can exist in different conformations (I) hydrogen peroxide, HOOH (2) ammonia, NH, (3) hydroxylamine, H,NOH (4) methyl alcohol, H,COH. (h) Draw two structural formulas for each compound in (a) possessing conformations, M... 

To a solution of allylic alcohol (688 mg, 1.05 mmol) in benzene (25 mL) was added vanadyl acetylacetonate (58 mg, 0.22 imnol) and te/7-buty I hydrogen peroxide as a 1.0 M solution in toluene (2.2 mL, 2.2 mmol). The resulting blood-red slurry was stirred rapidly for 2 h, quenched with saturated sodium thiosulfate (25 mL), and the organic layer collected and dried over sodium sulfate. The solvents were removed under reduced pressure and the resulting brown residue was purified by flash chromatography (45% EtOAc/hexanes) to afford the epoxide as a 1.2 1 mixture of diastereomers (605 mg, 86%). 

B.i. Hydrogen Peroxide. Table 3.1 showed the reduction potential of oxygen in the following reactions ... 

Pretreated (enzymatic and enzymatic-I-hydrogen peroxide) knitted wool fabrics were treated with argon and atmospheric air plasma to improve adsorption capacity (Demir et al., 2010). After plasma treatment, a chitosan solution was appUed for antimicrobial effect. The treated fabrics were evaluated in terms of washing stabiUty as well as antimicrobial activity. The surface morphology was characterized by SEM images and Fourier transform infrared (FilR) analysis. The results indicate that the atmospheric plasma treatment had an etching effect and increased the fiinctionahty of wool surface. Atmospheric plasma treatment also enhanced the adhesion of chitosan to the surface and improved the antimicrobial activity. 

Rooth, T., Ullberg, M., Karlsson, E., Persson, I. Hydrogen peroxide in BWRs An experimental determination of the actual level. Proc. 5. BNES Conf. Water Chemistry of Nuclear Reactor Systems, Bournemouth, UK, 1989, Vol. 2, p. 55-60 Ruiz, C. R, Lin, C. C., Robinson, R., Burns, W. G., Curtis, A. R. Model calculations of water radiolysis in BWR primary coolant. Proc. 5. BNES Conf. Water Chemistry of Nuclear Reactor Systems, Bournemouth 1989, Vol. 1, p. 131-140 Wunderlich, F., Eberle, R., Gartner, M., Gross, H. Brennstabe von Leichtwasserreaktoren. Auslegung und Betriebsverhalten. KTG Seminar Band 5, Verlag TUV Rheinland, Koln, 1990... 

ASTM. 1994. GllO, Standard practice for evaluating intergranular corrosion resistance of heat treatable aluminum alloys by immersion in sodium chloride I-hydrogen peroxide solution. Annual Book of ASTM Standards, 03.02 470-472. 

Chlorine, bromine and iodine form halic(V) acids but only iodic(V) acid, HIO3, can be isolated. Solutions of the chloric) V) and bromic) V) acids can be prepared by the addition of dilute sulphuric acid to barium chlorate(V) and bromate(V) respectively, and then filtering (cf. the preparation of hydrogen peroxide). These two acids can also be prepared by decomposing the corresponding halic(I) acids, but in this case the halide ion is also present in the solution. 

Method(B). Add3g. (3ml.)ofbenzonitrileto50ml.of lo-volumes hydrogen peroxide in a beaker, stir mechanically and add i ml. of 10% aqueous sodium hydroxide solution. Warm the stirred mixture at 40° until the oily suspension of the nitrile has been completely replaced by the crystalline benzamide (45-60 minutes). Cool the solution until crystallisation of the benzamide is complete, and then filter at the pump and recrystallise as above. One recrystallisation gives the pure benza-mide, m.p. 129-130° yield of purified material, 2-2-5 S ... 

Fenton s reagent. To a solution of tartaric acid or a tartrate add 1 drop of freshly prepared ferrous sulphate solution, i drop of hydrogen peroxide solution and then excess of NaOH solution an intense violet coloration is produced, due to the ferric salt of dihydroxyfumaric acid, HOOC C(OH) C(OH)COOH. 

With the aid of a small pipette or a fine-bore dropping-tube (Fig. 30, p. 60), add about 4 drops of the filtered enzyme solution to the amine acetate solution. Using another dropping-tube add i drop of 20 volume hydrogen peroxide solution and shake well. Note the colour change which takes place. 

Dissolve about o i g. of />-phenylene diamine in about 10 ml. of water. Place 5 ml. of milk in each of two test-tubes A and B. Boil the milk in B thoroughly for 2 minutes and then cool. In each test-tube place 5 drops of the phenylenc diamine solution and then add i drop of 20 vol. hydrogen peroxide solution, and mix. A green coloration is produced in A, and then very rapidly changes to a slate-blue. No coloration is produced in B. This test therefore readily differentiates fresh from boiled milk. 

Diphenic acid. Phenanthrene upon oxidation in acetic acid solution at 85° with 30 per cent, hydrogen peroxide gives diphenic acid (diphenyl-2 2 -di-carboxyHc acid) no phenanthraquinone is formed under these experimental conditions. The reaction is essentially an oxidation of phenanthrene with peracetic acid. (For another method of preparation, see Section I V,74.)... 

In addition to CuCfi, some other compounds such as Cu(OAc)2, Cu(N03)2-FeCl.i, dichromate, HNO3, potassium peroxodisulfate, and Mn02 are used as oxidants of Pd(0). Also heteropoly acid salts comtaining P, Mo, V, Si, and Ge are used with PdS04 as the redox system[2]. Organic oxidants such as benzo-quinone (BQ), hydrogen peroxide and some organic peroxides are used for oxidation. Alkyl nitrites are unique oxidants which are used in some industrial... 

Ammonia, anhydrous Mercury, halogens, hypochlorites, chlorites, chlorine(I) oxide, hydrofluoric acid (anhydrous), hydrogen peroxide, chromium(VI) oxide, nitrogen dioxide, chromyl(VI) chloride, sulflnyl chloride, magnesium perchlorate, peroxodisul-fates, phosphorus pentoxide, acetaldehyde, ethylene oxide, acrolein, gold(III) chloride... 

Oxidation. Maleic and fumaric acids are oxidized in aqueous solution by ozone [10028-15-6] (qv) (85). Products of the reaction include glyoxyhc acid [298-12-4], oxalic acid [144-62-7], and formic acid [64-18-6], Catalytic oxidation of aqueous maleic acid occurs with hydrogen peroxide [7722-84-1] in the presence of sodium tungstate(VI) [13472-45-2] (86) and sodium molybdate(VI) [7631-95-0] (87). Both catalyst systems avoid formation of tartaric acid [133-37-9] and produce i j -epoxysuccinic acid [16533-72-5] at pH values above 5. The reaction of maleic anhydride and hydrogen peroxide in an inert solvent (methylene chloride [75-09-2]) gives permaleic acid [4565-24-6], HOOC—CH=CH—CO H (88) which is useful in Baeyer-ViUiger reactions. Both maleate and fumarate [142-42-7] are hydroxylated to tartaric acid using an osmium tetroxide [20816-12-0]/io 2LX.e [15454-31 -6] catalyst system (89). 

Thallic oxide can be prepared by reaction of thallium with oxygen or hydrogen peroxide and an alkaline thallium(I) solution. However, it is more easily made from the oxidation of thaHous nitrate by chlorine ia aqueous potassium hydroxide solution. It is insoluble in water but dissolves in carboxyUc acids to give carboxylates. 

Hydrogen Peroxide Solutions, Storage andHandling, E. I. du Pont de Nemours Co., Inc., Wilmington, Del., 1983. 

Cyclohexenone has been prepared by dehydrohalogenation of 2-bromocyclohexanone, by the hydrolysis and oxidation of 3-chlorocyclohexene, by the dehydration of a-hydroxycyclohexa- ione, by the oxidation of cyclohexene with chromic acid or hydrogen peroxide in the presence of a vanadium catalyst, by I lie addition of acroleiti to ethyl acetoacctate followed by cycliza-lion, hydroly.sis, and decar])oxylation, by the reduction of N,N-dimelliyliiniline with sodium and ethanol itt liquid ammonia... 

Triazole has been prepared by the oxidation of substituted 1,2,4-triazoles, by the treatment of urazole with phosphorus pentasulfide, by heating equimolar quantities of formyl-hydrazine and formamide, by removal of the amino function of 4-amino-l,2,4-triazole, by oxidation of l,2,4-triazole-3(5)-thiol with hydrogen peroxide, by decarboxylation of 1,2,4-triazole-3(5)-carboxylic acid, by heating hydrazine salts with form-amide,by rapidly distilling hydrazine hydrate mixed with two molar equivalents of formamide, i by heating N,N -diformyl-hydrazine with excess ammonia in an autoclave at 200° for 24 hours, and by the reaction of 1,3,5-triazine and hydrazine monohydrochloride. ... 

Constitution. When coniine is distilled with zinc dust or heated with silver acetate/ a new base, coiiyrine, CgH N, differing from coniine by six atoms of hydrogen, is formed. This on oxidation yields pyridine-2-carboxylic acid and, since it is not identical with 2-isopropylpyridine, must be 2-propylpyridine (I). When coniine is heated with hydriodic acid at 300° it yields w-octane (II). These and other observations due mainly to A. W. Hofmann, made it clear by 1885 that coniine was probably a-propylpiperidine (III), and this has been amply confirmed by other reactions of the alkaloid and by syntheses. Thus, Wolffenstein showed that on oxidation with hydrogen peroxide, coniine is converted into amino-w-propylvaleraldehyde (IV) ... 

M. and M. Polonovski found that when scopolamine is treated with hydrogen peroxide, there is formed in addition to scopolamine iV-oxide [a]i, — 14° (H2O), [B. HBr, m.p. 153°] the quaternary base scopinium, isolated in the form of its bromide, m.p. 209-10°. The latter is reduced by sodium amalgam to a tertiary base, stereoisomeric with scopine and related to the latter as -tropine is to tropine and, therefore, named -SCOPINE. It yields crystalline salts B. HCl, m.p. 257-8°, aurichloride. 

The former passes into the second on further oxidation with hydrogen peroxide, indicating that it is an a-keto-carboxylic acid. Acid (b) loses carbon dioxide on fusion and gives a neutral substance, CjaHj OgN, m.p. 238°, which was shown to be 6 7-methylenedioxy-A-methylphenanthri-done (I), by comparison with a synthetic specimen. The position of the carboxyl group in (b) could not be determined by synthetic methods but is probably at since dihydrolycorineanhydromethine, Cl 7 7 2 ) m.p. 87-5° [picrate, m.p. 174° (dec.) methiodide, m.p. 236° (dec.)] on distillation with zinc dust yields a mixture of phenanthridine, 1-methyl-phenanthridine and 6 7-methylenedioxyphenanthridine, m.p. 142° [picrate, m.p. 257° (dec.)], the identity of the two latter being established by comparison with the synthetic products. These results indicate for lycorineanhydromethine formula (II). 

AMcycUc perfluoroketones undergo similar oxidation reactions as aromaUc fluoroaldehydes (equation 61). a lower concentration of hydrogen peroride oxidizes the ketones to a-hydroxy hydroperoxides [72], whereas concentrated hydrogen peroxide converts them to I,l -dihydroxydi(petfluorocycloalkyl) peroxides [16, 73] (equation 64). 

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