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Sodium oxidations with

Compounds can also combine to form new compounds, such as in the combination of sodium oxide with water to form sodium hydroxide ... [Pg.120]

A base can be prepared by the reaction of sodium oxide with water. Give the reaction and the name of the base product. [Pg.238]

CH3CH2OCH2CH2OH. A colourless liquid with a pleasant odour b.p. 135 C. Manufactured by heating ethylene oxide with ethanol and a catalyst, or by treating ethylene glycol with diethyl sulphate and sodium hydroxide. Used extensively as a solvent in nitrocellulose lacquers. [Pg.168]

Piperitone is of considerable technical im portance. It is a colourless oil of a pleasant peppermint-like smell. (-)-Piperilone has b.p. 109-5-110-5 C/I5mm. Piperitone yields thymol on oxidation with FeCl. On reduction with hydrogen in presence of a nickel catalyst it yields menthone. On reduction with sodium in alcoholic solution all forms of piperitone yield racemic menthols and womenthols together with some racemic a-phel)andrene. [Pg.316]

Thus potassium is obtained by heating potassium chloride with sodium, and barium by reduction of barium oxide with aluminium. [Pg.122]

Evidence for the solvated electron e (aq) can be obtained reaction of sodium vapour with ice in the complete absence of air at 273 K gives a blue colour (cf. the reaction of sodium with liquid ammonia, p. 126). Magnesium, zinc and iron react with steam at elevated temperatures to yield hydrogen, and a few metals, in the presence of air, form a surface layer of oxide or hydroxide, for example iron, lead and aluminium. These reactions are more fully considered under the respective metals. Water is not easily oxidised but fluorine and chlorine are both capable of liberating oxygen ... [Pg.271]

Ether so obtained is anhydrous, and almost entirely free from other impurities. On standing, however, it undergoes slight atmospheric oxidation, with the formation of traces of diethyl peroxide, (CaH jaOa. The formation of this peroxide can be largely checked, however, by storing the distilled ether over fresh sodium wire, preferably in the dark. [Pg.83]

The pinacolone may be employed for the preparation of trimethylacetlc acid (plvallc acid) by oxidation with sodium hypobromite solution ... [Pg.350]

Benzoquinone ( quinone ) is obtained as the end product of the oxidation of aniline by acid dichromate solution. Industrially, the crude product is reduced with sulphur dioxide to hydroquinone, and the latter is oxidised either with dichromate mixture or in very dilute sulphuric acid solution with sodium chlorate in the presence of a little vanadium pentoxide as catalyst. For the preparation in the laboratory, it is best to oxidise the inexpensive hydroquinone with chromic acid or with sodium chlorate in the presence of vanadium pent-oxide. Naphthalene may be converted into 1 4-naphthoquinone by oxidation with chromic acid. [Pg.745]

Most manganese today is obtained from ores found in Russia, Brazil, Australia, Republic of S. Africa, Gabon, and India. Pyrolusite and rhodochrosite are among the most common manganese minerals. The metal is obtained by reduction of the oxide with sodium, magnesium, aluminum, or by elctrolysis. [Pg.59]

Several methods are available for producing thorium metal it can be obtained by reducing thorium oxide with calcium, by electrolysis of anhydrous thorium chloride in a fused mixture of sodium and potassium chlorides, by calcium reduction of thorium tetrachloride mixed with... [Pg.174]

We shall describe a specific synthetic example for each protective group given above. Regiosdective proteaion is generally only possible if there are hydroxyl groups of different sterical hindrance (prim < sec < tert equatorial < axial). Acetylation has usually been effected with acetic anhydride. The acetylation of less reactive hydroxyl groups is catalyzed by DMAP (see p.l44f.). Acetates are stable toward oxidation with chromium trioxide in pyridine and have been used, for example, for protection of steroids (H.J.E. Loewenthal, 1959), carbohydrates (M.L. Wolfrom, 1963 J.M. Williams, 1967), and nucleosides (A.M. Micbelson, 1963). The most common deacetylation procedures are ammonolysis with NH in CH OH and methanolysis with KjCO, or sodium methoxide. [Pg.158]

Oxidation of 4 ten butylthiane (see Problem 16 23 for the structure of thiane) with sodium metaperiodate gives a mixture of two compounds of molecular formula CpHigOS Both products give the same sulfone on further oxidation with hydrogen peroxide What is the relationship between the two compounds ... [Pg.697]

Oxidation with Benedict s reagent (Section 25 19) Sugars that con tain a free hemiacetal function are called reducing sugars They react with copper(ll) sulfate in a sodium citrate/sodium carbonate buffer (Benedict s reagent) to form a red precipitate of copper(l) oxide Used as a qualitative test for reducing sugars... [Pg.1063]

Removal of the ketal protecting groups, followed by oxidation with sodium dichromate ia acetic acid gave... [Pg.101]

The concentration of aqueous solutions of the acid can be deterrnined by titration with sodium hydroxide, and the concentration of formate ion by oxidation with permanganate and back titration. Volatile impurities can be estimated by gas—Hquid chromatography. Standard analytical methods are detailed in References 37 and 38. [Pg.505]

Resorcinol or hydroquinone production from m- or -diisopropylben2ene [100-18-5] is realized in two steps, air oxidation and cleavage, as shown above. Air oxidation to obtain the dihydroperoxide (DHP) coproduces the corresponding hydroxyhydroperoxide (HHP) and dicarbinol (DC). This formation of alcohols is inherent to the autooxidation process itself and the amounts increase as DIPB conversion increases. Generally, this oxidation is carried out at 90—100°C in aqueous sodium hydroxide with eventually, in addition, organic bases (pyridine, imidazole, citrate, or oxalate) (8) as well as cobalt or copper salts (9). [Pg.488]

The polyalkylene glycol polymer employs a starter that consists of a relatively reactive alcohol and a smaller amount of its potassium or sodium salt. With propylene oxide, for instance, initiation of the polymeri2ation then involves the starter in the following steps ... [Pg.245]


See other pages where Sodium oxidations with is mentioned: [Pg.281]    [Pg.761]    [Pg.142]    [Pg.761]    [Pg.165]    [Pg.202]    [Pg.139]    [Pg.81]    [Pg.189]    [Pg.281]    [Pg.761]    [Pg.142]    [Pg.761]    [Pg.165]    [Pg.202]    [Pg.139]    [Pg.81]    [Pg.189]    [Pg.94]    [Pg.168]    [Pg.259]    [Pg.365]    [Pg.205]    [Pg.257]    [Pg.285]    [Pg.298]    [Pg.321]    [Pg.220]    [Pg.393]    [Pg.413]    [Pg.1020]    [Pg.99]    [Pg.93]    [Pg.477]    [Pg.12]    [Pg.277]    [Pg.213]    [Pg.378]    [Pg.466]    [Pg.437]   
See also in sourсe #XX -- [ Pg.16 , Pg.308 ]




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Alcohols, secondary, oxidation with sodium bromate

Alcohols, secondary, oxidation with sodium bromite

Alcohols, secondary, oxidation with sodium dichromate

Alcohols, secondary, oxidation with sodium hypochlorite

Alcohols, secondary, oxidation with sodium permanganate

Dextran oxidation with sodium

Oxidation with Sodium Dichromate

Oxidation with Sodium Hypochlorite

Oxidation with Sodium Periodate and Potassium Permanganate

Oxidation with sodium chlorite

Oxidation with sodium hypobromite

Oxidation with sodium periodate

Oxidation with sodium periodate-ruthenium trichlorid

Oxidation with sodium peroxide

Oxidation, of primary alcohols with sodium hypobromite

Oxidation, of primary alcohols with sodium hypochlorite

Oxidation—continued with sodium dichromate

Oxidation—continued with sodium persulfate

Oxidative with sodium periodate

Phenylacetylene, oxidative coupling reaction with sodium hypobromite

Pyridine 1-oxide reaction with sodium acetylide

Reactions sodium oxides with water

Sialic acid oxidation with sodium

Sodium 1-oxides, reactions with

Sodium azide, reaction with iron oxide

Sodium bromate, oxidation with

Sodium hypochlorite, alcohol oxidation with

Sodium oxidation

Sodium oxidative cleavage with

Sodium oxide

Studies of Superconducting Oxides with the Sodium Chloride Structure

Thioanisole, oxidation, by dinitrogen reaction with sodium metaperiodate

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