Barium chlorate oxidant

Quantitatively, sulfur in a free or combined state is generally determined by oxidizing it to a soluble sulfate, by fusion with an alkaH carbonate if necessary, and precipitating it as insoluble barium sulfate. Oxidation can be effected with such agents as concentrated or fuming nitric acid, bromine, sodium peroxide, potassium nitrate, or potassium chlorate. Free sulfur is normally determined by solution in carbon disulfide, the latter being distilled from the extract. This method is not useful if the sample contains polymeric sulfur. 

Syn-Dihydroxylation. When the reaction was first discovered, the syn-dihydroxylation of alkenes was carried out by using a stoichiometric amount of osmium tetroxide in dry organic solvent.56 Hoffman made the observation that alkenes could react with chlorate salts as the primary oxidants together with a catalytic quantity of osmium tetroxide, yielding syn-vicinal diols (Eq. 3.11). This catalytic reaction is usually carried out in an aqueous and tetrahydrofuran solvent mixture, and silver or barium chlorate generally give better yields.57... 

When barium chlorate burns with fuel components, the oxygen acts as an oxidizer, and the burning is accompanied by the light emission of a green-colored flame. 

Butyl hydroperoxide,37 barium chlorate,38 or potassium ferricyanide39 can also be used as oxidants in catalytic procedures. Scheme 12.6 provides some examples of oxidations of alkenes to glycols by permanganate and by osmium tetroxide. 

The aqueous solution of barium sulfide oxidizes slowly in the air forming elemental sulfur and various anions of sulfur including sulfite, thiosulfate, polysulfides and sulfate. The yellow color of barium sulfide solution is attributed to the presence of dissolved elemental sulfur that results from its slow oxidation in the air. In the presence of an oxidizing agent, barium sulfate is formed. Violent to explosive oxidation may occur when heated with strong oxidants such as phosphorus pentoxide or potassium chlorate. 

Ammonium nitrate Ammonium perchlorate Barium chlorate (hydrate) Barium chromate Barium nitrate Barium peroxide Iron oxide Iron oxide Lead chromate Lead oxide (red lead) Lead peroxide Potassium chlorate Potassium nitrate Potassium perchlorate Sodium nitrate Strontium nitrate... 

Barium nitrate - Ba(N03)2 - and barium chlorate - Ba(C o3)2 are used most often to produce green flames, serving both as the oxidizer and color source. Barium chlorate can produce a deep green, but it is somewhat unstable and can form explosive mixtures with good fuels. Barium nitrate produces an acceptable green color, and it is considerably safer to work with due to its... 

Chromium Chlorate, Cr(C10g)3, which is obtained by the double decomposition of barium chlorate and chrome alum, forms a violet solution which becomes green at 65° C. and decomposes on boiling, yielding chromium hydroxide and oxides of chlorine. Tire dcconr-position is facilitated by potassium ferricyanide. The salt is used iir calico printing and for increasing the permanence of aniline black. 

Barium Diuranate, BaUjO, is obtained by heating barium uranyl acetate, or by heating together the green oxide and barium chlorate. It is obtained in a hydrated condition when ammonia is added to mixed solutions of barium chloride and uranyl nitrate, or when excess of baryta water is added to uranyl nitrate solution. It is a deep yellow crystalline powder. 

Sodium chlorate, NaC103 potassium chlorate, KCI03 silver chlorate, AgCIOj and barium chlorate, Ba(CIOj)2, oxidize organic compounds only in the presence of catalysts, usually osmium tetroxide [310, 714, 715, 716, 718] or vanadium pentoxide [716, 718]. Because such oxidations do not occur without catalysts, it is likely that the real oxidants are osmium tetroxide and vanadium pentoxide, respectively, and that the function of the chlorates is reoxidation. 

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