Mercury oxide-sulfuric acid

Acetaldehyde is the product of the Wacker process. At the end of the fifties oxidation of ethene to ethanal replaced the addition of water to acetylene, because the acetylene/coal-based chemistry became obsolete, and the ethene/petrochemistry entered the commercial organic chemicals scene. The acetylene route involved one of the oldest organometallics-mediated catalytic routes started up in the 1920s the catalyst system comprised mercury in sulfuric acid. Coordination of acetylene to mercury(II) activates it toward nucleophilic attack of water, but the reaction is slow and large reactor volumes of this toxic catalyst were needed. An equally slow related catalytic process, the zinc catalysed addition of carboxylic acids to acetylene, is still in use in paint manufacture. 

ABSOLUTE ALCOHOL or ABSOLUTE ETHANOL (64-17-5) Forms explosive mixture with air (flash point 55°F/13°C). Reacts, possibly violently, with strong oxidizers, bases, acetic anhydride, acetyl bromide, acetyl chloride, aliphatic amines, bromine pentafluoride, calcium oxide, cesium oxide, chloryl perchlorate, disulfuryl difluoride, ethylene glycol methyl ether. Iodine heptafluoride, isocyanates, nitrosyl perchlorate, perchlorates, platinum, potassium- er -butoxide, potassium, potassium oxide, potassium peroxide, phosphonis(III) oxide, silver nitrate, silver oxide, sulfuric acid, oleum, sodium, sodium hydrazide, sodium peroxide, sulfmyl cyanamide, tetrachlorosilane, i-triazine-2,4,6-triol, triethoxydialuminum tribromide, triethylaluminum, uranium fluoride, xenon tetrafluoride. Mixture with mercury nitrate(II) forms explosive mercury fulminate. Forms explosive complexes with perchlorates, magnesium perchlorate (forms ethyl perchlorate), silver perchlorate. Flow or agitation of substance may generate electrostatic charges due to low conductivity. 

TELLURIUM (13494-80-9) Finely divided powder or dust may be flammable and explosive. Violent reaction with strong oxidizers, bromine pentafluoride, halogens, interhalogens, iodine pentafluoride, hexalithium disilicide, lithium silicide, nitrosyl fluoride, oxygen difluoride, sodium peroxide, sulfur, zinc. Incompatible with cadmium, cesium, hafnium, strong bases, chemically active metals, iodic acid, iodine oxide, lead chlorite, lead oxide, mercury oxides, nitric acid, peroxyformic acid, platinum, silver bromate/iodate/ fluoride, nitryl fluoride, sodium nitrate. 

In general ketones are more stable than their enol precursors and are the products actually isolated when alkynes undergo acid catalyzed hydration The standard method for alkyne hydration employs aqueous sulfuric acid as the reaction medium and mer cury(II) sulfate or mercury(II) oxide as a catalyst... 

Propyn-l-ol Alkali metals, mercury(II) sulfate, oxidizing materials, phosphorus pentoxide, sulfuric acid... 

From Acetylene. Although acetaldehyde has been produced commercially by the hydration of acetylene since 1916, this procedure has been almost completely replaced by the direct oxidation of ethylene. In the hydration process, high purity acetylene under a pressure of 103.4 kPa (15 psi) is passed into a vertical reactor containing a mercury catalyst dissolved in 18—25% sulfuric acid at 70—90°C (see Acetylene-DERIVED chemicals). 

At ordinary temperatures, mercury is stable and does not react with air, ammonia (qv), carbon dioxide (qv), nitrous oxide, or oxygen (qv). It combines readily with the halogens and sulfur, but is Htde affected by hydrochloric acid, and is attacked only by concentrated sulfuric acid. Both dilute and concentrated nitric acid dissolve mercury, forming mercurous salts when the mercury is in excess or no heat is used, and mercuric salts when excess acid is present or heat is used. Mercury reacts with hydrogen sulfide in the air and thus should always be covered. 

Manufacture and Processing. Until World War II, phthaUc acid and, later, phthaUc anhydride, were manufactured primarily by Hquid-phase oxidation of suitable feedstocks. The favored method was BASF s oxidation of naphthalene [91-20-3] by sulfuric acid ia the presence of mercury salts to form the anhydride. This process was patented ia 1896. During World War I, a process to make phthaUc anhydride by the oxidation of naphthalene ia the vapor phase over a vanadium and molybdenum oxide catalyst was developed ia the United States (5). Essentially the same process was developed iadependendy ia Germany, with U.S. patents being granted ia 1930 and 1934 (6,7). 

Bis(2,4,6-trinitrophenyl)methane when treated with NaAc in acetic acid produced (580) as a thermostable explosive (80MIP41600). The conversion of o-nitrotoluene into 2,1-benzisoxazole was effected by mercury(II) oxide catalysis. A mercury containing intermediate was isolated and was demonstrated to be converted into 2,1-benzisoxazole (67AHC(8)277). The treatment of o-nitrotoluene derivative (581) with sulfuric acid gave (582) in 35% yield (72MI41607). 

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