Mercury II oxide

Dibromine monoxide, BtjO, is prepared, similar to the corresponding dichlorine compound, by the action of a solution of bromine in carbon tetrachloride on yellow mercury(II) oxide ... 

The metal is slowly oxidised by air at its boiling point, to give red mercury(II) oxide it is attacked by the halogens (which cannoi therefore be collected over mercury) and by nitric acid. (The reactivity of mercury towards acids is further considered on pp. 436, 438.) It forms amalgams—liquid or solid—with many other metals these find uses as reducing agents (for example with sodium, zinc) and as dental fillings (for example with silver, tin or copper). 

Mercury(II) oxide, HgO, occurs in both yellow and red forms the yellow form is precipitated by addition of hydroxide ion to a solution containing mercury(II) ions, and becomes red on heating. Mercury(II) oxide loses oxygen on heating. 

Mercuryill) chloride is obtained in solution by dissolving mercury(II) oxide in hydrochloric acid the white solid is obtained as a sublimate by heating mercury(II) sulphate and solid sodium chloride ... 

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... 

Moissanite, see Silicon carbide Molybdenite, see Molybdenum disulfide Molybdite, see Molybdenum(VI) oxide Molysite, see Iron(III) chloride Montroydite, see Mercury(II) oxide Morenosite, see Nickel sulfate 7-water Mosaic gold, see Tin disulfide Muriatic acid, see Hydrogen chloride, aqueous solutions... 

Iodoform Acetone, lithium, mercury(II) oxide, mercury(I) chloride, silver nitrate... 

Mercury(II) oxide Chlorine, hydrazine hydrate, hydrogen peroxide, hypophosphorous acid, magnesium, phosphorus, sulfur, butadiene, hydrocarbons, methanethiol... 

SuIfona.tlon, Sulfonation is a common reaction with dialkyl sulfates, either by slow decomposition on heating with the release of SO or by attack at the sulfur end of the O—S bond (63). Reaction products are usually the dimethyl ether, methanol, sulfonic acid, and methyl sulfonates, corresponding to both routes. Reactive aromatics are commonly those with higher reactivity to electrophilic substitution at temperatures > 100° C. Tn phenylamine, diphenylmethylamine, anisole, and diphenyl ether exhibit ring sulfonation at 150—160°C, 140°C, 155—160°C, and 180—190°C, respectively, but diphenyl ketone and benzyl methyl ether do not react up to 190°C. Diphenyl amine methylates and then sulfonates. Catalysis of sulfonation of anthraquinone by dimethyl sulfate occurs with thaHium(III) oxide or mercury(II) oxide at 170°C. Alkyl interchange also gives sulfation. 

Hydrazino groups are also converted into H-compounds with mercury(II) oxide (74CR(C)-(278)427) in other reactions they have given hydrazones, or have been converted into pyrazoles and fused heterocyclic rings (77JAP(K)7785194), e.g. (72) -> (73). 

Again, as with pyridopyrimidines, the main reaction is oxidation of di- or poly-hydro derivatives to fully aromatic structures, often merely by air or oxygen. In some cases the reagent of choice is mercury(II) oxide, whilst other reagents used include sulfur, bromine, chloranil, chromium trioxide-acetic acid, hydrogen peroxide, and potassium ferricyanide, which also caused oxidative removal of a benzyl group in the transformation (306) (307)... 

Oxidative procedures have been utilized for the synthesis of both monocyclic five-membered heterocycles and their ring-fused analogs, although the ease of synthesis of the precursors for the latter ring closures results in wider application of this procedure. A variety of oxidizing agents have been used and the conversion of the benzylidene hydrazidines (221) into the 4-arylamino-l,2,4-triazole (222) was effected with mercury(II) oxide (77BCJ953). 

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). 

Intramolecular alkylnitrene addition to an alkenic moiety situated S,e to the electron deficient center has been utilized for the preparation of bi- and tri-cyclic aziridines (Scheme 11) (68JA1650). Oxidation of the primary alkylamine can be effected cleanly with NCS, LTA or mercury(II) oxide. 

Merkuri-jodid, n. mer curic iodide, mercury (II) iodide, -nitrat, n. mercuric nitrate, mercury-(II) nitrate. -oxyd, n. mercuric oxide, mercury (II) oxide, -rhodanid, n. mercuric thiocyanate, mercury(II) thiocyanate, -salz, n. mercuric salt, mercury (II) salt, -sulfati n. mercuric sulfate, mercury (II) sulfate, -sulfidt ti. mercuric sulfide, mercury (II) sulfide. -sulfozyamd, n. mercuric thiocyanate. 

Merkur-oxyd, n. niercury oxide, specif, mercuric oxide, mercury(II) oxide, -silber, n. silver amalgam, -sulfid, n. mercury sulfide, specif, mercuric sulfide, mercury(II) sulfide. 

Many different methods can be used to resolve compounds into their elements. Sometimes, but not often, heat alone is sufficient. Mercury(II) oxide, a compound of mercury and oxygen, decomposes to its elements when heated to 600°C. Joseph Priestley, an English... 

Mercury(II) oxide, a red powder, can be decomposed by heating to produce liquid mercury and oxygen gas. When a sample of this compound is decomposed, 3.87 g of oxygen and 48.43 g of mercury are produced. In a second experiment, 15.68 g of mercury is allowed to react with an excess of oxygen and 16.93 g of red mercury(II) oxide is produced. Show that these results are consistent with the law of constant composition. 

Another important primary battery is the mercury cell. It usually comes in very small sizes and is used in hearing aids, watches, cameras, and some calculators. The anode of this cell is a zinc-mercury amalgam the reacting species is zinc. The cathode is a plate made up of mercury(II) oxide, HgO. The electrolyte is a paste containing HgO and sodium or potassium hydroxide. The electrode reactions are... 

Mercury (II) oxide, 3-4 Mercury-in-glass thermometers, 7-8 Mercury thermometers, 2 Metabolic energy, 218 Metal A substance having characteristic... 

Dibenz[c,e]azepine 6-oxide (4, R = H) has been prepared in high yield (95 %) by oxidation of the cyclic hydroxainic acid 3 (R = H) with mercury(II) oxide.6 Oxidation of the unsym-metrically substituted derivative 3 (R = Ph) is regiospecific and yields only 5-phenyl-5//-dibenz[e,e]azepine 6-oxide (4, R = Ph 60% mp 188-189 C). 

The dibenzodiazepines 5 are hydrogenated to the 5,6-dihydro compounds by hydrazine/Raney nickel.149,153 The process is reversed by heating with mercury(II) oxide in diethyl ether.153... 

The oxime 4 undergoes ring closure to the (methylamino)benzoxadiazepine 5 under the influence of mercury(II) oxide.315... 

When mercury(II) oxide is heated, it decomposes into liquid mercury, driving off oxygen gas in the process. 

Thiols that are treated by mercury (II) oxide give rise to a very violent detonation if no solvent is used. 

Mixtures with mercury (II) oxide and manganese dioxide prepared at — 80°C ignited at 20° and reacted violently at 15°C, respectively. Copper(II) oxide reacted vigorously at 25 °C without ignition. 

Interaction is explosive when catalysed by sunlight or UV irradiation, or in presence of mercuiyQ oxide, mercury(II) oxide or silver oxide. 

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