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Mercuration 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. [Pg.294]

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. [Pg.295]

Mercury(II) oxide, or mercuric oxide, is a bright red powder. It decomposes on heating. What are the products of the decomposition of HgO ... [Pg.123]

Forms unstable explosive products in reaction with acetaldehyde + desiccants (forms polyethyUdine peroxide) acetic acid (forms peracetic acid) acetic + 3-thietanol acetic anhydride acetone (forms explosive peroxides) alcohols (products are shock-and heat-sensitive) carboxylic acids (e.g., formic acid, acetic acid, tartaric acid), diethyl ether, ethyl acetate, formic acid -f- metaboric acid, ketene (forms diacetyl peroxide) mercur f(II) oxide + nitric acid (forms mercur f(II) peroxide) thiourea -f- nitric acid polyacetoxyacryUc acid lactone + poly(2-hydroxyacrylic acid) + sodium hydroxide. [Pg.745]

SYNS C.I. 77760 MERCURIC OXIDE, RED MERCURIC OXIDE, soUd (DOT) MERCURIC OXIDE, YELLOW MERCURY(II) OXIDE OXYDE de MER-CURE (FRENCH) QUECKSILBEROXID (GERMAN) RED OXIDE of MERCURY RED PRECIPITATE SANTAR YELLOW MERCURIC OXIDE YELLOW OXIDE of MERCURY YELLOW PRECIPITATE... [Pg.870]

These workers also allowed /8-hydroxyethyl mercuric chloride to react to form supposedly the oxypalladation adduct postulated in the Pd(II) oxidation they obtained acetaldehyde as the product (34). [Pg.141]

A third primary dry cell is the zinc-mercuric oxide cell depicted in Figure 17.7. It is commonly given the shape of a small button and is used in automatic cameras, hearing aids, digital calculators, and quartz-electric watches. This battery has an anode that is a mixture of mercury and zinc and a steel cathode in contact with solid mercury(II) oxide (HgO). The electrolyte is a 45% KOH solution that saturates an absorbent material. The anode half-reaction is the same as that in an alkaline dry cell,... [Pg.724]

Potassium permanganate. Dimethyl sulfide-Chlorine. Dimethyl sulfoxide. Dimethyl sulfoxide-Chlorine. Dimethylsulf-oxide Sulfur trioxide. Dipyridine chro-mium(VI) oxide. Iodine. Iodine-Potassium iodide. Iodine tris(trifluoroacetate). Iodosobenzene diacetate. Isoamyl nitrite. Lead tetraacetate. Manganese dioxide. Mercuric acetate. Mercuric oxide. Osmium tetroxide—Potassium chlorate. Ozone. Periodic acid. Pertrifluoroacetic acid. Potassium ferrate. Potassium ferricyanide. Potassium nitrosodisulfonate. Ruthenium tetroxide. Selenium dioxide. Silver carbonate. Silver carbonate-Celite. Silver nitrate. Silver oxide. Silver(II) oxide. Sodium hypochlorite. Sulfur trioxide. Thalli-um(III) nitrate. Thallium sulfate. Thalli-um(III) trifluoroacetate. Triphenyl phosphite ozonide. Triphenylphosphine dibromide. Trityl fluoroborate. [Pg.297]

Pyrazine 93 was prepared by reductive cyclodimerization of 2-nitro-methylenehexahydroazocine.125 o-( 1 -Perhydroazocinyl)acetophenone was ring opened by Hg(II)fEDTA) to the aminoaldehyde 94.126 The reaction probably proceeds via JV-aryliminium ions in a manner similar to that of photocyclization of 64. Mercuric acetate oxidation of /V-methylperhydro-azocine, followed by HC1 and H2S, afforded trithiane (95).127 This was... [Pg.136]

Alkyl-l,3,2-dioxaborinanes, prepared by asymmetric hydroboration of prostereogenic olefins with monoisopinocampheylborane and subsequent removal of the chiral auxiliary, react with methoxy(phenylthio)methyllithium followed by treatment with mercuric(II) chloride, to give a-methoxyalkyl derivatives. Oxidation of these intermediates in a pH 8 phosphate buffer provides x-chiral aldehydes (method ) which are transformed by further oxidation into the corresponding a-chiral acids (method ) and by reduction into /i-chiral alcohols (method )14. [Pg.274]

Chart II. Mercuric acetate oxidation of dihydrooleavamine and methoxycarbonyl dihydrooleavamine. [Pg.85]

Genetics and Biochemistry. Early studies with purified SG-1 spores (80) showed that Mn(II) oxidation by the spores was inhibited by heat or various inhibitors, including mercuric chloride, sodium azide, and potassium cyanide. This work was... [Pg.405]

Because many ions and compounds have very similar names, there is great potential for confusing them. Write the correct chemical formulas to distinguish between (a) calcium sulfide and calcium hydrogen sulfide, (b) hydrobromic acid and bromic acid, (c) aluminum nitride and aluminum nitrite, (d) iron(II) oxide and iron(III) oxide, (e) ammonia and ammonium ion, (f) potassium sulfite and potassium bisulfite, (g) mercurous chloride and mercuric chloride, (h) chloric acid and perchloric add. [Pg.75]

Synonyms Cl 77760 Mercuric oxide (INCI) Mercuric oxide, red Mercury oxide Mercury (II) oxide Mercury oxide, red Red precipitate Classification Inorganic oxide Empirical HgO... [Pg.1187]

Ionic reactions between solvo-acids and solvo-bases may lead to insoluble products such as thallium sulphate formed from mercury(II) sulphate and thallium bromide in molten mercury(II) bromide. Similarly anhydrous copper(II) sulphate can be prepared by using a copper(II) halide. Perchlorates, nitrates and phosphates of many other elements can be prepared in a similar manner. By allowing mer-cury(II) oxide to react with the sulphate in mercury(II) bromide solution a red, insoluble product of composition (Hg0)2HgS04 is formed. Analogous compounds are formed from the sulphide, selenide and telluride of mercury in molten mercuric bromide. [Pg.100]

The mercury(II) oxide (mercuric oxide) RE is limited to use in highly alkaline solutions due to the stability of the oxide. While mercury(II) oxide is the only stable oxide, it can exist as either red or yellow powders that differ in solubility (37). The potential of the mer-cury(II) oxide RE is independent of the electrolyte, but depends on the activities of both OH and H2O (36). The potential can be calculated as follows (36) ... [Pg.91]

MF readily decomposes by action of many other chemical agents. It is relatively resistant to the action of dilute acids, e.g., nitric acid. Concentrated nitric acid decomposes it producing carbon monoxide, nitrogen(II) oxide, acetic acid, and mercuric nitrate [1,3, 35]. The reaction is fast when using fuming nitric acid [15]. Concentrated hydrochloric acid decomposes MF according to the following equation [3] ... [Pg.47]

Salter (1869) hsts this as mercuric oxide (mercury(II) oxide, HgO), stating that it was possible to make brick red or orange-yellow colours. [Pg.321]

See other pages where Mercuration II oxide is mentioned: [Pg.168]    [Pg.651]    [Pg.651]    [Pg.553]    [Pg.1032]    [Pg.168]    [Pg.651]    [Pg.651]    [Pg.553]    [Pg.1032]    [Pg.353]    [Pg.934]    [Pg.934]    [Pg.733]    [Pg.136]    [Pg.515]    [Pg.55]    [Pg.561]    [Pg.664]    [Pg.737]    [Pg.54]    [Pg.950]    [Pg.174]    [Pg.175]    [Pg.643]    [Pg.643]    [Pg.61]    [Pg.24]    [Pg.142]    [Pg.143]    [Pg.143]    [Pg.97]   
See also in sourсe #XX -- [ Pg.26 , Pg.211 , Pg.255 ]



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1-oxide mercuration

II) Oxide

Mercuric oxide oxidation

Mercurous oxide

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