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Silver , oxidation

The conversion of primary alcohols and aldehydes into carboxylic acids is generally possible with all strong oxidants. Silver(II) oxide in THF/water is particularly useful as a neutral oxidant (E.J. Corey, 1968 A). The direct conversion of primary alcohols into carboxylic esters is achieved with MnOj in the presence of hydrogen cyanide and alcohols (E.J. Corey, 1968 A,D). The remarkably smooth oxidation of ethers to esters by ruthenium tetroxide has been employed quite often (D.G. Lee, 1973). Dibutyl ether affords butyl butanoate, and tetra-hydrofuran yields butyrolactone almost quantitatively. More complex educts also give acceptable yields (M.E. Wolff, 1963). [Pg.134]

The halide anion of quaternary ammonium iodides may be replaced by hydroxide by treatment with an aqueous slurry of silver oxide Silver iodide precipitates and a solu tion of the quaternary ammonium hydroxide is formed... [Pg.938]

Nitrobenzene Nitric acid, nitrous oxide, silver perchlorate... [Pg.1210]

Silicon Alkali carbonates, calcium, chlorine, cobalt(II) fluoride, manganese trifluoride, oxidants, silver fluoride, sodium-potassium alloy... [Pg.1212]

Silver sulfate decomposes above 1085°C into silver, sulfur dioxide, and oxygen. This property is utilized ia the separation of silver from sulfide ores by direct oxidation. Silver sulfate is reduced to silver metal by hydrogen, carbon, carbon monoxide, zinc, and copper. [Pg.90]

Silver(II) Oxide. Silver(II) oxide [1301 -96-8, 35366-11-1], AgO, is prepared by persulfate oxidation of Ag20 in basic medium at 90°C or by the... [Pg.90]

Fire Hazards - Flash Point Not flammable Flammable Limits in Air (%) Not flammable Fire Extinguishing Agents Not pertinent Fire Extinguishing Agents Not To Be Used Not pertinent Special Hazards of Combustion Products Not pertinent Behavior in Fire Decomposes to silver oxide, silver, and carbon dioxide. The reaction is non violent Ignition Temperature Not pertinent Electrical Hazard Not pertinent Burning Rate Not pertinent. [Pg.341]

Answer the following questions and, for each yes response, write a balanced cell reaction and calculate the standard cell emf. (a) Can the oxygen present in air oxidize silver metal in acidic solution (b) Can the oxygen in air oxidize silver metal in basic solution ... [Pg.646]

Silver bromide Silver chloride Silver perchlorate Silver cyanide Silver fluoride Silver iodide Silver permar>gate Silver nitrate Silver carbonate Silver oxide Silver sulphate Silver sulphide Silver phosphate... [Pg.459]

Promoters may influence selectivity by poisoning undesired reactions or by increasing the rates of desired intermediate reactions so as to increase the yield of the desired product. If they act in the first sense, they are sometimes referred to as inhibitors. An example of this type of action involves the addition of halogen compounds to the catalyst used for oxidizing ethylene to ethylene oxide (silver supported on alumina). The halogens prevent complete oxidation of the ethylene to carbon dioxide and water, thus permitting the use of this catalyst for industrial purposes. [Pg.201]

See other metal oxides, silver compounds 0037. Silver peroxochromate... [Pg.24]

Hydrogen sulfide is rapidly oxidised, and may ignite in contact with a range of metal oxides, including barium peroxide, chromium trioxide, copper oxide, lead dioxide, manganese dioxide, nickel oxide, silver(I) oxide, silver(II) oxide, sodium peroxide, and thallium(III) oxide. In the presence of air, contact with mixtures of calcium oxide or barium oxide with mercury oxide or nickel oxide may cause vivid incandescence or explosion. [Pg.1652]

Catalyst, alumina, 34, 79 35, 73 ammonium acetate, 31, 25, 27 copper chromite, 31, 32 36, 12 cuprous oxide-silver oxide, 36, 36, 37 ferric nitrate, hydrated, 31, 53 piperidine, 31, 35 piperidine acetate, 31, 57 Raney nickel, 36, 21 sulfuric acid, 34, 26 Catechol, 33, 74 Cetylmalonic acid, 34, 16 Cetylmalonic ester, 34,13 Chlorination, by sulfuryl chloride, 33, 45 ... [Pg.46]

Creosol, 33, 17 Crotonaldehyde, 33, IS 34, 29 diethyl acetal, 32, 5 Cupric acetate monohydrate, 36, 77 Cuprous oxide-silver oxide, 36, 36, 37 Cyanamide, 34, 67 36, 8 Cyanoacetamide, 32, 34 Cyanoacetic acid, 31, 25 Cyanoacetylurea, 37, 16 >-Cyanobenzaldehyde, 30, 100 >-Cyanobenzaldiacetate, 36, 59 3-Cyano-5,6-dimethyl-2(l)-pyridone, 32,34 N-2-Cyanoethylaniline, 36, 6 N-2-Cyanoethyl- -anisidine, 36, 7 Cyanoethylation, of aniline, 36, 6 of ethyl phenylcyanoacetate, 30, 80 N-2-Cyanoethyl-m-chloroaniline, 36, 7 Cyanogen, 32, 31 Cyanogen iodide, 32, 29 Cyanogen iodide, complex with sodium iodide, 32, 31... [Pg.47]

Nitrites Nitrobenzene Nitroethane Nitrogen trichloride Organic nitrites in contact with ammonium salts, cyanides Nitric acid, nitrous oxide, silver perchlorate Hydroxides, hydrocarbons, metal oxides Ammonia, As, hydrogen sulfide, nitrogen dioxide, organic matter, ozone, phosphine, phosphorus, KCN, KOH, Se, dibutyl ether... [Pg.1479]

While it feels as though all the mouth fills with this pain, in fact the pain only manifests itself through those teeth filled with metal, the metal being silver dissolved in mercury to form a solid - we call it a silver amalgam. Corrosion of the filling s surface causes it to bear a layer of oxidized silver, so the tooth filling also represents a redox couple, with silver and silver oxide coexisting. [Pg.280]

Silver(l) oxide Silver oxide (8) Silver oxide (Ag20) (9) (20667-12-3) Triphenylarsine Arsine, triphenyl- (8,9) (603-32-7)... [Pg.186]

Ethylene oxidation to ethylene oxide. Silver catalyst placed in the pores of the tube (8wt% Ag). [Pg.139]

Diazirines have been prepared by dehydrogenation of diaziri-dines with mercuric oxide, silver oxide, or dichromate-sulfuric acid. The present procedure corresponds to that of Schmitz and Ohme. The procedure for the preparation of the 3,3-penta-methylenediaziridine has been reported by H. J. Abendroth. ... [Pg.107]

In the 1940s and 1950s, a considerable amount of research was funded to find and develop the chemists impossible dream a process for the direct oxidation of ethylene to EO, without any by-products. Finally, Union Carbide found the silver bullet that did the joE)—a catalyst made of silver oxide. Silver oxide is the only substance found having sufficient activity and selectivity. (Activity relates to the amount of conversion, selectivity relates to the right yield.) Moreover, ethylene is the only olefin affected in this way. The others, propylene, butylene, etc., tend to oxidize completely, forming carbon dioxide and water. But when silver oxide is used as a catalyst with ethylene, the dominant reaction is the formation of EO. Some ethylene still ends up being further oxidized, as much as 25% in some processes, as shown in Figure 10—2. [Pg.147]

Aromatic cation-radicals can also react with NOj", giving nitro compounds. Such reactions proceed either with a preliminary prepared cation-radical or starting from nncharged componnd if iodine and silver nitrite are added. As for mechanisms, two of them seem feasible—first, single electron transfer from the nitrite ion to a cation-radical and second, nitration of ArH with the NOj radical. This radical is quantitatively formed when iodine oxidizes silver nitrite in carbon tetrachloride (Neelmeyer 1904). [Pg.255]

Partial oxidation of 158 by bromine yields bromine-free 159 together with mono-, di-, and tribromo derivatives. Other useful reagents are nitrous acid (54JCS286) or the one-electron oxidants silver acetate (in substoichio-metric quantity) and cerium(IV) ammonium nitrate (only for the methyl ether of 158 86BCJ511). [Pg.117]

Compounds Silver nitrate silver chloride silver oxide silver sulfide... [Pg.632]

Synonyms silver peroxide argentic oxide silver suboxide Divasil... [Pg.843]

Rh (NHo) 5C1] (OH) 2, is produced by mixing the chloride with moist silver oxide. Silver chloride is precipitated, and a strongly alkaline liquid produced containing the hydroxide. The base absorbs carbon dioxide from the air, removes ammonia from ammonium salts, and precipitates metallic hydroxides from solutions of the metallic salts. It is only known in solution, and on evaporation of the liquid it is slowly transformed in the cold, more rapidly on heating, into a mixture of aquo-pentammino-rhodium chloride and aquo-pentammino-rhodium hydroxide, thus ... [Pg.204]


See other pages where Silver , oxidation is mentioned: [Pg.450]    [Pg.90]    [Pg.87]    [Pg.36]    [Pg.1518]    [Pg.1315]    [Pg.15]    [Pg.20]    [Pg.23]    [Pg.187]    [Pg.166]    [Pg.64]    [Pg.214]    [Pg.214]    [Pg.842]    [Pg.200]    [Pg.200]    [Pg.185]   
See also in sourсe #XX -- [ Pg.222 ]

See also in sourсe #XX -- [ Pg.183 ]

See also in sourсe #XX -- [ Pg.183 ]

See also in sourсe #XX -- [ Pg.183 ]

See also in sourсe #XX -- [ Pg.222 ]




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1,3-Diferrocenylimidazolium tetraphenylborate, reaction with silver oxide

Activations silver® oxide

Alcohols, secondary, oxidation with silver carbonate

Alcohols, secondary, oxidation with silver oxide

Alcohols, silver-mediated oxidation

Aldehyde, silver-mediated oxidation

Aldehydes silver® oxide

Aldehydes, reaction with silver oxide

Aldehydes, unsaturated, oxidation with silver oxide

Alkene Oxidation over Copper, Silver, and Gold Catalysts

Alkyl bromides synthesis, silver® oxide

Alkylation (Chapter with silver oxide

Amidation reactions, silver-mediated oxidation

Amines, silver-mediated oxidation

Ammonia silver oxide

Annealing, silver oxide

Aryl halides silver® oxide

Arylations silver® oxide

Arylboronic acids silver® oxide

Barriers silver oxide batteries

Batteries silver vanadium oxide

Battery Applications of Silver Vanadium Oxide

Battery silver oxide

Bromine-silver® oxide

Button batteries zinc/silver oxide primary

Cadmium-silver oxide cells

Cadmium/silver oxide batteries

Carbon monoxide oxidation silver oxide catalyst

Carboxylic acids with silver oxide

Cathodes silver oxide

Charging silver-oxide batteries

Cross-coupling silver® oxide

Cyclic ether synthesis silver® oxide

Cyclizations silver® oxide

Dehydrogenation of 3,3-pentamethylenediaziridine to 3,3-pentamethylenediazirine with silver oxide

Diazo ketones Wolff rearrangements, silver® oxide

Diazoketones reaction with silver oxide

Direct arylations silver® oxide

Divalent silver oxide

Electrochemical Syntheses of Binary Silver Oxides

Electrolytes zinc/silver oxide cells

Electrolytes zinc/silver oxide reserve batteries

Electrophilic catalyst, silver oxide

Ethylene oxidation on silver

Ethylene silver-catalyzed direct oxidation

Eusiderin use of silver oxide

F Pyrrolidine Silver oxide

Functionalizations silver oxide

Glass manufacturing, chemicals used silver oxide

Halides silver® oxide

Heterocycles silver© oxide

Hunsdiecker reactions silver© oxide

Hydroquinone oxidations silver oxide

Hydroquinones silver® oxide

Imines, silver-mediated oxidation

Impedance silver-oxide batteries

Indoles silver® oxide

Iodine and silver oxide

Iodine-silver oxide

Iron-silver oxide cells

Iron/silver oxide batteries

Lewis acids silver® oxide

Lithium-silver vanadium oxide

Lithium-silver vanadium oxide cells

Lithium/silver vanadium oxide batteries

Lithium/silver vanadium oxide batteries applications

Magnesium oxide silver

Magnetization, silver oxide composite

Mannosylation silver oxide activation

Mechanism silver carbonate oxidation

Metal catalysts, silver-mediated oxidation

Metal hydride-silver oxide cells

Methanol oxidation silver

Methylation silver oxide assisted

Nanoparticle silver oxide

Neolignan use of silver oxide

Nitriles silver oxide

OXYGEN Silver oxide

Oxidation by silver oxide

Oxidation by silver salts

Oxidation over Copper, Silver and Gold Catalysts

Oxidation silver catalysts

Oxidation silver dichromate

Oxidation with silver carbonate

Oxidation with silver carbonate on Celite

Oxidation with silver oxide

Oxidations silver trifluoroacetate/iodin

Oxidative 2- phenols, silver© oxide

Oxidative coupling 2- phenols, silver® oxide

Oxidative coupling silver nitrate

Oxidative coupling silver oxide

Oxidative decarboxylation, silver-mediated

Oxidative silver nitrate

Oxidative silver oxide

Oxide lead silver ores

Oxidized silver, spectra

Oxidizing agents silver compounds

Ozone, decomposition silver oxide

Ozonides with silver oxide

Phenols with silver oxide

Prenylation methods by silver oxide method

Primary batteries silver oxide cells

Primary silver vanadium oxide cells

Pyrroles silver -mediated oxidative

Pyrroles, silver-mediated oxidation

Reactions oxidation reaction, silver

Rechargeable silver vanadium oxide cells

Reserve batteries zinc/silver oxide

Selectivity ethylene oxidation over supported silver

Separators silver oxide batteries

Silver -catalysed oxidation

Silver 3 oxidation state

Silver II) oxide

Silver acetate allylic oxidation

Silver acetate iodine, oxidations with

Silver acetate oxidations with

Silver alloys, oxidation

Silver ammonia complex oxide

Silver carbonate oxidant

Silver carbonate oxidation

Silver carbonate, oxidizing agent

Silver catalysis oxidation

Silver catalysts ethylene oxidation

Silver catalysts ethylene oxidation over

Silver catalyzed oxidations

Silver chlorate oxidant

Silver chloride oxide

Silver complexes oxidative effects

Silver dichromate, tetrakis oxidation

Silver dichromate, tetrakis oxidation alcohols

Silver ethylene oxidation

Silver ethylene oxidation over

Silver ions, oxidation

Silver iron oxide

Silver nickel oxide

Silver nitrate oxidation

Silver oxidant

Silver oxidant

Silver oxidation with

Silver oxide

Silver oxide

Silver oxide Subject

Silver oxide Wolff rearrangement

Silver oxide carboxylic acids

Silver oxide catalyst

Silver oxide cell

Silver oxide composites

Silver oxide composites, preparation

Silver oxide compounds

Silver oxide elimination reaction

Silver oxide initiator

Silver oxide method

Silver oxide method in prenylation methods

Silver oxide oxidant

Silver oxide oxidation

Silver oxide oxidation

Silver oxide oxidative demethylation with

Silver oxide preparation

Silver oxide primary batteries

Silver oxide quinone synthesis

Silver oxide reaction

Silver oxide reaction with acyl chloride

Silver oxide secondary batteries

Silver oxide secondary batteries characteristics

Silver oxide secondary batteries electrodes

Silver oxide with active hydrogen

Silver oxide with silyl enol ethers

Silver oxide, Hofmann elimination

Silver oxide, Hofmann elimination reaction

Silver oxide, Hofmann elimination reaction and

Silver oxide, basic-strength

Silver oxide, catalyst preparation

Silver oxide, chemisorption

Silver oxide, decomposition

Silver oxide, reaction with boron

Silver oxide, reaction with boron alkyls

Silver oxide, reduction

Silver oxide-supported metal catalysts

Silver oxide/zinc battery

Silver oxides, structure

Silver oxids

Silver salt oxidation

Silver salts Komblum oxidation

Silver tetrafluoroborate DMSO oxidation of alcohols

Silver trifluoroacetate alkane oxidation

Silver vanadium oxide

Silver vanadium oxide cells

Silver zinc oxide

Silver(I) Oxide

Silver-catalyzed oxidative

Silver-catalyzed oxidative decarboxylation

Silver-copper reaction, oxidation-reduction

Silver-mediated oxidation reactions

Silver-mediated oxidation reactions oxidative decarboxylation

Silver-mediated oxidation reactions promoters

Silver-oxide overlayer

Silver/nickel oxide interface

Sulfonylations silver® oxide

Tetrakis silver dichromate oxidant

The Silver Vanadium Oxide Battery

Thiophenes silver® oxide

With silver oxide

Zinc-Silver Oxide Storage Batteries

Zinc-silver oxide and related cells

Zinc-silver oxide cells

Zinc-silver oxide system

Zinc/silver oxide primary batteries

Zinc/silver oxide primary batteries electrolytes

Zinc/silver oxide reserve batteries applications

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