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Salts carbonic

The much simpler steroid, 253, was fortuitously found to fulfill this role when injected into animals. Its lack of oral activity was overcome by incorporation of the 7a-thioacetate group. Reaction of the ethisterone intermediate, 77b, with a large excess of an organomagnesium halide leads to the corresponding acetylide salt carbonation with CO2 affords the carboxyllic acid, 251. This is then hydrogenated and the hydroxy acid cy-clized to the spirolactone. Oppenauer oxidation followed by treatment with chloranil affords the 4,6-dehydro-3-ketone (254). Conjugate addition of thiolacetic acid completes the synthesis of spironolactone (255), an orally active aldosterone antagonist. ... [Pg.206]

Please pass the sodium chloride It is amazing that food is seasoned with an ionic compound that is composed of two deadly elements— sodium and chlorine. The gain or loss of electrons can make a big difference in properties. Reacting sodium hydrogen carbonate, which is baking soda, with hydrochloric acid (HCI), the acid found in your stomach, produces salt, carbon dioxide, and water, according to the following equation ... [Pg.61]

When alkyl oxalyl chlorides were employed instead of acyl halides, symmetrical dibenzyl ketones were formed in good yields(44). Transition metal carbonyls or metal salts/carbon monoxide have generally been used for... [Pg.232]

Naji A., Willmann P., and Billaud D. Electrochemical Intercalation of Lithium into Graphite Influence of the Solvent Composition and the Nature of the Lithium Salt. Carbon, 36, 1347-1352 (1998). [Pg.246]

Solid state reactions are also very common in producing oxide materials and are based on thermal treatment of solid oxides, hydroxides and metal salts (carbonates, oxalates, nitrates, sulphates, acetates, etc.) which decompose and react forming target products and evolving gaseous products. Solid-state chemistry states that, like in the case of precipitation, powder characteristics depend on the speed of the nucleation of particles and their growth however, these processes in solids are much slower than in liquids. [Pg.501]

The most characteristic reaction of butadiene catalyzed by palladium catalysts is the dimerization with incorporation of various nucleophiles [Eq. (11)]. The main product of this telomerization reaction is the 8-substituted 1,6-octadiene, 17. Also, 3-substituted 1,7-octadiene, 18, is formed as a minor product. So far, the following nucleophiles are known to react with butadiene to form corresponding telomers water, carboxylic acids, primary and secondary alcohols, phenols, ammonia, primary and secondary amines, enamines, active methylene compounds activated by two electron-attracting groups, and nitroalkanes. Some of these nucleophiles are known to react oxidatively with simple olefins in the presence of Pd2+ salts. Carbon monoxide and hydrosilanes also take part in the telomerization. The telomerization reactions are surveyed based on the classification by the nucleophiles. [Pg.151]

Cyclic Salt Carbonates Silicates Evaporites Pollution ... [Pg.528]

Uses Manufacture of viscose rayon, cellophane, flotation agents, ammonium salts, carbon tetrachloride, carbanilide, paints, enamels, paint removers, varnishes, tallow, textiles, rocket fuel, soil disinfectants, electronic vacuum tubes, herbicides grain fumigants solvent for fats, resins, phosphorus, sulfur, bromine, iodine, and rubber petroleum and coal tar refining solvent and eluant for organics adsorbed on charcoal for air analysis. [Pg.257]

Concentrated nitric acid and other oxidizing agents decompose nickel tetracarbonyl forming their nickel salts, carbon dioxide and water ... [Pg.626]

Methanearsonic Acid, Sodium Salts Medranearsonic Acid, Sodium Salts Carbon Monoxide Morpholine... [Pg.68]

The purification of the alkali hydroxides.—Numerous impurities have been reported in commercial sodium and potassium hydroxides. Several have commented on the presence of peroxide, particularly in caustic potash.19 Various salts—carbonate, sulphate, nitrate, nitrite, chloride, and phosphate—as well as alumina, silica, organic matters, and metal oxides—e.g. arsenic, vanadium, iron, etc., have been reported. More or less of the other alkalies may also be present. [Pg.499]

Corbonic Acid, H2C03. The soln of C02 in H O exhibits feeble acid props it is unstable, however, and has never been isolated it is known only in the form of its salts (carbonates), acid salts 0bicarbonates), amides (carbamic acid or urea), and as acid chlorides (carbonyl chloride). This is also an old term for carboxylic acid Ref Hackh s(1944), 169... [Pg.456]

The base One equivalent, at least, of a base relative to the aryl halide must be present to achieve the alkene substitution catalytically. Most often a tertiary amine is employed. Secondary amines also appear to be suitable but primary amines usually are not. The base strength of the amine is important since only quite basic amines such as triethylamine work well. Acetate salts, carbonates and bicarbonates also are suitable bases but solubility may cause difficulties in some instances. The addition of a phase transfer agent such as a quaternary ammonium salt has often solved this problem. The inorganic bases, of course, may cause other problems such as ester hydrolysis, aldol condensations and other undesired side reactions. [Pg.844]

It also reacts with carbonates to give normal salts, carbon dioxide and water, and with reactive metals to give a normal salt and hydrogen gas. The reaction between zinc and sulfuric acid is often used to prepare hydrogen gas in the laboratory (Figure 12.8). [Pg.212]

Carbonates react with acids to form salts, carbon dioxide and water (Chapter 8, p. 123). For example, calcium carbonate reacts with dilute hydrochloric acid to form calcium chloride, carbon dioxide and water. [Pg.222]

Chemical weathering The conversion of minerals and other rock components into new, usually finer-grained materials through chemical reactions that typically involve water, natural acids, salts, carbon dioxide, and/or oxygen (compare with weathering and physical weathering). [Pg.443]

Chemistry (Theoretical and Applied).—Air. Water. Chemical theory. Acids, alkalies and salts. Carbon and its oxides fuels. Soaps. Textile fabrics. Water softeners. Sugars, starch, alcohol, acetic acid. Proteins. Fats. Yitamines. Yeasts, moulds and bacteria. Study of certain foods. Preservation and sterilisation of food stuffs. The practical work will be partly illustrative of the lectures, and partly experimental craft work, i.e. —... [Pg.113]

Metal carbonate + acid salt + carbonic acid NaHC03 + HCl - NaCI + H2CO3 (Note H2CO3 H2O + CO2)... [Pg.108]

Techniques based on the use of alkaline salts, carbonate solution in particnlar, offer the following advantages ... [Pg.48]


See other pages where Salts carbonic is mentioned: [Pg.152]    [Pg.353]    [Pg.78]    [Pg.29]    [Pg.25]    [Pg.296]    [Pg.25]    [Pg.230]    [Pg.4]    [Pg.790]    [Pg.166]    [Pg.745]    [Pg.149]    [Pg.535]    [Pg.876]    [Pg.935]    [Pg.181]    [Pg.59]    [Pg.2059]    [Pg.2059]    [Pg.826]    [Pg.13]    [Pg.650]    [Pg.236]    [Pg.106]    [Pg.194]    [Pg.790]   
See also in sourсe #XX -- [ Pg.690 ]




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Benzylic carbons, pyridinium salts

Binary mixed-salt solutions, carbon

Carbon binary salts

Carbon dioxide, addition salts

Carbon nucleophiles salts

Carbonate salts

Carbonate salts

Carbonate salts qualitative analysis

Carbonate salts solubility

Carbonate, inorganic salts

Carbonic acid calcium salt

Carbonic acid half ester salts

Carbonic acid magnesium salt

Carbonic acid magnesium salt anhydrous

Carbonic acid monopotassium salt

Carbonic acid monosodium salt

Carbonic acid salts

Carbonic acid, ammonium salt

Carbonic acid, diammonium salt

Carbonic acid, dicesium salt

Carbonic acid, dilithium salt

Carbonic acid, dipotassium salt

Carbonic acid, dirubidium salt

Carbonic acid, disodium salt

Carbonic acid, dithallium -salt

Carbonic acid, mono-ammonium salt

Carbon—lead bond silver salts

Cesium carbonate: Carbonic acid, dicesium salt

Enolate salts, carbonation

Fuel cell, high-temperature molten salt carbonate

Interaction of Carbon with Molten Salts-Chloride-Carbonate Melts

Mixed-salt solutions, carbon dioxide

Mixed-salt solutions, solubility carbon dioxide

Molten Salt Electrochemical Processes Directed Toward a Low Carbon Society

Molten salt media carbonization

Phosphonium salts, carbon-phosphorus

Phosphonium salts, carbon-phosphorus bond formation

Precipitation of carbonate salts

Salt catalysts, carbon-sulfur bond

Salting-out of carbon dioxide

Salts calcium carbonate

Salts of Carbonic Acid

Salts of oxoacids carbonates and hydrogencarbonates

Synthesis via coupling aromatic diazonium salts with carbon nucleophilic 4 atom fragments

Ternary mixed-salt solutions carbon dioxide solubility

Uranyl carbonates, ammonium salts

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