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Hydrochloric acid hydrogen carbonate

Cleavage of the optically active cyclopropyl compounds (I M = Li)5 by methanol in ether or ether/1,2-dimethoxyethane and (I M = SnMe3)6 by concentrated hydrochloric acid in carbon tetrachloride and by anhydrous hydrogen bromide in CC14 also take place with retention of optical activity and configuration, viz. [Pg.122]

Potassium carbonate Sodium carbonate Hydrochloric acid Hydrogen Ammonia... [Pg.232]

The group reagents used for the classification of most common cations are hydrochloric acid, hydrogen sulphide, ammonium sulphide, and ammonium carbonate. Classification is based on whether a cation reacts with these reagents by the formation of precipitates or not. It can therefore be said that classification of the most common cations is based on the differences of solubilities of their chlorides, sulphides, and carbonates. [Pg.191]

Group reagent there is no common reagent for the cations of this group. Group reaction cations of the fifth group do not react with hydrochloric acid, hydrogen sulphide, ammonium sulphide or (in the presence of ammonium salts) with ammonium carbonate. Special reactions or flame tests can be used for their identification. [Pg.285]

Some teachers may prefer not to carry out a complete separation of cations, but to hand out separate unknown mixtures containing cations of one analytical group only. In this case precipitation is made of the particular group reagent (hydrochloric acid, hydrogen sulphide, ammonia, ammonium sulphide or ammonium carbonate) and the precipitate is examined by Group Separation Tables V. 12 to V. 19 as well as V.23 to V.28 for each group respectively. [Pg.552]

Liver is the principal site of chloroform metabolism which involves two major pathways, both of which are catalyzed by the cytochrome P-450 enzymes in the presence of NADPH. The oxidative pathway produces phosgene and the reductive pathway produces the dichloromethyl free radical. Other metabolites of chloroform include chloro-methanol, hydrochloric acid, hydrogen chloride, and digluathionyl dithiocarbonate, with carbon dioxide as the predominant end product of metabolism. [Pg.562]

Pure Folpet is a white crystalline solid with a reported melting point of 177 °C. Solubility in water is only 1 ppm at room temperature. In the dry state, it is stable at room temperature, but it is hydrolysed in an aqueous solution at a rate that depends on the pH. Degradation products and hydrolysis in water can be carbon dioxide, hydrochloric acid, hydrogen sulfide, phthalamic acid, and phthalic acid. [Pg.23]

Destruction is accomplished by pyrolysis rather than oxidation therefore, typical products and by-products produced by incineration such as carbon monoxide, carbon dioxide, and oxides of nitrogen are not formed in significant concentrations. The principal products from soil-affixed TCDD using the Huber process are hydrogen, chlorine, hydrochloric acid, elemental carbon, and granular free-flowing soil material. [Pg.302]

CARBON OXYCHLORIDE (75-44-5) COCI2 Highly toxic and corrosive gas. Deconqioses slowly with water, producing hydrochloric acid and carbon oxides. Deconqjoses above 572°F/300°C, forming toxic and corrosive gases of hydrogen chloride and carbon monoxide chlorine. Reacts violently with strong oxidizers, amines, alkalis, anhydrous ammonia, isopropanol, chemically active metals aluminum, silicon tetrahydride, sodium. Forms shock-sensitive material with potassium. Incompatible with tert-alcohols. [Pg.219]


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See also in sourсe #XX -- [ Pg.65 ]




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Hydrochloric

Hydrochloric acid

Hydrochloric acid carbonate

Hydrogen carbonate-carbonic acid

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