Reaction with ammonium hydrogen carbonate

The equations that represent the reactions with water support the prediction that NH4NO3 dissolves to form an acidic solution and Na3P04 dissolves to form a basic solution. Calcium chloride is the salt of a strong base-strong acid, so neither ion reacts with water and the solution is neutral. Both ions in ammonium hydrogen carbonate react with water. Because Kt, for HCOs" is greater than for NH4, the salt dissolves to form a weakly basic solution. 

Fulop and co-workers [124] have reported the synthesis of some new (ami-noalkyl) naphthols and (aminoalkyl) quinolinols 85 in good yields through a one-pot, microwave-assisted three-component modified Mannich reaction of naphthol or quinolinol with two equivalents of an aldehyde using ammonium carbamate or ammonium hydrogen carbonate as solid ammonia sources. It was observed that aliphatic aldehydes did not lead to the formation of the desired (aminoalkyl) quinolinols 85 (Scheme 64). 

The bulk material may ignite or explode in storage. Traces of water may initiate the reaction. A rapid exothermic decomposition above 175°C releases oxygen and chlorine. Moderately explosive in its solid form when heated. Explosive reaction with acetic acid + potassium cyanide, amines, ammonium chloride, carbon or charcoal + heat, carbon tetrachloride + heat, N,N-dichloromethyl-amine + heat, ethanol, methanol, iron oxide, rust, 1-propanethiol, isobutanethiol, turpentine. Potentially explosive reaction with sodium hydrogen sulfate + starch + sodium carbonate. Reaction with acetylene or nitrogenous bases forms explosive products. 

Violent reactions with ammonium salts, chlorate salts, beryllium fluoride, boron diiodophosphide, carbon tetrachloride + methanol, 1,1,1-trichloroethane, 1,2-dibromoethane, halogens or interhalogens (e.g., fluorine, chlorine, bromine, iodine vapor, chlorine trifluoride, iodine heptafluoride), hydrogen iodide, metal oxides + heat (e.g., beryllium oxide, cadmium oxide, copper oxide, mercury oxide, molybdenum oxide, tin oxide, zinc oxide), nitrogen (when ignited), silicon dioxide powder + heat, polytetrafluoroethylene powder + heat. 

AMMONIUM HYDROGEN CARBONATE (1066-33-7) Violent reaction with acids, forming carbon dioxide. Reacts with strong bases, forming ammonia. Reacts with fluorine, magnesium, sodium hypochlorite. 

A simple method has been developed for synthesis of thiiranes from epoxides via a one-pot reaction of epoxides with diethyl phosphite in the presence of ammonium acetate or ammonium hydrogen carbonate, sulfur, and acidic alumina under solvent-free conditions using microwave irradiation (Scheme 8.68) [178]. 

The simple hydrothermal method can be used to control the ID and 2D nanostructures of the oxides. The reaction was a conversion of nitrates mixture into carbonate hydrate phase, with the presence of ammonium hydrogen carbonate solution, at a reaction temperature of200 °C for 3 h. Morphological architectures of the rare earth oxides obtained were controlled by the thermal treatment at... 

A further reaction shown by poly(acrylic acid) and poly(methacrylic acid) is with ammonia to form cyclic imides. Polymethacrylimide is prepared commercially by heating a copolymer of methacrylic acid and methacrylonitrile with an ammonia-producing compound (e.g. urea or ammonium hydrogen carbonate) at about 200°C ... 

Acidic Properties. As a typical acid, it reacts readily with alkaUes, basic oxides, and carbonates to form salts. The largest iadustrial appHcation of nitric acid is the reaction with ammonia to produce ammonium nitrate. However, because of its oxidising nature, nitric acid does not always behave as a typical acid. Bases having metallic radicals ia a reduced state (eg, ferrous and staimous hydroxide becoming ferric and stannic salts) are oxidized by nitric acid. Except for magnesium and manganese ia very dilute acid, nitric acid does not Hberate hydrogen upon reaction with metals. 

A) A mixture of 333 parts of 4-(1 -piperazinyDphenol dihydrobromide, 11.2 parts of acetic acid anhydride, 42 parts of potassium carbonate and 300 parts of 1,4-dioxane is stirred and refluxed for 3 days. The reaction mixture is filtered and the filtrate is evaporated. The solid residue is stirred in water and sodium hydrogen carbonate is added. The whole is stirred for 30 minutes. The precipitated product is filtered off and dissolved in a diluted hydrochloric acid solution. The solution is extracted with trichloromethane. The acid aqueous phase is separated and neutralized with ammonium hydroxide. The product is filtered off and crystallized from ethanol, yielding 5.7 parts of 1 acetyl-4-(4-hydroxyphenyl)piperazine MP 181.3°C. 

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