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Dinitrogen tetroxide decomposition

Hence dinitrogen tetroxide (sometimes mixed with an organic solvent) can be used to prepare anhydrous metal nitrates (many heavy metal nitrates are hydrated when prepared in aqueous solution, and they cannot be dehydrated without decomposition). [Pg.233]

The decomposition of dinitrogen tetroxide produces nitrogen dioxide N2 04(g) -> 2 N02(g)... [Pg.1009]

Dinitrogen pentoxide is a colorless crystalline solid which sublimes without melting at 32.5 °C at atmospheric pressure." Dinitrogen pentoxide is inherently unstable and readily decomposes to oxygen and dinitrogen tetroxide at room temperature as shown in Equation (9.1). The rate of decomposition is temperature dependent with a half-life of 10 days at 0 °C and 10 hours at 20 It is stable for 2 weeks at —20 °C and up to 1 year at temperatures below —60 °C. [Pg.351]

On a laboratory scale the dehydration of nitric acid with phosphorous pentoxide is a convenient route to dinitrogen pentoxide (Equation 9.2). Isolation is achieved by sublimation and collection in a cold trap at -78 °C, but the quality and yield of dinitrogen pentoxide is poor if the system is not continually flushed with a stream of ozone, a consequence of facile decomposition to dinitrogen tetroxide. [Pg.352]

The nitrate salt prepared by this method is hydrated. It cannot be dehydrated fully without decomposition. Anhydrous CuNOs may be prepared by dissolving copper metal in a solution of dinitrogen tetroxide, N2O4, in ethyl acetate. Upon crystaUization, an N2O4 adduct of Cu(N03)2 that probably has the composition [NO [Cu(N03)3] is obtained. This adduct, on heating at 90°C, yields blue anhydrous copper(II) nitrate which can be sublimed in vacuum at 150°C and coUected. [Pg.270]

It is a practice in some countries to add a small amount of sodium hydrogen carbonate to the powder dough, to neutralize dinitrogen tetroxide evolved during the decomposition of the powder. This would lead to formation of sodium nitrate... [Pg.555]

In previous chapters, we ve generally assumed that chemical reactions result in complete conversion of reactants to products. Many reactions, however, do not go to completion. Take, for example, the decomposition of the colorless gas dinitrogen tetroxide (N2O4) to the dark brown gas nitrogen dioxide (NO2). [Pg.528]

Addison N. Hodge, The Explosive Decomposition of Triethylammonium Nitrate-Dinitrogen Tetroxide Mixtures , Chem Ind 1953, 1315 CA 48,3691 (1954)... [Pg.863]

The decomposition of nitronium perchlorate between 70° and 112° C. has been reported by Cordes (2) to proceed to the gaseous products NO2, Cl2, C102, NO3CI, and 02. As a result of some screening experiments we were aware that at 65° C. in sealed tubes, nitrosonium perchlorate was a major decomposition product. We were also aware that dinitrogen tetroxide, at least in the liquid phase, would quantitatively convert nitronium perchlorate to nitrosonium perchlorate. Thus, a mechanism involving only gaseous products appeared unlikely. [Pg.88]

A mechanism for the decomposition of NO2CIO4 in the presence of its decomposition products, as in a sealed tube, would include the dinitrogen tetroxide-catalyzed conversion of NO2CIO4 to NOCIO4 in addition to Reactions 1 and 2. [Pg.96]

This problem can best be solved by algebraic methods. The reaction that we are interested in is the decomposition of some of the dinitrogen tetroxide, to reach a new steady state. Let us introduce the unknown quantity x to represent the number of moles of dinitrogen tetroxide in the liter flask which decompose as the new equilibrium is reached ... [Pg.399]

The great rate at which a chemical reaction may occur has been mentioned above in the discussion of the NOg-NgO equilibrium. It was pointed out that the decomposition of dinitrogen tetroxide or reformation of these molecules from nitrogen dioxide molecules occurs within... [Pg.407]

Iron Pentacarbonyl. In its reactions with liquid dinitrogen tetroxide this compound follows the pattern outlined above, and the remarks on reactions of nickel carbonyl probably apply here also. The solvate, Fe(N03)3.N204, is produced (4). This has the structure N0+[Fe(N03)4] in the solid state it is volatile without decomposition, and is believed to be a five-coordinate complex, Fe(N0)(N03)4, in the vapor state. We have not yet succeeded in isolating the simple trinitrate, Fe(N03)3, by removal of N2O4. [Pg.137]

Dinitrogen tetroxide, N2O4, a light-brown gas or liquid (bp 21.5-22.5 °C), is commercially available and is prepared from nitrososulfuric acid and potassium nitrate [453] or, more simply, by the thermal decomposition... [Pg.18]

A very simple and gentle oxidation of primary alcohols to aldehydes is their treatment in chloroform or carbon tetrachloride with a solution of dinitrogen tetroxide, obtained either commercially or by thermal decomposition of lead nitrate. The reaction is carried out at 0 °C through room temperature and gives high yields (91-98%) of benzaldehydes (equation 206) [454]. [Pg.115]

If the energy required is not too great, some other reactions that absorb energy will occur because they take energy from their surroundings. An example is the decomposition of dinitrogen tetroxide, which occurs at room temperature. [Pg.280]

Oxidation of amides (White deamination) [follows 1, 327], White223 has described the benzoylatien of 2-phenylethylamine (1), the reaction of (2) with dinitrogen tetroxide to give (3), which on thermal decomposition at 77° affords 2-phenylethyl benzoate (4). [Pg.364]

Combustible liquid (flash point 230°F/110°C cc). Ignites spontaneously in air. Sunlight causes rapid decomposition. Reacts with water or steam, producing toxic and flammable vapors. Violent reaction with strong oxidizers, dinitrogen tetroxide. Incompatible with strong acids, hydroxylamine. [Pg.728]


See other pages where Dinitrogen tetroxide decomposition is mentioned: [Pg.499]    [Pg.499]    [Pg.7]    [Pg.248]    [Pg.1779]    [Pg.334]    [Pg.88]    [Pg.408]    [Pg.512]    [Pg.41]    [Pg.396]    [Pg.411]    [Pg.193]    [Pg.334]    [Pg.896]    [Pg.40]    [Pg.197]    [Pg.259]    [Pg.329]    [Pg.329]    [Pg.405]    [Pg.437]    [Pg.461]    [Pg.525]    [Pg.695]    [Pg.697]    [Pg.740]    [Pg.1027]    [Pg.1027]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 ]




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