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Nitrogen-nitrogen

Released material Nitrogen Nitrogen Nitrogen Nitrogen... [Pg.521]

Residue from Nitrogen Nitrogen Nitrogen c7 Vanadium Nickel... [Pg.212]

No cleavage of nitrogen-nitrogen, nitrogen-carbon, or carbon-halogen bonds. [Pg.46]

With the heats of formation of the amino, and alkyl amino radicals, it is possible to calculate the dissociation energies for a number of carbon-nitrogen, nitrogen-nitrogen and nitrogen-hydrogen bonds. These are shown in Table 10, together with the relevant heats of formation of the parent compounds, in which the bonds occur. [Pg.140]

C. G. Overberger, J.-P. Ansehne, andj. G. Lombardino, Organic Compounds with Nitrogen—Nitrogen Bonds, The Ronald Press Co., New York, 1966, Chapt. 4. [Pg.233]

Gaseous and Hquid nitrogen Nitrogen, min % (mol/mol) Oxygen Water, ppm (v/v) Dew point, °C Total hydrocarbon a content... [Pg.79]

Many azo dyes, such as tartrazine (Section 4.04.4.1.3), are susceptible to reduction by bacterial reductases in the intestinal flora. Azo reduction is believed to proceed through a hydrazo intermediate that undergoes subsequent reductive cleavage of the nitrogen-nitrogen bond to yield the arylamine derivatives (B-80MI40406). [Pg.302]

In the modified Raschlg process , used by Bayer A.G. and by Mobay Chem. Co. for large scale production of hydrazine, the intermediacy of an oxaziridine could be clearly evidenced (81MI50800). In this process ammonia and hypochlorite are reacted in the presence of acetone to form ketazine (302). Nitrogen-nitrogen bond formation is faster by a factor of about 1000 in the presence of acetone than in its absence. Thus acetone does not merely trap hydrazine after formation, but participates in the N —N bond forming reaction. Very fast formation of oxaziridine (301), which is isolable, is followed by its likewise fast reaction with ammonia. [Pg.235]

IV-Nitrosqanilides are an alternative source of aryl radicals. There is a close mechanistie relationship to the decomposition of azo compounds. The JV-nitrosoanilides rearrange to intermediates that have a nitrogen-nitrogen double bond. The intermediate then decomposes to generate aryl radieals. ... [Pg.674]

Repeat your analysis for pyridazine. Do any of the resonanee eontributors provide an adequate deseription of its geometry Does pyridazine incorporate a nitrogen-nitrogen double bond (Refer to hydrazine and to diimide as examples of moleeules ineorporating NN single and double bonds, respeetively.)... [Pg.39]

Stickstoff-. nitrogen, nitrogenous, nitric, nitrous, nitride of. -ammonium, n. ammonium nitride. [Pg.428]

Hydrazones can be reduced to the hydrazine, and, if continued, hydrogenolysis of the nitrogen-nitrogen bond ensues. Raney nickel (14,15,31,133,134, 178,185), platinum (42,52,139,155,167), and rhodium (130) have each been... [Pg.168]

Nitrogen Nitrogen is virtually insoluble in pure sodium (10 p.p.m. at 500°C and 1 MN/m ). It is, however, quite soluble in molten lithium (2 (XX) p.p.m. at 3(X)°C and l(X)kN/m ) and can accelerate the already corrosive action of lithium, particularly on steels. Zirconium and yttrium have been used to getter nitrogen. [Pg.431]

Energy from radiation can cause chemical bonds to break. To break the nitrogen-nitrogen bond in N2 gas, 941 kj/mol is required. [Pg.159]


See other pages where Nitrogen-nitrogen is mentioned: [Pg.7]    [Pg.106]    [Pg.106]    [Pg.7]    [Pg.135]    [Pg.251]    [Pg.683]    [Pg.636]    [Pg.101]    [Pg.8]    [Pg.995]    [Pg.995]    [Pg.320]    [Pg.419]    [Pg.826]    [Pg.216]    [Pg.243]    [Pg.124]    [Pg.74]    [Pg.82]    [Pg.188]    [Pg.219]    [Pg.46]    [Pg.340]    [Pg.255]    [Pg.168]    [Pg.168]    [Pg.169]    [Pg.846]    [Pg.74]    [Pg.190]    [Pg.298]    [Pg.728]    [Pg.1012]    [Pg.128]    [Pg.615]   


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