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Nitrogen atoms, combination

The valence electrons of nitrogen and fluorine are five and seven respectively. In this case, to complete its octet nitrogen needs three more electrons and fluorine needs one more electron. Therefore one nitrogen atom combines with three fluorine atoms. [Pg.33]

The nitrogen atom in the N02 molecule has an incomplete octet, having a single unpaired electron. The unpaired electrons of the nitrogen atoms combine to form a single bond. [Pg.44]

The nitrogen atom has five electrons in its valence shell, so it needs to be involved in three covalent single bonds in order to obtain the stability that is conferred by having an octet of electrons. If two nitrogen atoms combine with each other so as to form a diatomic molecule, then each atom provides the three extra electrons that are needed by the other to satisfy the octet. [Pg.42]

A photoelectron spectrum of the nitrogen molecule is shown in Fig. 10.2 and the electronic structure is shown in Fig. 10.3.1 H 1 The two 2 orbitals of the nitrogen atoms combine to form the two orbitals indicated as 1 (bonding orbital) and 2 (antibonding orbital). The six Ip orbitals combine to form six orbitals. Of these six, three (marked 3, 4, and 5) are bonding orbitals. The electrons ejected from orbital 1 do not appear in the spectrum of Fig. 10.2 because the light energy used is smaller than the ionization potential of these electrons. [Pg.165]

One important use of catalysts is in catalytic converters on automobiles, which reduce the emission of exhaust gas pollutants such as carbon monoxide (CO), nitrogen oxides (NO., where x is variable), and unburned hydrocarbons. (See the chapter-opening diagrams and photograph for this chapter.) Air is introduced into the exhaust emissions from the automobile engine this mixture of gases then passes over the catalyst, which on its surface adsorbs molecules of CO, NO , and O2. The NO dissociates into N and O atoms, whereas the O2 dissociates into its atomic species. Pairs of nitrogen atoms combine to form N2 molecules, and carbon monoxide is oxidized to form... [Pg.121]

Cobalt compounds have been in use for centuries, notably as pigments ( cobalt blue ) in glass and porcelain (a double silicate of cobalt and potassium) the metal itself has been produced on an industrial scale only during the twentieth century. Cobalt is relatively uncommon but widely distributed it occurs biologically in vitamin B12 (a complex of cobalt(III) in which the cobalt is bonded octahedrally to nitrogen atoms and the carbon atom of a CN group). In its ores, it is usually in combination with sulphur or arsenic, and other metals, notably copper and silver, are often present. Extraction is carried out by a process essentially similar to that used for iron, but is complicate because of the need to remove arsenic and other metals. [Pg.401]

For a function to transform according to a specific irreducible representation means that the function, when operated upon by a point-group symmetry operator, yields a linear combination of the functions that transform according to that irreducible representation. For example, a 2pz orbital (z is the C3 axis of NH3) on the nitrogen atom... [Pg.590]

In deoxyhemoglobin, histidine F8 is liganded to the heme iron ion, but steric constraints force the Fe His-N bond to be tilted about 8° from the perpendicular to the plane of the heme. Steric repulsion between histidine F8 and the nitrogen atoms of the porphyrin ring system, combined with electrostatic repulsions between the electrons of Fe and the porphyrin 77-electrons, forces the iron atom to lie out of the porphyrin plane by about 0.06 nm. Changes in... [Pg.485]

It would be expected that the stabilization of the adsorbed species by an extended conjugated system should increase with the number of aromatic rings in the adsorbed azahydrocarbon. However, data suitable for comparison are available only for phenanthridine, benzo-[/]quinoline, and benzo[h] quinoline. The large difference in the yields of biaryl obtained from the last two bases could be caused by steric interaction of the 7,8-benz-ring with the catalyst, which would lower the concentration of the adsorbed species relative to that with benzo[/]quinoline. The failure of phenanthridine to yield any biaryl is also noteworthy since some 5,6-dihydrophenanthridine was formed. This suggests that adsorption on the catalyst via the nitrogen atom is possible, but that steric inhibition to the combination of the activated species is involved. The same effect could be responsible for the exclusive formation of 5,5 -disubstituted 2,2 -dipyridines from 3-substi-tuted pyridines, as well as for the low yields of 3,3, 5,5 -tetramethyl-2,2 -bipyridines obtained from 3,5-lutidine and of 3,3 -dimethyl-2,2 -... [Pg.196]

The Lewis structures of the oxides of nitrogen are shown in Figure 21.6. Two of these species, NO and NO are paramagnetic, with one impaired electron. When nitrogen dioxide is cooled, it dimerizes the unpaired electrons combine to form a single bond between the two nitrogen atoms ... [Pg.564]

This section treats seven-membered ring systems with maximum unsaturation containing within the ring two or more oxygen, sulfur or nitrogen atoms, or a combination of these.1... [Pg.299]


See other pages where Nitrogen atoms, combination is mentioned: [Pg.10]    [Pg.3]    [Pg.137]    [Pg.11]    [Pg.151]    [Pg.13]    [Pg.12]    [Pg.48]    [Pg.794]    [Pg.70]    [Pg.10]    [Pg.3]    [Pg.137]    [Pg.11]    [Pg.151]    [Pg.13]    [Pg.12]    [Pg.48]    [Pg.794]    [Pg.70]    [Pg.2424]    [Pg.326]    [Pg.179]    [Pg.191]    [Pg.11]    [Pg.52]    [Pg.74]    [Pg.386]    [Pg.286]    [Pg.47]    [Pg.200]    [Pg.76]    [Pg.38]    [Pg.328]    [Pg.27]    [Pg.148]    [Pg.230]    [Pg.133]    [Pg.136]    [Pg.185]    [Pg.197]    [Pg.197]    [Pg.173]    [Pg.152]    [Pg.826]    [Pg.949]    [Pg.424]    [Pg.250]    [Pg.718]   
See also in sourсe #XX -- [ Pg.150 , Pg.151 ]




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Atomic combinations

Atoms Combined

Atoms, combination

Nitrogen atom

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