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Nitrogen chemical properties

Among the non-metals, nitrogen and chlorine, for example, are gases, but phosphorus, which resembles nitrogen chemically, is a solid, as is iodine which chemically resembles chlorine. Clearly we have to consider the physical and chemical properties of the elements and their compounds if we are to establish a meaningful classification. [Pg.1]

Ammonia is a colourless gas at room temperature and atmospheric pressure with a characteristic pungent smell. It is easily liquefied either by cooling (b.p. 240 K) or under a pressure of 8-9 atmospheres at ordinary temperature. Some of its physical and many of its chemical properties are best understood in terms of its structure. Like the other group head elements, nitrogen has no d orbitals available for bond formation and it is limited to a maximum of four single bonds. Ammonia has a basic tetrahedral arrangement with a lone pair occupying one position ... [Pg.216]

Chemical Properties. Although the chemical properties of the trivalent lanthanides are quite similar, some differences occur as a consequence of the lanthanide contraction (see Table 3). The chemical properties of yttrium are very similar too, on account of its external electronic stmcture and ionic radius. Yttrium and the lanthanides are typical hard acids, and bind preferably with hard bases such as oxygen-based ligands. Nevertheless they also bind with soft bases, typicaUy sulfur and nitrogen-based ligands in the absence of hard base ligands. [Pg.540]

Chemical Properties The formation of salts with acids is the most characteristic reaction of amines. Since the amines are soluble in organic solvents and the salts are usually not soluble, acidic products can be conveniendy separated by the reaction with an amine, the unshared electron pair on the amine nitrogen acting as proton acceptor. Amines are good nucleophiles reactions of amines at the nitrogen atom have as a first step the formation of a bond with the unshared electron pair of nitrogen, eg, reactions with acid anhydrides, haUdes, and esters, with carbon dioxide or carbon disulfide, and with isocyanic or isothiocyanic acid derivatives. [Pg.198]

Chemical Properties. The presence of both a carbocycHc and a heterocycHc ring faciUtates a broad range of chemical reactions for (1) and (2). Quaternary alkylation on nitrogen takes place readily, but unlike pyridine both quinoline and isoquinoline show addition by subsequent reaction with nucleophiles. Nucleophilic substitution is promoted by the heterocycHc nitrogen. ElectrophiHc substitution takes place much more easily than in pyridine, and the substituents are generally located in the carbocycHc ring. [Pg.389]

Figure 5. Niels Bohr came up with the idea that the energy of orbiting electrons would be in discrete amounts, or quanta. This enabled him to successfully describe the hydrogen atom, with its single electron, In developing the remainder of his first table of electron configurations, however, Bohr clearly relied on chemical properties, rather than quantum theory, to assign electrons to shells. In this segment of his configuration table, one can see that Bohr adjusted the number of electrons in nitrogen s inner shell in order to make the outer shell, or the reactive shell, reflect the element s known trivalency. Figure 5. Niels Bohr came up with the idea that the energy of orbiting electrons would be in discrete amounts, or quanta. This enabled him to successfully describe the hydrogen atom, with its single electron, In developing the remainder of his first table of electron configurations, however, Bohr clearly relied on chemical properties, rather than quantum theory, to assign electrons to shells. In this segment of his configuration table, one can see that Bohr adjusted the number of electrons in nitrogen s inner shell in order to make the outer shell, or the reactive shell, reflect the element s known trivalency.
The German physicist Lothar Meyer observed a periodicity in the physical properties of the elements at about the same time as Mendeleev was working on their chemical properties. Some of Meyer s observations can be reproduced by examining the molar volume for the solid element as a function of atomic number. Calculate the molar volumes for the elements in Periods 2 and 3 from the densities of the elements found in Appendix 2D and the following solid densities (g-cuU ) nitrogen, 0.88 fluorine, 1.11 neon, 1.21. Plot your results as a function of atomic number and describe any variations that you observe. [Pg.178]

With its oxygen functionality, graphite oxide has chemical properties more akin to those of layered disulfides or sheet silicates than to those of graphite (Gi, T1,A2). Many studies have been of an extremely applied nature the possibility of fluorination (LI, N1), redox potentials in the presence of hydrogen peroxide (V2), the apparent density (L2), the adsorption isotherms with nitrogen (L3), and the diffusion of Cs in graphite oxide (R2). [Pg.283]

In all cases where the chemical properties of these preparations have been studied the active material appears to be predominantly carbohydrate in nature, containing in the case of the A factor 50-70% of reducing sugar, 5.7% nitrogen and giving by colorimetric estimations 25-30% of glucosamine on hydrolysis. [Pg.204]

Another early suggestion was that some of the fullerene carbon atoms could be replaced by another element such as nitrogen or boron.1811 Such heterofullerenes are envisaged to have strongly altered chemical properties in comparison to the all-carbon structures.1811 For example, as the substitution number of an electronegative element such... [Pg.183]

The comparison of physical and chemical properties of Parylene-N and Parylene-F is shown in Table 18.4. Parylene-N is considerably less stable in air than in nitrogen as a result of oxidative degradation. However, the similarity between its behavior in air and in nitrogen suggests that Parylene-F has very good thermal oxidative stability, which is most likely the result of the high stability of the C—F bond, and provides evidence that oxidative attack starts at the benzylic C—H bonds in Parylene-N.15... [Pg.279]


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See also in sourсe #XX -- [ Pg.892 ]

See also in sourсe #XX -- [ Pg.10 ]




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