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Electronic orbitals

Once the 2s and 2p orbitals are filled the next level is the 3s followed by the 3p 3py and 3p orbitals Electrons in these orbitals are farther from the nucleus than those in the 2s and 2p orbitals and are of higher energy... [Pg.10]

The molecular orbital approach to chemical bonding rests on the notion that as elec trons m atoms occupy atomic orbitals electrons m molecules occupy molecular orbitals Just as our first task m writing the electron configuration of an atom is to identify the atomic orbitals that are available to it so too must we first describe the orbitals avail able to a molecule In the molecular orbital method this is done by representing molec ular orbitals as combinations of atomic orbitals the linear combination of atomic orbitals molecular orbital (LCAO MO) method... [Pg.61]

Its powerful oxidizing properties result from the tight binding of its valence sheU 7-orbital electrons. No commercial source is available. [Pg.235]

The emission of y rays follows, in the majority of cases, what is known as P decay. In the P-decay process, a radionuclide undergoes transmutation and ejects an electron from inside the nucleus (i.e., not an orbital electron). For the purpose of simplicity, positron and electron capture modes are neglected. The resulting transmutated nucleus ends up in an excited nuclear state, which prompdy relaxes by giving offy rays. This is illustrated in Figure 2. [Pg.673]

Bahn, /. way, road, track path orbit trajectory railway breadth (of cloth), bahnbrechend, p.a. pioneer, epoch-making. Bahn-brecher, m. pioneer, -durchmesser, m. orbital diameter, -ebene, /. orbital plane, -elektron, n. orbital electron, bahnen, v.t. beat, smooth, clear (a way). Bahn-hof, m. (railway) station, -impuls, m. linear momentum orbital moment, -sdileife, -schlinge, /., orbital loop, -spur, /, track, -tibergang, m. orbital transition, -zug, m. railway train. [Pg.55]

Volume around nucleus occupied by orbiting electrons... [Pg.4]

There are three common ways by which nuclei can approach the region of stability (1) loss of alpha particles (a-decay) (2) loss of beta particles (/3-decay) (3) capture of an orbital electron. We have already encountered the first type of radioactivity, a-decay, in equation (/0). Emission of a helium nucleus, or alpha particle, is a common form of radioactivity among nuclei with charge greater than 82, since it provides a mechanism by which these nuclei can be converted to new nuclei of lower charge and mass which lie in the belt of stability. The actinides, in particular, are very likely to decay in this way. [Pg.417]

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.
For 7-ray energies below 1 MeV (the range of interest) there are two principal modes of interaction with matter — Compton scattering and photoelectron absorption. Compton scattering is the elastic scattering of the 7 photon by an orbital electron in which part of the incident 7-energy is imparted to the recoiling electron. [Pg.380]

Unsaturated organic molecules, such as ethylene, can be chemisorbed on transition metal surfaces in two ways, namely in -coordination or di-o coordination. As shown in Fig. 2.24, the n type of bonding of ethylene involves donation of electron density from the doubly occupied n orbital (which is o-symmetric with respect to the normal to the surface) to the metal ds-hybrid orbitals. Electron density is also backdonated from the px and dM metal orbitals into the lowest unoccupied molecular orbital (LUMO) of the ethylene molecule, which is the empty asymmetric 71 orbital. The corresponding overall interaction is relatively weak, thus the sp2 hybridization of the carbon atoms involved in the ethylene double bond is retained. [Pg.52]

The ground term of the cP configuration is F. That of is also F. Those of and d are " F. We shall discuss these patterns in Section 3.10. For the moment, we only note the common occurrence of F terms and ask how they split in an octahedral crystal field. As for the case of the D term above, which splits like the d orbitals because the angular parts of their electron distributions are related, an F term splits up like a set of / orbital electron densities. A set of real / orbitals is shown in Fig. 3-13. Note how they comprise three subsets. One set of three orbitals has major lobes directed along the cartesian x or y or z axes. Another set comprises three orbitals, each formed by a pair of clover-leaf shapes, concentrated about two of the three cartesian planes. The third set comprises just one member, with lobes directed equally to all eight corners of an inscribing cube. In the free ion, of course, all seven / orbitals are degenerate. In an octahedral crystal field, however, the... [Pg.46]

Electron propagator theory generates a one-electron picture of electronic structure that includes electron correlation. One-electron energies may be obtained reliably for closed-shell molecules with the P3 method and more complex correlation effects can be treated with renormalized reference states and orbitals. To each electron binding energy, there corresponds a Dyson orbital that is a correlated generalization of a canonical molecular orbital. Electron propagator theory enables interpretation of precise ab initio calculations in terms of one-electron concepts. [Pg.49]

The n orbital amplitudes of ethene are identical on both carbons. Unsymmetrical substitutions polarize the n orbital. Electron acceptors or electrophiles attack the carbon with the larger r amplitude. The polarization of frontier orbitals is important for regioselectivities of reactions. Here, mechanism of the n orbital polarization of ethene by methyl substitution [4] is described (Scheme 5). [Pg.60]

C22-0011. Identify the nuclides that decay in the following manner (a) A nuclide undergoes 3 and y decay to give Z = 58 and A = 140 (b) A nuclide undergoes a decay to give polonium-218 and (c) A nuclide captures an orbital electron to give tellurium with 73 neutrons. [Pg.1573]


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Electron orbitals

Electron, orbiting

Orbital electrons

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