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Orbital outer shell

Phosphorus and sulfur are the third-row analogs of nitrogen and oxygen, and the bonding in both can be described using hybrid orbitals. Because of their positions in the third row, however, both phosphorus and sulfur can expand their outer-shell octets and form more than the typical number of covalent bonds. Phosphorus, for instance, often forms five covalent bonds, and sulfur occasionally forms four. [Pg.20]

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 octet rule tells us that eight electrons fill the outer shell of an atom to give a noble-gas ns1ns(l valence-shell configuration. However, when the central atom in a molecule has empty d-orbitals, it may be able to accommodate 10, 12, or even more electrons. The electrons in such an expanded valence shell may be present as lone pairs or may be used by the central atom to form additional bonds. [Pg.198]

In bivalent nickel, palladium, or platinum there are eight electrons in the outer d subshell. Putting them two to an orbital, they occupy a minimum of four of the five d orbitals, leaving only one d orbital available for bond formation through combination with s, px, py, and pz of the next outer shell. It is found that only four strong bond orbitals can be formed. These four lie in a plane and are directed towards the four comers of a... [Pg.156]

In NF3, with each atom having four orbitals in its outer shell, there is no way for one fluorine atom to be attached to the nitrogen atom by a double bond and the other two by single bonds and to provide orbitals for the... [Pg.335]

Here the phosphorus atom has four shared electron pairs and one unshared pair, using five orbitals. (In PC15, eg, the transargononic phosphorus atom has five shared pairs in its outer shell.) However, because of the electroneutrality principle such a structure is allowed only for structure 1. Transargononic structures do not occur for first-row atoms, so this phenomenon is not found in NF3. These ideas concerning the bonding in NF3 and PF3 are implicit in the discussion by Marynick, Rosen and Liebman61 of the inversion barriers of these molecules. [Pg.337]

The symbol ( S—]+ represents tercovalent argononic sulfur. Like Si, it is argononic in that, counting shared as well as unshared electron pairs, it has four pairs in its outer shell, giving it the electron number of argon. A tercovalent argononic sulfur atom resembles a normal (neutral) tercovalent phosphorus atom. The bond orbitals of S + are similar to those of S. ... [Pg.619]

The most common reaction of carbanions is combination with a positive species, usually a proton, or with another species that has an empty orbital in its outer shell (a Lewis acid-base reaction) ... [Pg.237]

In the Brpnsted picture, the acid is a proton donor, but in the Lewis picture the proton itself is the acid since it has a vacant orbital. A Brpnsted acid becomes, in the Lewis picture, the compound that gives up the actual acid. The advantage of Lewis theory is that it correlates the behavior of many more processes. For example, AICI3 and BF3 are Lewis acids because they have only 6 electrons in the outer shell and have room for 8. Both SnCU and SO3 have eight, but their central elements, not being in the first row of the periodic table, have room for 10 or 12. Other Lewis acids are simple cations, like Ag. The simple reaction A + B- A—B is not very common in organic chemistry, but the scope of the Lewis picture is much larger because reactions of the types... [Pg.339]

Electrons that are in filled sets of orbitals between the nucleus and outer shell electrons shield the outer shell electrons partially from the effect of the protons in the nucleus this effect is called nuclear shielding. [Pg.79]

So, in summary, the principal differences between Cl2(g) and NaCl(S) lie in the location and the interactions of electrons in the atoms outer shells. We say these electrons reside in an atom s frontier orbitals, meaning that we can ignore the inner electrons, which are tightly bound to the nucleus. [Pg.59]

In the modern periodic table, horizontal rows are known as periods, and are labeled with Arabic numerals. These correspond to the principal quantum numbers described in the previous section. Because the outer shells of the elements H and He are 5 rather than p orbitals, these elements are usually considered differently from those in the rest of the table, and thus the 1st period consists of the elements Li, Be, B, C, N, O, F, and Ne, and the 2nd Na to Ar. Periods 1 and 2 are known as short periods, because they contain only eight elements. From the discussion above, it can be seen that these periods correspond to the filling of the p orbitals (the 2p levels for the first period, and the 3p for the second), and they are consequently referred to as p-block elements. The 3rd and 4th periods are extended by an additional series of elements inserted after the second member of the period (Ca and Sr respectively), consisting of an extra ten elements (Sc to Zn in period 3 and Y... [Pg.245]

It is seen from their orbital structures that hydrogen and fluorine both need to share 1 electron to complete their outer shells. Therefore the orbital representation of HF molecule is ... [Pg.12]

Soft Low-charge density Large ionic radius Easily excited outer shell electrons Cu+ High polarizability Low electronegativity Low-energy vacant orbitals Easily oxidized RSH, RS-, CN", CO... [Pg.16]

As concerns the spontaneous transmutations undergone by the radioactive elements, the facts appear to indicate (or, at least, can be brought into some sort of order by supposing) the atom to consist of a central nucleus and an outer shell, as suggested by Sir Ernest Rutherford. The nucleus may be compared to the sun of a solar system. It is excessively small, but in it the mass of the atom is almost entirely concentrated. It is positively charged, the charge being neutralised by that of the free electrons which revolve like planets about it, and which by their orbits account for the... [Pg.3]

Since the overlap of an inner shell on one ion with the outer shell on another ion is at least on order of magnitude less than the outer-shell-outer-shell overlaps, only the 5 orbital in Equation 11 for I" will participate appreciably in the overlap deformation. Using this approximation, Equation 11 becomes... [Pg.138]

We recall that the amount of s character in the bonding orbitals of Te is a = 0.18. Assuming that only the outer shell electrons effect a change in electron density at the Te nucleus and that the electron density at the Te nucleus is proportional to the summation over all outer shell orbitals of the number of electrons in an orbital, weighted by the 5 character of the orbital, we have for the ratio of electron densities at the Te nucleus in Na2Te04 and Te ... [Pg.155]

The 3d orbitals in TM ions have a relatively large radius and are unshielded by outer shells, so that strong ion-lattice coupling tend to occur in TM ions. As a result, the spectra of TM ions present both broad (S > 0) and sharp (S 0) bands, opposite to the spectra of (RE) + ions, discussed in section 6.2.1, which only showed sharp bands (S 0). [Pg.211]


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See also in sourсe #XX -- [ Pg.59 , Pg.460 ]




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Outer-shell orbital radius

Shells orbitals

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