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Gain stability

Fluorine (F, atomic number 9) has seven outer electrons, one unpaired. Because it needs to obtain only one electron to fill its outer shell and gain stability, it is highly reactive. Neon (Ne, atomic number 10), on the other hand, has a filled outer shell. Like helium and its other column mates, the noble gases, neon does not readily react with any element. [Pg.806]

The density section of the tool, also seen in Figure 4-281, uses a 1.7 curie (Ci) of 137-cesium (Ce) gamma ray source in conjunction with two gain-stabilized scintillation detectors to provide a high-quality, borehole compensated density measurement. [Pg.986]

Polar bonds gain stability from the electrical attraction between the negative and positive fractional charges around the bonded atoms. Bonds between oxygen and other second-row elements exemplily this trend ... [Pg.641]

Starting with a dilute solution, for each doubling of the activities of the free ions on the left of these reactions, the activities of the ion pairs on the right sides must quadruple. As concentration increases, the ion pairs become progressively more important and eventually can come to overwhelm the free ions in solution. The higher temperature of the Red Sea brine also favors complexing because ion pairs gain stability relative to free ions as temperature increases. [Pg.101]

PCR is an alternative method to the much more used regression method PLS (Section 4.7). PCR is a strictly defined method and the model often gives a very similar performance as a PLS model. Usually PCR needs more components than PLS because no information ofy is used for the computation of the PCA scores this is not necessarily a disadvantage because more variance of X is considered and the model may gain stability. [Pg.163]

Exercise 1. Compute the range of gains stabilizing Gn(s) in the reactors in Table 1 and plot this ratio vs the reactor volume. [Pg.19]

Because the outermost shell of a carbon atom contains only four electrons, these atoms can gain stability by losing four electrons, adding four electrons, or sharing four additional electrons from another atom. When an atom loses electrons to another atom, adds electrons from another atom, or shares electrons with another atom, a chemical bond is formed. A chemical bond acts to hold atoms together. The strengths of the bonds vary, depending... [Pg.20]

The actinide elements are all radioactive. Their nuclei are unstable mainly because of their very high charges the attractive forces operating between the neutrons and protons do not fully balance the interproton repulsion. The nuclei consequently emit alpha particles, 4He2+, to gain stability, i.e. to lose mass. Examples of radioactive decay are given in Table 8.9. [Pg.169]

As indicated earlier, a dramatic difference is observed in the chemistry of Os(II) and Os(III), the former gaining stabilization from 1t acids and the latter from electron-rich Os(II) must depend entirely on the sixth ligand for stabilization through tt backbonding. [Pg.335]

Conformations of primary, secondary, and tertiary amides of (R,R)-tartaric acid, both symmetrically and asymmetrically substituted, have been studied ciys-tallographically [22, 24, 29, 30-40] Moreover, ab initio studies up to MP2 / 6-31G //RHF/6-31G level [41] for both the diamide and N,N,N ,N -tctramcthyl-diamide of (/ ,/ [-tartaric acid have been carried out [20, 22]. X-ray results have shown that primary and secondary amides of (R,R [-tartaric acid tend to adopt a conformation with the extended carbon chain - the Taa structure. In this Taa conformation both the a-hydroxy-amide moieties form planes and the structure gains stabilization from hydrogen bonding between donors, the NH, and acceptors, the proximal OH groups. Moreover, the Taa structure is favorably stabilized by the attraction of antiparallel local dipoles formed along distal C H and Csp2=0 bonds [18, 21, 22],... [Pg.190]

The conversion of higher substituted to less substituted olefins is not favored thermodynamically. This obstacle can be overcome when the newly formed C=C bond gains stabilization by conjugation with another double bond, e.g. C=0, or an aromatic unit, or by equilibration into a more stable product in a consecutive reaction. The E-Z geometry of the starting olefin may have a significant effect on the configuration and enantioselectivity in the product. [Pg.431]

A large negative value of AEa implies that a cation gains stability by forming an activated complex with pentagonal bipyramidal or square pyramidal symmetry. On this basis, cations such as Fe2+, Co2+, Ti3+, and V3+, as well as the 3d5 cations with zero CFSE, are predicted to show rapid reaction rates of substitution or leaching from a crystal structure. [Pg.335]

X = 0 is stable this state loses stability at Da = DaT simultaneously, the nontrivial solution gets physically meaningful values and gains stability. [Pg.115]

To gain stability, neutrons undergo decay reactions alpha emission, beta emission, positron emission, and electron capture are possible. [Pg.109]

Hemiacetal formation is reversible, and hemiacetals are stabilized by the same special structural features as those of hydrates. However, hemiacetals can also gain stability by being cyclic—when the carbonyl group and the attacking hydroxyl group are part of the same molecule. The reaction is now an intramolecular (within the same molecule) addition, as opposed to the intermolecular (between two molecules) ones we have considered so far. [Pg.145]

You will already realize from earlier chapters that, for an atom to gain stability when it forms a compound, it tries to gain or lose electrons to make its outer electronic... [Pg.105]

II. DIFFERENT MEANS FOR GAINING STABILITY A. Charge Segregation... [Pg.480]

Magnetic properties of polycyclic anions serve as a probe for the mode of delocalization of the added electrons. These anions gain stability either by minimizing paratropicity or by... [Pg.480]

It can be seen that compounds 27 and 28, which have relatively long tethers, behave like 22. Therefore, their two-electron reduction yields antiaromatic species, 27b2 and 28b2, which eventually cleave the solvent (giving 29 and 30 after reaction) as a means of gaining stability. [Pg.491]


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See also in sourсe #XX -- [ Pg.7 ]




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Finite-gain stability

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