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Definitions, charges

The possible formation of a dipole is a feature of covalent bonding but it is obvious that an ionic bond results in a definite unequal distribution of electrons within a molecule and such molecules (or ions) are extremely polar. However, the fact that they carry a definite charge enables additional separation techniques to be applied. The rate of migration in an electric field (electrophoresis) and the affinity for ions of opposite charge (ion-exchange chromatography) are extremely valuable techniques in the separation of ionic species. [Pg.93]

Experimental conditions were 727, 756, and 794 K isothermal reactor temperature 827-, 1220-, and 2619-kPa hydrogen pressure 138- and 345-kPa hydrocarbon pressure and 1 to 26 liquid hourly space velocity. (See Section II for definition.) Charge stocks consisted of three C6 component blends (blends included 53/19/23/5, 25/75/0/0, and 0/0/50/50 wt. % hexane/methylcyclopentane/cyclohexane/benzene), C6 to C7 component naphthas (322-366 K TBP Kirkuk, Mid-Continent, and Nigerian), a C6 to C8 component naphtha (322-416 K TBP Mid-Continent), and C6 to C12 component naphthas (322-461 K TBP Arab Light, Mid-Continent, and... [Pg.227]

Photolysis of allyl iodide in thiophene gives a mixture of 2-allyl- (63.8%) and 3-allyl-(36.2%) thiophenes (77JOC1570). This is in contrast to homolytic phenylation, where almost exclusive 2-phenylation takes place (Section 3.14.2.9). It has been suggested that the rate-determining step in the allyl substitution reaction has a small but definite charge-transfer character. [Pg.795]

There is no thermodynamic equilibrium between the ideally polarizable electrode (more exactly the metal phase) and the solution phase because there is no common component capable of changing its charge and being transferred between the phases, conditions necessary for equilibrium. The state of an ideally polarizable electrode is well defined only if an external source is used to maintain a constant polarization potential, i.e., the double-layer capacitor charged with a definite charge. The polarization potential is an independent parameter of the system. [Pg.204]

The traditional description of individual properties of molecules is based on the assumption of a definite charge distribution in them determined by the symmetry of the nuclear framework. The light electrons, moving in the field of heavy nuclei, adjust (adiabatically) their space distribution to the nuclear configuration, which results from the self-consistent electrostatic interaction of the electrons and nuclei. [Pg.2]

In batch distillation (whether of the simple or countercurrent type) a definite charge is put into the still and treated. A distinction should be made between fractional and unfractionated distillation. In the latter, the whole distillate is collected in one lot, and the initial material is thus separated into two fractions the distillate and... [Pg.245]

The difference in electron binding energies between the elements can be understood by studying the forces that hold the atoms together. Each element in the periodic table has a specific number of protons in its atomic nucleus and hence, a definite charge. Due to the electrostatic attraction between the atomic nucleus and the electrons, the binding... [Pg.30]

Deviations from normal copolymerization behavior can be caused not only by a penultimate chain end effect but also by the formation of charge transfer complexes. Definitive charge transfer complexes can be formed by two monomer molecules of widely different polarities, i.e., an electron donor and an electron acceptor. The presence of such complexes can frequently be inferred from accentuated bands in the visible and ultraviolet spectra. [Pg.782]

Now, if an eigenstate of the Hamiltonian is also an eigenstate of J, which is automatically the case for a state of definite charge when the number of charges equals the number of orbitals, then... [Pg.226]

In a consideration of the general properties of the bond of carbon to silicon, we must also consider the influence of the basic portion of the molecule. In a covalent bond between carbon and silicon there should be a definite charge distribution, since silicon more readily donates its electron than does carbon. Consequently, the electron cloud that forms the -Si-C-bond is somewhat denser close to the carbon atom, because the charge of its nucleus is not shielded by a full L-shell, and hence exerts a stronger Coulomb attraction on the electrons responsible for the bond. As a result, the carbon atom is more electronegative than the silicon atom, with the same substituents on both atoms. [Pg.292]

Let s use this approach to find the electrostatic potential that attracts a point charge Q at a distance a. from a conducting planar surface. By definition, charges move freely in a conducting surface. As long as no electric current is flowing, the charges in a conductor experience no electrostatic force within the... [Pg.399]

Solution The three points mentioned are correspondingly disposed just inside the inner sphere (domain I, < EJ, between the two spheres (domain II, R Gauss theorem to solve the problem. First, we have to solve the... [Pg.264]


See other pages where Definitions, charges is mentioned: [Pg.553]    [Pg.200]    [Pg.12]    [Pg.12]    [Pg.124]    [Pg.261]    [Pg.253]    [Pg.75]    [Pg.62]    [Pg.15]    [Pg.174]    [Pg.28]    [Pg.478]    [Pg.154]    [Pg.5]    [Pg.12]    [Pg.216]    [Pg.3253]    [Pg.67]    [Pg.39]   
See also in sourсe #XX -- [ Pg.16 , Pg.17 ]




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