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Ionization definition

In this equation, the electronegativity of an atom is related to its ionization potential, 1, and its electron affinity, E. Mulhken already pointed out that in this definition the ionization potential, and the electron affinity, E, of valence states have to be used. This idea was further elaborated by Hinze et al. [30, 31], who introduced the concept of orbital electronegativity. [Pg.330]

According to the Arrhenius definitions an acid ionizes m water to pro duce protons (H" ) and a base produces hydroxide ions (HO ) The strength of an acid is given by its equilibrium constant for ionization m aqueous solution... [Pg.49]

Achiral (Section 7 1) Opposite of chiral An achiral object is supenmposable on its mirror image Acid According to the Arrhenius definition (Section 1 12) a substance that ionizes in water to produce protons Accord mg to the Br0nsted-Lowry definition (Section 1 13) a sub stance that donates a proton to some other substance According to the Lewis definition (Section 1 17) an electron pair acceptor... [Pg.1274]

Plasma can be broadly defined as a state of matter in which a significant number of the atoms and/or molecules are electrically charged or ionized. The generally accepted definition is limited to situations whereia the numbers of negative and positive charges are equal, and thus the overall charge of the plasma is neutral. This limitation on charge leaves a fairly extensive subject area. The vast majority of matter ia the universe exists ia the plasma state. Interstellar space, interplanetary space, and even the stars themselves are plasmas. [Pg.106]

The fundamental parameters in the two main methods of achieving ignition are basically the same. Recent advances in the field of combustion have been in the development of mathematical definitions for some of these parameters. For instance, consider the case of ignition achieved by means of an electric spark, where electrical energy released between electrodes results in the formation of a plasma in which the ionized gas acts as a conductor of electricity. The electrical energy Hberated by the spark is given by equation 2 (1), where V = the potential, V 7 = the current. A 0 = the spark duration, s and t = time, s. [Pg.516]

Equilibriiun reactions The interaction of ionizable compounds in which the products obtained tend to revert to the substance from which they were formed until a balance is reached in which both reactants and pacts are present in definite ratios. [Pg.437]

Next we turn to the magnitudes of the p constants. Evidently if p = 0, there is no substituent effect on reactivity. Moreover because p = -I-1.000 by definition for the aqueous ionization of benzoic acids, we have a scale calibration of sorts. Wiberg gives examples of p as a measure of the extent of charge development in the transition state. McLennan" has pointed out that p values must first be adjusted for the transmission factor before they can be taken as measures of charge devel-... [Pg.331]

Besides the already mentioned Fukui function, there are a couple of other commonly used concepts which can be connected with Density Functional Theory (Chapter 6). The electronic chemical potential p is given as the first derivative of the energy with respect to the number of electrons, which in a finite difference version is given as half the sum of the ionization potential and the electron affinity. Except for a difference in sign, this is exactly the Mulliken definition of electronegativity. ... [Pg.353]

The values of Hn and E are zero for water, by virtue of the constants 1.74 and 2.60. In these definitions, pKa refers to the acid ionization constant of the conjugate acid of the nucleophile, and E° to the standard electrode potential for the two-electron half-reaction ... [Pg.231]

Figure 7.13. The definitions of ionization potential, Ie, work function, , Fermi level, EF, conduction level, Ec, valence level Ev, and x-potential Xe without (a) and with (b) band bending at the semiconductor-vacuum interface. Figure 7.13. The definitions of ionization potential, Ie, work function, <t>, Fermi level, EF, conduction level, Ec, valence level Ev, and x-potential Xe without (a) and with (b) band bending at the semiconductor-vacuum interface.
Previous theoretical kinetic treatments of the formation of secondary, tertiary and higher order ions in the ionization chamber of a conventional mass spectrometer operating at high pressure, have used either a steady state treatment (2, 24) or an ion-beam approach (43). These theories are essentially phenomenological, and they make no clear assumptions about the nature of the reactive collision. The model outlined below is a microscopic one, making definite assumptions about the kinematics of the reactive collision. If the rate constants of the reactions are fixed, the nature of these assumptions definitely affects the amount of reaction occurring. [Pg.146]

For a given molecule and a given intemuclear separation a would have a definite value, such as to make the energy level for P+ lie as low as possible. If a happens to be nearly 1 for the equilibrium state of the molecule, it would be convenient to say that the bond is an electron-pair bond if a is nearly zero, it could be called an ionic bond. This definition is somewhat unsatisfactory in that it does not depend on easily observable quantities. For example, a compound which is ionic by the above definition might dissociate adiabatically into neutral atoms, the value of a changing from nearly zero to unity as the nuclei separate, and it would do this in case the electron affinity of X were less than the ionization potential of M. HF is an example of such a compound. There is evidence, given bdow, that the normal molecule approximates an ionic compound yet it would dissociate adiabatically into neutral F and H.13... [Pg.71]

Learning various kinds of chemical reactions and physical processes is an important element of all chemistry curricula. Earlier in this chapter we conunented on how students could recite the verbal definition of a strong acid but yet failed to select a visual representation that best illustrates the complete ionization of hydrogen chloride molecules. Another part of this study, conducted by Smith and Metz (1996), was probing students microscopic representation of the reaction... [Pg.67]

Thus, acids and bases are defined as aqueous solutions of substances and not as the substances themselves. It follows that ionization is a necessary characteristic of Arrhenius acids and bases. Another restriction of this definition is that acid-base behaviour is not recognized in non-aqueous solution. [Pg.15]

There is little information for fluoro-substituted sulfinyl groups. Values of a and ffp for SOCFj based on benzoic acid ionization are 0.63 and 0.69 respectively , compared with values of about 0.52 and 0.49 for SOMe (Table 3). Thus the electronegative fluorine somewhat enhances the electron-attracting influence of the sulfinyl function and makes the order more definitely sulfur lone pair to engage in 7t(pp) conjugation. Values of and ffp for SOCF3 based on anilinium ion dissociation are 0.76 and 1.05 respectively . An increase of 0.13 as between and [Pg.509]

In the current era neutral compounds are important simply because there are so many of them especially in screening collections made in automated chemistry for HTS. Other things being equal, a compound with an ionizable moiety is preferred to a neutral compound. By definition a neutral compound will not give an acid or basic pJCj value. Some essentially neutral compounds can form aqueous unstable salts. This most commonly occurs when an extremely poorly basic compound is dissolved in organic solvent and the salt is precipitatated, e.g. by bubbling in HCl gas. [Pg.269]


See other pages where Ionization definition is mentioned: [Pg.249]    [Pg.526]    [Pg.515]    [Pg.511]    [Pg.235]    [Pg.344]    [Pg.5]    [Pg.501]    [Pg.509]    [Pg.889]    [Pg.14]    [Pg.356]    [Pg.99]    [Pg.37]    [Pg.150]    [Pg.857]    [Pg.83]    [Pg.189]    [Pg.193]    [Pg.501]    [Pg.889]    [Pg.287]    [Pg.369]    [Pg.409]    [Pg.730]   
See also in sourсe #XX -- [ Pg.46 ]

See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.19 , Pg.91 , Pg.157 ]

See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.19 , Pg.91 , Pg.157 ]

See also in sourсe #XX -- [ Pg.287 ]




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