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Electron involving

A selected list of redox indicators will be found in Table 8.26. A redox indicator should be selected so that its if" is approximately equal to the electrode potential at the equivalent point, or so that the color change will occur at an appropriate part of the titration curve. If n is the number of electrons involved in the transition from the reduced to the oxidized form of the indicator, the range in which the color change occurs is approximately given by if" 0.06/n volt (V) for a two-color indicator whose forms are equally intensely colored. Since hydrogen ions are involved in the redox equilibria of many indicators, it must be recognized that the color change interval of such an indicator will vary with pH. [Pg.1160]

Studies aimed at characterizing the mechanisms of electrode reactions often make use of coulometry for determining the number of electrons involved in the reaction. To make such measurements a known amount of a pure compound is subject to a controlled-potential electrolysis. The coulombs of charge needed to complete the electrolysis are used to determine the value of n using Faraday s law (equation 11.23). [Pg.506]

In almost all cases X is unaffected by any changes in the physical and chemical conditions of the radionucHde. However, there are special conditions that can influence X. An example is the decay of Be that occurs by the capture of an atomic electron by the nucleus. Chemical compounds are formed by interactions between the outer electrons of the atoms in the compound, and different compounds have different electron wave functions for these outer electrons. Because Be has only four electrons, the wave functions of the electrons involved in the electron-capture process are influenced by the chemical bonding. The change in the Be decay constant for different compounds has been measured, and the maximum observed change is about 0.2%. [Pg.446]

Closo Clusters 2n + 2 Systems). The assignment of valence electrons and the factoring out of those electrons involved in exopolyhedral bonds provides 2n framework electrons for a B H molecule, two electrons short of the 2n + 2 closo count. In fact, stable neutral B H molecules are not... [Pg.229]

Here, with six electrons involved, it is the disrotatory mode (Hiickel system) in which the transition state is stabilized. There are numerous examples of interconversion of 1,3,5-... [Pg.614]

Classify the following reactions as electrocyclizations, sigmatropic rearrangements, cycloadditions, etc., and give the correct symbolism for the electrons involved in each concerted process. Some of the reactions proceed by two sequential processes. [Pg.656]

Notice that the orbital array is of the Mobius topology with a phase change depicted between the C-1 and C-2 positions. This corresponds to an allowed photochemical process since there are six electrons involved in bonding changes. [Pg.777]

It follows from the preceding discussion that the unbranched H bond can be regarded as a 3-centre 4-electron bond A-H B in which the 2 pairs of electrons involved are the bond pair in A-H and the lone pair on B. The degree of charge separation on bond formation will depend on the nature of the proton-donor group AH and the Lewis base B. The relation between this 3-centre bond formalism and the 3-centre bond descriptions frequently used for boranes, polyhalides and compounds of xenon is particularly instructive and is elaborated in... [Pg.63]

Faraday s Law the quantity of charge (Q) passed in an electrochemical reaction is directly proportional to the number of moles (n) of substance reacted. Thus Q = zFn, where z is the number of electrons involved in one molecule of the reaction and F is the Faraday constant. [Pg.1368]

The amounts of different substances liberated or dissolved by the same quantity of electricity are proportional to their relative atomic (or molar) masses divided by the number of electrons involved in the respective electrode... [Pg.503]

Coulometric analysis is an application of Faraday s First Law of Electrolysis which may be expressed in the form that the extent of chemical reaction at an electrode is directly proportional to the quantity of electricity passing through the electrode. For each mole of chemical change at an electrode (96487 x n) coulombs are required i.e. the Faraday constant multiplied by the number of electrons involved in the electrode reaction. The weight of substance produced or consumed in an electrolysis involving Q coulombs is therefore given by the expression... [Pg.529]

Here p is the coordination number of the complex ion formed, Xb is the ligand and n is the number of electrons involved in the electrode reaction. The concentration of the complex ion does not enter into equation (15), so that the observed half-wave potential will be constant and independent of the concentration of the complex metal ion. Furthermore, the half-wave potential is more negative the smaller value of Kinstabi, i.e. the more stable the complex ion. The half-wave potential will also shift with a change in the concentration... [Pg.601]

A more general and fundamental view is obtained by a consideration of (a) the number of electrons involved in the partial ionic equation representing the reaction, and (b) the change in the oxidation number of a significant element in the oxidant or reductant. Both methods will be considered in some detail. [Pg.847]

At the end of the paper, condensed tables of the higher approximations have been carried out with respect to atomic and molecular systems. For atoms, the tables are arranged after the number of electrons involved, which means that, e.g., N = 2 refers to the series of He-like ions H", He, Li+, Be2+, etc. For molecules, there is a table for H2 a table for other simple molecules (LiH, BeH+, H20, NH3, etc.) with all or almost all electrons treated, and finally a special table for the n electron systems in the two latter cases, the references to the best SCF data available are also contained for comparison. [Pg.324]

See also Oxidation, Reduction). Some dissolved substances in water occur either in an oxidized or a reduced form, and their state can be changed by either the acquisition of electrons (reduction) or the loss of electrons (oxidation). This transfer system is an reduction-oxidation system, or redox. (Red. - Oxid. n+ = ne—, where n is number of electrons involved), and can be used to measure and... [Pg.752]

In the ionization of the p-nitroanilinium ion, the free base is stabilized by delocalization of electrons involving the canonical structure 19. An analogous structure is not possible for... [Pg.495]

Shislov and coworkers13 studied the photochemical transformation of the paramagnetic particles of irradiated polycrystalline DMSO-d6 in order to evaluate the energy of the electrons involved in the formation of the anion-radical pair. [Pg.892]

The electrons involved in the actual reaction (which are designated here by dots and referred to here as the active electrons) can be treated according to the general prescription of the four-electron three-orbital problem with the VB wave functions (Ref. 5)... [Pg.55]

The electronegative O atoms of the carboxylic acid group withdraw electrons from the whole ring, thereby reducing its overall electron density. Moreover, resonance preferentially removes electrons from the ortho and para positions. To focus on the essentials, only the lone pairs of electrons involved in resonance are shown ... [Pg.864]

Phenyltrimethylammonium Ion, N+(CH3)S-CaHe.—In this ion, as in toluene, we ignore the electrons involved in bonds from nitrogen to the attached groups, and consider only the inductive effect. The positive charge on the nitrogen atom increases its electron affinity to a value still greater than that for neutral nitrogen, so that we... [Pg.198]

We may apply the statistical theory to determine the number of outer electrons involved in bond formation by determining... [Pg.404]


See other pages where Electron involving is mentioned: [Pg.1685]    [Pg.107]    [Pg.468]    [Pg.484]    [Pg.505]    [Pg.234]    [Pg.275]    [Pg.26]    [Pg.247]    [Pg.313]    [Pg.7]    [Pg.612]    [Pg.621]    [Pg.649]    [Pg.176]    [Pg.908]    [Pg.23]    [Pg.94]    [Pg.88]    [Pg.90]    [Pg.1253]    [Pg.1253]    [Pg.1254]    [Pg.1355]    [Pg.67]    [Pg.32]    [Pg.314]    [Pg.4]    [Pg.232]   
See also in sourсe #XX -- [ Pg.293 ]




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Auger decay/electrons involved transitions

Chain processes, free radical, in aliphatic systems involving an electron

Chain processes, free radical, in aliphatic systems involving an electron transfer

Chain processes, free radical, in aliphatic systems involving an electron transfer reaction

Coupling Reactions Involving Electron-transfer Processes

Electrode processes involving multiple electron transfer

Electron involving iron-sulfur

Electron involving quinone-like compound

Electron pulse, species involved

Electron transfer kinetics involving cytochrome

Electron transfer reactions involving

Electron tunneling in reactions involving chlorophyll and its synthetic analogues

Electron-Deficient C2 Fragments (Cycloadditions Involving Azomethines, Nitrones, Nitrile Oxides, and Dienes)

Electron-Transfer Reactions Involving Transition-Metal Ions

Electron-transfer reaction, free radical chain involving

Electron-transfer reaction, free radical chain processes in aliphatic systems involving

Elementary Processes Involving More Than Four Electrons

Excitation, electronic excited states involved

Excitation, electronic interaction mechanisms involved

Fast electron transfer involving cytochrome

Flavins Are Used in Reactions Involving One or Two Electron Transfers

Involving electron-deficient

Involving electron-deficient heteroatoms

Number of electrons involved

Photochemical reactions involving electronically excited oxygen

Reactions Involving Carbenes, Nitrenes, and Other Electron-Deficient Intermediates

Reactions Involving Radicals, Electron-Deficient Species, Reducing Agents, and at Surfaces

Rearrangement involving electron-deficient

Rearrangements Involving Electronically Deficient Nitrogen Atoms

Transformation, chemical, involving electrons

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