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Electron flow electronegativity

Space-Charge-Limited Diode. This method is equally applicable to electropositive and electronegative adsorbed layers. In a diode the maximum current which can be drawn from the cathode is given by the emission formula in Sec. V,A. Electrons emitted from the cathode at low current densities build up an electron atmosphere or space charge at the surface, and this space charge presents an electrostatic barrier to electrons flowing to... [Pg.89]

The concepts, which are used in the design of synthetic routes, are based on the chemist s notion of electron density in molecular space. Most of these ideas have been arrived at by trial-and-error, or intuition, and refined by actual syntheses. An elaborate scheme, based on the concept of bond polarity, which is related to intrinsic differences in electronegativity, has grown into a book-keeping procedure to envisage electron flow during chemical reaction. An example of a polar bond occurs in chloromethane ... [Pg.242]

The electron flow starts from the polarized sigma bond. Metal hydrides can serve as good electron sources, but their behavior varies with the electronegativity of the metal. Alkali metal hydrides, NaH and KH, are ionic and function primarily as bases reacting with acidic protons to form hydrogen gas little reduction occurs. [Pg.155]

These two electron sinks are the least common of the six that make up the set of multiple-bonded electron sinks with no attached leaving group. They behave very similarly to the conjugate acceptors previously discussed. The electronegative C-ewg group replaces the electronegative Y in accepting the electron flow from the nucleophile. [Pg.171]

In this pathway electrons flow from the source to the multiply bonded carbon, break the pi bond, and produce a stable anion. An electronegative carbon atom, C-ewg, can replace an electronegative heteroatom, Y, and the electron flow does not change. When... [Pg.187]

An electronegative heteroatom, Y, can be replaced by an electronegative carbon atom, C-ewg. The electron-withdrawing group is extremely necessary, for without a means to stabilize the carbanion formed, the electron flow cannot occur. The enhancement of nucleophilicity by hydrogen bonding may occur in a protic solvent whenever the nucleophile bears a reasonably acidic hydrogen. [Pg.204]

If this quantity is positive, transferring an electron from B to A requires less energy than from A to B. The A group is then a Lewis acid. The direction of electron flow can be determined by the difference in absolute electronegativities, whose magnitude is a measure of the driving force for the transfer. 0... [Pg.88]

Steps 1, 3, and 5 cannot be slow as they are just proton transfers between oxygen atoms, and proton transfer between electronegative atoms is always fast. That leaves only steps 2 and 4 as possible rate-determining steps. The bimolecular addition of the weak nucleophile water to the low concentration of protonated ester (step 2) is the most attractive candidate, as step 4—the unimolecular loss of ethanol and re-formation of the carbonyl group—should be fast. What p value would be expected for the reaction if step 2 were the rate-determining step It would be made up of two parts. There would be an equilibrium p value for the protonation step and a reaction p value for the addition of water. Step 1 involves electrons flowing out of the molecule and step 2 involves electrons flowing in so the p values for these two steps would... [Pg.1046]

What is the result if an electron-withdrawing group or atom is attached to a carbonyl carbon The structural difference between acetic acid (18, pK of 4.76) and chloroacetic acid (19, pK of 2.87) is the presence of the chlorine on the sp carbon that is attached to the sp carbon of the carbonyl (the so-called a-carbon). The pKg values indicate that 19 is more acidic. A bond polarization model of 19 (see 19A) shows a different electron flow and a different induced dipole when compared to 18A. Chlorine is more electronegative than carbon and this makes the C-Cl bond polarized with a 6- Cl and a 6+ C. The result of this polarized bond is that the carbon of the C-Cl unit is adjacent to the... [Pg.212]


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See also in sourсe #XX -- [ Pg.254 ]




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