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electronegativity
(redirected from electronegative)

   Also found in: Dictionary/thesaurus, Medical, Wikipedia, Hutchinson 0.04 sec.
electronegativity (ĭlĕk'trōnĕgətĭv`ətē), in chemistry, tendency for an atom to attract a pair of electrons that it shares with another atom (see chemical bond chemical bond, mechanism whereby atoms combine to form molecules . There is a chemical bond between two atoms or groups of atoms when the forces acting between them are strong enough to lead to the formation of an aggregate with sufficient stability to be regarded as
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). For example, the molecule hydrogen chloride, HCl, consists of a hydrogen atom, H, and a chlorine atom, Cl, sharing a pair of electrons. If the pair of electrons are not shared equally, i.e., if they spend more time with one atom than with the other, the favored atom is said to be more electronegative. In the case of HCl, measurements indicate that the molecule has a dipole moment, that is, the chlorine end is relatively negative and the hydrogen end is relatively positive. This means that the electron pair spends more time with the chlorine atom than with the hydrogen atom and thus chlorine is more electronegative than hydrogen. Nonmetals have much higher electronegativities than metals; of the nonmetals, fluorine is the most electronegative, followed by oxygen, nitrogen, and chlorine. The larger the difference in electronegativity between two atoms, the more polar the bond between them. In the extreme case of a bond between a metal and a nonmetal, a complete transfer of electrons takes place.


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Fluorine atoms are highly electronegative, which gives the CF bond a large dipole moment.
The ALAD 2 allele has been shown to modify the toxicokinetics of lead by coding for a more electronegative enzyme that may bind positively charged lead ions more tightly than does the ALAD-1 protein (Wetmur 1994; Wetmur et al.
174 TRAYLOR PS,J CHEM S CH,vol ,page 0279,1984,cites= 23,STERICALLY PROTECTED HEMINS WITH ELECTRONEGATIVE SUBSTITUENTS - EFFICIENT CATALYSTS FOR HYDROXYLATION AND EPOXIDATION
 
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