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Electronegativity, symbolized as χ, is the tendency for an atom of a given chemical element to attract shared electrons (or electron density) when forming a chemical bond. [1] An atom's electronegativity is affected by both its atomic number and the distance at which its valence electrons reside from the charged nucleus. The higher the ...
The tendency of an atom in a molecule to attract the shared pair of electrons towards itself is known as electronegativity. It is a dimensionless quantity because it is only a tendency. [17] The most commonly used scale to measure electronegativity was designed by Linus Pauling. The scale has been named the Pauling scale in his honour.
The polarization of a single σ covalent bond due to the electronegativity difference. Transfer of shared π-bond electron pairs to one atom under the influence of a strong external field. Permanent effect. Temporary effect. Always observed. Only observed in the presence of an electrophilic reagent. Induced charges are partial charges (δ + or ...
Covalent and ionic bonding form a continuum, with ionic character increasing with increasing difference in the electronegativity of the participating atoms. Covalent bonding corresponds to sharing of a pair of electrons between two atoms of essentially equal electronegativity (for example, C–C and C–H bonds in aliphatic hydrocarbons).
This connection comes from the Mulliken electronegativity scale. By inserting the energetic definitions of the ionization potential and electron affinity into the Mulliken electronegativity, it is seen that the Mulliken chemical potential is a finite difference approximation of the electronic energy with respect to the number of electrons, i.e.,
It is more pronounced than the lanthanide contraction because the 5f electrons are less effective at shielding than 4f electrons. [1] It is caused by the poor shielding effect of nuclear charge by the 5f electrons along with the expected periodic trend of increasing electronegativity and nuclear charge on moving from left to right.
A list of the electron affinities was used by Robert S. Mulliken to develop an electronegativity scale for atoms, equal to the average of the electrons affinity and ionization potential. [2] [3] Other theoretical concepts that use electron affinity include electronic chemical potential and chemical hardness.
With respect to acidity, a common trend to note is that, inductively, an electron-withdrawing substituent in the vicinity of an acidic proton will lower the pKa (i.e. increase the acidity) and, correspondingly, an electron-donating substituent will raise the pKa. [7] The reorganization of charge due to field effects will have the same result.