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In chemistry, polarity is a separation of electric charge leading to a molecule or its chemical groups having an electric dipole moment, with a negatively charged end and a positively charged end. Polar molecules must contain one or more polar bonds due to a difference in electronegativity between the bonded atoms.
Another class of oxonium ions encountered in organic chemistry is the oxocarbenium ions, obtained by protonation or alkylation of a carbonyl group e.g. R−C= + −R′ which forms a resonance structure with the fully-fledged carbocation R− + −O−R′ and is therefore especially stable:
An example of a polar surface is the rocksalt (111) surface. [2] In general, a polar surface is less stable than a nonpolar surface because a dipole moment increases the surface Gibbs energy. Also, oxygen polar surfaces are more stable than metal polar surfaces because oxygen ions are more polarizable, which lowers the surface energy. [9]
Definition [ edit ] Electric polarizability is the relative tendency of a charge distribution, like the electron cloud of an atom or molecule , to be distorted from its normal shape by an external electric field .
Ionic bonding is a type of chemical bonding that involves the electrostatic attraction between oppositely charged ions, or between two atoms with sharply different electronegativities, [1] and is the primary interaction occurring in ionic compounds.
In organic chemistry, the term stereoelectronic effect is also used to emphasize the relation between the electronic structure and the geometry (stereochemistry) of a molecule. The term polar effect is sometimes used to refer to electronic effects, but also may have the more narrow definition of effects resulting from non-conjugated substituents.
The canonical umpolung reagent is the cyanide ion. The cyanide ion is unusual in that a carbon triply bonded to a nitrogen would be expected to have a (+) polarity due to the higher electronegativity of the nitrogen atom. Yet, the negative charge of the cyanide ion is localized on the carbon, giving it a (-) formal charge.
The phosphite ion, PO 3− 3, is a strong base, and so always carries at least one proton. In this case the proton is attached directly to the phosphorus atom with the structure HPO 2− 3. In forming this ion, the phosphite ion is behaving as a Lewis base and donating a pair of electrons to the Lewis acid, H +. Predominance diagram for chromate