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In the simple aromatic ring of benzene, the delocalization of six π electrons over the C 6 ring is often graphically indicated by a circle. The fact that the six C-C bonds are equidistant is one indication that the electrons are delocalized; if the structure were to have isolated double bonds alternating with discrete single bonds, the bond would likewise have alternating longer and shorter ...
Because proper (symmetry-adapted) molecular orbitals are fully delocalized and do not admit a ready correspondence with the "bonds" of the molecule, as visualized by the practicing chemist, the most common approach is to instead consider the interaction between filled and unfilled localized molecular orbitals that correspond to σ bonds, π ...
Such electrons can therefore easily change from one energy state to a slightly different one. Thus, not only do they become delocalized, forming a sea of electrons permeating the structure, but they are also able to migrate through the structure when an external electrical field is applied, leading to electrical conductivity.
The charged components that make up ionic solids cannot exist in the high-density sea of delocalized electrons characteristic of strong metallic bonding. Some molecular salts, however, feature both ionic bonding among molecules and substantial one-dimensional conductivity , indicating a degree of metallic bonding among structural components ...
However, in benzene the remaining six bonding electrons are located in three π (pi) molecular bonding orbitals that are delocalized around the ring. Two of these electrons are in an MO that has equal orbital contributions from all six atoms. The other four electrons are in orbitals with vertical nodes at right angles to each other.
The bond results because the metal atoms become somewhat positively charged due to loss of their electrons while the electrons remain attracted to many atoms, without being part of any given atom. Metallic bonding may be seen as an extreme example of delocalization of electrons over a large system of covalent bonds, in which every atom ...
Hyperconjugation can be used to rationalize a variety of chemical phenomena, including the anomeric effect, the gauche effect, the rotational barrier of ethane, the beta-silicon effect, the vibrational frequency of exocyclic carbonyl groups, and the relative stability of substituted carbocations and substituted carbon centred radicals, and the thermodynamic Zaitsev's rule for alkene stability.
Antiaromaticity is a chemical property of a cyclic molecule with a π electron system that has higher energy, i.e., it is less stable due to the presence of 4n delocalised (π or lone pair) electrons in it, as opposed to aromaticity.