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The octet rule is a chemical rule of thumb that reflects the theory that main-group elements tend to bond in such a way that each atom has eight electrons in its valence shell, giving it the same electronic configuration as a noble gas. The rule is especially applicable to carbon, nitrogen, oxygen, and the halogens; although more generally the ...
Most homoleptic organo-main group compounds adopt a characteristic oxidation state: RLi, R 2 Be, R 3 B/R 3 Al, R 4 Si, R 3 P, R 2 S. Members where the simplest stoichiometry violates the octet rule often aggregate by formation of bridging alkyl groups. When the alkyl group bridges two main group elements, the bonding is called three-center two ...
Alternatively, electron-deficiency describes molecules or ions that function as electron acceptors. Such electron-deficient species obey the octet rule, but they have (usually mild) oxidizing properties. [4] 1,3,5-Trinitrobenzene and related polynitrated aromatic compounds are often described as electron-deficient. [5]
Under the framework of valence bond theory, resonance is an extension of the idea that the bonding in a chemical species can be described by a Lewis structure. For many chemical species, a single Lewis structure, consisting of atoms obeying the octet rule, possibly bearing formal charges, and connected by bonds of positive integer order, is sufficient for describing the chemical bonding and ...
Octet rule is used with Lewis structures for main group elements, especially the lighter ones such as carbon, nitrogen, and oxygen, 18-electron rule [2] in inorganic chemistry and organometallic chemistry of transition metals, Hückel's rule for the π-electrons of aromatic compounds,
Only one of the two pairs of electrons is occupying a molecular orbital that involves bonding to the central atom, the second pair being non-bonding and occupying a molecular orbital composed of only atomic orbitals from the two ligands. This model in which the octet rule is preserved was also advocated by Musher. [3]
General structure of a sulfide with the blue marked functional group. In organic chemistry, a sulfide (British English sulphide) or thioether is an organosulfur functional group with the connectivity R−S−R' as shown on right. Like many other sulfur-containing compounds, volatile sulfides have foul odors. [1]
The 18-electron rule is the equivalent of the octet rule in main group chemistry and provides a useful guide for predicting the stability of organometallic compounds. [34] It predicts that organometallic species "in which the sum of the metal valence electrons plus the electrons donated by the ligand groups total 18 are likely to be stable."