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In chemistry, isovalent or second order hybridization is an extension of orbital hybridization, the mixing of atomic orbitals into hybrid orbitals which can form chemical bonds, to include fractional numbers of atomic orbitals of each type (s, p, d). It allows for a quantitative depiction of bond formation when the molecular geometry deviates ...
In chemistry, orbital hybridisation (or hybridization) ... For molecules with lone pairs, the bonding orbitals are isovalent sp x hybrids. For example, ...
Isovalent hybridization is used to explain bond angles of those molecules that is inconsistent with the generalized simple sp, sp 2 and sp 3 hybridization. For molecules containing lone pairs, the true hybridization of these molecules depends on the amount of s and p characters of the central atom which is related to its electronegativity.
In chemical bonds, an orbital overlap is the concentration of orbitals on adjacent atoms in the same regions of space. Orbital overlap can lead to bond formation. Linus Pauling explained the importance of orbital overlap in the molecular bond angles observed through experimentation; it is the basis for orbital hybridization.
In more advanced courses, an alternative explanation for this phenomenon considers the greater stability of orbitals with excess s character using the theory of isovalent hybridization, in which bonds and lone pairs can be constructed with sp x hybrids wherein nonintegral values of x are allowed, so long as the total amount of s and p character ...
C. Carbon–carbon bond; Carbon-carbon bond activation; Carbon–fluorine bond; Carbon–nitrogen bond; Carbon–oxygen bond; Carbon–hydrogen bond; Catch bond
Orbital hybridization. The s-character of an orbital relates to how close electrons are to the nucleus. In the case of a radical, s-character more specifically relates to how close the single electron is to the nucleus. Radicals decrease in stability as they are closer to the nucleus, because the electron affinity of the orbital increases.
Using the language of orbital hybridization, the bonds of molecules like PF 5 and SF 6 were said to be constructed from sp 3 d n orbitals on the central atom. Langmuir, on the other hand, upheld the dominance of the octet rule and preferred the use of ionic bonds to account for hypervalence without violating the rule (e.g. " SF 2+