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Hybridisation theory is an integral part of organic chemistry, one of the most compelling examples being Baldwin's rules. For drawing reaction mechanisms sometimes a classical bonding picture is needed with two atoms sharing two electrons. [5] Hybridisation theory explains bonding in alkenes [6] and methane. [7]
In chemistry, Bent's rule describes and explains the relationship between the orbital hybridization and the electronegativities of substituents. [1] [2] The rule was stated by Henry A. Bent as follows: [2] Atomic s character concentrates in orbitals directed toward electropositive substituents.
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 ...
Linear organic molecules, such as acetylene (HC≡CH), are often described by invoking sp orbital hybridization for their carbon centers. Two sp orbitals. According to the VSEPR model (Valence Shell Electron Pair Repulsion model), linear geometry occurs at central atoms with two bonded atoms and zero or three lone pairs (AX 2 or AX 2 E 3) in ...
[18]: 1165 Examples of this include the octacyanomolybdate (Mo(CN) 4− 8) and octafluorozirconate (ZrF 4− 8) anions. [18]: 1165 The nonahydridorhenate ion (ReH 2− 9) in potassium nonahydridorhenate is a rare example of a compound with a steric number of 9, which has a tricapped trigonal prismatic geometry. [13]: 254 [18]
In organic chemistry, molecules which have a trigonal pyramidal geometry are sometimes described as sp 3 hybridized. The AXE method for VSEPR theory states that the classification is AX 3 E 1. Phosphine, an example of a molecule with a trigonal pyramidal geometry.
A typical example of the first group is the solvent and anaesthetic diethyl ether, commonly referred to simply as "ether" (CH 3 −CH 2 −O−CH 2 −CH 3). Ethers are common in organic chemistry and even more prevalent in biochemistry, as they are common linkages in carbohydrates and lignin. [2]
Structure of xenon oxytetrafluoride, an example of a molecule with the square pyramidal coordination geometry. Square pyramidal geometry describes the shape of certain chemical compounds with the formula ML 5 where L is a ligand. If the ligand atoms were connected, the resulting shape would be that of a pyramid with a square base.