For example, in methane, the C hybrid orbital which forms each carbon– hydrogen bond consists of 25% s character and 75% p character and is thus described as sp 3 (read as s-p-three) hybridised. Hybrid orbitals are assumed to be mixtures of atomic orbitals, superimposed on each other in various proportions. In heavier atoms, such as carbon, nitrogen, and oxygen, the atomic orbitals used are the 2s and 2p orbitals, similar to excited state orbitals for hydrogen. In the case of simple hybridization, this approximation is based on atomic orbitals, similar to those obtained for the hydrogen atom, the only neutral atom for which the Schrödinger equation can be solved exactly. Orbitals are a model representation of the behavior of electrons within molecules. The amount of p character or s character, which is decided mainly by orbital hybridisation, can be used to reliably predict molecular properties such as acidity or basicity. Hybridisation theory explains bonding in alkenes and methane. For drawing reaction mechanisms sometimes a classical bonding picture is needed with two atoms sharing two electrons. Hybridisation theory is an integral part of organic chemistry, one of the most compelling examples being Baldwin's rules. It gives a simple orbital picture equivalent to Lewis structures. This concept was developed for such simple chemical systems, but the approach was later applied more widely, and today it is considered an effective heuristic for rationalizing the structures of organic compounds. Each hybrid is denoted sp 3 to indicate its composition, and is directed along one of the four C-H bonds. Pauling supposed that in the presence of four hydrogen atoms, the s and p orbitals form four equivalent combinations which he called hybrid orbitals. The angle between any two bonds is the tetrahedral bond angle of 109☂8' (around 109.5°). In reality, methane has four C-H bonds of equivalent strength. Pauling pointed out that a carbon atom forms four bonds by using one s and three p orbitals, so that "it might be inferred" that a carbon atom would form three bonds at right angles (using p orbitals) and a fourth weaker bond using the s orbital in some arbitrary direction. History and uses Ĭhemist Linus Pauling first developed the hybridisation theory in 1931 to explain the structure of simple molecules such as methane (CH 4) using atomic orbitals. Usually hybrid orbitals are formed by mixing atomic orbitals of comparable energies. Hybrid orbitals are useful in the explanation of molecular geometry and atomic bonding properties and are symmetrically disposed in space. For example, in a carbon atom which forms four single bonds the valence-shell s orbital combines with three valence-shell p orbitals to form four equivalent sp 3 mixtures in a tetrahedral arrangement around the carbon to bond to four different atoms. In chemistry, orbital hybridisation (or hybridization) is the concept of mixing atomic orbitals to form new hybrid orbitals (with different energies, shapes, etc., than the component atomic orbitals) suitable for the pairing of electrons to form chemical bonds in valence bond theory. Mixing (superposition) of atomic orbitals in chemistry
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