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  2. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    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 ...

  3. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    For this molecule, carbon sp 2 hybridises, because one π (pi) bond is required for the double bond between the carbons and only three σ bonds are formed per carbon atom. In sp 2 hybridisation the 2s orbital is mixed with only two of the three available 2p orbitals, usually denoted 2p x and 2p y. The third 2p orbital (2p z) remains unhybridised.

  4. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    Shape of water molecule showing that the real bond angle 104.5° deviates from the ideal sp 3 angle of 109.5°. 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]

  5. Trigonal pyramidal molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Trigonal_pyramidal...

    3, and the sulfite ion, SO 2− 3. 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.

  6. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–carbon_bond

    In fact, the carbon atoms in the single bond need not be of the same hybridization. Carbon atoms can also form double bonds in compounds called alkenes or triple bonds in compounds called alkynes. A double bond is formed with an sp 2-hybridized orbital and a p-orbital that is not involved in the hybridization. A triple bond is formed with an sp ...

  7. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    For example, the double-bond carbons in alkenes like C 2 H 4 are AX 3 E 0, but the bond angles are not all exactly 120°. Likewise, SOCl 2 is AX 3 E 1, but because the X substituents are not identical, the X–A–X angles are not all equal. Based on the steric number and distribution of Xs and Es, VSEPR theory makes the predictions in the ...

  8. “What’s The Creepiest Display Of Intelligence You’ve Seen By ...

    www.aol.com/23-creepiest-displays-intelligence...

    Image credits: TheBurn1nator No doubt about it, it’s a fact that humans are the most intelligent creatures on the planet. But, while we have a rich history of adapting to and comprehending the ...

  9. Tetrahedral carbonyl addition compound - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_carbonyl...

    Since three-membered rings are very strained (bond angles forced to be 60˚), sp 3 hybridization is more favorable than sp 2 hybridization. For the sp 3 hybridized hydrate the bonds have to be distorted by about 49˚, while for the sp 2 hybridized ketone the bond angle distortion is about 60˚.