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By necessity of having five bonds on carbon but only four valence electron pairs available for bonding, they feature delocalized 3c-2e σ bonding and are thus regarded as type of non-classical carbocation. Like carbenium ions, carbonium ions are often invoked as intermediates in the upgrading of hydrocarbons in refineries.
The carbon–carbon single bond is a sigma bond and is formed between one hybridized orbital from each of the carbon atoms. In ethane , the orbitals are sp 3 - hybridized orbitals, but single bonds formed between carbon atoms with other hybridizations do occur (e.g. sp 2 to sp 2 ).
All other C-C bond lengths are normal (ca. 1.5 Å). [1] In chemistry, a carbonium ion is a cation that has a pentacoordinated carbon atom. [2] They are a type of carbocation. In older literature, the name "carbonium ion" was used for what is today called carbenium. Carbonium ions charge is delocalized in three-center, two-electron bonds. The ...
In the first step, the leaving group departs, forming a carbocation (C +). In the second step, the nucleophilic reagent (Nuc:) attaches to the carbocation and forms a covalent sigma bond. If the substrate has a chiral carbon, this mechanism can result in either inversion of the stereochemistry or retention of configuration. Usually, both occur ...
A saturated compound is a chemical compound (or ion) that resists addition reactions, such as hydrogenation, oxidative addition, and binding of a Lewis base. The term is used in many contexts and for many classes of chemical compounds. Overall, saturated compounds are less reactive than unsaturated compounds.
The bond lengths between carbon atoms in a phenyl group are approximately 1.4 Å. [6] In 1 H-NMR spectroscopy, protons of a phenyl group typically have chemical shifts around 7.27 ppm. These chemical shifts are influenced by aromatic ring current and may change depending on substituents.
The 1,2-rearrangement belongs to a broad class of chemical reactions called rearrangement reactions. A rearrangement involving a hydrogen atom is called a 1,2-hydride shift. If the substituent being rearranged is an alkyl group, it is named according to the alkyl group's anion: i.e. 1,2-methanide shift, 1,2-ethanide shift, etc.
A strong chemical bond is formed from the transfer or sharing of electrons between atomic centers and relies on the electrostatic attraction between the protons in nuclei and the electrons in the orbitals. The types of strong bond differ due to the difference in electronegativity of the constituent elements.