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The rule states that with the addition of a protic acid HX or other polar reagent to an asymmetric alkene, the acid hydrogen (H) or electropositive part gets attached to the carbon with more hydrogen substituents, and the halide (X) group or electronegative part gets attached to the carbon with more alkyl substituents. This is in contrast to ...
The "size" of the charge in an ionic bond depends on the number of electrons transferred. An aluminum atom, for example, with a +3 charge has a relatively large positive charge. That positive charge then exerts an attractive force on the electron cloud of the other ion, which has accepted the electrons from the aluminum (or other) positive ion.
In atomic physics, a partial charge (or net atomic charge) is a non-integer charge value when measured in elementary charge units. It is represented by the Greek lowercase delta (𝛿), namely 𝛿− or 𝛿+. Partial charges are created due to the asymmetric distribution of electrons in chemical bonds.
There are several functional groups that contain an alkene such as vinyl group, allyl group, or acrylic group. Hydrocarbons may form charged structures: positively charged carbocations or negative carbanions. Carbocations are often named -um. Examples are tropylium and triphenylmethyl cations and the cyclopentadienyl anion.
The anion is the species that retains the electrons from the bond while the cation is stripped of the electrons from the bond. The anion usually forms on the most electronegative atom, in this example atom A. This is because the most electronegative atom will naturally attract electrons towards itself more strongly, leading to its negative charge.
The electron cloud in a σ-bond between two unlike atoms is not uniform and is slightly displaced towards the more electronegative of the two atoms. This causes a permanent state of bond polarization, where the more electronegative atoms has a fractional negative charge (δ –) and the less electronegative atom has a fractional positive charge ...
In chemistry, π backbonding is a π-bonding interaction between a filled (or half filled) orbital of a transition metal atom and a vacant orbital on an adjacent ion or molecule. [ 1 ] [ 2 ] In this type of interaction, electrons from the metal are used to bond to the ligand , which dissipates excess negative charge and stabilizes the metal.
The rightmost structure in the diagram has a charge of -2 on the nitrogen atom. Applying the principle of electroneutrality this can be identified as only a minor contributor. Additionally as the most electronegative atom should carry the negative charge, then the triple bonded structure on the left is predicted to be the major contributor. [7]