Vinyl Carbocation Definition

Allylic carbon atom can form stable carbocations due to electron delocalization.

Vinyl carbocation definition.

A vinylic carbocation which has an empirical formula of c h is a carbocation that has a positive charge only on the alkene carbon atom. The rate of this step and therefore the rate of the overall substitution reaction depends on the activation energy for the process in which the bond between the carbon and the leaving group breaks and a carbocation forms. A carbocation may have one or more positive charges. A carbocation with a two coordinate positive carbon derived from formal removal of a hydride ion h from an alkene is known as a vinyl cation.

The general formula for vinyl group is r ch ch 2 in which both carbon atoms are bonded with double bond and r is attached at vinylic position. In the absence of geometric constraints most substituted vinyl cations carry the formal positive charge on an sp hydridized carbon atom of linear geometry. The carbocation carbon has sp hybridization. General vinylic carbocation structure.

Stability of carbocation intermediates. More generally a vinylic cation is any disubstituted trivalent carbon where the carbon bearing the positive charge is part of a double bond and is sp hybridized. The vinyl cation puts positive charge at an sp hybridized carbon atom. Vinylic compounds can produce vinylic polymers such as pvc pvf pvac etc.

Vinylic carbocations are very unstable due to lack of p character. A carbocation in which the carbon atom having the open octet and positive formal charge is part of a carbon carbon double bond. Any trivalent disubstituted carbon is generally a vinylic carbocation in which the carbon atom which is bearing the positive charge is found to be double bonded and will always exist as sp hybridized. The vinyl cation is a carbocation with the positive charge on an alkene carbon.

Allylic carbon meaning the double bonded carbon atoms can be classified as vinylic and allylic carbon atoms. These carbocations are generally unstable because p orbitals of the carbon atom are free due to loss of electrons. Because of the high s character of the orbital the positive charge resides closer to the positively charged nucleus which makes it a particularly high energy cation. The term carbocation can be defined as an ion containing a positively charged carbon atom.

Therefore carbocations are very often reactive. Its empirical formula is c 2 h 3.