# Perpendicular orbitals in aryl and vinyl carbocations? [duplicate]

This point (iv) has been given under reasons for extremely low reactivity of aryl and vinyl halides. I cannot understand it. First of all, isn't the positive carbon atom in phenyl as well as vinyl carbocation sp-hybridized. But in the point, the positively charged carbon atom of the phenyl carbocation is referred to as sp2-hybridized. I cannot understand why. Also I cannot understand the "perpendicular part". That the orbitals are perpendicular and so the carbocation is not formed. But how are they perpendicular and how does this hinder the formation of carbocation. I cannot understand the last diagram (for vinyl carbocation). Please help.

## marked as duplicate by Mithoron, andselisk♦, Todd Minehardt, Mathew Mahindaratne, Nuclear ChemistFeb 10 at 15:24

• No, I do not think my question is a duplicate. My concerns are a bit different. If you read my question properly, you can understand. My question is mainly about why the perpendicularity of the orbitals destabilizes the carbocation, the hybridization of the carbon atoms and the meaning of the last diagram. – MrAP Feb 9 at 19:46

While the dissociation drawn in your reference for halogen is unlikely, I would however object the idea that aryl cations can not exist. The intermediate generation of the aryl diazonium ion at low temperatures, typically followed by release of nitrogen gas (triple bond $$\ce{N#N}$$) is one of rare cases where this high energy situation may be compensated, offering a wide array of subsequent chemistry.