The high s character means that the electrons are closer to the nucleus, so we must add more energy to remove these electrons and break the bond. Therefore, carbocations are very often reactive. This is because a carbon atom with a positive charge can have only three bonds around it. I don't know how much detail you need to go into, but if you need to know more, google hyperconjugation.
Whereas the tertiary has three methyl groups stabilising the charge which makes the cation more solid.
General aryl carbocation structure. For example, carbanion contains a negative charge on the carbon atom. If electrons were money, carbocations would be the beggars of organic chemistry. A carbocation may have one or more positive charges. The simplest case is called the phenyl carbocation. The south was like that is not how we treat our slaves.
The attempt at a solution I noticed nothing can stabilize or delocalize the positive charge because then it'd lose aromaticity but till it has aromatic nature it should show stability.
A tertiary carbonation will be more stable compared to both primary and also secondary, the actual delocalised charge will be stabilized from the heavier teams. I just bought a pair of lace-up boots, why is phenyl carbocation unstable, and they're beautiful, but every time I take a step, the top part where the laces go over the the tongue squeaks. Vintage Collectible Tupperware Red SLI-SAW-ALL Gadget. My itunes is no longer my default player and I want it to be.