Benzene contains 6 pi (π) electrons.
Benzene's structure, a cyclic molecule with alternating single and double bonds, leads to a delocalized π electron system above and below the plane of the ring. This delocalization is what gives benzene its unique stability and properties.
Here's a breakdown:
- Benzene's formula is C6H6.
- Each carbon atom is sp2 hybridized.
- The sp2 hybridization leaves one unhybridized p orbital on each carbon atom. These p orbitals are perpendicular to the plane of the ring.
- These six p orbitals overlap sideways to form a continuous π system.
- Each double bond contributes two π electrons. Since benzene can be represented with three double bonds, it has 3 x 2 = 6 π electrons.
- According to Hückel's rule, aromatic compounds have (4n+2) π electrons, where n is an integer. For benzene, n=1, so it follows Hückel's rule (4(1)+2 = 6).
This delocalization of the 6 π electrons is crucial for benzene's stability and resistance to addition reactions.