What is a true solution, in simple terms please?
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The delocalized cloud of π electrons in benzene is formed by the overlap of 6<u> p-orbitals</u>.
So, option B is correct one.
In the case of hydrocarbons, delocalisation occurs in benzene rings , where a hexagon of six carbon atoms has decalized electrons spread over the whole ring.
All of the carbon atoms in the benzene rings are orbitals around the ring produces a framework of six sigma bonds, while the unhybridized p-orbitals which are perpendicular to this plane over in side-to-side fashion to form three pi-bonds.
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