Furan undergoes electrophilic aromatic substitution more readily than benzene; mild reagents and conditions are sufficient. For example,

Question:

Furan undergoes electrophilic aromatic substitution more readily than benzene; mild reagents and conditions are sufficient. For example, furan reacts with bromine to give 2-bromofuran.
(a) Propose mechanisms for the bromination of furan at the 2-position and at the 3-position, Draw the resonance forms of each sigma complex, and compare their stabilities.
(b) Explain why furan undergoes bromination (and other electrophilic aromatic substitutions) primarily at the 2-position.