Heterocyclic aromatic compounds undergo electrophilic aromatic substitution in a similar fashion to that undergone by benzene with the formation of a resonance-stabilized intermediate. Draw all of the resonance contributors expected when the above compound undergoes bromination

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Explanation:

When we talk about electrophilic substitution, we are talking about a substitution reaction in which the attacking agent is an electrophile. The electrophile attacks an electron rich area of a compound during the reaction.

The five membered furan ring is aromatic just as benzene. This aromatic structure is maintained during electrophilic substitution reaction. The attack of the electrophile generates a resonance stabilized intermediate whose canonical structures have been shown in the image attached.

it’s previous models   because when i picked that son of a gun’s answer it was wrong look for previous models because they might make it a different letter