Heterocyclic aromatic compounds undergo electrophilic aromatic substitution in a similar fashion to that undergone by benzene wi
th the formation of a resonance-stabilized intermediate. Draw all of the resonance contributors expected when the above compound undergoes bromination
1 answer:
Answer:
See explanation
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.
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Answer:
Explanation:
Cesium Lewis dot structure would look like this:
·Cs, because it only has one valence electron. But, since it has a plus, that means we lost an electron. So, we have to get rid of the dot and you have: