Usually at the 2- or 3- position, Thiophene undergoes electrophilic aromatic substitution. Draw the intermediates and all resonance structures for the reaction at each position, and then decide what position should be more reactive depending on your intermediates.

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Usually at the 2- or 3- position, Thiophene undergoes electrophilic aromatic substitution. Draw the intermediates and all resonance structures for the reaction at each position, and then decide what position should be more reactive depending on your intermediates.

The image shows a chemical structure of Thiophene, which is a heterocyclic compound. It consists of a five-membered ring with four carbon atoms and one sulfur atom. The sulfur atom is represented by "S" at the top of the ring. The numbered positions "2" and "3" indicate the locations of the carbon atoms in the ring adjacent to the sulfur.

The diagram has alternating single and double bonds, illustrating the aromatic nature of the compound. The structure is crucial for understanding the properties and reactions of Thiophene in organic chemistry.
Transcribed Image Text:The image shows a chemical structure of Thiophene, which is a heterocyclic compound. It consists of a five-membered ring with four carbon atoms and one sulfur atom. The sulfur atom is represented by "S" at the top of the ring. The numbered positions "2" and "3" indicate the locations of the carbon atoms in the ring adjacent to the sulfur. The diagram has alternating single and double bonds, illustrating the aromatic nature of the compound. The structure is crucial for understanding the properties and reactions of Thiophene in organic chemistry.
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