Question

Dimerisation of cyclopentadiene yields a stable compound represented by

Answer 1

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$\huge\mathfrak{Answer:}$

When cyclopenta-1,3-diene loses a H+ ion from the 5th carbon, the resulting carboanion is aromatic because of its structure: its cyclic, planar, has a delocalised conjugated pi system which has 4n+2 pi electrons, so it's aromatic.

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Answer 2

Answer:

When cyclopenta-1,3-diene loses a H+ ion from the 5th carbon, the resulting carboanion is aromatic because of its structure: its cyclic, planar, has a delocalised conjugated pi system which has 4n+2 pi electrons, so it's aromatic.

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