Aromaticity varies systematically across benzene, thiophene, pyrrole, furan, and pyridine.

the verdict

SUPPORTED

the evidence backs this

Recorded sources

2 sources for · 0 against

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The retrieved literature supports the systematic variation of aromaticity across benzene, thiophene, pyrrole, furan, and pyridine based on structural features and heteroatom contributions.

The analysis

The claim is specific, empirical, and testable. Papers [0] and [9] directly discuss and quantify the systematic variations in aromaticity and related electronic properties across these specific cyclic compounds (benzene, pyrrole, furan, thiophene). Therefore, the evidence clearly supports the claim.

Evidence for · 2

The predictive power of aromaticity: quantitative correlation between aromaticity and ionization potentials and HOMO–LUMO gaps in oligomers of benzene, pyrrole, furan, and thiophene

Recorded source metadata

Renana Gershoni-Poranne, Anuja P. Rahalkar, Amnon Stanger. The predictive power of aromaticity: quantitative correlation between aromaticity and ionization potentials and HOMO–LUMO gaps in oligomers of benzene, pyrrole, furan, and thiophene. 2018. https://doi.org/10.1039/c8cp02162g

Paper 0 establishes quantitative correlations between aromaticity and electronic properties across oligomers of benzene, pyrrole, furan, and thiophene.

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More for · 1

A Computational Study of the Relative Aromaticity of Pyrrole, Furan, Thiophene and Selenophene, and Their Diels-Alder Stereoselectivity

Recorded source metadata

V. Yadav. A Computational Study of the Relative Aromaticity of Pyrrole, Furan, Thiophene and Selenophene, and Their Diels-Alder Stereoselectivity. 2020. https://doi.org/10.26434/chemrxiv.12734039

Paper 9 examines the varying aromatic character and relative aromaticity trends across five-membered heterocycles including pyrrole, furan, and thiophene based on heteroatom lone-pair overlap.

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first checked01 Aug 2026

judged → SUPPORTED · 8601 Aug 2026

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