Physical Chemistry 2 Quiz
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A researcher is studying the electronic structure of a series of aromatic compounds using UV-Vis spectroscopy. The compounds differ in their substitution patterns and conjugation lengths.
Compound A (benzene) shows λmax at 254 nm, while compound B (naphthalene) shows λmax at 286 nm. Compound C (anthracene) shows λmax at 375 nm. If compound D is tetracene (four fused benzene rings), what would be the most reasonable prediction for its λmax and the underlying reason?
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