The 1 H NMR spectrum of an unknown compound shows absorptions at (no multiplicities given) =

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The 1H NMR spectrum of an unknown compound shows absorptions at (no multiplicities given) δ = 7.3 (5H), 2.3 (1 H), and 0.9 (6 H) ppm. One of the following five structures satisfies these data. Which one? (The 1H NMR signal for ethane is at δ = 0.9 ppm, that for benzene at δ = 7.3 ppm.)

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Organic Chemistry structure and function

ISBN: 978-1429204941

6th edition

Authors: K. Peter C. Vollhardt, Neil E. Schore

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