Compound Y (C 10 H 18 O 5 ) exhibits one 1H NMR signal at 1.4
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Compound Y (C10H18O5) exhibits one 1H NMR signal at δ 1.4 (a singlet), three signals in its broadband proton decoupled 13C NMR spectrum at δ 28, 87, and 151, and has the following IR spectrum (Figure 1). Propose a structure for Y that is consistent with this data and explain your reasoning.
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Related Book For 
Organic Chemistry
ISBN: 978-1118875766
12th Edition
Authors: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
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