When methyl 5-oxopentanoate is treated with vinyl Grignard, a compound is produced whose formula is C,H1002. In the IR spectrum of C7H1002, an intense absorption appears at 1740 cm-1 and a weaker absorption appears at 1650 cm-1. Seven signals appear in the 13C NMR spectrum of C,H1002. The DEPT spectrum shows that there is one carbon that is bonded to no hydrogens, two CH carbons, and four CH2 carbons. Draw the structure of C,H1002. 1.AMGB., THF → C7H10O2 `OCH3 2. NH4CI, H2O Methyl 5-oxopentanoate o=/

When methyl 5-oxopentanoate is treated with vinyl Grignard, a compound is produced whose formula is C,H1002. In the IR spectrum of C7H1002, an intense absorption appears at 1740 cm-1 and a weaker absorption appears at 1650 cm-1. Seven signals appear in the 13C NMR spectrum of C,H1002. The DEPT spectrum shows that there is one carbon that is bonded to no hydrogens, two CH carbons, and four CH2 carbons. Draw the structure of C,H1002. 1.AMGB., THF → C7H10O2 `OCH3 2. NH4CI, H2O Methyl 5-oxopentanoate o=/

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.26P: Compound I (C11H14O2) is insoluble in water, aqueous acid, and aqueous NaHCO3, but dissolves readily...

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