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=/

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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=/
Transcribed Image Text: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=/
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