A compound, C4H6O, exhibits IR absorption at 1705 cm³. Its carbon NMR shifts are given below. The number of hydrogens at each carbon, determined by DEPT, is given in parentheses after the chemical shift. Draw its structure. 13C NMR: 8 14.0 (3), 134.4 (2), 146.0 (0), 194.7 (1)
A compound, C4H6O, exhibits IR absorption at 1705 cm³. Its carbon NMR shifts are given below. The number of hydrogens at each carbon, determined by DEPT, is given in parentheses after the chemical shift. Draw its structure. 13C NMR: 8 14.0 (3), 134.4 (2), 146.0 (0), 194.7 (1)
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![14. A compound, C4H6O, exhibits IR absorption at 1705 cm³¹. Its carbon NMR shifts are given below. The number of
hydrogens at each carbon, determined by DEPT, is given in parentheses after the chemical shift. Draw its
structure.
13C NMR: 8 14.0 (3), 134.4 (2), 146.0 (0), 194.7 (1)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F9090d5e4-d7bb-4a15-856d-17cb06b171d4%2F29703b66-1f6f-4b53-a535-6d1ba75849f8%2Favlcgla_processed.png&w=3840&q=75)
Transcribed Image Text:14. A compound, C4H6O, exhibits IR absorption at 1705 cm³¹. Its carbon NMR shifts are given below. The number of
hydrogens at each carbon, determined by DEPT, is given in parentheses after the chemical shift. Draw its
structure.
13C NMR: 8 14.0 (3), 134.4 (2), 146.0 (0), 194.7 (1)
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