4. A compound having the molecular formula CsH1002 exhibits the following 'H-NMR-Figure 4a Figure 4a Figure 4b Multiplet @ 1.46 ppm Multiplet @ 1.22 ppm Triplet @ 2.20 ppm Triplet @ 0.78 ppm O PPM and 13C-NMR-Figure 4b spectra. Identify the compound. The spin multiplicities are indicated below. 'H-NMR (400 MHz, CDCI3 at 300K) ô: 11.8 (s), 2.20 (t), 1.46 (m), 1.22 (m), 0.78 (t). BC-NMR (400 MHz, CDC13 at 300K) 8: 180.8 (s), 33.8 (t), 26.8 (t), 22.4 (t), 3.58 (q).

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4. A compound having the molecular formula CsH10O2 exhibits the following 'H-NMR-Figure 4a
Figure 4a
Figure 4b
Multiplet
@ 1.46 ppm
Multiplet
@ 1.22 ppm
Triplet
@ 2.20 ppm
Triplet
@ 0.78 ppm
PPM
and 13C-NMR-Figure 4b spectra. Identify the compound. The spin multiplicities are indicated
below.
'H-NMR (400 MHz, CDCI3 at 300K) 8: 11.8 (s), 2.20 (t), 1.46 (m), 1.22 (m), 0.78 (t).
13C-NMR (400 MHz, CDCI3 at 300K) 8: 180.8 (s), 33.8 (t), 26.8 (t), 22.4 (t), 3.58 (q).
Transcribed Image Text:4. A compound having the molecular formula CsH10O2 exhibits the following 'H-NMR-Figure 4a Figure 4a Figure 4b Multiplet @ 1.46 ppm Multiplet @ 1.22 ppm Triplet @ 2.20 ppm Triplet @ 0.78 ppm PPM and 13C-NMR-Figure 4b spectra. Identify the compound. The spin multiplicities are indicated below. 'H-NMR (400 MHz, CDCI3 at 300K) 8: 11.8 (s), 2.20 (t), 1.46 (m), 1.22 (m), 0.78 (t). 13C-NMR (400 MHz, CDCI3 at 300K) 8: 180.8 (s), 33.8 (t), 26.8 (t), 22.4 (t), 3.58 (q).
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