Triplet @ 2.20 ppm 0.78 ppm and C-NMR-Figure 4b spectra. Identify the compound. The spin multiplicities are indicated below. 2.5 'H-NMR (400 MHz, CDCI, at 300K) 8: 11.8 (s), 2.20 (t), 1.46 (m), 1.22 (m), 0.78 (t). "C-NMR (400 MHz, CDCI, at 300K) 8: 180.8 (s), 33.8 (t), 26.8 (t), 22.4 (t), 3.58 (q). Triplet

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Chapter1: Chemical Foundations
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4. A compound having the molecular formula C,H,O, exhibits the following H-NMR-Figure 4a
Figure 4a
Figure 4b
ми
Multiplet
@ 1.22 ppm
Triplet
@ 2.20 ppm
Triplet
@0.78 ppm
and C-NMR-Figure 4b spectra. Identify the compound. The spin multiplicities are indicated
below.
2.5
'H-NMR (400 MHz, CDCI, at 300K) 8: 11.8 (s), 2.20 (t), 1.46 (m), 1.22 (m), 0.78 (t).
PC-NMR (400 MHz, CDCI, at 300K) 8: 180.8 (s), 33.8 (t), 26.8 (t), 22.4 (t), 3.58 (q).
Multiplet
@ 1.46 ppm
Transcribed Image Text:Answer as soon as possible within 10 minutes with proper explanation in handwritten form. Don't answer after 11:54 PM Otherwise I will downvote and report !! Thank you 4. A compound having the molecular formula C,H,O, exhibits the following H-NMR-Figure 4a Figure 4a Figure 4b ми Multiplet @ 1.22 ppm Triplet @ 2.20 ppm Triplet @0.78 ppm and C-NMR-Figure 4b spectra. Identify the compound. The spin multiplicities are indicated below. 2.5 'H-NMR (400 MHz, CDCI, at 300K) 8: 11.8 (s), 2.20 (t), 1.46 (m), 1.22 (m), 0.78 (t). PC-NMR (400 MHz, CDCI, at 300K) 8: 180.8 (s), 33.8 (t), 26.8 (t), 22.4 (t), 3.58 (q). Multiplet @ 1.46 ppm
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