Answer as soon as possible within 10 minutes withproper explanation in handwritten form. Don't answerafter 11:54 PM Otherwise I will downvote and report !!Thank you4. A compound having the molecular formula C,H,O, exhibits the following H-NMR-Figure 4aFigure 4aFigure 4bмиMultiplet@ 1.22 ppmTriplet@ 2.20 ppmTriplet@0.78 ppmand C-NMR-Figure 4b spectra. Identify the compound. The spin multiplicities are indicatedbelow.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

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

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

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy

Section13.11: Characteristics Of 13c Nmr Spectroscopy

Problem 18P: Propose structures for compounds that fit the following descriptions: (a) A hydrocarbon with seven...

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