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please draw structure also! Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 'H NMR Spectra, the integral is

please draw structure also!
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Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 'H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Mass Spectrum (not shown): [M] =235 (100%) m/z IR Spectrum (not shown): 3240, 3090, 2990, 2970, 1715, 1601, 1500 cm (all listed are strong (s) unless otherwise indicated) "H NMR Spectrum (400 MHz, CDC13, 25 C) brs m 6 7 1H 1H 111 PPM 1H 3H2H 1H SH 13C NMR Spectrum, proton-decoupled (100 MHz, CDC13, 25 C) 2x (CH2) (CH) C (C) (C) (C) (C) (C) (CH) (CH) (CH) (CH) 200 180 160 140 120 100 PPM 80 60 40 20 Part 1: Enter the number of each atom based on your structure's molecular formula in the boxes below. Enter each atom count as a whole number. Enter O if the atom(s) listed are not in your structure Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For 'H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Mass Spectrum (not shown): [M] =235 (100%) m/z IR Spectrum (not shown): 3240, 3090, 2990, 2970, 1715, 1601, 1500 cm (all listed are strong (s) unless otherwise indicated) "H NMR Spectrum (400 MHz, CDC13, 25 C) brs m 6 7 1H 1H 111 PPM 1H 3H2H 1H SH 13C NMR Spectrum, proton-decoupled (100 MHz, CDC13, 25 C) 2x (CH2) (CH) C (C) (C) (C) (C) (C) (CH) (CH) (CH) (CH) 200 180 160 140 120 100 PPM 80 60 40 20 Part 1: Enter the number of each atom based on your structure's molecular formula in the boxes below. Enter each atom count as a whole number. Enter O if the atom(s) listed are not in your structure

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