HAMA (NMR ΓΙ' arbitrary intensity ' το ΤΤΤΤΤΤΤΙΤΙ το ppm IMS αδιά Which of the following...
arbitrary intensity Which of the following molecules produces the spectra above?
HNMR arbitrary intensity - 220 2200 200 160 160 180 120 100 200 5 Which of the following molecules produces the spectra above? (1 pt)
HNMR --CNMR arbitrary intensity 200 100 100 100 120100 2 020 20 ppm MS Which compound below gives the spectra above? (1 pt)
3 of 8 arbitrary intensity Bogo Voz 6 ppm Which compound below gives the spectra above? uro in
arbitrary intensity L200 220200100100 1201002 Which compound below gives the spectra above? ML Å w
34 2h H-NMR Spectrum of Ester A НЕ НЕ на PPM tr H-NMR Spectrum of Product B НЕ зН зн на НL 0 PPM ) Write a comple te curved arrow mechanism for the bromination reaction below. Include the formation of all intermediates (10 points). нооно а 5) Name the following molecules (8 points total). но, (q 6) When an ester A is treated with one equivalent of sodium methoxide, product B is formed. The 'H-NMR spectra of A and...
Which of the following compounds, with the molecular formula
C9H18O2 is consistent with the 1H NMR and the 13C NMR spectra shown
below?
NEW HARBINGER SELF-HELP WORKBOOK 30 diple 10. Which of the following compounds, with me 'H NMR and C NMR spectra shown below? following compounds, with molecular formula C His Or, is consistent with the 3 i 2 i do . 160' 140 120 100 PPM 8060.40.20 17027 o 9 0 பல ல PPM P207 < a IV...
Which peak would NOT be in either the decoupled 13C or 1H NMR spectra of the molecule shown below? a)a singlet around 65 ppm (13C) b)a quartet around 2. 1 ppm (1M) c)a doublet around 1. 1 ppm (1H) d)a singlet around 170 ppm (13C) e) a singlet around 220 ppm (13C) f) a singlet around 3. 5 ppm (1H) 2) For which pair of molecules below would decoupled l3C NMR spectroscopy not be effective in easily telling apart?
7. Which compound below be H-1 NMR 0.9 ppm (quartet fits the following spectral data? (6 points) 1.2 ppm (sextet 2 hydrogens), 2.1 ppm (triplet, hydrogens), 4.3 ppm (singlet 3 hydrogens) C-13 NMR 5 signals 25 ppr ppm (CH2); 61 ppm: (CH3) 198 Ppm (C). IR strong peak 1735 cm Ignals 25 ppm (CH): 35 ppm (CH2), 46 ppm (CH2); 61 ppm: em Mass Spee parent M+ = 102 Mass Spec paren ou 0 H2 CH3 HjC Holo H3C- CC...
16. Propose a structure for a molecule of formula CaHsCl which gave the following 1H NMR spectrum. PPM 17. Propose a structure for a molecule whose mass spectrum shows a parent ion at m/z 148, an IR peak at 1680 cm'and gives the following H and 13C NMR spectra 3H зн 2H 2H 2H 3 5 2 7 6 4 PPM 160 140 180 60 220 200 20 0 120 100 80 40 PPM -