Using the information we can deduce the structure.
Extra Spectroscopy Practice D Ere just synthesized a new compound, and the following spectroscopic data is...
A compound of unknown structure gave the following
spectroscopic data:
Mass spectrum: M+ = 88.1
IR: 3600cm-1
1H NMR: 1.4 (2H, quartet, J=7Hz); 1.2 (6H, singlet); 1.0 (1H,
singlet); 0.9 (3H, triplet, J=7Hz)
13C NMR: 74, 35, 27, 25
a. assuming that the compound contains C and H but may or may not
contain O, give three possible molecular formulas.
b. how many protons (H) does the compound contain?
c. what functional group(s) does the compound contain?
d. how many...
The following spectroscopic data corresponds to an an unknown compound with the molecular formula C4H8O2. Deduce and draw the structure of the compound that corresponds to the data 1H NMR: δ 4.07 (quartet, 2H), 1.97 (singlet, 3H), 1.18 (triplet, 3H) ppm. "C NMR: δ 170, 60, 20, 14 ppm.
The following spectroscopic data below corresponds to an unknown carbonyl compound with the molecular formula C8H12O. Deduce and draw the structure of the compound that corresponds to the data. The letter \"m\" refers to an uninterpretable multiplet in the spectra. 1H NMR: δ 0.94 (t, 3H), 1.48 (sextet, 2H), 2.21 (q, 2H), 5.8-7.1 (m, 4H), and 9.56 (d, 1H) ppm. 13C NMR: δ 13.6, 21.9, 35.2, 129.0, 135.2, 146.7, 152.5, 193.2 ppm.
The following spectroscopic data below corresponds to an unknown carbonyl compound with the molecular formula C_8H_12O. Deduce and draw the structure of the compound that corresponds to the data. The letter "m" refers to an uninterpretable multiplet in the spectra. ^1H NMR: delta 0.94 (t, 3H), 1.48 (sextet, 2H), 2.21 (q, 2H), 5.8-7.1 (m, 4H), and 9.56 (d, 1H) ppm. ^13 C NMR: delta 13.6, 21.9, 35.2, 129.0, 135.2. 146.7, 152.5, 193.2 ppm.
The following spectroscopic data below corresponds to an unknown carbonyl compound with the molecular formula CH120. Deduce and draw the structure of the compound that corresponds to the data. The letter "m" refers to an uninterpretable multiplet in the spectra. TH NMR: 8 1.60 (m, 4H), 2.15 (s, 3H), 2.19 (m, 4H), and 6.78 (t, 1H) ppm. 13C NMR: 8 21.8, 22.2, 23.2, 25.0, 26.2, 139.8, 140.7, 198.6 ppm.
The following spectroscopic data corresponds to an unknown compound with the molecular formula C3H8O. Deduce and draw the structure of the compound that corresponds to the data. 1H NMR: δ 3.8 (septet, 1H), 3.6 (singlet, 1H), 1.0 (doublet, 6H) ppm. 13C NMR: δ 65, 24 ppm.
Question 5 (a) Given the following spectroscopic data, identify and draw the compound. Explain your reasoning i. ii. MS molecular ion: 102 'H NMR peaks a. 1.15 t (3H) b. 1.25 (3H) c. 2.35q (2H) d. 4.159 (2H) [Marks: 4] (b) For 1-cyclohexyl-eth-1-ene, sketch and label the: Infrared spectrum ii. 3C NMR spectrum
Putting It Together: Spectroscopy 1. You identity a new compound X Mass spectroscopy suggests a molecular forma following IR and proton NMR spectra are recorded: troscopy suggests a molecular formula of CH120, and the Wavelength (m) 0.05 Absorbance 80.40 0.60 204 4000 3500 3000 2500 100 500 400 200 2000 1800 1600 1400 1200 1000 Frequency (cm ) 200 500 TAHT 31 2H 1 H 6.0 5.0 4.0 8 (ppm) Deduce the structure of compound X, and explain the assignment...
Based on the following
spectroscopic data of an unknown compound with molecular formula
C8H6S, (i) determine the chemical structure of this compound; (ii)
assign all the signals in the 1H-NMR spectrum & 13C-NMR
spectrum. NMR is complete
۳۳-۳-rr-T-------- IR Spectrum (KBr disc) 4000 3000 1200 800 2000 1600 V (cm) M ** = 13 Mass Spectrum بالليليللليلعليا % of base peak CgHES 40 80 200 240 280 120 m 160 /e 13C NMR Spectrum (100.0 MHz, CDCI, solution) expansion DEPT...
Spectroscopic Analysis Unknown 1: Molecule Number a) Determine the empirical formula from the microanalysis data, showing your working: Empirical Formula b) Does the mass spectrum imply the molecular formula is the same as the empirical formula? Why/Why not? Molecular Formula c) Use the 'double bond equivalents' formula to determine the degree on unsaturation for this molecule: d) What structural information can you garner from the IR spectrum? e) What structural information can you garner from the 'H NMR spectrum? Specify...