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12. Choose the correct structure of the compound (Formula: CioH1202) with the following spectral data Then,...
6. Given the spectral data below, provide a structure. Note you must assign all of the...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+ 164 (no significant M+2 signal) (6 pts.) 3H, s зн, 2H, d 2H, d 2H, q 8 6 5 PPM 140 120 100 180 160 80 PPM 60 40 0.8 0.6 0.4 3000 2000...
6. Given the spectral data below, provide a structure. Note you must assign all of the...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+ = 164 (no significant M+2 signal) (6 pts.) 3HS 2H. d 2Hd 2Hg 8 7 6 5 4 3 2 1 0 PPM 180 160 140 120 100 PPM 80 60 40 20 0...
Draw the structure that fits the following data. Molecular formula: C6H12O 1H NMR spectral data: 13C...
Draw the structure that fits the following data. Molecular
formula: C6H12O 1H NMR spectral data: 13C NMR spectrum:
PLEASE HELP
the structure that fits the following data. Molecular formula: C6H12O H NMR spectral data: ppm 0.90 1.53 2.34 9.72 Integration6 4 1 1 Multiplicity triplet multiplet multiplet doublet C NMR spectrum:
Provide the correct structure for your unknown based on the spectroscopic data provided. Provide the correct...
Provide the correct structure for your unknown based on the
spectroscopic data provided. Provide the correct name for your
compound. Either the IUPAC name, or a commonly accepted name (i.e.,
ethyl acetate in place of ethyl ethanoate) will be accepted.IR
spectrum: Assign as many peaks as possible. In particular, you
should assign peaks that were important in making your structural
interpretation (i.e. functional group peaks such as OH, C=O, N-H,
etc.).
1H-NMR spectrum: Assign all the peaks in the spectrum...
4. The proton NMR and IR spectra of Compound B are shown on the next page....
4. The proton NMR and IR spectra of Compound B are shown on the next page. Using the molecular formula C,H,O: (a) Calculate the index of unsaturation. (b) Assign at least three absorption bands in the IR spectrum to functional groups. (C) By considering this value in your analysis of the spectra, give the correct structure for unknown B. Integration values are given above the peaks. (d) Label all peaks in the NMR spectrum, i.e., Ha, Hb, etc., and place...
Draw the structure that fits the following data. Molecular formula: C6H12O 1H NMR spectral data: 13C NMR spectrum: P...
Draw the structure that fits the following data. Molecular
formula: C6H12O 1H NMR spectral data: 13C NMR spectrum:
PLEASE HELP
the structure that fits the following data. Molecular formula: C6H12O H NMR spectral data: ppm 0.90 1.53 2.34 9.72 Integration6 4 1 1 Multiplicity triplet multiplet multiplet doublet C NMR spectrum:
5 Given the spectral data below, provide a structure. Note you must assign all of the...
5 Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below receive full credit. Also assign any key sionals in the IR OMS that assisted you in deriving your answer. (6 pts.) 6H. d 3H, d 2H. 1H, sextet PPM Relative Intensity M+s 164 m /z wavenumber im-11
CHE 310 Homework 9 Due WED NOV 20 6. Given the spectral data below, provide a...
CHE 310 Homework 9 Due WED NOV 20 6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer MS: M+-164 (no significant M+2 signal) (6 pts) 2H, 2H, d 2H. per 43 PPM 180 10 10 120 100 80 60 40 20 Relative Transmittance 2000 Wavenumber(cm-1)
6. Given the spectral data below, provide a structure. Note you must assign all of the...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
6. Given the spectral data below, provide a structure. Note you must assign all of the...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+ 164 (no significant M+2 signal) (6 pts.) 3H, s зн, 2H, d 2H, d 2H, q 8 6 5 PPM 140 120 100 180 160 80 PPM 60 40 0.8 0.6 0.4 3000 2000...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+ = 164 (no significant M+2 signal) (6 pts.) 3HS 2H. d 2Hd 2Hg 8 7 6 5 4 3 2 1 0 PPM 180 160 140 120 100 PPM 80 60 40 20 0...
Draw the structure that fits the following data. Molecular
formula: C6H12O 1H NMR spectral data: 13C NMR spectrum:
PLEASE HELP
the structure that fits the following data. Molecular formula: C6H12O H NMR spectral data: ppm 0.90 1.53 2.34 9.72 Integration6 4 1 1 Multiplicity triplet multiplet multiplet doublet C NMR spectrum:
Provide the correct structure for your unknown based on the
spectroscopic data provided. Provide the correct name for your
compound. Either the IUPAC name, or a commonly accepted name (i.e.,
ethyl acetate in place of ethyl ethanoate) will be accepted.IR
spectrum: Assign as many peaks as possible. In particular, you
should assign peaks that were important in making your structural
interpretation (i.e. functional group peaks such as OH, C=O, N-H,
etc.).
1H-NMR spectrum: Assign all the peaks in the spectrum...
4. The proton NMR and IR spectra of Compound B are shown on the next page. Using the molecular formula C,H,O: (a) Calculate the index of unsaturation. (b) Assign at least three absorption bands in the IR spectrum to functional groups. (C) By considering this value in your analysis of the spectra, give the correct structure for unknown B. Integration values are given above the peaks. (d) Label all peaks in the NMR spectrum, i.e., Ha, Hb, etc., and place...
Draw the structure that fits the following data. Molecular
formula: C6H12O 1H NMR spectral data: 13C NMR spectrum:
PLEASE HELP
the structure that fits the following data. Molecular formula: C6H12O H NMR spectral data: ppm 0.90 1.53 2.34 9.72 Integration6 4 1 1 Multiplicity triplet multiplet multiplet doublet C NMR spectrum:
5 Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below receive full credit. Also assign any key sionals in the IR OMS that assisted you in deriving your answer. (6 pts.) 6H. d 3H, d 2H. 1H, sextet PPM Relative Intensity M+s 164 m /z wavenumber im-11
CHE 310 Homework 9 Due WED NOV 20 6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer MS: M+-164 (no significant M+2 signal) (6 pts) 2H, 2H, d 2H. per 43 PPM 180 10 10 120 100 80 60 40 20 Relative Transmittance 2000 Wavenumber(cm-1)
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
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