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From the given spectrums, what is the structure. label the
carbons and hydrogens
MASS of Base...
Identify the compound C8H9NO2 from its 1H, 13C/DEPT, COSY, HMQC, and INADEQUATE spectra and show all...
Identify the compound C8H9NO2 from its 1H, 13C/DEPT, COSY, HMQC,
and INADEQUATE spectra and show all correlations.
'H NMR 600 MHz 5480 5470 Hz 5200 5190 Hz 4910 4900 Hz 4370 4360 Hz 2590 2580 Hz 790 780 Hz 9.0 8.5 8.0 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 ppm 13C/DEPT 150.9 MHz 160 150 140 130 120 110 100 90 80 70 60 50 40 30 ppm 274 CHAPTER 5 Two-Dimensional NMR Spectroscopy Exercise...
label the spectrum OTBS Meo Yome Me H NMR spectrum (CDC13, 400 MHz) 8.5 8.0 7.5...
label the spectrum
OTBS Meo Yome Me H NMR spectrum (CDC13, 400 MHz) 8.5 8.0 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 f1 (ppm) 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 -0.5 18C NMR spectrum (CDCI, 100 MHz) 210 200 190 180 170 160 150 140 130 120 110 100 fi (ppm) 90 80 70 60 50 40 30 20 10 -10
please help me figure out what the compound is. thanks MASS % of Base Peak 1387...
please help me figure out what the compound is.
thanks
MASS % of Base Peak 1387 S47 677 957 123 50 60 70 80 90 100 110 120 130 140 awamp % Transmittance -2958 -2870 -16701 -13811 -1246 -903 STS TTT 4000 3000 1000 2000 Wavenumber (cm-') 'H NMR 300 MHz N 1750 1740 Hz 640 Hz 570 560 Hz 300 290 Hz 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 ppm 13C/DEPT NMR 75.5 MHz 200 180...
What is the molecular structure? 2 4 CHAPTER 8 ASSIGNED PROBLEMS Problem 8.43A MASS I 20...
What is the molecular structure?
2
4 CHAPTER 8 ASSIGNED PROBLEMS Problem 8.43A MASS I 20 sen par 43 100 131 85 109 95 1827 ? 185 50 200 50 100 150 200 m/z IR 100 90 E 70 4000 3000 2000 1000 Wavenumber (cm-1) 'H NMR 600 MHz 1260 1240 Hz 780 760 740 Hz 4.5 4.0 3.5 3.0 2.5 2.0 1.5 Ppm 1C/DEPT NMR 150.9 MHz 170 160 150 140 130 120 110 100 90 80 70 60...
A variety of spectra for an organic compound with molecular formula C10H16O are presented below. The experimental accurate mass using (+) APCI source is 153.1280 u. The 1H, 13C, COSY, HSQC and HMBC NM...
A variety of spectra for an organic compound with molecular
formula C10H16O are presented below. The
experimental accurate mass using (+) APCI source is 153.1280 u. The
1H, 13C, COSY, HSQC and HMBC NMR spectra are given in the following
slides. Propose a structure for this unknown and answer or address
the following questions or requirements:
a. Using the most abundant isotopes of C, H and O, what are the
errors in ppm and milli-Daltons for the experimental accurate
mass?...
A variety of spectra for an organic compound with molecular formula C10H16O are presented below. The experimental accurate mass using (+) APCI source is 153.1280 u. The 1H, 13C, COSY, HSQC and HMBC NM...
A variety of spectra for an organic compound with molecular
formula C10H16O are presented below. The
experimental accurate mass using (+) APCI source is 153.1280 u. The
1H, 13C, COSY, HSQC and HMBC NMR spectra are given in the following
slides. Propose a structure for this unknown and answer or address
the following questions or requirements:
d. If there are still any questionable assignments, propose
additional NMR experiments which would solve those questions and
briefly explain specifically what correlations you...
1.Identify the compound whose spectral data are shown. 2. Describe the coupling observed and show the...
1.Identify the compound whose spectral data are shown.
2. Describe the coupling observed and show the splitting diagram
for each hydrogen.
3. Determine the value of each coupling constants.
4. Label and assign each 1 H and 13 C signal to your answer.
100 3 % of Base Peak 90 80 100 120 m/z 5 SA % Transmittance --1689 -3047 --14197 --1273 -957 E9EE- -702 3000 1000 4000 'H NMR 300 MHz 2000 Wavenumber (cm-1) 2720 2700 Hz 2600 2580...
H2 Ha a) Given that the 'H NMR spectrum was acquired at 300 MHz, convert the ppm values...
H2 Ha a) Given that the 'H NMR spectrum was acquired at 300 MHz, convert the ppm values for the alkenyl region to Hz and provide the cis proton coupling constant to 1 decimal place. CEC Ha OH b) Please provide the chemical shift values for i) Both alkyne carbons i) The aromatic carbon bearing the substituent ii)H iv) H v) H vi) H H NMR spectrum as 25 1C NMR spectrum 9911 1C NMR spectrum 90 60 10 170...
Use the spectra below to determine the molecular formula and chemical structure of the unknown compound....
Use the spectra below to determine the molecular formula and
chemical structure of the unknown compound.
MASS 142 % of Base Peak 1147 40 50 70 80 5 100 % Transmittance Jari- 3000 1000 4000 'H NMR 300 MERE 2000 Wavenumber (cm) 3.0 25 20 15 Ppm 4.0 3.5 C/DEPT NMR 75.5 MHz ppm 60 50 40 80 70 90 100 110 120 170 160 150 140 130 ppm 4.5 4.0 3.5 3.0 2.5 2.0 1.5 ppm COSY 300 MHz...
Find structure of C8H8O by labeling the bonds of the IR structure, identifying the hydrogens (proton...
Find structure of C8H8O by labeling the bonds of the IR
structure, identifying the hydrogens (proton label, chemical shift,
# of protons and multiplicity), and identify the carbon labels and
chemical shift.
Diagnostic IR frequencies (cm-1). Wavenumber, cm: Stretching or Bending Type of Bond (e.g. O-H) Table of H Chemical shifts. If assignment is uncertain, group the labels, list a range of chemical shifts, and list as a multiplet. Proton Label Chemical shift, ppm No. of Protons Multiplicity Table of...
Identify the compound C8H9NO2 from its 1H, 13C/DEPT, COSY, HMQC,
and INADEQUATE spectra and show all correlations.
'H NMR 600 MHz 5480 5470 Hz 5200 5190 Hz 4910 4900 Hz 4370 4360 Hz 2590 2580 Hz 790 780 Hz 9.0 8.5 8.0 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 ppm 13C/DEPT 150.9 MHz 160 150 140 130 120 110 100 90 80 70 60 50 40 30 ppm 274 CHAPTER 5 Two-Dimensional NMR Spectroscopy Exercise...
label the spectrum
OTBS Meo Yome Me H NMR spectrum (CDC13, 400 MHz) 8.5 8.0 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 f1 (ppm) 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 -0.5 18C NMR spectrum (CDCI, 100 MHz) 210 200 190 180 170 160 150 140 130 120 110 100 fi (ppm) 90 80 70 60 50 40 30 20 10 -10
please help me figure out what the compound is.
thanks
MASS % of Base Peak 1387 S47 677 957 123 50 60 70 80 90 100 110 120 130 140 awamp % Transmittance -2958 -2870 -16701 -13811 -1246 -903 STS TTT 4000 3000 1000 2000 Wavenumber (cm-') 'H NMR 300 MHz N 1750 1740 Hz 640 Hz 570 560 Hz 300 290 Hz 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 ppm 13C/DEPT NMR 75.5 MHz 200 180...
What is the molecular structure?
2
4 CHAPTER 8 ASSIGNED PROBLEMS Problem 8.43A MASS I 20 sen par 43 100 131 85 109 95 1827 ? 185 50 200 50 100 150 200 m/z IR 100 90 E 70 4000 3000 2000 1000 Wavenumber (cm-1) 'H NMR 600 MHz 1260 1240 Hz 780 760 740 Hz 4.5 4.0 3.5 3.0 2.5 2.0 1.5 Ppm 1C/DEPT NMR 150.9 MHz 170 160 150 140 130 120 110 100 90 80 70 60...
A variety of spectra for an organic compound with molecular
formula C10H16O are presented below. The
experimental accurate mass using (+) APCI source is 153.1280 u. The
1H, 13C, COSY, HSQC and HMBC NMR spectra are given in the following
slides. Propose a structure for this unknown and answer or address
the following questions or requirements:
a. Using the most abundant isotopes of C, H and O, what are the
errors in ppm and milli-Daltons for the experimental accurate
mass?...
A variety of spectra for an organic compound with molecular
formula C10H16O are presented below. The
experimental accurate mass using (+) APCI source is 153.1280 u. The
1H, 13C, COSY, HSQC and HMBC NMR spectra are given in the following
slides. Propose a structure for this unknown and answer or address
the following questions or requirements:
d. If there are still any questionable assignments, propose
additional NMR experiments which would solve those questions and
briefly explain specifically what correlations you...
1.Identify the compound whose spectral data are shown.
2. Describe the coupling observed and show the splitting diagram
for each hydrogen.
3. Determine the value of each coupling constants.
4. Label and assign each 1 H and 13 C signal to your answer.
100 3 % of Base Peak 90 80 100 120 m/z 5 SA % Transmittance --1689 -3047 --14197 --1273 -957 E9EE- -702 3000 1000 4000 'H NMR 300 MHz 2000 Wavenumber (cm-1) 2720 2700 Hz 2600 2580...
H2 Ha a) Given that the 'H NMR spectrum was acquired at 300 MHz, convert the ppm values for the alkenyl region to Hz and provide the cis proton coupling constant to 1 decimal place. CEC Ha OH b) Please provide the chemical shift values for i) Both alkyne carbons i) The aromatic carbon bearing the substituent ii)H iv) H v) H vi) H H NMR spectrum as 25 1C NMR spectrum 9911 1C NMR spectrum 90 60 10 170...
Use the spectra below to determine the molecular formula and
chemical structure of the unknown compound.
MASS 142 % of Base Peak 1147 40 50 70 80 5 100 % Transmittance Jari- 3000 1000 4000 'H NMR 300 MERE 2000 Wavenumber (cm) 3.0 25 20 15 Ppm 4.0 3.5 C/DEPT NMR 75.5 MHz ppm 60 50 40 80 70 90 100 110 120 170 160 150 140 130 ppm 4.5 4.0 3.5 3.0 2.5 2.0 1.5 ppm COSY 300 MHz...
Find structure of C8H8O by labeling the bonds of the IR
structure, identifying the hydrogens (proton label, chemical shift,
# of protons and multiplicity), and identify the carbon labels and
chemical shift.
Diagnostic IR frequencies (cm-1). Wavenumber, cm: Stretching or Bending Type of Bond (e.g. O-H) Table of H Chemical shifts. If assignment is uncertain, group the labels, list a range of chemical shifts, and list as a multiplet. Proton Label Chemical shift, ppm No. of Protons Multiplicity Table of...
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