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Name: 6. Use the spectral data given to identify the structure of the unknown compound with...
Amswer all parts please QUICKLY 6. Use the spectral data given to identify the structure of the unknown compound wit...
Amswer all parts please QUICKLY
6. Use the spectral data given to identify the structure of the unknown compound with chemical formula (C12H1602). (20 points) TOODE UV Spectum: 2 = 240 nm MW = 192 g/mol, ( Ombre HH2DSIMH IR resonance: 1610, 1729 cm', 13C NMR Spectrum (1000 MHz, CDCI, solution) DEPT CH CH CH proton decoupled solvent 200 160 120 B0 40 08 (ppm) TH NMR Spectrum (400 MHZ COCI, solution) expansion 9 8.0 7.5 PPM 10 9 8...
thanks for the help! Consider an unknown compound with the following molecular formula and spectral data:...
thanks for the help!
Consider an unknown compound with the following molecular formula and spectral data: CH3O2 a. Calculate the degrees of unsaturation for the formula. b. Draw a structure consistent with the spectral data. IR Spectrum CHO, 4000 3000 1800 1200 800 8 Mass Spectrum M12 8 8 No significant UV absorption above 220 mm 9 C6H802 240 220 40 80 120 160 200 13C NMR Spectrum (100 MHE, COCI, DEPT со сно сне prolon de coupled 200 TH...
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure...
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure for this compound in the box at the bottom of the page. Peak assignments written on the spectra may be worth partial credit. (5 marks) r IR Spectrum liquid film) 1735 1717 4000 3000 1200 800 2000 1600 V (cm) 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI Chit Cht solvent proton decoupled 100 no Sloml proton decoupled 200 160 120 80 40...
Use the spectral data provided to determine the structure of the following organic conpounds. IR Spectrum...
Use the spectral data provided to determine the structure of
the following organic conpounds.
IR Spectrum ouid im) 3410 4000 3000 2000 1600 1200 V (om: 800 100 Mass Spectrum 43 80 60 M (15) 71 20 40 120 80 160 200 240 280 m/e 13C NMR Spectrum (50.0 M, COCI, solution) DEPT CHt CH,t CHt solvent proton decoupled 0 8 (ppm) 40 80 120 200 160 'H NMR Spectrum (200 MHz, CDCI, solution) expansion exchanges with Dy0 50 pom...
Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and...
Deduce the following structure of the compound given their IR, H1
NMR, 13C NMR spectra, and assign IR functional group absorptions
and assign the structure's protons and carbons to their respective
spectral resonances.
Compound 4 Da- U6)+20 IR Spectrum Oquid fim) 1760 800 1200 2000 1600 3000 4000 v (cm) Mass Spectrum 100 43 No significant UV absorption above 220 nm M146 (1% ) 87 20 CH1004 280 40 80 120 m/e 160 200 240 13C NMR Spectrum (1000 MHz,...
Attached are four spectra for isomer with the MF= c12h14o4. Determine the structure for each molecule...
Attached are four spectra for isomer with the MF=
c12h14o4. Determine the structure for each molecule and draw them
below.
problem 63 IR Spectrum (CCI, solution) 1765 4000 3000 1200 800 2000 V (cm ) Mass Spectrum UV Spectrum & 8 8 g 8 of base 2 mar 269 nm (10910€ 2.7) humax 263 nm (10910 2.7) M -222 (< 1) 169 sahent: methanol 8 C12H1404 240 280 40 80 120 160 200 13C NMR Spectrum (50.0 MHz, COCI, solution)...
What is the structure of C14H12 with mw 180 based on the data given? I realize...
What is the structure of C14H12 with mw 180 based on the data
given?
I realize the structure on there is wrong but I am having
trouble interpreting the 1H NMR. I don't have much experience with
13C or 1H NMR and our professor does not explain this very well.
Could someone please explain the significance of dublets and
quartets in 1H NMR? Thank-you!
Problem 152 Trans IR Spectrum (CHCl solution 4000 3000 2000 v (cm 1600 ) 1200 8000...
9. Assign structures to compounds A through E on the basis of the spectral data given....
9. Assign structures to compounds A through E on the basis of the spectral data given. Clearly explain your reasons for making each assignment. d) Compound D: CH1002 NMR SPECTRUM TH NMR Spectrum (400 MHz, CDCI, solution) expansion 7.2 7.0 ppm TMS 10 9 8 7 6 5 4 3 2 1 shem 8 (ppm) IR SPECTRUM IR Spectrum (liquid film) 1760 4000 3000 1200 800 2000 v (cm 1600 ) Mass Spectrum and UV absorptions 108 Mass Spectrum UV...
Please include the following information allow with the molecular structure of the unknown compound: 1. IR-Include...
Please include the following information allow with the
molecular structure of the unknown compound:
1. IR-Include the major peaks and indicate the stretch
wavenumber and what bond it is.
2. UV-VIs- If there is a lambda max given, please briefly
indicate what structural element is contributing to it.
3. HNMR-Include proton label, chemical shift, multiplicity, and
integration.
4. CNMR- include the carbon label and the chemical shift.
Some additional information about the unknown compound:
Iodoform Test: Clear solution
Chromic Acid...
Identify the structure Problem 120 mm IR Spectrum liquid film) 1734 4000 3000 2000 1200 800...
Identify the structure
Problem 120 mm IR Spectrum liquid film) 1734 4000 3000 2000 1200 800 1600 V (cm) 100 Mass Spectrum M 128 80 60 40F wodowe No significant UV absorption above 220 mm 83 100 113 C-H1202 40 80 120 200 240 280 160 m/e 13C NMR Spectrum (100.0 MHZ. CDCI, solution) DEPT Chat Chat Cht W proton decoupled 200 160 120 80 40 O 8 (ppm) H NMR Spectrum (400 MHE, COCI, solution) expansions oppm 1936 ppi...
Amswer all parts please QUICKLY
6. Use the spectral data given to identify the structure of the unknown compound with chemical formula (C12H1602). (20 points) TOODE UV Spectum: 2 = 240 nm MW = 192 g/mol, ( Ombre HH2DSIMH IR resonance: 1610, 1729 cm', 13C NMR Spectrum (1000 MHz, CDCI, solution) DEPT CH CH CH proton decoupled solvent 200 160 120 B0 40 08 (ppm) TH NMR Spectrum (400 MHZ COCI, solution) expansion 9 8.0 7.5 PPM 10 9 8...
thanks for the help!
Consider an unknown compound with the following molecular formula and spectral data: CH3O2 a. Calculate the degrees of unsaturation for the formula. b. Draw a structure consistent with the spectral data. IR Spectrum CHO, 4000 3000 1800 1200 800 8 Mass Spectrum M12 8 8 No significant UV absorption above 220 mm 9 C6H802 240 220 40 80 120 160 200 13C NMR Spectrum (100 MHE, COCI, DEPT со сно сне prolon de coupled 200 TH...
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure for this compound in the box at the bottom of the page. Peak assignments written on the spectra may be worth partial credit. (5 marks) r IR Spectrum liquid film) 1735 1717 4000 3000 1200 800 2000 1600 V (cm) 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI Chit Cht solvent proton decoupled 100 no Sloml proton decoupled 200 160 120 80 40...
Use the spectral data provided to determine the structure of
the following organic conpounds.
IR Spectrum ouid im) 3410 4000 3000 2000 1600 1200 V (om: 800 100 Mass Spectrum 43 80 60 M (15) 71 20 40 120 80 160 200 240 280 m/e 13C NMR Spectrum (50.0 M, COCI, solution) DEPT CHt CH,t CHt solvent proton decoupled 0 8 (ppm) 40 80 120 200 160 'H NMR Spectrum (200 MHz, CDCI, solution) expansion exchanges with Dy0 50 pom...
Deduce the following structure of the compound given their IR, H1
NMR, 13C NMR spectra, and assign IR functional group absorptions
and assign the structure's protons and carbons to their respective
spectral resonances.
Compound 4 Da- U6)+20 IR Spectrum Oquid fim) 1760 800 1200 2000 1600 3000 4000 v (cm) Mass Spectrum 100 43 No significant UV absorption above 220 nm M146 (1% ) 87 20 CH1004 280 40 80 120 m/e 160 200 240 13C NMR Spectrum (1000 MHz,...
Attached are four spectra for isomer with the MF=
c12h14o4. Determine the structure for each molecule and draw them
below.
problem 63 IR Spectrum (CCI, solution) 1765 4000 3000 1200 800 2000 V (cm ) Mass Spectrum UV Spectrum & 8 8 g 8 of base 2 mar 269 nm (10910€ 2.7) humax 263 nm (10910 2.7) M -222 (< 1) 169 sahent: methanol 8 C12H1404 240 280 40 80 120 160 200 13C NMR Spectrum (50.0 MHz, COCI, solution)...
What is the structure of C14H12 with mw 180 based on the data
given?
I realize the structure on there is wrong but I am having
trouble interpreting the 1H NMR. I don't have much experience with
13C or 1H NMR and our professor does not explain this very well.
Could someone please explain the significance of dublets and
quartets in 1H NMR? Thank-you!
Problem 152 Trans IR Spectrum (CHCl solution 4000 3000 2000 v (cm 1600 ) 1200 8000...
9. Assign structures to compounds A through E on the basis of the spectral data given. Clearly explain your reasons for making each assignment. d) Compound D: CH1002 NMR SPECTRUM TH NMR Spectrum (400 MHz, CDCI, solution) expansion 7.2 7.0 ppm TMS 10 9 8 7 6 5 4 3 2 1 shem 8 (ppm) IR SPECTRUM IR Spectrum (liquid film) 1760 4000 3000 1200 800 2000 v (cm 1600 ) Mass Spectrum and UV absorptions 108 Mass Spectrum UV...
Please include the following information allow with the
molecular structure of the unknown compound:
1. IR-Include the major peaks and indicate the stretch
wavenumber and what bond it is.
2. UV-VIs- If there is a lambda max given, please briefly
indicate what structural element is contributing to it.
3. HNMR-Include proton label, chemical shift, multiplicity, and
integration.
4. CNMR- include the carbon label and the chemical shift.
Some additional information about the unknown compound:
Iodoform Test: Clear solution
Chromic Acid...
Identify the structure
Problem 120 mm IR Spectrum liquid film) 1734 4000 3000 2000 1200 800 1600 V (cm) 100 Mass Spectrum M 128 80 60 40F wodowe No significant UV absorption above 220 mm 83 100 113 C-H1202 40 80 120 200 240 280 160 m/e 13C NMR Spectrum (100.0 MHZ. CDCI, solution) DEPT Chat Chat Cht W proton decoupled 200 160 120 80 40 O 8 (ppm) H NMR Spectrum (400 MHE, COCI, solution) expansions oppm 1936 ppi...
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