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determine structure and formula using the provided spectrums
Mass spectrum 100- 60- 20- myz 25 50...
determine the compound structure based on the spectrums. please explain. IR Spectrum liquid rim) 1600 1200...
determine the compound structure based on the
spectrums. please explain.
IR Spectrum liquid rim) 1600 1200 800 4000 3000 2000 V (cm') 100 콩2 No significant LV absorption above 220 nm 40 3 C6H1004 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (S0.0 MH, CDC, solution) proton decoupled 40 0 δ(ppm) 200 160 120 80 H NMR Spectrum (200 MHz, CDCi solution) 10 9 8 76 5 4 3 2 1 0 8 (ppm)
Find the compounds using NMR and IR: Problem 85 IR Spectrum (liquid fiim) 1720 1600 2000...
Find the compounds using NMR and IR:
Problem 85 IR Spectrum (liquid fiim) 1720 1600 2000 v (cm) 800 3000 1200 4000 100 Mass Spectrum 73 140 138 80 No significant UV 60 115 absorption above 220 nm 40 M 194/196 (1% ) 20 CeH1102Br 120 160 200 240 280 40 80 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH, Cн, сн! solvent proton decoupled 8 (ppm) 160 120 40 200 80 H NMR Spectrum (200 MHz, CDCI,...
Find the compounds using IR and NMR: Problem 25 2251 IR Spectrum (liquid film) 800 1600...
Find the compounds using IR and NMR:
Problem 25 2251 IR Spectrum (liquid film) 800 1600 1200 4000 3000 2000 v (cm) 100 Mass Spectrum M 117 80 77 60 91 40 20 CgH7N 200 80 120 160 240 280 40 m/e expansion 13C NMR Spectrum (100.0 MHz, CDCI, solution) 130 129 ppm DEPT CH Cн,! сн! expansion 130 129 ppm solvent proton decoupled (ppm) 40 200 160 120 80 H NMR Spectrum (400 MHz. CDCI, solution) TMS 10 7...
What would the structure look like using the mass spec with a parent peak of 162, IR, C-NMR and H-NMR? TRETTENCEI...
What would the structure look like using the mass spec with a
parent peak of 162, IR, C-NMR and H-NMR?
TRETTENCEI Singlet doublet Singlet triplet muitplet PPM halides 13C NMR: Broadband in provided below. DEPT data is in the provided table. 200 180 160 140 120 100 PPM 80 60 40 20 0 DEPT-135 positive DEPT-90 positive PPM 191 149 138 137 135 128 126 positive positive positive positive positive positive positive positive positive positive
determine the compound structure based on the spectrums 2114 3296 R Spectrum 4000 2000 1 V...
determine the compound structure based on the
spectrums
2114 3296 R Spectrum 4000 2000 1 V (cm) 3000 1600 1200 100 Mass Spectrum Du)-26)12-9-しキ N° significant uv absorption abave 220 nm 40 M-83 CsHgN 40 80 120 160 200 240 280 m/e 13 C NMR Spectrum (100 0 MHz, CDCi, solution) proton decoupied δ(ppm) 0 40 80 120 160 200 H NMR Spectrum (400 MHE, CDci, soudon) with 2H 2H 1H 2H 2H 1.5 8 (ppm) 10 9 8 7...
help me with the structure please i can't find the right structure. please help IR Spectrum...
help me with the structure please
i can't find the right structure. please help
IR Spectrum ad 4000 2000 1800 1200 800 Mass Spectrum CHO 280 40 60 120 160 200 240 mle 13C NMR Spectrum (50.0 MH2 CDC, son WA DEPT CH CH. CH proton decoupled 200 16012080 400 (ppm) 'H NMR Spectrum (200 M CDO, O 10 9 8 7 6 5 4 3 2 6 (ppm) IR Spectrum udim 4000 3000 2000 1800 1200 300 Mass Spectrum...
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...
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224 (25%) m/z IR Spectrum (not...
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224
(25%) m/z
IR Spectrum (not shown): 3060, 2985, 1600, 1495 cm-1 (all listed
are strong (s) unless otherwise indicated)
Please explain how you determine the organic compound for the
info given. Please check your compound with Chemdraw to verify your
answer before posting your answer (if you have Chemdraw).
Thanks!
NMR Spectrum (400 MHz, CDCI, 25 C) t (J 8Hz) PPM 1H1H 1H 3H C NMR Spectrum (with DEPT,...
determine the structure guven the information below. please state all information that supports this structure. IR...
determine the structure guven the information below. please
state all information that supports this structure.
IR Spectrum KB 1927 4000 3000 1200 2000 1600 V tom) 800 100 Mass Spectrum 80 60 No significant UV absorption above 220 nm 40 104 M 119 C4HNO, 4000 120 160 200 240 280 13C NMR Spectrum 11000 MLDO DEPT icht produit 200 160 120 80 40 0 (ppm) 'H NMR spectrum OU DOWN Na teremo preko wwch charge with the Dyosh 41 m...
Problem 3 IR Spectrum (quam 4000 3000 2000 1600 V (cm) 1200 800 Mass Spectrum So...
Problem 3 IR Spectrum (quam 4000 3000 2000 1600 V (cm) 1200 800 Mass Spectrum So base per 107/109 152/54 M 180/182 CgH9O2Br 40 80 120 160 mle 200 240 280 13C NMR Spectrum (50.0 CDC, on DEPT CHIC CHA over proton decoupled 200 160 120 80 400 8 (ppm) 'H NMR Spectrum (200 M COCI, solution 40 pm 10 9 8 7 6 5 4 3 2 8 (ppm)
determine the compound structure based on the
spectrums. please explain.
IR Spectrum liquid rim) 1600 1200 800 4000 3000 2000 V (cm') 100 콩2 No significant LV absorption above 220 nm 40 3 C6H1004 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (S0.0 MH, CDC, solution) proton decoupled 40 0 δ(ppm) 200 160 120 80 H NMR Spectrum (200 MHz, CDCi solution) 10 9 8 76 5 4 3 2 1 0 8 (ppm)
Find the compounds using NMR and IR:
Problem 85 IR Spectrum (liquid fiim) 1720 1600 2000 v (cm) 800 3000 1200 4000 100 Mass Spectrum 73 140 138 80 No significant UV 60 115 absorption above 220 nm 40 M 194/196 (1% ) 20 CeH1102Br 120 160 200 240 280 40 80 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH, Cн, сн! solvent proton decoupled 8 (ppm) 160 120 40 200 80 H NMR Spectrum (200 MHz, CDCI,...
Find the compounds using IR and NMR:
Problem 25 2251 IR Spectrum (liquid film) 800 1600 1200 4000 3000 2000 v (cm) 100 Mass Spectrum M 117 80 77 60 91 40 20 CgH7N 200 80 120 160 240 280 40 m/e expansion 13C NMR Spectrum (100.0 MHz, CDCI, solution) 130 129 ppm DEPT CH Cн,! сн! expansion 130 129 ppm solvent proton decoupled (ppm) 40 200 160 120 80 H NMR Spectrum (400 MHz. CDCI, solution) TMS 10 7...
What would the structure look like using the mass spec with a
parent peak of 162, IR, C-NMR and H-NMR?
TRETTENCEI Singlet doublet Singlet triplet muitplet PPM halides 13C NMR: Broadband in provided below. DEPT data is in the provided table. 200 180 160 140 120 100 PPM 80 60 40 20 0 DEPT-135 positive DEPT-90 positive PPM 191 149 138 137 135 128 126 positive positive positive positive positive positive positive positive positive positive
determine the compound structure based on the
spectrums
2114 3296 R Spectrum 4000 2000 1 V (cm) 3000 1600 1200 100 Mass Spectrum Du)-26)12-9-しキ N° significant uv absorption abave 220 nm 40 M-83 CsHgN 40 80 120 160 200 240 280 m/e 13 C NMR Spectrum (100 0 MHz, CDCi, solution) proton decoupied δ(ppm) 0 40 80 120 160 200 H NMR Spectrum (400 MHE, CDci, soudon) with 2H 2H 1H 2H 2H 1.5 8 (ppm) 10 9 8 7...
help me with the structure please
i can't find the right structure. please help
IR Spectrum ad 4000 2000 1800 1200 800 Mass Spectrum CHO 280 40 60 120 160 200 240 mle 13C NMR Spectrum (50.0 MH2 CDC, son WA DEPT CH CH. CH proton decoupled 200 16012080 400 (ppm) 'H NMR Spectrum (200 M CDO, O 10 9 8 7 6 5 4 3 2 6 (ppm) IR Spectrum udim 4000 3000 2000 1800 1200 300 Mass 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...
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224
(25%) m/z
IR Spectrum (not shown): 3060, 2985, 1600, 1495 cm-1 (all listed
are strong (s) unless otherwise indicated)
Please explain how you determine the organic compound for the
info given. Please check your compound with Chemdraw to verify your
answer before posting your answer (if you have Chemdraw).
Thanks!
NMR Spectrum (400 MHz, CDCI, 25 C) t (J 8Hz) PPM 1H1H 1H 3H C NMR Spectrum (with DEPT,...
determine the structure guven the information below. please
state all information that supports this structure.
IR Spectrum KB 1927 4000 3000 1200 2000 1600 V tom) 800 100 Mass Spectrum 80 60 No significant UV absorption above 220 nm 40 104 M 119 C4HNO, 4000 120 160 200 240 280 13C NMR Spectrum 11000 MLDO DEPT icht produit 200 160 120 80 40 0 (ppm) 'H NMR spectrum OU DOWN Na teremo preko wwch charge with the Dyosh 41 m...
Problem 3 IR Spectrum (quam 4000 3000 2000 1600 V (cm) 1200 800 Mass Spectrum So base per 107/109 152/54 M 180/182 CgH9O2Br 40 80 120 160 mle 200 240 280 13C NMR Spectrum (50.0 CDC, on DEPT CHIC CHA over proton decoupled 200 160 120 80 400 8 (ppm) 'H NMR Spectrum (200 M COCI, solution 40 pm 10 9 8 7 6 5 4 3 2 8 (ppm)
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