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Please help determining this structure and explain how you
got to that structure please because I’m...
Problem 112: treat the peaks at 2.3 ppm as two singlets, as the 1BC NMR confirms. Problem 112 I...
Problem 112: treat the peaks at 2.3 ppm as two singlets, as the 1BC NMR confirms. Problem 112 IR Spectrum 4000 3000 2000 1600 1200 V (cm) Mass Spectrum uv Spectrum 100 A,s. 265 nm (log10ε 2.6) λ max 271 nm 0og10ε 2.6 ) M* 150 solvent: methanol 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (100.0 MHz, CDC, solution) 24 20 ppm 24 proton decoupled 200 160 120 80 40 δ (ppm) H NMR Spectrum 400...
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)
Problem 79 4000 3000 2000 1600 1200 800 V (cm) Mass Specrum uv Spectrum 100 80...
Problem 79 4000 3000 2000 1600 1200 800 V (cm) Mass Specrum uv Spectrum 100 80 60 40t 3 20 max 260 nm (logroE 2.5) 91 solvent: methanol C11H16 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz, CDC, solution) proton decoupled 200 160 120 40 0 δ(ppm) H NMR Spectrum (200 MHz, CDci, solution) 7.5 7.0 ppm
Deduce the structure based on the information below: Concepts: organic spectroscopy, organic chemistry - Problem 53...
Deduce the structure based on the information below:
Concepts: organic spectroscopy, organic chemistry
- Problem 53 IR Spectrum (liquid film) 4000 3000 1600 1200 . 800 2000 V (cm Mass Spectrum % of baso peak No significant UV absorption above 220 nm 115 M+ 146 40 80 200 240 120 160 m/e 280 13C NMR Spectrum (50.0 MHz, CDC, solution) solvent proton decoupled 200 160 120 80 40 0 8 (ppm) TH NMR Spectrum (200 MHZ, CDCI, solution) TMS LIIIIIIIIIIIIIIIII...
What is the structure based on these spectroscopy graphs & how did you get this structure?...
What is the structure based on these spectroscopy graphs
& how did you get this structure?
IR spectrum liquid fim) 2000 1600 1200 V (cm) 100 31 Mass Spectrum No significant UV absorption above 210 nm 40 C3H602 40 80 120 160 200 240 280 13C NMR Spectrum (S0.0 MHL COC, solution) proton decoupled 80 40 0 δ(ppm) 200 160 120 3 H NMR Spectrum (100 MHz, CDCl3 solution) 2. δ (Dom) 10 9 8 7 6 5 4 3...
Can you please dumb this down and do it step by step closely with full explanation? I have the si...
Can you please dumb this down and do it step by step closely
with full explanation? I have the simple walkthrough already but
it's not helping much!
Thanks so much in advance!
problem 3 R Spectrum 2984 (iquid flm) 1741 1243 1600 1200 800 0.0 3000 100 Mass Spectrum0.5 60 아る29 20 UV spectrum solvent: ethanol 154 mg/10 mls palh length: 1.00 cm M 88 C4H802 1.5 250 300 350 40 80 120 160 200 240 280 λ(nm) m/e 13C...
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,...
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...
V (em) 100 Mass Spectrum No significant UV absorption above 210 nm 40E 8 C3H6 O2 40 80 120 160 20...
determine the compound structure based on the
spectrums.
V (em) 100 Mass Spectrum No significant UV absorption above 210 nm 40E 8 C3H6 O2 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (500 Mrz. Coci, solution) protion coupled proton decoupled 200 80 40 0 δ(ppm) 160 120 H NMR Spectrum (100 MHz, CDC, soluton) TMS expansion 4x 10 9 8 6 5 4 3 2 1 0 6 (ppm)
V (em) 100 Mass Spectrum No significant UV...
Determine the structure of the molecule with formula CeH,OCI from the following spectra and explain your...
Determine the structure of the molecule with formula CeH,OCI from the following spectra and explain your reasoning: 3. 875 1773 1738 IR Spectrum (liquid film) 800 2000 ,1600 1200 V (em1) 3000 4000 13C NMR Spectrum 100.0 MHz, CDA, solutanj 132 13t ppm preien decoupled r82 131 Dpmsolent 160 200 120 80 40 δ(ppm) 0 H NMR Spectrum (ad0 MH2. COc soution) exparslon 80 7.5 7.0 ppm TMS 10 9 87 654 3 2 1 δ (ppm)
Problem 112: treat the peaks at 2.3 ppm as two singlets, as the 1BC NMR confirms. Problem 112 IR Spectrum 4000 3000 2000 1600 1200 V (cm) Mass Spectrum uv Spectrum 100 A,s. 265 nm (log10ε 2.6) λ max 271 nm 0og10ε 2.6 ) M* 150 solvent: methanol 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (100.0 MHz, CDC, solution) 24 20 ppm 24 proton decoupled 200 160 120 80 40 δ (ppm) H NMR Spectrum 400...
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)
Problem 79 4000 3000 2000 1600 1200 800 V (cm) Mass Specrum uv Spectrum 100 80 60 40t 3 20 max 260 nm (logroE 2.5) 91 solvent: methanol C11H16 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz, CDC, solution) proton decoupled 200 160 120 40 0 δ(ppm) H NMR Spectrum (200 MHz, CDci, solution) 7.5 7.0 ppm
Deduce the structure based on the information below:
Concepts: organic spectroscopy, organic chemistry
- Problem 53 IR Spectrum (liquid film) 4000 3000 1600 1200 . 800 2000 V (cm Mass Spectrum % of baso peak No significant UV absorption above 220 nm 115 M+ 146 40 80 200 240 120 160 m/e 280 13C NMR Spectrum (50.0 MHz, CDC, solution) solvent proton decoupled 200 160 120 80 40 0 8 (ppm) TH NMR Spectrum (200 MHZ, CDCI, solution) TMS LIIIIIIIIIIIIIIIII...
What is the structure based on these spectroscopy graphs
& how did you get this structure?
IR spectrum liquid fim) 2000 1600 1200 V (cm) 100 31 Mass Spectrum No significant UV absorption above 210 nm 40 C3H602 40 80 120 160 200 240 280 13C NMR Spectrum (S0.0 MHL COC, solution) proton decoupled 80 40 0 δ(ppm) 200 160 120 3 H NMR Spectrum (100 MHz, CDCl3 solution) 2. δ (Dom) 10 9 8 7 6 5 4 3...
Can you please dumb this down and do it step by step closely
with full explanation? I have the simple walkthrough already but
it's not helping much!
Thanks so much in advance!
problem 3 R Spectrum 2984 (iquid flm) 1741 1243 1600 1200 800 0.0 3000 100 Mass Spectrum0.5 60 아る29 20 UV spectrum solvent: ethanol 154 mg/10 mls palh length: 1.00 cm M 88 C4H802 1.5 250 300 350 40 80 120 160 200 240 280 λ(nm) m/e 13C...
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,...
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...
determine the compound structure based on the
spectrums.
V (em) 100 Mass Spectrum No significant UV absorption above 210 nm 40E 8 C3H6 O2 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (500 Mrz. Coci, solution) protion coupled proton decoupled 200 80 40 0 δ(ppm) 160 120 H NMR Spectrum (100 MHz, CDC, soluton) TMS expansion 4x 10 9 8 6 5 4 3 2 1 0 6 (ppm)
V (em) 100 Mass Spectrum No significant UV...
Determine the structure of the molecule with formula CeH,OCI from the following spectra and explain your reasoning: 3. 875 1773 1738 IR Spectrum (liquid film) 800 2000 ,1600 1200 V (em1) 3000 4000 13C NMR Spectrum 100.0 MHz, CDA, solutanj 132 13t ppm preien decoupled r82 131 Dpmsolent 160 200 120 80 40 δ(ppm) 0 H NMR Spectrum (ad0 MH2. COc soution) exparslon 80 7.5 7.0 ppm TMS 10 9 87 654 3 2 1 δ (ppm)
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