Solution :
4) The given NMR spectrum belongs to 1-butanal (CH3CH2CH2CHO).
The four signals are due to four types of protons (a to d).
CH3 a CH2 b CH2 c CH d O
>> A triplet at 1.0 ppm is due to proton a of CH3 group.
>> A multiplet at 1 5 ppm is due to proton b of CH2.
>> A triplet at 2.2 ppm is due to proton c of CH2 group.
>> The chemical shift of proton d at 9.8 ppm due to presence of alhehydic proton.
5) The C-13 spectrum suggest the presence of 3-pentanone.
CH3CH2COCH2CH3
Both CH3 are equivalent, hence gives quartet at 10 ppm and both CH2 gives triplet at 25 ppm.
NMR Day 1 4) C,H,0 HOP-04-01 12 11 10 9 ppm (signal at -2.2ppm is considered...
NMR Day 1 7) C6H14. Chemical Shifts Observed: 1.22 ppm Quartet 0.855 ppm Singlet (very intense) 0.84 ppm Triplet NMR Day 1 8) CHg 10 9 8 7 6 4 3 2 1 5 ppm HSP-00-541 (signal at 7ppm is often referred to as a Multiplet)
NMR Day 2 Version 2 6) CH.02 :50 richt aclaped Ihlamultiplet 12 10 8 6 HSP-01-671 ppm (signal at -8.12ppm is a doublet; signals at -7.5-79ppm are a -triplet overlapped with a multiplet, respectively)
4. (4 points) Which of the structures shown below is consistent with its H-NMR spectrum? (formula = C9H110Br) 1 = multiplet 2 = multiplet 3 multiplet 4 triplet 5 - triplet 6 = quintet 11 TTTTTTTTTTT 10 9 8 7 6 5 3 2 ppm
4. (4 points) Which of the structures shown below is consistent with its H-NMR spectrum? (formula = C9H11OBr) 1 = multiplet 2 = multiplet 3 = multiplet 4 = triplet 5 = triplet 6 = quintet 11 10 9 8 7 s 4 3 į i o ppm
Determine the structure of the following given the spectrum and molecular formula CzH02 11 10 9 8 7 6 HSP-03-871 ppm C,H1202 TTTTTTT 11 10 9 8 7 5 2 1 . HSP-03-401 ppm C.H. 11 10 9 8 7 6 5 3 2 10 HSP-00-525 ppm H C HO 12 11 10 9 8 7 4 3 2 1 0 - 1 6 5 ppm HSP-02-753
this is the 1H NMR and 13C NMR of a structure. can someone help me find out exactly the structure ?? and also detailed as possible? & also can you identity if the structure is an alkane, alkyl, or an aromatic compoubd with no O or N? please thank you Unknown # 14 'H NMR: 90 MHz in CDC13 11 10 9 8 7 6 4 3 2 1 5 ppm HSP-03-605 Unknown # 14 1H NMR: 90 MHz in...
Data Interpretation - 'H NMR > 14 12 10 8 6 4 2 0 HSP-49-414 ppm What types of compounds do peaks at 7.6 - 8.7 correspond to? O Alcohols O Aldehydes O Aromatics O Carboxylic acids The peaks at 7.6 - 8.7 are a triplet and two doublets, which altogether integrate to 4 protons. What does this suggest about the structure of the molecule? O No structural information can be determined from this. The presence of a mono-substituted phenyl...
Fill out the chart. Help me understand what is going on here. 1H NMR Structure: Peak Chemical Shift (8) Multiplicity H Peak Chemical Shift (8) Multiplicity H 7 Ha OH 2 8 3 9 Name: 4 10 1,4 butanedoil 5 11 6 12 'H NMR Peak Chemical Shift (8) Multiplicity H Peak Chemical Shift (8) Multiplicity H 7 Structure: 2 8 WOH 3 9 4 10 Name: 5 11 6 12 Specify the multiplicity as a singlet (s), doublet (d),...
`C-CH₂ leach H₂C som aratet auntel 11 10 9 8 § 4 2 6 5 ppm HSP-00-231 (
Please help with all 10 1) Predict the structure of the compounds for the IR and 'H- a) CH1002 s, 3H s, 3H d, 2H d. 2H 11 10 HSP-03-442 ppm TRANSMETTRNCEI 1500 2000 1000 300g NAVENURSERI-1 Ca Hio o b) GIÁO S, 1H S, 3H s, 3H d, 1H d, 1H + S, IH 13 12 11 10 9 8 7 6 5 4 3 2 1 HSP-06-376 ppm 2000 1500 4000 1000 RAVENUHBERII c) CH1002 s, 1H t,...