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NMR Day 2 Version 2 6) CH.02 :50 richt aclaped Ihlamultiplet 12 10 8 6 HSP-01-671...
NMR Day 1 4) C,H,0 HOP-04-01 12 11 10 9 ppm (signal at -2.2ppm is considered a triplet; -1.5ppm is considered a multiplet) NMR Day 1 5) CsH100 NMR Day 1 6) C4H30 11 10 9 8 7 6 5 4 3 2 1 HSP-03-535 ppm
HNMR Question
2H, d 3H, m 1H, S 12 10 8 HSP-01-671 ppm
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)
Please deduce the following structures
8 6 2 12 10 ppm HSP-02-265
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...
II. Number of Signals 2. Predict the number of unique protons that would generate peaks in an NMR spectrum. Look at Figure 13.6 and example problem 13.2 for guidance. Then for each of these unique proton signals, predict the ppm range where you would find it and the integration value or signal area. Look at figure 13.7 in your textbook. Finally, determine the splitting pattern (multiplicity) of the signal. This is predicted using the n+1 rule. Watch the video for...
and draw the Structures Determine the Hydrogen Deficiency Index Challenges: C4H8O2 1.2 8: 3H triplet 3.0 8: 2H quartet 3.6 8: 3H singlet CoH14 1.3 8: 9H singlet 7.2 8:5H multiplet C&H;N 3.7 8:2H singlet 7.2 8:5H singlet C.H.CI,O2 1.4 8: 3H triplet 4.3 8: 2H quartet 5.9 8: 1H singlet CsH1002 1.2 8:6H doublet 2.0 8:3H singlet 5.0 8: 1H septet 'H NMR Practice Problems Best thing is to first determine the Hydrogen Deficiency Index so you know the...
II. Number of Signals 2. Predict the number of unique protons that would generate peaks in an NMR spectrum. Look at Figure 13.6 and example problem 13.2 for guidance. Then for each of these unique proton signals, predict the ppm range where you would find it and the integration value or signal area. Look at figure 13.7 in your textbook. Finally, determine the splitting pattern (multiplicity) of the signal. This is predicted using the n+1 rule. Watch the video for...
Using the NMR, IR, and MS figure out what the compoud is.
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identify the molecular structure througu NMR, IR and MS
CHEM 100L Lab 3 NMR Problems Unknown 1 CH 0 M-a 102 Relative Intensity 20 30 40 50 70 80 60 m/z water, not part of sample 1-2975-2877 9H, singlet 2H, 3H, quartet triplet ppm Unknown 2 C,H,O tensity 119 Relative 3200-2600 1680V 3H, singlet 2x 2H, doublet 1H, singlet ppm Unknown 3 C,HO, Relative Intensity 3090 3035...
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6. Reaction Coordinate Diagrams (10 points) (a) Sketch an accurate energy diagram that meets the following criteria (4 points) SM - OM Int - P SM - Int is endergonic and the slowest step. overall SM + P is exergonic. al Free Energy (G) Reaction Coordinate (b) Label the transitions states in your diagram (2 points) (c) Indicate AG. for the overall transformation (2 points) (d) Indicate E. for each step...