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Main Concepts. SymmetryChemical ShiftIntegrationSplitting Patterns. How Symmetry Effects Interpretation. A molecule's symmetry determines how many signals you seeNeed to determine how many unique proton signals a molecule hasA molecule that is completely symmetric will have only one signalIn a
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1. H1 NMR Interpretation Lecture for Chem 2140
Spring 2012
2. Main Concepts Symmetry
Chemical Shift
Integration
Splitting Patterns
3. How Symmetry Effects Interpretation A molecule’s symmetry determines how many signals you see
Need to determine how many unique proton signals a molecule has
A molecule that is completely symmetric will have only one signal
In a molecule with no symmetry, every set of protons (on a carbon) will give a signal
In molecule with some symmetry, some protons are equivalent and will give one signal
4. Methane (CH4)
5. Propane (CH3-CH2-CH3)
6. Benzene
7. Phenol
8. Hydroquinone
9. Chemical Shift Refers to a shift from the standard tetramethylsilane (TMS) set at zero
Downfield: Away from zero/standard
Occurs for compounds that are more “deshielded” (i.e. near electronegative groups)
Upfield: Toward zero/standard
Occurs for compounds that are more “shielded”
10. Typical Chemical Shifts
11. Chemical Shifts to Scale
12. Integration The area “under the curve” of a signal (just like calculus)
Each signal’s area is directly proportional to number of protons for that signal
One signal is set as the standard
All other signals are relative to the standard
The standard can be set to any number of protons
Automatically set to “1” if not changed (i.e. if CH2 peak is set to 1, then all other signals are 2x the number given)
13. How Integration Relates to Symmetry A molecule’s symmetry determines how many unique proton signals are in the spectrum
Thus, if there are equivalent protons (on different carbons), those protons give only one peak
Similarly, integration accounts for ALL protons in a given peak
14. Splitting Patterns Different signals have different splitting patterns
These patterns come from protons coupling with neighboring protons
Each signal spits the neighboring proton (i.e. a methyl group has 3 equivalent protons all giving the same signal, thus neighboring protons split by 3 signals)
Only non-equivalent protons will couple (and thus) split each other
Equivalent protons are equal and give off the same signal
15. N+1 Rule The # of adjacent neighbors (N) of a given proton signal + 1 = splitting
0 neighbors = singlet (0+1 = 1)
1 = doublet (1+1 = 2)
2 = triplet (2+1 = 3)
3 = quartet (3+1 = 4)
4+= multiplet (4++1 =5+)
16. Pascal’s Triangle and Splitting
17. Ethyl Acetate
18. Pentanoic Acid
19. 3-Chloro 1-Iodopropane
20. 2-Chloropropane
21. Exchangeable Protons Protons that are attached to N, O, or S are often exchangeable with water
These protons may or may not appear in a spectra
Normally don’t integrate perfectly
Normally singlets and do not effect splitting