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1 H-NMR SPECTROSCOPY 2008. Unknown C 4 H 8 O 2 1 H-NMR.

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Presentation on theme: "1 H-NMR SPECTROSCOPY 2008. Unknown C 4 H 8 O 2 1 H-NMR."— Presentation transcript:

1 1 H-NMR SPECTROSCOPY 2008

2 Unknown C 4 H 8 O 2

3 1 H-NMR

4 1 H-NMR - Theory 3.1 Nuclear Spin States 3.2 Nuclear Magnetic Moments 3.3 Absorption of Energy

5 1 H-NMR - Theory

6 3.4 Absorption / Resonance

7 1 H-NMR 3.7 The Spectrometer The FID (Free Induction Decay) Fourier Transform (time domain signal converted to frequency domain signal)

8 1 H-NMR – Chemical Shift Chemical equivalence Hybridization effects Electronegativity Effects Shielding (vs deshielded) hexane

9 1 H-NMR Chemical Shift Hybridization effects Electronegativity Effects

10 1 H-NMR – Chemical Shift

11 Acidic and Exchangeable Protons - Chemical Shift Ranges Exchangable proton Chemical Shift Range (ppm) AcidsRCOOH10.5 - 12 PhenolsArOH4.0-7.0 (as high as 9.0) AlcoholsROH0.5 – 5.0 AminesRNH20.5 – 5.0 AmidesRCONH25.0 - 9.0

12 1 H-NMR – Chemical Shift Magnetic Anisotropy (3.12)

13 1 H-NMR – Coupling Spin-Spin Splitting (3.13)

14 1 H-NMR – Coupling Spin-Spin Splitting (3.13)

15 1 H-NMR – Coupling Spin-Spin Splitting (3.13)

16 1 H-NMR – Coupling The Coupling Constant (3.17)

17 1 H-NMR – Coupling The Coupling Constant (3.17)

18 1 H-NMR – Coupling The Coupling Constant (3.17)

19 1 H-NMR – Coupling The Coupling Constant (3.17)

20 1 H-NMR – Coupling The Coupling Constant (3.17)

21 C 6 H 5 -CH=CH-CO 2 CH 3 C 10 H 10 O 2 1 H-NMR – Coupling - The Coupling Constant (3.17) 3089.8 3073.8 2587.62571.6

22 1 H-NMR - Aromatics (3.19C)

23 1 H-NMR 4-n-propylphenol

24 1 H-NMR - Aromatics Chemical Shift Calculation 6.75 vs 7.03 ppm

25 1 H-NMR – Unknown (C 6 H 4 Br)

26 1 H-NMR – Unknown (C 6 H 6 BrN)

27 C7H7OBr 1 H-NMR – Unknown (C 7 H 7 BrO)

28 Unknown A (C 7 H 14 ) Unknown B (C 7 H 14 ) 1 H-NMR – Unknown isomers


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