Download presentation
Presentation is loading. Please wait.
Published byJuniper Logan Modified over 9 years ago
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
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.