B EUIDE TO 'H NMR CHEMICAL SHIFT VALUES ce (NMR) is 2 commonly used technique for x ogee ‘compound structure determination. In 1H NMR, aj Fe hich spin to flip. The environment of the proton in the molecule affects where the signal is seen on the r 130 125 120 MS 110 WS 100 95 90 85 80 75 10 65 60 55 50 45 40 35 30 25 20 15 10 05 0 a Illa ll ri cs 1 er eer Ess Gees Gees Giemet iiemain dasenaa ras mains Vicia aes ee leo ag aH sage cm anpectncanmoee aft ompoundchem | Facebook: wwauracebookonvcompounschem EY PYGY(S) Nobels ene ©OSOSPECTROSCOPY REFERENCE TABLES ‘H-NMR Sn-H R-oH ia dethielded (donnfiel) Shielded Cupfield) wa Sb veges Epics ZN Soa x-d-H Xe Fae Allylic GH PAZIIIIZIZ EMI LyA GUIDE TO °C NMR CHEMICAL SHIFT VALUES Nuclear Magnetic Resonance (NMR) is 2 commonly used technique for organic compound structure determination. In ™C NMR, applying an external ‘magnetic field causes the nuclei spin to flip. The environment of the carbon atom in the molecule affects where the signalis seen on the resultant spectrum. CHEMICAL SHIFT (5, ppm) Only 1% of carbon atoms are carbon-13, ators which have one more neutron than carbon-12, NMR doesn’t 12 Oo, 13 BR cre Se caries ws rece tet tore ihe recpeicy sonnel to pt cmt? moins 0 BS yese seme te Corel ty tprcierrnsar en rks Mane omens on aden ‘carbons in a single molecule being carbon-13 atoms is very low, no splitting of peaks is seen, unlike in H-NMR. © COMPOUND INTEREST 2015- WW-COMPOUNDCHEM-COM | Twitter: @compoundchem | Facebook: wiv facebook convcompoundchem \(YGYS) CU) This graphics shared under a Creative Commons Antribution-NonCommerdal-NoDerivatives licence,