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Monday, 12 January 2015

13C NMR 1- OCTYNE










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13C NMR ETHYL BENZENE










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13C NMR......1- HEXYNE





Absorption by triply bonded (sp-hybridized) carbon falls between the regions for sp3-hybridized carbon, as shown for 1-hexyne.

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Interpretation of methylene-proton NMR signals of 1,3-dimethyl-substituted alkyl chains





Unraveling the unknown: Interpretation of methylene-proton NMR signals of 1,3-dimethyl-substituted alkyl chains allows for the assignment of the relative ...





Assignment of Relative Configuration of Desoxypropionates by 1H NMR Spectroscopy: Method Development, Proof of Principle by Asymmetric Total Synthesis of Xylarinic Acid A and Applications (pages 7071–7081)
Dr. Yvonne Schmidt, Dipl.-Chem. Konrad Lehr, Lucie Colas and Prof. Dr. Bernhard Breit
Article first published online: 27 APR 2012 | DOI: 10.1002/chem.201103988
Thumbnail image of graphical abstract
Unraveling the unknown: Interpretation of methylene-proton NMR signals of 1,3-dimethyl-substituted alkyl chains allows for the assignment of the relative configuration of the two adjacent stereogenic centers (see figure). The new method is applicable in various NMR solvents and general trends and rules for assignment are shown. Natural products with unknown configuration can be assigned by using the information gained from already published spectra.
Corrected by:
Vol. 18Issue 4514226Article first published online: 25 OCT 2012







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Heterocyclic aldehyde


1H-NMR and 13C-NMR for a heterocyclic aldehyde. Notice the correlation between the chemical shifts in the two spectra. The proton spectrum has a sweep width of 10 ppm, and the carbon spectrum has a width of 200 ppm.


The peak areas of the 13C-NMR are not proportional to the number of carbons giving rise to the peaks. Carbons with no protons attached to them usually give rise to small peaks. In the proton spin decoupled 13C-NMR each carbon signal appears as a unsplit singlet. The heterocyclic aldehyde has 5 carbons all in different environments so the spectrum will show 5 peaks.

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