The corresponding portion of the Audio

Slides:



Advertisements
Similar presentations
NMR - Recall From Last Week
Advertisements

13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy
Nuclear Magnetic Resonance Yale Chemistry 800 MHz Supercooled Magnet.
Return to Question of Equivalent hydrogens. Stereotopicity – Equivalent or Not? Are these two hydrogens truly equivalent? Seemingly equivalent hydrogens.
1 Features of an NMR spectrum: SHAPE Spin Coupling: Neighboring nuclei “split” NMR signals Usually n neighbors splits the signal into n+1 peaks Multiplicity.
Chemistry 125: Lecture 60 March 23, 2011 NMR Spectroscopy Chemical Shift and Diamagnetic Anisotropy, Spin-Spin Coupling This For copyright notice see final.
Chemistry 125: Lecture 66 April 9, 2010 Oxidizing/Reducing Reagents Bookeeping & Mechanism This For copyright notice see final page of this file.
Che 440/540 Proton Nuclear Magnetic Resonance (NMR) Spectroscopy.
Chemistry 125: Lecture 60 March 24, 2010 NMR Spectroscopy Isotropic J and Dynamics This For copyright notice see final page of this file.
Nuclear Magnetic Resonance
13.6 Interpreting Proton NMR Spectra. 1. number of signals 2. their intensity (as measured by area under peak) 3. splitting pattern (multiplicity) Information.
Interpreting 1H (Proton) NMR Spectra
NMR Theory and C-13 NMR. Nuclear Magnetic Resonance Powerful analysis – Identity – Purity No authentic needed Analyze nuclei – 1 H, 13 C, 31 P, etc –
13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy Based on McMurry’s Organic Chemistry, 7 th edition.
Nuclear Magnetic Resonance Spectroscopy. The Use of NMR Spectroscopy Used to map carbon-hydrogen framework of molecules Most helpful spectroscopic technique.
Nuclear Magnetic Resonance Spectroscopy
1 st -order spin-spin coupling We observe 1 st -order NMR spectra when the frequency difference between the chemical shifts of any given pair of nuclei.
A SSIGNMENT OF S PIN S YSTEMS NMR - The Coupling Constant 4-1 CHEM 430 – NMR Spectroscopy1 For each compound: Describe all spin systems Determine the number.
13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy Based on McMurry’s Organic Chemistry, 6 th edition.
Chromatography (Separations) Mass Spectrometry Infrared (IR) Spectroscopy Nuclear Magnetic Resonance (NMR) Spectroscopy X-ray Crystallography (visual solid.
Chapter 14 NMR Spectroscopy Organic Chemistry 6th Edition Dr. Halligan
To insert an Audio file on all slides click Insert click the Audio drop down arrow and select the type of audio you want. An audio file placed on the.
NMR Spectroscopy A proton NMR spectrum. Information from peaks: Size (integration), position and multiplicity.
Chapter 13 Structure Determination: Nuclear Magnetic Resonance Spectroscopy.
Nuclear Magnetic Resonance Spectroscopy A proton NMR spectrum. Information from peaks: magnitude (integration), position and multiplicity.
CHEM 344 Organic Chemistry Lab January 26 th & 27 th 2009 Structural Determination of Organic Compounds Lecture 3 – More NMR.
Nuclear Magnetic Resonance Spectroscopy
Structure Elucidation Method
13.6 Interpreting 1H NMR Spectra
CHEM 344 Spectroscopy of Organic Compounds Lecture 2 6 th and 10 th September 2007.
NMR Chapter 13 1 H-NMR Spectroscopy CHEMISTRY 220 Spring 2003.
CH 9-5: NMR Topic 3 - “Signal Splitting” The magnetic field of a specific H nucleus will be “influenced” by the H nuclei on adjacent carbon atoms. This.
Chapter 16 Nuclear Magnetic Resonance Spectroscopy.
NMR = Nuclear Magnetic Resonance
The Use of NMR Spectroscopy
Nuclear Magnetic Resonance
13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy
Proton Relationships Substitution test is the most reliable:
13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy
Nuclear Magnetic Resonance Spectroscopy
Nuclear Magnetic Resonance Spectroscopy
16.1 Intro to NMR Spectroscopy
Nuclear Magnetic Resonance Spectroscopy
NMR Nuclear Magnetic Resonance
continued on next slide
Only three of a maximum possible four stereoisomers exists for the molecule shown. These include a pair of enantiomers and a single meso compound. Meso.
The Use of NMR Spectroscopy
Nuclear Magnetic Resonance Spectroscopy
Copyrights apply.
                                                                                                                                                                                                                                                
continued on next slide
continued on next slide
Nuclear Magnetic Resonance Spectroscopy
13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy
13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy
A Summarized Look into…
Example Expect the signal for this hydrogen to be split into seven by the six equivalent neighbors. Expect the peak for the methyl hydrogens to be split.
Chapter 14 NMR: Connectivity
1H NMR Interpretation Number of Signals (Resonances)
Nuclear Magnetic Resonance Spectroscopy
Diamagnetic Anisotropy, Spin-Spin Coupling
Nuclear Magnetic Resonance Spectroscopy
Nuclear Magnetic Resonance (NMR) Spectroscopy
Nuclear Magnetic Resonance Spectroscopy
13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy
Organization news Archives of Physical Medicine and Rehabilitation
continued on next slide
The Use of NMR Spectroscopy
continued on next slide
Volume 22, Issue 4, Pages vii-viii (April 2015)
Presentation transcript:

Chemistry 125: review session April 6, 2011 This slide was used in reviewing NMR. The corresponding portion of the Audio file comes between 1:58 and 2:13. This For copyright notice see final page of this file

Question 8 diastereotopic ! enantiotopic ? enantiotopic different  C H D C C N H D B A same  (unless chiral, resolved solvent) enantiotopic no mirror plane mirror plane TMS D B C Could this 3 Hz doublet be due to long-range splitting by A? (> 3 Hz for larger field) different  There is no reciprocal 3 Hz quintet for A! Just the 7 Hz triplet from C! 1:3:3:1 7 Hz 1:2:1 Question 8