PPT-NMR Nuclear Magnetic Resonance Spectroscopy

Author : calandra-battersby | Published Date : 2018-11-02

Nuclear Magnetic Resonance Spectroscopy Over the past fifty years nuclear magnetic resonance spectroscopy commonly referred to as nmr has become the preeminent technique

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NMR Nuclear Magnetic Resonance Spectroscopy: Transcript


Nuclear Magnetic Resonance Spectroscopy Over the past fifty years nuclear magnetic resonance spectroscopy commonly referred to as nmr has become the preeminent technique for determining the structure of organic compounds . Eluci. dation . Method. Janine A. . Ferrer. IV- BS Chemistry for Teachers. Nuclear Magnetic. Resonance. Spectroscopy. A spectroscopic technique that provides information about the carbon-hydrogen framework of a molecule.. Infrared Spectroscopy . Mass Spectrometry . Carbon-13 NMR. Proton NMR. Chromatography . 1. Infrared Spectroscopy. Absorption of infrared radiation causes bonds to vibrate. Different bonds absorb different wavelengths. These can be identified using the table on the data sheet. . 10-9. The NMR spectroscopy of . 13. C is of greater potential utility than that of . 1. H NMR.. The . 13. C spectra of an organic compound is much simpler than the . 1. H spectra because spin-spin coupling between adjacent carbon atoms and between carbon and hydrogen atoms can be avoided.. Department of Chemistry. Dylan W. Benningfield. Electron Spin Resonance (ESR). Electron spin resonance (ESR. ). Electron . paramagnetic resonance (EPR) . Study of paramagnetic materials. Radicals, bi-radicals, triplet states, unfilled conduction bands, transition metal ions, impurities in semi-conductors, etc.. David . J. . Keeble. Magnetic Resonance. Magnetic moments?. Magnetic. What matters is matter with moments. Matter: Leptons and quarks . The simplest fundamental particle is the lepton the . electron. Nuclear Magnetic Resonance. An NMR Spectrometer. 1. H and . 13. C. both have spin = ±1/2. 1. H is 99% at natural abundance. 13. C is 1.1% at natural abundance. The nuclei that are most useful to. organic chemists are:. Part-2. Prepared By. Dr. Khalid Ahmad . Shadid. Islamic University in . Madinah. Department of Chemistry. Chemical Shifts. Chemical shift: The relative energy of resonance of a nucleus resulting from its local environment. Part 1. Magnetic Resonance Imaging. A great multidisciplinary application of physics and other sciences. And example of a “pure science” discovery given a practical application. Based on NMR – Nuclear Magnetic Resonance – discovered in the 1940s. Fall . 2017. First Order Spectra. For a spectrum to be 1. st. order, the . D. n. between the chemical shifts of any given pair of nuclei must be much larger than the value of the coupling constant . Introduction to Spectroscopy. 2. Spectroscopy. is the study of the interaction of matter with the electromagnetic spectrum. Electromagnetic radiation displays the properties of both particles and waves. For . CHEM 481 Lab. Objectives. Student should gain better understanding of NMR spectroscopy.. . Student should gain experience in the acquisition, processing, and displaying NMR data.. . Student should gain experience in interpreting NMR data in order to establish structure for unknown organic molecules.. Fall . 2017. FACTORS THAT INFLUENCE PROTON SHIFTS. Local Fields. Shielding by e. -. that surround the resonating nuclei arise from . local fields . They are a simple function of e. -. density affected by induction, resonance and hybridization effects. Created by Sibrina N. Collins, Lei Yang, Kari Young, . Arpita. . Saha. , Gerard Rowe, Robert Holbrook and posted on . VIPEr. (. www.ionicviper.org. ) on July 18, 2014. Copyright Sibrina N. Collins, Lei Yang, Kari Young, . Chemistry 1060 Laboratory. Analysis. Purity determination. Thin Layer Chromatography (TLC). Separation and identification. stationary . phase – silica gel. mobile . phase – organic solvent. Relative attraction to the two phases.

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