Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Identification of functional groups

Proton and carbon-13 nmr spectroscopy provides detailed information on all types of hydrogen and carbon atoms, thus enabling identification of functional groups and types of linkages ia the lignin stmcture. Detailed a ssignments of signals ia proton and carbon-13 nmr spectra have been pubHshed... [Pg.141]

Solvent selection ana screening approaches can be divided into two levels of analysis. The first level focuses on identification of functional groups or chemical famihes that are hkely to give favorable solvent-key component molecular interactions. The second level of analysis identifies and compares individual-candidate solvents. The various methods of analysis are described briefly and illustrated with an example of choosing a solvent for the methanol-acetone separation. [Pg.1317]

Until the second half of the twentieth century, the structure of a substance—a newly discovered natural product, for example—was determined using information obtained from chemical reactions. This information included the identification of functional groups by chemical tests, along with the results of experiments in which the substance was broken down into smaller, more readily identifiable fragments. Typical of this approach is the demonstration of the presence of a double bond in an alkene by catalytic hydrogenation and subsequent determination of its location by ozonolysis. After-considering all the available chemical evidence, the chemist proposed a candidate structure (or structures) consistent with the observations. Proof of structure was provided either by converting the substance to some already known compound or by an independent synthesis. [Pg.519]

Infrared absorption spectra of heteropyrans have been used mainly for the identification of functional groups. Assignments of the bands belonging to heterocyclic bond vibrations (C=C, C—S, C—Se, C—Te) have not been common. As a rule, 4W-heteropyrans exhibit maxima at higher wave numbers than 2//-isomers. Typical IR absorption maxima for heteropyrans are shown in Table X. [Pg.235]

Neutral loss scan3 Scan with constant loss of neutral group identification of functional groups High Medium... [Pg.149]

Infrared absorption spectra have frequently been used in structure proof of imidazo[2,l-h]thiazoles, but identification of functional groups is the... [Pg.298]

Feldman HJ, Dumontier M, Lng S et al. (2005) CO a chemical ontology for identification of functional groups and semantic comparison of small molecules. FEES Lett 579 4685-4691... [Pg.146]

Molecular Photography in the Undergraduate Laboratory Identification of Functional Groups Using Scanning Tunneling Microscopy 74... [Pg.126]

It was noted that more refinement in spectral resolution was still needed. The combination of proton enhanced C-13 spectra combined with magic angle spinning made possible the identification of functional groups in the four DGEBA epoxy systems. A peak between 70-73 ppm were evidenced in all four systems indicative of the carboxyl-methine ether carbon of the reacted epoxide groups and adjacent methylene groups. [Pg.102]

PI Thomas, L. C., The Identification of Functional Groups in Organophosphorus Compounds, Academic London, (1974). [Pg.525]

The IR spectrum is extremely useful for the identification of functional groups in the unknown. The tables given in the chapter on IR spectroscopy should be consulted. Briefly IR is helpful in identifying the following ... [Pg.237]

A comparison of the data in Fig. 2 (Plate A, filled circles) and Fig. 5 (Plate B, open symbols) reveals that the performance of the heat-treated wood-based carbon, even under some preloading conditions, is similar to single solute TCE uptake by coal-based activated carbons in the absence of preloading [9]. The observed effect may result from some combination of optimum surface acidity, optimal type of surface functional group, and/or pore structure effects. The WVB carbon has a mesoporous pore structure, which has been observed to minimize the impacts of preloading in preliminary comparative experiments designed to isolate this effect (data not shown). Future work will employ carbon surface characterization techniques that will allow identification of functional groups and more accurate correlation with surface reactivity. [Pg.559]

The only trap is in the reduction of the cyclic keto-ester where you need to recall that NaBH4 reduces ketones but doesn t reduce esters. Correct identification of functional groups matters. [Pg.35]

FI. J. Feldman, M. Dumontier, S. Ling,., N Haider, C.W.V. Hogue (2005) CO A Chemical Ontology for Identification of Functional Groups and Semantic Comparison of Small Molecules, FEES Letters, 579, 4685-4691. [Pg.90]

Owing to the orientation dependence that it imparts to the NMR frequency, the chemical-shift anisotropy (CSA) has proven useful not only in studies of slow dynamics but also for characterizing segmental orientation distributions and fast segmental reorientations. While static powder patterns provide this CSA information in the most accessible form, site resolution by MAS is indispensable in all but the simplest unlabeled systems. The two requirements can be combined in two-dimensional (2D) separation experiments. Recently, a robust sequence, termed separation of undistorted powder-patterns by effortless recoupling (SUPER), was introduced that makes CSA measurements under standard MAS conditions routine.28 It enables identification of functional groups and measurements of orientation distributions, segmental dynamics, and conformations. [Pg.3]

Identification of Functional Groups. Representative ESCA spectra of the C(ls) and F(1s) regions are shown in Figs. 2 and 3. Qualitatively similar spectra were obtained for films prepared from TFE, HTP, and PF2B. Only one distinct peak is seen in the F(ls) region, corresponding to covalently bonded fluorine. [Pg.149]

Understanding of specific reactions for identification of functional groups and organic compounds... [Pg.330]

These parts of organic molecules are called functional groups. The identification of functional groups and the ability to predict reactivity based on functional group properties is one of the cornerstones of organic chemistry. [Pg.75]


See other pages where Identification of functional groups is mentioned: [Pg.32]    [Pg.325]    [Pg.333]    [Pg.211]    [Pg.314]    [Pg.334]    [Pg.334]    [Pg.338]    [Pg.541]    [Pg.26]    [Pg.372]    [Pg.42]    [Pg.273]    [Pg.521]    [Pg.72]    [Pg.4]    [Pg.171]    [Pg.126]    [Pg.210]    [Pg.3470]    [Pg.817]    [Pg.164]    [Pg.99]   


SEARCH



Functional group identification

© 2024 chempedia.info