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Conjugate classes

A few comments on the polar effects of the substituents reported in Tables IX—XI are now relevant. With the exception of 4-chloro-5-nitroquinoline (see Section IV, C, l,c), they involve only positions not subject to primary steric effects. The relations to the reaction center are of the conjugative cata, amphi) as well as of the non-conjugative class meta, epi, pros) as shown in Chart 3 by structures 45 and 46. [Pg.331]

The kinetic effects of some substituents on the fused benzene ring (CHg, NOg, OCHg, Cl) havc been determined recently for the reaction between the methoxide ion and the series of compounds aj-R-2-chlorobenzothiazole. Some of these effects are compared in Table XVIII with those observed at the 6-position of 2-chloroquino-lines and quinoxalines which are of the conjugative class. The data for... [Pg.349]

While glucuronide and sulfate molecular ion species are not seen in the PB mass spectra, the SAX-LC separation groups the compounds by conjugate class. Phenols elute first, followed by glucuronides, and then sulfates. Thus, tentative identification of unknown metabolites is possible based upon identification of the aglycone and the retention time window. [Pg.243]

The resistance of cereals is classified into different groups type I is resistance to primary infection, type II resistance to the spread of infection, type III is the resistance to infection of grains, type IV is tolerance against Fusarium head bhght (FHB) and trichothecenes, type V is the resistance to the accumulation of trichothecenes Class 1 is chemical modification (such as conjugation). Class 2 is inhibition of biosynthesis. [Pg.965]

CH = CH — CH = CH — are said to have conjugated double bonds and react somewhat differently from the other diolefins. For instance, bromine or hydrogen is often added so that a product of the type -CHBr-CH=CH-CHBr- is formed. Also, these hydrocarbons participate in the Diels-Alder reaction see diene reactions). They show a tendency to form rubber-like polymers. Hydrocarbons not falling into these two classes are said to have isolated double... [Pg.142]

The Huckel method and is one of the earliest and simplest semiempirical methods. A Huckel calculation models only the 7t valence electrons in a planar conjugated hydrocarbon. A parameter is used to describe the interaction between bonded atoms. There are no second atom affects. Huckel calculations do reflect orbital symmetry and qualitatively predict orbital coefficients. Huckel calculations can give crude quantitative information or qualitative insight into conjugated compounds, but are seldom used today. The primary use of Huckel calculations now is as a class exercise because it is a calculation that can be done by hand. [Pg.33]

Fully conjugated cyclopolyynes, so-called cyciocarbons, constitute another class of carbon modifications besides diamond, graphite, and the recently discovered fullerenes (see section 5.6). Syntheses of these unstable rings might be possible by mild elimination, extrusion, or... [Pg.338]

Thus cyclobutadiene like cyclooctatetraene is not aromatic More than this cyclo butadiene is even less stable than its Lewis structure would suggest It belongs to a class of compounds called antiaromatic An antiaromatic compound is one that is destabi lized by cyclic conjugation... [Pg.451]

Frosts circle (Section 11 19) A mnemonic that gives the Huckel TT MOs for cyclic conjugated molecules and 10ns Functional class nomenclature (Section 4 2) Type of lUPAC nomenclature in which compounds are named according to functional group families The last word in the name... [Pg.1284]

Methacryhc acid and its ester derivatives are Ctfjy -unsaturated carbonyl compounds and exhibit the reactivity typical of this class of compounds, ie, Michael and Michael-type conjugate addition reactions and a variety of cycloaddition and related reactions. Although less reactive than the corresponding acrylates as the result of the electron-donating effect and the steric hindrance of the a-methyl group, methacrylates readily undergo a wide variety of reactions and are valuable intermediates in many synthetic procedures. [Pg.246]

TT-conjugated. Only classes / and 2 have been used in copiers and printers. [Pg.134]


See other pages where Conjugate classes is mentioned: [Pg.332]    [Pg.334]    [Pg.339]    [Pg.58]    [Pg.25]    [Pg.213]    [Pg.195]    [Pg.232]    [Pg.174]    [Pg.387]    [Pg.332]    [Pg.334]    [Pg.339]    [Pg.58]    [Pg.25]    [Pg.213]    [Pg.195]    [Pg.232]    [Pg.174]    [Pg.387]    [Pg.1184]    [Pg.1188]    [Pg.1190]    [Pg.97]    [Pg.406]    [Pg.107]    [Pg.79]    [Pg.206]    [Pg.124]    [Pg.545]    [Pg.297]    [Pg.134]    [Pg.409]    [Pg.412]    [Pg.257]    [Pg.489]    [Pg.427]    [Pg.443]    [Pg.245]    [Pg.110]    [Pg.243]    [Pg.158]    [Pg.469]    [Pg.35]    [Pg.42]    [Pg.134]    [Pg.327]   
See also in sourсe #XX -- [ Pg.58 ]




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Classes of Dienes Conjugated and Otherwise

Conjugate Elements and Classes

Conjugation class

Conjugation class

Proteins, classes conjugated

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