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Disappearing peak

Table 1-28 lists the mean vibration frequencies characteristic of CH bonds (t/CH, 5CH, yCH) as a function of the substitution pattern. For the v(CH) vibrations, the highest frequency peak disappears in the spectra of 5-substituted derivatives, whereas it is unchanged by substitution at the 2-or 4-positions. This band has been assigned to the v(CH) vibration connected with the CH bond at the 5-position (173). [Pg.64]

The peak near 3085 cm disappears only for 2.4-disubstituted derivatives. Its frequency is slightly higher for 2- than for 4-substituted compounds. The vC(2)H and vC(4,H vibrations seem to be nearly equivalent and usually give rise to an unique peak, except in the case of 5-bromo-and 5-isopropylthiazoles in CCI4 solution, where this peak is split into two bands. [Pg.64]

Deuterium does not give a signal under the conditions of H NMR spectroscopy Thus replacement of a hydroxyl proton by deuterium leads to the disappearance of the OH peak of the alcohol Protons bonded to nitrogen and sulfur also undergo exchange with... [Pg.544]

Identify compound A (CgHioO) on the basis of its H NMR spectrum (Figure 15 10) The broad peak at 8 2 1 disappears when D2O is added... [Pg.663]

Retarders were originally arenecarboxylic acids. These acidic materials not only delay the onset of cross-linking but also slow the cross-linking reaction itself. The acidic retarders do not function weU in black-fiUed compounds because of the high pH of furnace blacks. Another type of retarder, A/-nitroso diphenylamine [86-30-6] was used for many years in black-fiUed compounds. This product disappeared when it was recognized that it trans-nitrosated volatile amines to give a several-fold increase in airborne nitrosamines. U.S. production peaked in 1974 at about 1.6 million kg. [Pg.226]

Figure 23-36 shows a computer calculation with these specific rates, but which does not agree quantitatively with the figure shown by Swern. The time scales appear to be different, but both predict a peak in the amount of oleic acid and rapid disappearance of the first two acids. [Pg.2114]

The progress of this reaction may be followed either by observing the disappearance of the band at 1845 cm. in the infrared or by following the replacement of the reactant proton magnetic resonance peak (carbon tetrachloride) at S 1.55 b the product peak at S 1.50. [Pg.49]

The XRD peaks characteristic of Co and Ni disappeared after the treatment, as did the broad ESR line, successfully leaving only the narrow asymmetric line with 26 G linewidth as shown in Fig. 8 [40]. The g-value of the narrow line is =2.002 0.001. The narrow ESR line shows Dysonian at all temperatures in the range of 4-300 K. Furthermore, the ESR intensity is quite independent of T and thus the density of conduction electrons is invariant as a function of temperature as shown in Fig. 9. These show that the material is highly metallic, even at low 7. [Pg.85]

Therefore, these synchrotron experiments show that the repeat distance for the smectic layer lies very close to, but is distinct from, that of the crystal. Moreover, the smectic peak disappears totally when the transformation is complete, indicating that the mesophase has been destroyed in the semicrystalline sample. [Pg.385]


See other pages where Disappearing peak is mentioned: [Pg.47]    [Pg.126]    [Pg.80]    [Pg.334]    [Pg.65]    [Pg.358]    [Pg.183]    [Pg.158]    [Pg.106]    [Pg.294]    [Pg.47]    [Pg.126]    [Pg.80]    [Pg.334]    [Pg.65]    [Pg.358]    [Pg.183]    [Pg.158]    [Pg.106]    [Pg.294]    [Pg.595]    [Pg.1452]    [Pg.1862]    [Pg.1928]    [Pg.2106]    [Pg.2486]    [Pg.223]    [Pg.541]    [Pg.819]    [Pg.319]    [Pg.348]    [Pg.353]    [Pg.399]    [Pg.49]    [Pg.41]    [Pg.182]    [Pg.436]    [Pg.116]    [Pg.273]    [Pg.354]    [Pg.256]    [Pg.171]    [Pg.541]    [Pg.819]    [Pg.185]    [Pg.129]    [Pg.298]    [Pg.385]    [Pg.520]   
See also in sourсe #XX -- [ Pg.80 ]




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Disappearance

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