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Spectrum, reference

Problem 13.18 How many peaks would you expect in the H NMR spectrum of 1,4-dimethyl-benzene (pom-xylene, or p-xylene) What ratio of peak areas would you expect on integration of the spectrum Refer to Table 13.3 for approximate chemical shifts, and sketch what the spectrum would look like. (Remember from Section 2.4 that aromatic rings have two resonance forms.)... [Pg.459]

Silene IR method temperature (K) IR bands observed0 (cm-1) Calculated Si=C stretching frequency (cm-1) Reference for observed spectrum Reference for calculated spectrum... [Pg.11]

Figure 23-1 A part of the electromagnetic spectrum. The letters Vy By G, Y, O, R over the visible part of the spectrum refer to the colors of the light. The position marked "Ka line of Cu" is the wavelength of X-rays and most widely employed in X-ray diffraction studies of proteins and other organic materials. Figure 23-1 A part of the electromagnetic spectrum. The letters Vy By G, Y, O, R over the visible part of the spectrum refer to the colors of the light. The position marked "Ka line of Cu" is the wavelength of X-rays and most widely employed in X-ray diffraction studies of proteins and other organic materials.
IR/Raman spectrum Reference 15. h Electron diffraction Reference 25. [Pg.776]

IR, cm 1 (medium) (reference) H-NMR, 8 (solvent) (reference) l3C-NMR (solvent) ( 8) Mass spectrum (reference)... [Pg.299]

Fig. 7.—Structural-reporter-group Regions of the Resolution-enhanced, 500-MHz, H-N.m.r. Spectrum of Compound 7. [The bold numbers in the spectrum refer to the corresponding residues in the structure. Signals of corresponding protons in the a and anomer of 7, occurring in this anomeric mixture in the ratio of 2 1, coincide, unless otherwise indicated. The relative-intensity scale of the N-acety 1-proton region (see insertion) differs from that of the other part of the spectrum, as indicated. The HOD resonance has been omitted from the spectrum its position is indicated by an arrow.]... Fig. 7.—Structural-reporter-group Regions of the Resolution-enhanced, 500-MHz, H-N.m.r. Spectrum of Compound 7. [The bold numbers in the spectrum refer to the corresponding residues in the structure. Signals of corresponding protons in the a and anomer of 7, occurring in this anomeric mixture in the ratio of 2 1, coincide, unless otherwise indicated. The relative-intensity scale of the N-acety 1-proton region (see insertion) differs from that of the other part of the spectrum, as indicated. The HOD resonance has been omitted from the spectrum its position is indicated by an arrow.]...

See other pages where Spectrum, reference is mentioned: [Pg.534]    [Pg.316]    [Pg.143]    [Pg.199]    [Pg.81]    [Pg.11]    [Pg.231]    [Pg.258]    [Pg.265]    [Pg.279]    [Pg.281]    [Pg.288]    [Pg.297]    [Pg.299]    [Pg.312]    [Pg.318]    [Pg.326]    [Pg.329]    [Pg.335]   
See also in sourсe #XX -- [ Pg.111 ]




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Authentic reference spectra

C NMR Spectra of Secondary Reference Compounds

Fourier transform infrared reference spectra

Hormones, spectra, reference

Major Reference Masses in the Spectrum

Mass reference spectrum

Mass spectrum reference spectra

Multiplicative scatter correction reference spectrum

NMR Spectra of Secondary Reference Compounds

Nuclear magnetic resonance reference spectra

Paper reference standard, spectrum

Proton reference spectra

Pure component reference spectra

Reference Masses in the Spectrum of Heptacosafluorotributylamine (Perfluorotributylamine)

Reference emission spectra

Solar irradiance reference spectra

Spectra References (Including Theory in Some Cases)

Spectra and Reference Library

Spectra of Solvents and Reference Compounds

Spectrum, reference solar

The AM 1.5 G Reference Spectrum

Vibrational Spectra of Reference Materials

Vibrational overtone spectra references

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