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Amides Benzene

Amine B.P. M.P. Acetamide Benz- amide Benzene- sulphon- amlde /)-Tolu- enesul- phon- amlde Benzal Derivative Pi crate 3-Nltro- phthal- Imlde 2 4- Dlnltro- phenyl Derivative Formyl Derivative Phenyl thio- urea... [Pg.658]

Bento amide Benzene- sulphon- amide p-Tolu- enesul- phon- amide Plcrate Formyl Derivative Other Derivatives... [Pg.659]

Benzamide Benzoyl amide Benzene Carbon Amide or Benzoic Acid Amidefcailed Benzamid or Benzol-saure-amid in Ger), CgH6.CO.NH2 mw 121.13,... [Pg.38]

Quinoline and Acridine and their homologues belong to the chromogens. The chromogen character is but slight and is only inconsiderably developed by introduction o amido-groups. The simple amido bases form yellow salts, which are, however, not dyestuifs. These are formed, however, by introduction of an amidated benzene residue. [Pg.207]

Amine Acet- amide Benz- amide Benzene sulfon- amide Picrate Melting point, C Position of nitro groups ... [Pg.336]

Amine Acet amide Ben amide Benzene sulion amide Picrate Melting point X Position ol nilro groups... [Pg.343]

Figure 3. NMR spectra (15.4 MHz) of at natural abundance for a mixture of common solvents, as indicated from left to right dimethylformamide (amide), benzene, ethanol (hydroxyl), ethanol (methylene), dimethylformamide (methyl), acetone, ethanol (methyl), tetramethylsilane. The D in each formula is to emphasize that for a molecular species containing at natural abundance all other hydrogen is Key A, proton-coupled B, proton-decoupled. (From Ref. A.)... Figure 3. NMR spectra (15.4 MHz) of at natural abundance for a mixture of common solvents, as indicated from left to right dimethylformamide (amide), benzene, ethanol (hydroxyl), ethanol (methylene), dimethylformamide (methyl), acetone, ethanol (methyl), tetramethylsilane. The D in each formula is to emphasize that for a molecular species containing at natural abundance all other hydrogen is Key A, proton-coupled B, proton-decoupled. (From Ref. A.)...
P. Ottiger, C. Pfaffen, R. Leist, S. Leutwyler, R.A. Bachorz. and W. Klopper, Strong N-H...7T hydrogen bonding in amide-benzene interactions,... [Pg.94]

Amine Acct amide Benz amide Benzene sulfon amide Picrate... [Pg.341]

Amine Acet amide Bena amide Benzene sullon amide Picrate Melting point C Position ol nitro groups... [Pg.343]

See other pages where Amides Benzene is mentioned: [Pg.71]    [Pg.59]    [Pg.301]    [Pg.30]    [Pg.73]    [Pg.78]    [Pg.30]    [Pg.262]    [Pg.96]    [Pg.1760]   
See also in sourсe #XX -- [ Pg.69 ]



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