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Naming, acid anhydrides sulfides

Naming, acid anhydrides—cont d prostaglandins, 1069 sulfides, 668 thioesters. 787 thiols, 667... [Pg.1308]

Compound Name Methyl Acetate Propionic Acid Propionic Anhydride Methyl Mercaptan Dimethyl Sulfide Formic Acid Methyl Alcohol Hexamethylenetetramine Methoxychlor Methoxychlor Diethylebe Glycol Monomethyl Ether Methylacetylene-Propadiene Mixture Methylacetylene-Propadiene Mixture Crotonaldehyde Methyl Acrylate Methyl Formal Methyl Alcohol Methallyl Chloride Methylamine N-Methylaniline Methyl Amyl Acetate Methyl Amyl Alcohol Methyl Isobutyl Carbinol N-Amyl Methyl Ketone O-Toluidine 0-Toluidine N-Methylaniline N-Methylaniline Propyleneiniiine. [Pg.152]

More complicated structures without symmetry were named end to end. This method was partieularly appropriate for the poly(oxides) of the form -(R-O-R -O h (and for the analogous sulfides, sulfones, ureas, and anhydrides) and for the poly(o-amino acids) and for the poly (o-hydroxy aeids). The constitutional hydrocarbon subunits were ordered alphabetieally in naming the polymer as, for example, in poly(methyleneoxy pentamethylene oxide). [Pg.876]


See other pages where Naming, acid anhydrides sulfides is mentioned: [Pg.260]    [Pg.194]    [Pg.194]    [Pg.763]    [Pg.194]    [Pg.3]   
See also in sourсe #XX -- [ Pg.668 ]

See also in sourсe #XX -- [ Pg.693 ]




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