Acidolysis of vinyl acetate by fatty acids

Acid number, 32, 3 Acidolysis, of ethyl a-chlorophenyl-acetate by acetic add, 36,4 of vinyl acetate by fatty acids, 30, 106... [Pg.82]

Acidolysis of vinyl acetate by fatty adds, 30, 106 Acrolein acetal, 32, 5 Acrolein diethyl acetal, 32, 5 Acrylic acid, frans-/3-( -NiTROpHE. NYL)-a-PHENYL-, 35, 89 Acrylonitrile, 30, 80 Acrylonitrile, triphenyl-, 31, 52 Acylation of ethanolamine with phthalic anhydride, 32, 19... [Pg.103]

Vinyl esters are prepared by the reaction of a fatty acid with either acetjfene in direct condensation or vinyl acetate by acidolysis. [Pg.85]

Transesterification has a number of important commercial uses. Methyl esters of fatty acids are produced from fats and oils. Transesterification is also the basis of recycling technology to break up poly(ethylene terephthalate) [25038-59-9] to monomer for reuse (29) (see Recycling, plastics). Because vinyl alcohol does not exist, poly(vinyl alcohol) [9002-89-5] is produced commercially by base-cataly2ed alcoholysis of poly(vinyl acetate) [9003-20-7] (see Vinyl polymers). An industrial example of acidolysis is the reaction of poly(vinyl acetate) with butyric acid to form poly(vinyl butyrate) [24991-31-9]. [Pg.388]

See also in sourсe #XX -- [ Pg.106 ]

See also in sourсe #XX -- [ Pg.30 , Pg.106 ]

See also in sourсe #XX -- [ Pg.30 , Pg.106 ]

See also in sourсe #XX -- [ Pg.30 , Pg.106 ]

See also in sourсe #XX -- [ Pg.106 ]

See also in sourсe #XX -- [ Pg.30 , Pg.106 ]

See also in sourсe #XX -- [ Pg.30 , Pg.106 ]

See also in sourсe #XX -- [ Pg.30 , Pg.106 ]

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