1- Benzoate 2-naphthoate ethylene

The overall transesterification reaction found to follow a second-order law. The reversibility of the transesterification was confirmed by heating a mixed sequence of 1-benzoate 2-naphthoate ethylene (BEN). Both forward reaction of the equimolar amounts of the reagents and reverse reaction come to equilibrium at the same molar ratio of the reactants and reaction products of roughly 0.25 0.50 0.25 for BEB, BEN, and NEN, respectively. [Pg.357]

Benzoate 2-naphthoate ethylene, 357 Benzoic acid, 393, 396, 398 Benzonitrile, 263, 286, 318 Benzophenone, 223, 312 3,3, 4,4 -Benzophenone dianhydride, 477, 481 3,3, 4,4 -Benzophenone tetracarboxylic dianhydride, 494 1 -B enzothiazol-3 -phenyl-pyrazoline, 32 Benzotriazole, 317... [Pg.580]

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