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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/26608


    Title: Kinetics of the nucleophilic substitution of benzyltributylammonium bromide with allyl, butyl, and benzyl chlorides and with benzyl acetate and benzyl ether
    Authors: Wang,TT;Chang,CH;Huang,TC
    Contributors: 化學工程與材料工程學系
    Keywords: N/A
    Date: 1996
    Issue Date: 2010-06-29 17:32:15 (UTC+8)
    Publisher: 中央大學
    Abstract: In this study, we investigated the kinetics of the nucleophilic substitutions, RX + (BzBu(3)NBr) reversible arrow RBr + (BzBu(3)NX), where R = allyl, Bu and Bz, when X = CI; and X = AcO and BzO when R = Bz. The forward and backward rate constants in addition to the activation energies for R = allyl and Bu were also determined. However, only the rate constants at 35 degrees C were determined for the benzyl compounds with toluene as the solvent to reduce the reaction rate. Moreover, the effects of the structures of the groups R and the leaving groups X on the reactivity were compared. Results in this study can provide valuable information for future studies involving the phase transfer catalyzed displacements. (C) 1996 John Wiley & Sons, Inc.
    Relation: INTERNATIONAL JOURNAL OF CHEMICAL KINETICS
    Appears in Collections:[National Central University Department of Chemical & Materials Engineering] journal & Dissertation

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