Nucleophilic solvent participation in the solvolysis of 4-methoxybenzyl bromide and chloride

Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/28385

Title:	Nucleophilic solvent participation in the solvolysis of 4-methoxybenzyl bromide and chloride
Authors:	Liu,KT;Duann,YF;Hou,SJ
Contributors:	中央大學
Keywords:	BENZYLIC SOLVOLYSES;SATURATED CARBON;SODIUM AZIDE;SCALE;ION;SUBSTITUTION;SECONDARY;REACTIVITIES;INTERVENTION;DERIVATIVES
Date:	1998
Issue Date:	2010-06-29 19:47:39 (UTC+8)
Publisher:	化學研究所
Abstract:	The solvolysis of 4-methoxybenzyl chloride (1) and bromide (3), and 1-(4-methoxyphenyl)ethyl chloride (4) in a variety of solvents were carried out. The observation of linear correlation using the dual-parameter Grunwald-Winstein equation, and the positive azide salt effect indicate significant nucleophilic solvent participation for 1 and 3, A smaller deviation of log k (in 100% 2,2,2-trifluoroethanol) for the bromide 3 than chloride 1 in the log k - Y-BnX plots reveals a lesser extent of nucleophilic participation and is also in harmony with the greater nucleofugality of the bromide ion. The use of a low k(Br)/k(Cl) ratio as evidence for the presence of solvent participation is discussed. The observed alpha-deuterium kinetic isotope effect of 1.08 to 1.21 measured for 1 and 3 is inconsistent with the magnitude generally considered for a concerted mechanism.
Relation:	JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
Appears in Collections:	[Graduate Institute of Chemistry] journal & Dissertation

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