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Synthesizing Stilbene by Olefin Metathesis Reaction Using Guided Inquiry To Compare and Contrast Wittig and Metathesis Methodologies

机译:用烯烃复分解反应合成斯蒂尔贝烯,采用指导调查比较和对比威特和复分解方法

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In this experiment, students are asked to conduct a catalytic cross-metathesis experiment and compare this reaction to the Wittig reaction within the confines of green 2 chemistry. Students synthesize stilbene from styrene using Grubbs second-generation catalyst. Products can be minimally characterized by IR spectroscopy and melting point, but using H-1 NMR spectroscopy is preferred. Students find that the Wittig reaction is selective for cis-stilbene while the metathesis reaction produces 98% trans-stilbene. Students determine the cis/trans selectivity, turnover number, and maximum turnover frequency of the reaction. The experiment is conducted alongside the synthesis of stilbene using Wittig chemistry from a published procedure.
机译:在这项实验中,要求学生进行催化交叉复分解实验,并将这种反应与绿色2化学的范围内的威丝反应进行比较。 学生使用Grubbs第二代催化剂从苯乙烯中合成斯蒂林。 通过IR光谱学和熔点可以微小地表征产品,但使用H-1 NMR光谱是优选的。 学生发现Wittig反应是Cis-stilbene的选择性,而复分解反应产生& 98%的反式斯蒂尔贝烯。 学生确定反应的CIS / Trans选择性,营收数和最大周转频率。 使用Wittig化学从公开的程序一起与SiLBENE合成进行实验。

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