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首页> 外文期刊>Journal of Chemical Education >Arrows on the Page Are Not a Good Gauge: Evidence for the Importance of Causal Mechanistic Explanations about Nucleophilic Substitution in Organic Chemistry
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Arrows on the Page Are Not a Good Gauge: Evidence for the Importance of Causal Mechanistic Explanations about Nucleophilic Substitution in Organic Chemistry

机译:页面上的箭头不是一个很好的衡量标记:有机化学中亲核替代的因果机制解释重要的证据

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摘要

This three-year study builds on prior work analyzing students' causal mechanistic explanations about acid-base reactions. Here we extend that work to characterize and investigate how students construct causal mechanistic explanations of simple nucleophilic substitution reactions. After an initial pilot study, we adopted a modified version of the original task prompt which was used in two subsequent years to compare responses from students enrolled in a transformed organic chemistry course (Organic Chemistry, Life, the Universe and Everything) and a traditional organic chemistry course. Student responses were sampled in the middle of the first semester organic chemistry, just after they had learned the material, and once again at the end of the course, to identify how responses changed over time. Our findings from this study include (1) eliciting causal mechanistic explanations requires careful scaffolding to activate productive elements of a response, and (2) students from a transformed course are more likely to construct a causal mechanistic explanation at the end of Organic Chemistry 2 than students from the control group, suggesting that if students are to retain the use of valuable knowledge, this must be supported by instruction and course expectations.
机译:这项三年的研究建立在现有工作中,分析了学生对酸碱反应的因果机制解释。在这里,我们扩展了这项工作,以表征和调查学生如何构建简单亲核代替反应的因果机制解释。在初步的试点研究之后,我们采用了一个修改版的原始任务提示版,其在后续几年中使用,以比较从转型的有机化学课程(有机化学,生命,宇宙和一切)和传统有机物中的学生的反应化学课程。在第一学期的有机化学中,学生回应是在他们学到了材料的第一学期,并且在课程结束时再次识别回应随着时间的推移的变化。我们本研究的发现包括(1)引出的因果机制解释需要仔细的脚手架,以激活反应的高效元素,(2)来自转化课程的学生更有可能在有机化学结束时构建有机化学结束的因果机制解释来自对照组的学生,建议如果学生保留使用有价值的知识,则必须得到指导和课程的预期支持。

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