Výsledky vyhledávání - "Amanda Bongers"

Building mental models of a reaction mechanism: the influence of static and animated representations, prior knowledge, and spatial ability

Autor: Amanda Bongers, Alison B. Flynn, Nicholas Streja, Berthorie Beauvoir, Georg Northoff

Publikováno v: Chemistry Education Research and Practice. 21:496-512

In chemistry, novices and experts use mental models to simulate and reason about sub-microscopic processes. Animations are thus important tools for learning in chemistry to convey reaction dynamics and molecular motion. While there are many animation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4ce4c0a865b2274ddeac06a678f15a04
https://doi.org/10.1039/c9rp00198k

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Working with mental models to learn and visualize a new reaction mechanism

Autor: Georg Northoff, Alison B. Flynn, Amanda Bongers

Publikováno v: Chemistry Education Research and Practice. 20:554-569

Creating and using models are essential skills in chemistry. Novices and experts alike rely on conceptual models to build their own personal mental models for predicting and explaining molecular processes. There is evidence that chemistry students la

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9e36055a7bdac22c4e3655c1d9048b8a
https://doi.org/10.1039/c9rp00060g

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Is learning scale-free? Chemistry learning increases EEG fractal power and changes the power law exponent

Autor: Georg Northoff, Amanda Bongers, Alison B. Flynn

Publikováno v: Neuroscience research. 156

Learning in chemistry and other areas of science involves developing one’s mental models of invisible processes and manipulating temporal and spatial domains during visual information processing. While some aspects learning have been well studied b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6476c4022f030d1f6d91fe75c149bcee
https://pubmed.ncbi.nlm.nih.gov/31722228

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Synthesis of Cyclic Azomethine Imines by Cycloaddition Reactions of N-Isocyanates and N-Isothiocyanates

Autor: Jean-François Vincent-Rocan, Indee Ranasinghe, Philippe Lemire, Andre M. Beauchemin, Amanda Bongers, Alyssa Perozzo

Publikováno v: Organic Letters. 18:3778-3781

Various nitrogen-substituted iso(thio)cyanates engage in [3 + 2]-cycloaddition reactions to form azomethine imines containing triazolone, triazole-thione, and pyrazole-thione cores. First, iminoisothiocyanates are shown to undergo aminothiocarbonylat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c2eb46b845cd82dfe024721d3fffc9f
https://doi.org/10.1021/acs.orglett.6b01788

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Intermolecular Aminocarbonylation of Alkenes using Concerted Cycloadditions of Iminoisocyanates

Autor: Nicolas Das Neves, Kaitlyn Lavergne, Lyanne Betit, Serge I. Gorelsky, Christian Clavette, Amy B. Toderian, Thomas Markiewicz, Wei Gan, Nimrat K. Obhi, Amanda Bongers, André M. Beauchemin, Patrick J. Moon

Publikováno v: The Journal of organic chemistry. 82(2)

The aminocarbonylation of alkenes is a powerful method for accessing the β-amino carbonyl motif that remains underdeveloped. Herein, the development of intermolecular aminocarbonylation reactivity of iminoisocyanates with alkenes is presented. This

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::064a8501cd3f3baf70d8b4e80eb7f80d
https://pubmed.ncbi.nlm.nih.gov/28002669

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ChemInform Abstract: Synthesis of Cyclic Azomethine Imines by Cycloaddition Reactions of N-Isocyanates and N-Isothiocyanates

Autor: Indee Ranasinghe, Andre M. Beauchemin, Jean-François Vincent-Rocan, Amanda Bongers, Philippe Lemire, Alyssa Perozzo

Publikováno v: ChemInform. 47

Various nitrogen-substituted iso(thio)cyanates engage in [3 + 2]-cycloaddition reactions to form azomethine imines containing triazolone, triazole–thione, and pyrazole–thione cores. First, iminoisothiocyanates are shown to undergo aminothiocarbon

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ff83c9b0228b9e8cf902e7098722a5fc
https://doi.org/10.1002/chin.201651031

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