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Lewis Acid-Base, Molecular Modeling, and Isotopic Labeling in a Sophomore Inorganic Chemistry Laboratory
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    Lewis Acid-Base, Molecular Modeling, and Isotopic Labeling in a Sophomore Inorganic Chemistry Laboratory
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    Department of Chemistry, Lafayette College, Easton, PA 18042
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    Journal of Chemical Education

    Cite this: J. Chem. Educ. 2004, 81, 5, 722
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    https://doi.org/10.1021/ed081p722
    Published May 1, 2004

    Abstract

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    Lewis acid–base theory is taught in most inorganic courses. These concepts are typically studied in the laboratory, usually by the formation of an adduct. The reaction of t-BuNH3Cl with NaBH4 is a standard laboratory that allows students to prepare an adduct by reacting a Lewis acid with a Lewis base. The long period of stirring required for this lab provides an opportunity to enrich the laboratory experience. Computational methods can be introduced to simulate IR spectra and to view the HOMO of the Lewis base and the LUMO of the Lewis acid. In addition to the computational exercise, NaBD4 can be used in the synthesis of the adduct in place of NaBH4. This allows the students to observe the effect of isotopic labeling on IR spectra. These additional activities greatly enhance the value of the lab.

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    This article is cited by 7 publications.

    1. Sarah E. Shaner, Kari L. Stone. Determination of Stretching Frequencies by Isotopic Substitution Using Infrared Spectroscopy: An Upper-Level Undergraduate Experiment for an In-Person or Online Laboratory. Journal of Chemical Education 2023, 100 (6) , 2347-2352. https://doi.org/10.1021/acs.jchemed.2c00905
    2. Robert J. Cleaver Casey C. Raymond . Carboxyborate: A Main Group Inorganic Laboratory Experience. 2020, 13-20. https://doi.org/10.1021/bk-2020-1371.ch002
    3. Navamoney Arulsamy. Ammonia Borane Acid–Base Complex: An Experiment Involving 1H and 11B NMR Spectroscopy and the Gas Laws. Journal of Chemical Education 2018, 95 (8) , 1381-1385. https://doi.org/10.1021/acs.jchemed.8b00038
    4. Amber J. Dood, Kimberly B. Fields, Jeffrey R. Raker. Using Lexical Analysis To Predict Lewis Acid–Base Model Use in Responses to an Acid–Base Proton-Transfer Reaction. Journal of Chemical Education 2018, 95 (8) , 1267-1275. https://doi.org/10.1021/acs.jchemed.8b00177
    5. Richard A. Kjonaas, Richard W. Fitch, and Robert J. Noll . Cross-Course Collaboration in the Undergraduate Chemistry Curriculum: Isotopic Labeling with Sodium Borodeuteride in the Introductory Organic Chemistry Laboratory. Journal of Chemical Education 2017, 94 (9) , 1334-1337. https://doi.org/10.1021/acs.jchemed.6b00949
    6. Craig D. Montgomery . A Mechanistic Study of the Migratory Insertion Reaction: A Computational Chemistry Exercise. Journal of Chemical Education 2013, 90 (10) , 1396-1400. https://doi.org/10.1021/ed300526k
    7. Amber J. Dood, Kimberly B. Fields, Daniel Cruz-Ramírez de Arellano, Jeffrey R. Raker. Development and evaluation of a Lewis acid–base tutorial for use in postsecondary organic chemistry courses. Canadian Journal of Chemistry 2019, 97 (10) , 711-721. https://doi.org/10.1139/cjc-2018-0479

    Journal of Chemical Education

    Cite this: J. Chem. Educ. 2004, 81, 5, 722
    Click to copy citationCitation copied!
    https://doi.org/10.1021/ed081p722
    Published May 1, 2004

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