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    Organic Chemistry Lab: Reduction and Spectroscopy

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    1. Sketch the NMR spectrum you would expect to observe for the following compounds:
    A. Acetone
    B. 1,1,2-tribromoethane

    2.Which of the isomeric butanols (C4H10) be prepared by reduction of a ketone with sodium borohydride?

    3. In trans-1,2-dibenzoylethylene, even though the conjugated C=O group frequency coincides directly with the expected C=C stretching fequency, we would not have expected to observe the late stretching mode in the infrared spectum. Why?

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    https://brainmass.com/chemistry/organic-chemistry-bonding/organic-chemistry-lab-reduction-spectroscopy-200919

    Solution Preview

    1,1,2-tribromo ethane

    A triplet corresponding to (1H)at 4.26 ...

    Solution Summary

    The solution examines reduction and spectroscopy. The NMR spectrum is sketched for acetone and 1,1,2-tribromoethane.

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