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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Solution Summary
The solution examines reduction and spectroscopy. The NMR spectrum is sketched for acetone and 1,1,2-tribromoethane.
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1,1,2-tribromo ethane
A triplet corresponding to (1H)at 4.26 ...
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