Which of the following compounds would give a H NMR spectrum with the following signals: a singlet (3H) at 3.4 ppm, a singlet (2H) at 4.5 ppm, and a multiplet (5H) at 7.2 ppm?
Which of the following compounds would give a H NMR spectrum with the following signals: a singlet (3H) at 3.4 ppm, a singlet (2H) at 4.5 ppm, and a multiplet (5H) at 7.2 ppm?
Chapter13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy
Section13.SE: Something Extra
Problem 53GP: The compound whose 1H NMR spectrum is shown has the molecular formula C3H6Br2. Propose a structure.
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