Chapter 14: Q19P (page 527)
Question: Draw a splitting diagram for \({{\bf{H}}_{\bf{b}}}\) in trans-1,3-dichloropropene, given that \({{\bf{J}}_{{\bf{ab}}}}{\bf{ = 13}}{\bf{.1}}\;{\bf{Hz}}\) and \({{\bf{J}}_{{\bf{bc}}}}{\bf{ = 7}}{\bf{.2 Hz}}\).
Chapter 14: Q19P (page 527)
Question: Draw a splitting diagram for \({{\bf{H}}_{\bf{b}}}\) in trans-1,3-dichloropropene, given that \({{\bf{J}}_{{\bf{ab}}}}{\bf{ = 13}}{\bf{.1}}\;{\bf{Hz}}\) and \({{\bf{J}}_{{\bf{bc}}}}{\bf{ = 7}}{\bf{.2 Hz}}\).
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Get started for freeCompound A exhibits two signals in its 1H NMR spectrum at 2.64 and 3.69 ppm and the ratio of the absorbing signals is 2:3. Compound B exhibits two signals in its 1H NMR spectrum at 2.09 and 4.27 ppm and the ratio of the absorbing signals is 3:2. Which compound corresponds to dimethyl succinate and which compound corresponds to ethylene diacetate?
What protons in alcohol A give rise to each signal in its 1HNMR spectrum? Explain all splitting patterns observed for absorptions between 0–7 ppm.
Question: Identify the structures of isomers E and F (molecular formula C4H802 ). Relative areas are given above each signal.
a.
b.
Question: How can you use 1H NMR spectroscopy to distinguish between CH2=C(Br)CO2CH3 and methyl (E)-3-bromopropenoate, BrCH=CHCO2CH3?
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