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 freeWhat protons in alcohol A give rise to each signal in its 1HNMR spectrum? Explain all splitting patterns observed for absorptions between 0–7 ppm.
Describe the 1HNMR spectrum of each compound. State how many NMR signals are present, the splitting pattern for each signal, and the approximate chemical shift.
a.
b.
c.
d.
Question: For each compound, which of the protons on the highlighted carbons absorbs farther downfield?
a.
b.
c.
Propose a structure for a compound of molecular formula C3H8O with an IR absorption at 3600 to 3200 cm-1 and the following NMR spectrum:
Draw all constitutional isomers of molecular formula \({{\bf{C}}_{\bf{3}}}{{\bf{H}}_{\bf{6}}}{\bf{C}}{{\bf{l}}_{\bf{2}}}\).
a. How many signals does each isomer exhibit in its \({}^{\bf{1}}{\bf{H}}\) NMR spectrum?
b. How many lines does each isomer exhibit in its \({}^{{\bf{13}}}{\bf{C}}\) NMR spectrum?
c. When only the number of signals in both \({}^{\bf{1}}{\bf{H}}\) and \({}^{{\bf{13}}}{\bf{C}}\) NMR spectroscopy is considered, is it possible to distinguish all of these constitutional isomers?
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