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 freeRank each group of protons in order of increasing chemical shift.
a.
b.
Question: Identify the carbon atoms that give rise to each NMR signal.
a.
b
Question. Compound O has a molecular formula C10H12O and shows an IR absorption at 1687 . The 1H -NMR spectrum of O is given below. What is the structure of O?
How many peaks are present in the NMR signal of each labelled proton?
a.
b.
c.
d.
Which of the highlighted carbon atoms in each molecule absorbs farther downfield?
a.
b.
c.
d.
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