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 freeSketch the NMR spectrum of CH3CH2Cl , giving the approximate location of each NMR signal.
Question: Because 31P has an odd mass number, 31P nuclei absorb in the NMR and, in many ways, these nuclei behave similarly to protons in NMR spectroscopy. With this in mind, explain why the 1 H NMR spectrum of methyl dimethyl phosphonate,CH3PO(OCH3)2 , consists of two doublets at 1.5 and 3.7 ppm.
Identify products A and B from the given 1HNMR data.
a. Treatment of CH2=CHCOCH3 with one equivalent of HCl forms compound A. A exhibits the following absorptions in its 1HNMR spectrum: 2.2 (singlet, 3 H), 3.05 (triplet, 2 H), and 3.6 (triplet, 2H) ppm. What is the structure of A?
b.Treatment of acetone [(CH3)2C=O] with dilute aqueous base forms B. Compound B exhibits four singlets in its 1HNMR spectrum at 1.3 (6 H), 2.2 (3 H), 2.5 (2 H), and 3.8 (1 H) ppm. What is the structure of B?
How many peaks are present in the NMR signal of each labelled proton?
a.
b.
c.
d.
a.
b.
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