Chapter 14: Q.21558-14-16P. (page 546)
Sketch the NMR spectrum of CH3CH2Cl , giving the approximate location of each NMR signal.
Chapter 14: Q.21558-14-16P. (page 546)
Sketch the NMR spectrum of CH3CH2Cl , giving the approximate location of each NMR signal.
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Get started for freeFor each compound, which of the protons on the highlighted carbons absorbs farther downfield?
a.
b.
c.
Label the protons in each highlighted CH2 group as enantiotopic, diastereotopic, or homotopic.
a.
b.
c.
Which compounds give a 1H NMR spectrum with two signals in a ratio of 2:3?
a.
b.
c.
d.
Question:Reaction of unknown A with HCl forms chlorohydrin B as the major product. A shows no absorptions in its IR spectrum at 1700 cm-1 or 3600-3200 cm-1 , and gives the following 1H NMR data: 1.4 (doublet, 3 H), 3.0 (quartet of doublets, 1 H), 3.5 (doublet, 1 H), 3.8 (singlet, 3 H), 6.9 (doublet, 2 H), and 7.2 (doublet, 2 H) ppm.
(a) Propose a structure for A, including stereochemistry.
(b) Explain why B is the major product in this reaction.
Draw a splitting diagram for Hb in trans-1,3-dichloropropene, given that Jab = 13.1 Hz and Jbc = 7.2 Hz.
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