Chapter 14: Q74P (page 527)
Chapter 14: Q74P (page 527)
All the tools & learning materials you need for study success - in one app.
Get started for freeHow many lines are observed in the 13C NMR spectrum of each compound?
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.
Question. Treatment of butan-2-one (CH3COCH2CH3) with a strong base followed by CH3l forms a compound Q, which gives a molecular ion in its mass spectrum at 86. The IR (> 1500 only) and 1H-NMR spectrum of Q is given below. What is the structure of Q?
Rank each group of protons in order of increasing chemical shift.
a.
b.
Identify A and B, isomers of molecular formula C3H4Cl2 , from the given 1HNMR data: Compound A exhibits signals at 1.75 (doublet, 3H,J = 6.9 Hz) and 5.89 (quartet, 1H, J = 6.9 Hz) ppm. Compound B exhibits signals at 4.16 (singlet, 2 H), 5.42 (doublet, 1H, J = 1.9 Hz), and 5.59 (doublet, 1H, J = 1.9 Hz) ppm.
What do you think about this solution?
We value your feedback to improve our textbook solutions.