Chapter 13: Q 42. (page 522)
Question: What major IR absorptions are present above 1500 for each compound?
Short Answer
Answer
The following bonds have a higher frequency above in the IR spectrum.
a.
b. O-H
c. C=O
d. C=O and O-H
Chapter 13: Q 42. (page 522)
Question: What major IR absorptions are present above 1500 for each compound?
Answer
The following bonds have a higher frequency above in the IR spectrum.
a.
b. O-H
c. C=O
d. C=O and O-H
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Get started for freeQuestion: Use the following information to propose a molecular formula for nootkatone, a compound partly responsible for the characteristic odor of grapefruit. Nootkatone contains the elements C, H, and O, has five degrees of unsaturation, and a molecular ion in its mass spectrum at m/z = 218.
Question:A low-resolution mass spectrum of the neurotransmitter dopamine gave a molecular ion at m/z= 153. Two possible molecular formulas for this molecular ion are and . A high-resolution mass spectrum provided an exact mass at 153.0680. Which of the possible molecular formulas is the correct one?
Question: Reaction of BrCH2CH2CH2CH2NH2 with NaH forms compound W, which gives the IR and mass spectra shown below. Propose a structure for W and draw a stepwise mechanism that accounts for its formation.
Question:Propose a structure consistent with each set of data.
a. a compound that contains a benzene ring and has a molecular ion at m/z= 107
b. a hydrocarbon that contains only sp3 hybridized carbons and a molecular ion at m/z= 84
c. a compound that contains a carbonyl group and gives a molecular ion at m/z= 114
d. a compound that contains C, H, N, and O and has an exact mass for the molecular ion at
101.0841
Question: Propose possible structure consistent with each set of data. Assume each compound has hybridized C-H absorption in its IR spectrum, and that other major IR absorption above 1500are list.
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