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Question: What major IR absorptions are present above 1500 cm-1for each compound?

Short Answer

Expert verified

Answer

The following bonds have a higher frequency above 1500cm-1 in the IR spectrum.

a. CC

b. O-H

c. C=O

d. C=O and O-H

Step by step solution

01

IR absorptions frequency

The IR absorption frequency will vary according to the functional group present in the compound. Each functional group has its particular range of frequency.

02

Determination IR frequency

The IR frequency is dependent upon the functional group present in the molecule.

a. Csp-H at 3300cm-1Csp3-H at 2850–3000cm-1C–C triple bond at 2250cm-1

Triple bonded carbons have the higher IR absorption

b. O–H at 3200–360 cm-1Csp–H at 2850–3000cm-1

Hydroxyl bond has the higher IR absorption

c. Csp3 –H at 2850–3000cm-1C=O at 1700cm-1

Carbonyl bond has the higher IR absorption

d. O–H at > 3000cm-1 Csp2–H at 3000–3150cm-1C=O at approx. 1700cm-1phenyl group at 1600, 1500cm-1.The OH of the RCOOH is even broader than the OH of alcohol (3500–2500cm-1).

The carboxylic group shows higher IR absorption

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Most popular questions from this chapter

Question: 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 C8H11NO2and C7H11N3O. 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 sp3hybridized C-H absorption in its IR spectrum, and that other major IR absorption above 1500cm-1are list.

  1. A compound having a molecular ion at 72 and an absorption in its IR spectrum at 1725 cm-1.
  2. A compound having a molecular ion at 55 and an absorption in its IR spectrum at 2250 cm-1.
  3. A compound having a molecular ion at 74 and an absorption in its IR spectrum at 3600-3200 cm-1.
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