Exam 12: Infrared Spectroscopy
Exam 1: Covalent Bonding and Shapes of Molecules115 Questions
Exam 2: Alkanes and Cycloalkanes95 Questions
Exam 3: Stereoisomerism and Chirality93 Questions
Exam 4: Acids and Bases94 Questions
Exam 5: Alkenes: Bonding, Nomenclature, and Properties86 Questions
Exam 6: Reactions of Alkenes98 Questions
Exam 7: Alkynes100 Questions
Exam 8: Haloalkanes, Halogenation, and Radical Reactions76 Questions
Exam 9: Nucleophilic Substitution and Beta-Elimination111 Questions
Exam 10: Alcohols98 Questions
Exam 11: Ethers, Epoxides, and Sulfides93 Questions
Exam 12: Infrared Spectroscopy67 Questions
Exam 13: Nuclear Magnetic Resonance Spectroscopy102 Questions
Exam 14: Mass Spectrometry65 Questions
Exam 15: An Introduction to Organometallic Compounds66 Questions
Exam 16: Aldehydes and Ketones119 Questions
Exam 17: Carboxylic Acids71 Questions
Exam 18: Functional Derivatives of Carboxylic Acids112 Questions
Exam 19: Enolate Anions and Enamines93 Questions
Exam 20: Dienes, Conjugated Systems, and Pericyclic Reactions69 Questions
Exam 21: Benzene and the Concept of Aromaticity85 Questions
Exam 22: Reactions of Benzene and Its Derivatives107 Questions
Exam 23: Amines88 Questions
Exam 24: Catalytic Carbon-Carbon Bond Formation77 Questions
Exam 25: Carbohydrates60 Questions
Exam 26: Lipids54 Questions
Exam 27: Amino Acids and Proteins70 Questions
Exam 28: Nucleic Acids52 Questions
Exam 29: Organic Polymer Chemistry60 Questions
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Label three peaks in the following spectrum with the bond that gives rise to them, and identify the functional group that is present in the compound (the compound has a formula of C5H10O2)? 
(Essay)
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Which of the following compounds gives an infrared spectrum with a peak at ~1750 cm-1, but no significant peaks at 3000-3500 cm-1 or 1050-1250 cm-1? 
(Multiple Choice)
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Which of the following functional groups is likely to be present in a molecule that has peaks in the infrared spectrum at 1630-1820 cm-1 (strong, broad) and 1000-1250 cm-1; but does not have peaks at 3200-3650 cm-1?
(Multiple Choice)
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Which of the following compounds gives an infrared spectrum with peaks at 1000-1250 cm-1 (strong), but does not have peaks at 3200-3650 or 1630-1820 cm-1 (sharp, weak peak)? 
(Multiple Choice)
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Which of the following bonds gives rise to an absorbance at approximately 2700-3300 cm-11 in the infrared spectrum?
(Multiple Choice)
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Which of the following compounds gives a carbonyl bond absorption at the highest frequency? 
(Multiple Choice)
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MATCH a structure from the list below to the following IR spectra. Place the letter of the structure in the blank provided.
-_____
Spectrum obtained from: SDBSWeb: http://www.aist.go.jp/RIODB/SDBS/
(Multiple Choice)
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The radio wave region of the electromagnetic spectrum would have sufficient energy to produce the following energy transition. 
(True/False)
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Label three peaks in the following spectrum with the bond that gives rise to them, and identify the functional group that is present in the compound (the compound has a formula of C6H14O)? 
(Essay)
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Which of the following relationships is not valid as applied to infrared spectroscopy?
(Multiple Choice)
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Which of the following compounds gives an infrared spectrum with peaks at 3300 cm-1 (sharp peak) and 2150 cm-1 (sharp peak)? 
(Multiple Choice)
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Examining the infrared spectrum of a compound allows us to determine the nature of the conjugated pi electron system in the compound.
(True/False)
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The vertical axis on an IR spectrum represents the percent transmission and the horizontal axis measures frequency (wavenumber).
(True/False)
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Which of the following compounds gives an infrared spectrum with a peak in the range of 1630-1820 cm-1 (strong peak), but does not have peaks at 3200-3650 or 1000-1250 cm-1? 
(Multiple Choice)
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What are the units of wavenumber,
, in infrared spectroscopy?
(Multiple Choice)
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Which of the following compounds gives a carbonyl bond absorption at the lowest frequency? 
(Multiple Choice)
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What range of wavelengths corresponds to the infrared region of the electromagnetic spectrum?
(Multiple Choice)
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Assume you are carrying out the conversion of 1-bromobutane to 1-butanol. How could you use IR spectroscopy to determine when the reaction is complete?
As the reaction progress the 3400-3640 cm-1IR band should increase in intensity.
(True/False)
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Which of the following compounds does not give an infrared spectrum with peak at ~1750 cm-1? 
(Multiple Choice)
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