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Select the potential energy diagram that best represents the following reaction: Select the potential energy diagram that best represents the following reaction: A) I B) II C) III D) IV E) V Select the potential energy diagram that best represents the following reaction: A) I B) II C) III D) IV E) V


A) I
B) II
C) III
D) IV
E) V

F) All of the above
G) D) and E)

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Draw all of the primary alcohols corresponding to the formula C5H12O,including stereoisomers.

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cis-3-Hexene is treated with meta-chloroperbenzoic acid and the product is then subjected to acid-catalyzed hydrolysis.What is the final product? cis-3-Hexene is treated with meta-chloroperbenzoic acid and the product is then subjected to acid-catalyzed hydrolysis.What is the final product? A) equal amounts I and II B) equal amounts I,II and V C) equal amounts III,IV and V D) equal amounts III and IV E) Only V


A) equal amounts I and II
B) equal amounts I,II and V
C) equal amounts III,IV and V
D) equal amounts III and IV
E) Only V

F) D) and E)
G) B) and D)

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What would be the major product of the following reaction sequence? What would be the major product of the following reaction sequence? A) I B) II C) III D) IV E) An equimolar mixture of I and II.


A) I
B) II
C) III
D) IV
E) An equimolar mixture of I and II.

F) None of the above
G) A) and B)

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What is the relationship between (1S,2R) -2-methylcyclohexanol and (1R,2S) -2-methylcyclohexanol? They are:


A) constitutional isomers.
B) enantiomers.
C) conformers
D) diastereomers.
E) identical.

F) B) and E)
G) None of the above

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What is the relationship between alcohols I and II? What is the relationship between alcohols I and II? They are: A) different conformations of the same compound. B) constitutional isomers. C) enantiomers. D) diastereomers. E) identical. They are:


A) different conformations of the same compound.
B) constitutional isomers.
C) enantiomers.
D) diastereomers.
E) identical.

F) A) and D)
G) A) and C)

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Which of the following statements is NOT true of ethers?


A) Ethers are generally unreactive molecules toward reagents other than strong acids.
B) Ethers generally have lower boiling points than alcohols of a corresponding molecular weight.
C) Ethers generally have much lower water solubilities than alcohols with a corresponding molecular weight.
D) Ethers can generally be cleaved by heating them with strong acids.
E) Ethers form peroxides when allowed to stand in the presence of oxygen.

F) A) and D)
G) A) and C)

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The reaction between 1-pentanol and HBr to yield 1-bromopentanol is probably:


A) an SN1-type reaction involving the protonated alcohol as the substrate.
B) an SN2-type reaction involving the protonated alcohol as the substrate.
C) an E1-type reaction involving the protonated alcohol as the substrate.
D) an E2-type reaction involving the protonated alcohol as the substrate.
E) an epoxidation reaction.

F) A) and C)
G) A) and E)

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The correct IUPAC name for tert-butyl alcohol is:


A) 1-Butanol
B) 2-Methyl-1-propanol
C) 2-Methyl-2-propanol
D) 2-Butanol
E) 1,1-Dimethyl-1-ethanol

F) C) and D)
G) A) and E)

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Give the correct IUPAC name corresponding to the following structure: Give the correct IUPAC name corresponding to the following structure:

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Propose a mechanism for the following transformation: Propose a mechanism for the following transformation:

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Which compound would have the greatest solubility in water?


A) Diethyl ether
B) Methyl propyl ether
C) 1-Butanol
D) 1,2-Butanediol
E) Pentane

F) All of the above
G) B) and E)

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Provide a reasonable synthetic strategy for the synthesis of trans-1,2-cyclohexanediol from bromocyclohexane

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The total number of primary alcohols corresponding to the formula C6H14O,counting stereoisomers separately,is:


A) 2
B) 4
C) 6
D) 8
E) 10

F) B) and C)
G) A) and B)

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The product of the following reaction The product of the following reaction A) I B) II C) III D) IV E) V


A) I
B) II
C) III
D) IV
E) V

F) A) and E)
G) D) and E)

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Select the structure of benzyl methyl ether. Select the structure of benzyl methyl ether. A) I B) II C) III D) IV E) V


A) I
B) II
C) III
D) IV
E) V

F) C) and D)
G) A) and B)

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What is the relationship between (1R,2R) -2-methylcyclohexanol and (1R,2S) -2-methylcyclohexanol? They are:


A) constitutional isomers.
B) enantiomers.
C) conformers
D) diastereomers.
E) identical.

F) B) and E)
G) A) and E)

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What is the relationship between alcohols I and II? What is the relationship between alcohols I and II? They are: A) conformers. B) constitutional isomers. C) enantiomers. D) diastereomers. E) identical. They are:


A) conformers.
B) constitutional isomers.
C) enantiomers.
D) diastereomers.
E) identical.

F) B) and C)
G) C) and D)

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A compound has the formula C6H14O.The 13C and 1H NMR spectral data for this compound are: 13C NMR Broadband decoupled 13C NMR: 29.7,29.8,46.4,60.0 δ DEPT-90: no peaks DEPT-135: positive peak at 29.8 δ; negative peaks at 29.7,60.0 δ 1H NMR 0.91 δ,singlet (9H) 1.53 δ,triplet (2H)J = 7.3 Hz 2.13 δ,broad singlet (exchangeable,1H) 3.70 δ,triplet (2H)J = 7.3 Hz

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What would be the major product(s) of the following reaction What would be the major product(s) of the following reaction A) C<sub>6</sub>H<sub>5</sub>Br + CH<sub>3</sub>OH B) C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>Br + CH<sub>3</sub>Br C) C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>OH + CH<sub>3</sub>Br D) C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>Br + CH<sub>3</sub>OH E) C<sub>6</sub>H<sub>5</sub>CH<sub>2</sub>CH<sub>2</sub>Br


A) C6H5Br + CH3OH
B) C6H5CH2Br + CH3Br
C) C6H5CH2OH + CH3Br
D) C6H5CH2Br + CH3OH
E) C6H5CH2CH2Br

F) None of the above
G) B) and E)

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