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Which of the following is the bond line drawing for 2-ethyl-1-methylcyclopentanol?


A)
Which of the following is the bond line drawing for 2-ethyl-1-methylcyclopentanol? A)    B)    C)    D)    E)
B)
Which of the following is the bond line drawing for 2-ethyl-1-methylcyclopentanol? A)    B)    C)    D)    E)
C)
Which of the following is the bond line drawing for 2-ethyl-1-methylcyclopentanol? A)    B)    C)    D)    E)
D)
Which of the following is the bond line drawing for 2-ethyl-1-methylcyclopentanol? A)    B)    C)    D)    E)
E)
Which of the following is the bond line drawing for 2-ethyl-1-methylcyclopentanol? A)    B)    C)    D)    E)

F) C) and D)
G) None of the above

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Which molecule would be considered a derivative of phenol?


A)
Which molecule would be considered a derivative of phenol? A)    B)    C)    D)    E)
B)
Which molecule would be considered a derivative of phenol? A)    B)    C)    D)    E)
C)
Which molecule would be considered a derivative of phenol? A)    B)    C)    D)    E)
D)
Which molecule would be considered a derivative of phenol? A)    B)    C)    D)    E)
E)
Which molecule would be considered a derivative of phenol? A)    B)    C)    D)    E)

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

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What is the inorganic compound that can be considered the structural basis for alcohols and ethers? Discuss two ways in which the physical properties of alcohols and ethers are similar to properties of this compound.

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Alcohols and ethers can be considered to...

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The product of dehydration of an alcohol is an


A) alkane.
B) alkene.
C) aromatic.
D) ether.
E) aldehyde.

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

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Which compound is the least soluble in water?


A) CH3CH2CH2CH2OH
B) CH3CH2CH2OH
C) CH3CH2CH2CH3
D) CH3CH2CH3
E) CH3CH2CH2CH2CH2CH2CH2CH3

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

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What is the IUPAC name of the compound shown? What is the IUPAC name of the compound shown?   A) 4-ethyl-1-hexanol B) 3-ethyl-6-hexanol C) 3-ethyl-1-hexanol D) 4,4-diethyl-1-butanol E) isooctanol


A) 4-ethyl-1-hexanol
B) 3-ethyl-6-hexanol
C) 3-ethyl-1-hexanol
D) 4,4-diethyl-1-butanol
E) isooctanol

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

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A

The molecule shown is a ________ alcohol because ________. The molecule shown is a ________ alcohol because ________.   A) primary;it has one -OH group B) primary;its -OH group is on the end of the molecule C) secondary;the carbon bonded to the -OH group is bonded to two other carbons D) secondary;each group bonded to the hydroxyl carbon contains two carbon atoms E) tertiary;the -OH is bonded to the number 3 carbon


A) primary;it has one -OH group
B) primary;its -OH group is on the end of the molecule
C) secondary;the carbon bonded to the -OH group is bonded to two other carbons
D) secondary;each group bonded to the hydroxyl carbon contains two carbon atoms
E) tertiary;the -OH is bonded to the number 3 carbon

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

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Enantiomers are a form of stereoisomer in which each molecule in the pair of isomers has


A) its functional groups situated in different configurations with respect to a double bond.
B) the same carbon skeleton and the same functional groups,but the functional groups are attached at different sites.
C) the same functional groups,but a different carbon skeleton.
D) a carbon atom bonded to four different groups and the isomers are mirror images.
E) a plane of symmetry perpendicular to the carbon skeleton so that the bottom half and top half of the molecule are mirror images.

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

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An alcohol is classified as primary,secondary or tertiary based on the


A) number of carbon atoms bonded to the carbon bearing the OH group.
B) number of carbon atoms in the molecule.
C) number of hydrogens present in the alcohol.
D) number of OH groups present in the molecule.
E) mass of the alcohol.

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

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List three properties of enantiomers that are the same and three properties that are different.

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Same: molecular formula,connections betw...

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Which functional group will cause a compound to have a boiling point greater than that predicted only by molar mass?


A) ether
B) alcohol
C) alkene
D) ketone
E) alkane

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

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Treatment of CH3CH2OH with an excess amount of oxidizing agent will produce


A) an aldehyde.
B) a ketone.
C) an alkene.
D) a carboxylic acid.
E) no reaction.

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

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All of the following properties of alcohols are affected by hydrogen bonding except


A) boiling point.
B) miscibility with water.
C) ability to dissolve polar substances.
D) molecular weight.
E) none of the above

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

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What is the IUPAC name for the compound shown? What is the IUPAC name for the compound shown?   A) 3-bromo-2-chloro-3-methylpentane B) 3-bromomethyl-2-chloro-pentane C) bromochlorohexane D) 3-bromo-4-chloro-3-methylpentane E) none of these


A) 3-bromo-2-chloro-3-methylpentane
B) 3-bromomethyl-2-chloro-pentane
C) bromochlorohexane
D) 3-bromo-4-chloro-3-methylpentane
E) none of these

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

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The major product resulting from the dehydration of The major product resulting from the dehydration of   Will be A) 1-pentene. B) 2-pentene. C) n-pentane. D) 1,2-pentanediol. E) 1,3-pentanediol. Will be


A) 1-pentene.
B) 2-pentene.
C) n-pentane.
D) 1,2-pentanediol.
E) 1,3-pentanediol.

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

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B

The reaction conditions which would result in formation of disulfides from thiols are


A) mild oxidizing.
B) gentle heat.
C) strong heat.
D) strong acid.
E) none of these

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

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The IUPAC name of the alcohol shown is The IUPAC name of the alcohol shown is   A) 2,3-dimethyl-1-pentanol. B) 2,3-dimethyl-5-pentanol. C) 3,4-dimethyl-1-pentanol. D) 3,4-dimethyl-5-pentanol. E) primary 2,3-dimethylpentanol.


A) 2,3-dimethyl-1-pentanol.
B) 2,3-dimethyl-5-pentanol.
C) 3,4-dimethyl-1-pentanol.
D) 3,4-dimethyl-5-pentanol.
E) primary 2,3-dimethylpentanol.

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

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Match the following. -disulfide


A) Match the following. -disulfide A)   B)   C) C  C   C  SSC  C  D) -O
B) Match the following. -disulfide A)   B)   C) C  C   C  SSC  C  D) -O
C) CMatch the following. -disulfide A)   B)   C) C  C   C  SSC  C  D) -O   C Match the following. -disulfide A)   B)   C) C  C   C  SSC  C  D) -O   CMatch the following. -disulfide A)   B)   C) C  C   C  SSC  C  D) -O   SSCMatch the following. -disulfide A)   B)   C) C  C   C  SSC  C  D) -O   CMatch the following. -disulfide A)   B)   C) C  C   C  SSC  C  D) -O
D) -OMatch the following. -disulfide A)   B)   C) C  C   C  SSC  C  D) -O   Match the following. -disulfide A)   B)   C) C  C   C  SSC  C  D) -O

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

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Which alcohol should be used to produce 4-methyl-2-pentene by dehydration?


A) 2-methyl-3-pentanol
B) 4-methyl-2-pentanol
C) 4-methyl-1-pentanol
D) 2-methyl-1-pentanol
E) 1-propanol and 2-propanol

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

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Which molecule shown is a primary alcohol?


A)
Which molecule shown is a primary alcohol? A)    B)    C)    D)    E)
B)
Which molecule shown is a primary alcohol? A)    B)    C)    D)    E)
C)
Which molecule shown is a primary alcohol? A)    B)    C)    D)    E)
D)
Which molecule shown is a primary alcohol? A)    B)    C)    D)    E)
E)
Which molecule shown is a primary alcohol? A)    B)    C)    D)    E)

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

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C

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