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The following represents what functional group? The following represents what functional group?   A)  ester B)  ether C)  alcohol D)  thiol E)  ketone


A) ester
B) ether
C) alcohol
D) thiol
E) ketone

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

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What is the name given to the Newman projection of the butane conformation shown here? What is the name given to the Newman projection of the butane conformation shown here?   A)  eclipsed B)  gauche C)  staggered D)  anti E)  skewed


A) eclipsed
B) gauche
C) staggered
D) anti
E) skewed

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

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The following Newman projection represents which molecule? The following Newman projection represents which molecule?   A)    B)    C)    D)    E)


A)
The following Newman projection represents which molecule?   A)    B)    C)    D)    E)
B)
The following Newman projection represents which molecule?   A)    B)    C)    D)    E)
C)
The following Newman projection represents which molecule?   A)    B)    C)    D)    E)
D)
The following Newman projection represents which molecule?   A)    B)    C)    D)    E)
E)
The following Newman projection represents which molecule?   A)    B)    C)    D)    E)

F) C) and E)
G) B) and E)

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What is the correct IUPAC name for the following molecule? What is the correct IUPAC name for the following molecule?   A)  1-ethyl-2-methylhexane B)  2-ethyl-1-methylcycloheptane C)  4-ethyl-5-methylcyclohexane D)  1-ethyl-2-methylcyclohexane E)  1-methyloctane


A) 1-ethyl-2-methylhexane
B) 2-ethyl-1-methylcycloheptane
C) 4-ethyl-5-methylcyclohexane
D) 1-ethyl-2-methylcyclohexane
E) 1-methyloctane

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

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Which of the following is considered to be a nucleophile?


A) CH3Cl
B) CH3CH2I
C)
Which of the following is considered to be a nucleophile? A)  CH<sub>3</sub>Cl B)  CH<sub>3</sub>CH<sub>2</sub>I C)    D)    E)
D)
Which of the following is considered to be a nucleophile? A)  CH<sub>3</sub>Cl B)  CH<sub>3</sub>CH<sub>2</sub>I C)    D)    E)
E)
Which of the following is considered to be a nucleophile? A)  CH<sub>3</sub>Cl B)  CH<sub>3</sub>CH<sub>2</sub>I C)    D)    E)

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

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The correct name of the following molecule would be: The correct name of the following molecule would be:   A)  2-ethyl-3,3-dimethylheptane B)  6-ethyl-5,5-dimethylheptane C)  3,4,4-trimethyloctane D)  2-butyl-3-methylpentane E)  2-sec-butyl-2-methylhexane


A) 2-ethyl-3,3-dimethylheptane
B) 6-ethyl-5,5-dimethylheptane
C) 3,4,4-trimethyloctane
D) 2-butyl-3-methylpentane
E) 2-sec-butyl-2-methylhexane

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

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The IUPAC name for [(CH3) 3C]2CHCH3 is:


A) 1,1-di-tert-butylethane
B) 3-tert-butyl-2,2-dimethylbutane
C) 2,2,3,4,4-pentamethylpentane
D) 2,4,4-trimethylheptane
E) None of the above.

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

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Arrange these acids in the order of increasing acidity. Arrange these acids in the order of increasing acidity.   A)  CH<sub>4</sub>,H<sub>2</sub>O,HF,NH<sub>3</sub> B)  HF,H<sub>2</sub>O,CH<sub>4</sub>,NH<sub>3</sub> C)  HF,H<sub>2</sub>O,NH<sub>3</sub>,CH<sub>4</sub>, D)  CH<sub>4</sub>,NH<sub>3</sub>,H<sub>2</sub>O,HF, E)  NH<sub>3</sub>,CH<sub>4</sub>,H<sub>2</sub>O,HF,


A) CH4,H2O,HF,NH3
B) HF,H2O,CH4,NH3
C) HF,H2O,NH3,CH4,
D) CH4,NH3,H2O,HF,
E) NH3,CH4,H2O,HF,

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

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What is the correct structure for tert-butyl bromide?


A)
What is the correct structure for tert-butyl bromide? A)    B)    C)    D)    E)
B)
What is the correct structure for tert-butyl bromide? A)    B)    C)    D)    E)
C)
What is the correct structure for tert-butyl bromide? A)    B)    C)    D)    E)
D)
What is the correct structure for tert-butyl bromide? A)    B)    C)    D)    E)
E)
What is the correct structure for tert-butyl bromide? A)    B)    C)    D)    E)

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

Correct Answer

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The following Newman projection corresponds to which molecule? The following Newman projection corresponds to which molecule?   A)  pentane B)  butane C)  3-ethylbutane D)  hexane E)  3-methylpentane


A) pentane
B) butane
C) 3-ethylbutane
D) hexane
E) 3-methylpentane

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

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All steroids are derivatives of the ring system shown.How many tertiary hydrogens are in this ring system? All steroids are derivatives of the ring system shown.How many tertiary hydrogens are in this ring system?   A)  none B)  2 C)  4 D)  5 E)  6


A) none
B) 2
C) 4
D) 5
E) 6

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

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Which of the following has the highest pKa?


A) HI
B) NH3
C) HNO3
D) CH3COOH
E) H2SO4

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

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What is the name given to the Newman projection of the butane conformation shown here? What is the name given to the Newman projection of the butane conformation shown here?   A)  anti B)  gauche C)  staggered D)  eclipsed E)  skewed


A) anti
B) gauche
C) staggered
D) eclipsed
E) skewed

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

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How many ester functional groups are in the potent anticancer compound Taxol? How many ester functional groups are in the potent anticancer compound Taxol?   A)  0 B)  1 C)  2 D)  3 E)  4


A) 0
B) 1
C) 2
D) 3
E) 4

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

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Consider the potential energy diagram for rotation about the C2-C3 bond in pentane.The position marked "A" most likely corresponds to which of the following Newman projections? Consider the potential energy diagram for rotation about the C2-C3 bond in pentane.The position marked  A  most likely corresponds to which of the following Newman projections?   A)    B)    C)    D)    E)


A)
Consider the potential energy diagram for rotation about the C2-C3 bond in pentane.The position marked  A  most likely corresponds to which of the following Newman projections?   A)    B)    C)    D)    E)
B)
Consider the potential energy diagram for rotation about the C2-C3 bond in pentane.The position marked  A  most likely corresponds to which of the following Newman projections?   A)    B)    C)    D)    E)
C)
Consider the potential energy diagram for rotation about the C2-C3 bond in pentane.The position marked  A  most likely corresponds to which of the following Newman projections?   A)    B)    C)    D)    E)
D)
Consider the potential energy diagram for rotation about the C2-C3 bond in pentane.The position marked  A  most likely corresponds to which of the following Newman projections?   A)    B)    C)    D)    E)
E)
Consider the potential energy diagram for rotation about the C2-C3 bond in pentane.The position marked  A  most likely corresponds to which of the following Newman projections?   A)    B)    C)    D)    E)

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

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B

What is the correct IUPAC name for the following molecule? What is the correct IUPAC name for the following molecule?   A)  6-propyl-5,7,8-trimethyldecane B)  5,7,8-trimethyl-6-propyldecane C)  3,4,6-trimethyl-5-propyldecane D)  5-propyl-3,4,6-trimethyldecane E)  None of the above.


A) 6-propyl-5,7,8-trimethyldecane
B) 5,7,8-trimethyl-6-propyldecane
C) 3,4,6-trimethyl-5-propyldecane
D) 5-propyl-3,4,6-trimethyldecane
E) None of the above.

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

Correct Answer

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C

Name the following functional group: Name the following functional group:   A)  ester B)  ketone C)  alcohol D)  carboxylic acid E)  anhydride


A) ester
B) ketone
C) alcohol
D) carboxylic acid
E) anhydride

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

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E

The following represents what functional group? The following represents what functional group?   A)  amide B)  thiol C)  ketone D)  nitrile E)  amine


A) amide
B) thiol
C) ketone
D) nitrile
E) amine

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

Correct Answer

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The following represents what functional group? The following represents what functional group?   A)  alcohol B)  aldehyde C)  carboxylic acid D)  amide E)  ketone


A) alcohol
B) aldehyde
C) carboxylic acid
D) amide
E) ketone

F) None of the above
G) All of the above

Correct Answer

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Which isomer of C7H16 shown would have the highest boiling point?


A)
Which isomer of C<sub>7</sub>H<sub>16</sub> shown would have the highest boiling point? A)    B)    C)    D)    E)
B)
Which isomer of C<sub>7</sub>H<sub>16</sub> shown would have the highest boiling point? A)    B)    C)    D)    E)
C)
Which isomer of C<sub>7</sub>H<sub>16</sub> shown would have the highest boiling point? A)    B)    C)    D)    E)
D)
Which isomer of C<sub>7</sub>H<sub>16</sub> shown would have the highest boiling point? A)    B)    C)    D)    E)
E)
Which isomer of C<sub>7</sub>H<sub>16</sub> shown would have the highest boiling point? A)    B)    C)    D)    E)

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

Correct Answer

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