Deck 14: Aromatic Compounds

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Question
What is the correct name for the following? <strong>What is the correct name for the following?  </strong> A) o-nitrophenone B) p-hydroxynitrobenzene C) 3-nitroacetophenone D) m-nitrophenol <div style=padding-top: 35px>

A) o-nitrophenone
B) p-hydroxynitrobenzene
C) 3-nitroacetophenone
D) m-nitrophenol
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Question
What is the correct name for the following? <strong>What is the correct name for the following?  </strong> A) o-bromoaniline B) 2-bromoaniline C) 1-amino-2-bromobenzene D) all of the above <div style=padding-top: 35px>

A) o-bromoaniline
B) 2-bromoaniline
C) 1-amino-2-bromobenzene
D) all of the above
Question
To be aromatic, a compound must be ___ , ___ , contain alternating double and single bonds and have
A(n) ___ of electrons.

A) noncyclic, coplanar, even number
B) cyclic, symmetric, odd number
C) cyclic, planar, Huckel
D) cyclic, aliphatic, Huckel
Question
___ is the general name for all monocyclic structures that contain alternating double and single bonds.

A) Annulenes
B) Cumulenes
C) Aromatics
D) Antiaromatics
Question
A new monocyclic ring is formed. The pi-electron energy of the ring is calculated and found to be 25 kJ/mole lower than the pi-electron energy of the corresponding open chain form of the ring with the same number of carbons and double bonds.

A) aromatic
B) antiaromatic
C) nonaromatic
Question
A new monocyclic ring is formed. The pi-electron energy of the ring is calculated and found to be the exact same as the pi-electron energy of the corresponding open chain form of the ring with the same number of carbons and double bonds.

A) aromatic
B) antiaromatic
C) nonaromatic
Question
Which of the following are aromatic? <strong>Which of the following are aromatic?  </strong> A) I B) II C) III D) I and II E) II and III F) I and III G) none of the above H) all of the above <div style=padding-top: 35px>

A) I
B) II
C) III
D) I and II
E) II and III
F) I and III
G) none of the above
H) all of the above
Question
Which of the following are aromatic?
<strong>Which of the following are aromatic?  </strong> A) I B) II C) III D) I and II E) II and III F) I and III G) none of the above H) all of the above <div style=padding-top: 35px>

A) I
B) II
C) III
D) I and II
E) II and III
F) I and III
G) none of the above
H) all of the above
Question
In NMR, aromatic hydogens resonate at ___ ppm while carbons resonate at ___ ppm. In IR spectroscopy, aromatic hydrogens absorb at ___ cm-1.

A) 3-4, 100-170, 1450-1600
B) 6-9.5, 100-170, 3030
C) 3-4, 100-170, 2250
D) 6-9.5, 100-170, 1450-1600
Question
Which of the following represents the two major fragments that are seen when monoalkylbenzenes fragment in a Mass Spectrometer? <strong>Which of the following represents the two major fragments that are seen when monoalkylbenzenes fragment in a Mass Spectrometer?  </strong> A) I and II B) I and III C) I and IV D) II and III E) III and IV F) II and IV <div style=padding-top: 35px>

A) I and II
B) I and III
C) I and IV
D) II and III
E) III and IV
F) II and IV
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Deck 14: Aromatic Compounds
1
What is the correct name for the following? <strong>What is the correct name for the following?  </strong> A) o-nitrophenone B) p-hydroxynitrobenzene C) 3-nitroacetophenone D) m-nitrophenol

A) o-nitrophenone
B) p-hydroxynitrobenzene
C) 3-nitroacetophenone
D) m-nitrophenol
m-nitrophenol
2
What is the correct name for the following? <strong>What is the correct name for the following?  </strong> A) o-bromoaniline B) 2-bromoaniline C) 1-amino-2-bromobenzene D) all of the above

A) o-bromoaniline
B) 2-bromoaniline
C) 1-amino-2-bromobenzene
D) all of the above
all of the above
3
To be aromatic, a compound must be ___ , ___ , contain alternating double and single bonds and have
A(n) ___ of electrons.

A) noncyclic, coplanar, even number
B) cyclic, symmetric, odd number
C) cyclic, planar, Huckel
D) cyclic, aliphatic, Huckel
cyclic, planar, Huckel
4
___ is the general name for all monocyclic structures that contain alternating double and single bonds.

A) Annulenes
B) Cumulenes
C) Aromatics
D) Antiaromatics
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5
A new monocyclic ring is formed. The pi-electron energy of the ring is calculated and found to be 25 kJ/mole lower than the pi-electron energy of the corresponding open chain form of the ring with the same number of carbons and double bonds.

A) aromatic
B) antiaromatic
C) nonaromatic
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6
A new monocyclic ring is formed. The pi-electron energy of the ring is calculated and found to be the exact same as the pi-electron energy of the corresponding open chain form of the ring with the same number of carbons and double bonds.

A) aromatic
B) antiaromatic
C) nonaromatic
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7
Which of the following are aromatic? <strong>Which of the following are aromatic?  </strong> A) I B) II C) III D) I and II E) II and III F) I and III G) none of the above H) all of the above

A) I
B) II
C) III
D) I and II
E) II and III
F) I and III
G) none of the above
H) all of the above
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8
Which of the following are aromatic?
<strong>Which of the following are aromatic?  </strong> A) I B) II C) III D) I and II E) II and III F) I and III G) none of the above H) all of the above

A) I
B) II
C) III
D) I and II
E) II and III
F) I and III
G) none of the above
H) all of the above
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9
In NMR, aromatic hydogens resonate at ___ ppm while carbons resonate at ___ ppm. In IR spectroscopy, aromatic hydrogens absorb at ___ cm-1.

A) 3-4, 100-170, 1450-1600
B) 6-9.5, 100-170, 3030
C) 3-4, 100-170, 2250
D) 6-9.5, 100-170, 1450-1600
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10
Which of the following represents the two major fragments that are seen when monoalkylbenzenes fragment in a Mass Spectrometer? <strong>Which of the following represents the two major fragments that are seen when monoalkylbenzenes fragment in a Mass Spectrometer?  </strong> A) I and II B) I and III C) I and IV D) II and III E) III and IV F) II and IV

A) I and II
B) I and III
C) I and IV
D) II and III
E) III and IV
F) II and IV
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