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Provide the product for the following reaction. Provide the product for the following reaction.     A)  I B)  II C)  III D)  IV E)  V Provide the product for 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 D)
G) C) and D)

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Which one of the following compounds is antiaromatic? Which one of the following compounds is antiaromatic?   A)  I B)  II C)  III D)  IV E)  none of these


A) I
B) II
C) III
D) IV
E) none of these

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

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Give the common name for o-xylene.


A) hydroxybenzene
B) aminobenzene
C) 1,2-dimethylbenzene
D) ethylbenzene
E) 1,3-dimethylbenzene

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

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Provide the structures of the intermediates and final product in the following reaction sequence. Provide the structures of the intermediates and final product in the following reaction sequence.

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Using a Frost circle, draw the molecular orbital energy diagram for the cyclopropenyl anion and predict if it is aromatic. Using a Frost circle, draw the molecular orbital energy diagram for the cyclopropenyl anion and predict if it is aromatic.

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blured image_TB4454_00...

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Using a Frost circle, draw the molecular orbital energy diagram for the cyclopentadienyl anion and predict if it is aromatic. Using a Frost circle, draw the molecular orbital energy diagram for the cyclopentadienyl anion and predict if it is aromatic.

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blured image_TB4454_00...

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What is the main difference between an aromatic and antiaromatic compound?


A) Aromatic compounds must be cyclic and planar, but not antiaromatic compounds
B) Aromatic compounds must be monocyclic.
C) Antiaromatic compounds must have a conjugated system with a p orbital at every vertex
D) Aromatic compounds must satisfy Hückel's rule.
E) none of these

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

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According to molecular orbital theory, how many π\pi -bonding molecular orbitals does benzene have?


A) 1
B) 2
C) 3
D) 4
E) 5

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

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C

Predict the product for the following reaction. Predict the product for the following reaction.     A)  I B)  II C)  III D)  IV E)  V Predict the product for the following reaction.     A)  I B)  II C)  III D)  IV E)  V


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

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

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Provide the reagent(s) necessary to convert toluene to benzoic acid.


A) Na2Cr2O7/H2SO4/H2O
B) 1. NBS, Δ\Delta 2.NaOH
C) 1. LiAlH4 2. H3O+
D) H2, Pd
E) 1. CO2, 2. H3O+

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

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A compound with molecular formula C9H12O displays the following 1H NMR and 13C NMR spectra. Propose a structure for this compound. A compound with molecular formula C<sub>9</sub>H<sub>12</sub>O displays the following <sup>1</sup>H NMR and <sup>13</sup>C NMR spectra. Propose a structure for this compound.    A compound with molecular formula C<sub>9</sub>H<sub>12</sub>O displays the following <sup>1</sup>H NMR and <sup>13</sup>C NMR spectra. Propose a structure for this compound.

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11ea894b_ad1e_5546_bba7_71a98916e37c_TB4454_00_TB4454_00

Both pyridine and pyrrole are nitrogen containing aromatic heterocyclic compounds. When treated with HCl, only pyridine forms the hydrochloride salt, whereas pyrrole is unreactive. Provide an explanation for this observed reactivity. Both pyridine and pyrrole are nitrogen containing aromatic heterocyclic compounds. When treated with HCl, only pyridine forms the hydrochloride salt, whereas pyrrole is unreactive. Provide an explanation for this observed reactivity.

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In pyridine, the nonbonding electron pai...

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Which one of the following compounds is most acidic? Which one of the following compounds is most acidic?   A)  I B)  II C)  III D)  I & III E)  II & III


A) I
B) II
C) III
D) I & III
E) II & III

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

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Which one of the following compounds is most acidic? Which one of the following compounds is most acidic?   A)  I B)  II C)  III D)  IV E)  none of these


A) I
B) II
C) III
D) IV
E) none of these

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

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Which one of the following compounds is aromatic? Which one of the following compounds is aromatic?   A)  I B)  II C)  III D)  IV


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

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

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Identify the functional group in styrene.


A) ether
B) alkene
C) carboxylic acid
D) aldehyde
E) ketone

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

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Provide the reagents necessary to carry out the following conversion. Provide the reagents necessary to carry out the following conversion.

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1. NBS/blured image
2....

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Which one of the following compounds is aromatic? Which one of the following compounds is aromatic?   A)  I B)  II C)  III D)  IV


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

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

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What is the common name for the following compound? What is the common name for the following compound?

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m-xylene

Using a Frost circle, draw the molecular orbital energy diagram for the tropylium cation and predict if it is aromatic. Using a Frost circle, draw the molecular orbital energy diagram for the tropylium cation and predict if it is aromatic.

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blured image_TB4454_00...

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