Deck 15: Benzene and Aromaticity: Electrophilic Aromatic Substitution

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Question
Which of the following carbocations would you expect to be most stable?

A)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
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Question
How would you name the following? <strong>How would you name the following?  </strong> A) 3-chloro-5-methylphenol B) 3-hydroxy-5-chlorotoluene C) 1-chloro-3-hydroxy-5-methylbenzene D) Meta-methy-meta-hydroxytoluene E) 3-hydroxy-5-methylchlorobenzene <div style=padding-top: 35px>

A) 3-chloro-5-methylphenol
B) 3-hydroxy-5-chlorotoluene
C) 1-chloro-3-hydroxy-5-methylbenzene
D) Meta-methy-meta-hydroxytoluene
E) 3-hydroxy-5-methylchlorobenzene
Question
Which of the following would not be aromatic (i.e.,which would not be unusually stable)?

A)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following molecules would you predict to be aromatic?

A)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What is the common name for the following compound? <strong>What is the common name for the following compound?  </strong> A) Toluene B) Anisole C) Aniline D) Phenol E) Cresol <div style=padding-top: 35px>

A) Toluene
B) Anisole
C) Aniline
D) Phenol
E) Cresol
Question
The best experimental proof of aromaticity is

A) a pleasant odor.
B) infrared CH absorption frequency.
C) NMR chemical shifts.
D) presence of resonance structures.
E) presence of conjugation.
Question
Which of the following is not a resonance structure involved in electrophilic aromatic bromination?

A)
<strong>Which of the following is not a resonance structure involved in electrophilic aromatic bromination?</strong> A)   B)   C)   D)   E) All of these are valid resonance structures. <div style=padding-top: 35px>
B)
<strong>Which of the following is not a resonance structure involved in electrophilic aromatic bromination?</strong> A)   B)   C)   D)   E) All of these are valid resonance structures. <div style=padding-top: 35px>
C)
<strong>Which of the following is not a resonance structure involved in electrophilic aromatic bromination?</strong> A)   B)   C)   D)   E) All of these are valid resonance structures. <div style=padding-top: 35px>
D)
<strong>Which of the following is not a resonance structure involved in electrophilic aromatic bromination?</strong> A)   B)   C)   D)   E) All of these are valid resonance structures. <div style=padding-top: 35px>
E) All of these are valid resonance structures.
Question
What would be the expected product of the following reactions? <strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following would you expect to be aromatic?

A)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following reactions of aromatics is reversible?

A) Nitration
B) Bromination
C) F-C alkylation
D) Sulfonation
E) F-C acylation
Question
Which of the following reactions has an aromatic transition state with (4n + 2)electrons involved?

A)
<strong>Which of the following reactions has an aromatic transition state with (4n + 2)electrons involved?</strong> A)   B)   C)   D) Two of these. E) All of these. <div style=padding-top: 35px>
B)
<strong>Which of the following reactions has an aromatic transition state with (4n + 2)electrons involved?</strong> A)   B)   C)   D) Two of these. E) All of these. <div style=padding-top: 35px>
C)
<strong>Which of the following reactions has an aromatic transition state with (4n + 2)electrons involved?</strong> A)   B)   C)   D) Two of these. E) All of these. <div style=padding-top: 35px>
D) Two of these.
E) All of these.
Question
What reagents are typically required to accomplish bromination of an aromatic ring?

A) Br2 + HBr
B) Br2 + heat
C) Br2 + light
D) Br2 + FeBr3
E) Br2 + H2SO4
Question
How many mononitrated (on the aromatic ring)derivatives of meta-xylene (= 1,3-dimethylbenzene)are possible? (Don't worry about how they might be made or which would be the major product.)

A) 1
B) 2
C) 3
D) 4
E) 5
Question
Which of the following would you expect to react fastest in an SN1 reaction (consider the mechanism)?

A)
<strong>Which of the following would you expect to react fastest in an S<sub>N</sub>1 reaction (consider the mechanism)?</strong> A)   B)   C)   D) All would react rapidly. E) None would react. <div style=padding-top: 35px>
B)
<strong>Which of the following would you expect to react fastest in an S<sub>N</sub>1 reaction (consider the mechanism)?</strong> A)   B)   C)   D) All would react rapidly. E) None would react. <div style=padding-top: 35px>
C)
<strong>Which of the following would you expect to react fastest in an S<sub>N</sub>1 reaction (consider the mechanism)?</strong> A)   B)   C)   D) All would react rapidly. E) None would react. <div style=padding-top: 35px>
D) All would react rapidly.
E) None would react.
Question
What is/are the major product(s)in the following reaction? <strong>What is/are the major product(s)in the following reaction?  </strong> A)   B)   C)   D) Both A and C E) No Reaction <div style=padding-top: 35px>

A)
<strong>What is/are the major product(s)in the following reaction?  </strong> A)   B)   C)   D) Both A and C E) No Reaction <div style=padding-top: 35px>
B)
<strong>What is/are the major product(s)in the following reaction?  </strong> A)   B)   C)   D) Both A and C E) No Reaction <div style=padding-top: 35px>
C)
<strong>What is/are the major product(s)in the following reaction?  </strong> A)   B)   C)   D) Both A and C E) No Reaction <div style=padding-top: 35px>
D) Both A and C
E) No Reaction
Question
Which would be the best systematic name of vanillan,the primary flavoring ingredient in vanilla? <strong>Which would be the best systematic name of vanillan,the primary flavoring ingredient in vanilla?  </strong> A) 4-formyl-2-methoxyphenol B) 3-formyl-6-hydroxyanisole C) 4-hydroxy-3-methoxybenzaldehyde D) 5-formyl-2-hydroxyanisole E) 4-formyl-5-methoxyphenol <div style=padding-top: 35px>

A) 4-formyl-2-methoxyphenol
B) 3-formyl-6-hydroxyanisole
C) 4-hydroxy-3-methoxybenzaldehyde
D) 5-formyl-2-hydroxyanisole
E) 4-formyl-5-methoxyphenol
Question
The reagents listed below all react readily with alkenes.Which one can react (slowly)irreversibly with an aromatic ring?

A) HBr + peroxides
B) CH3CO3H
C) HBr
D) H2/catalyst
E) H2O,H+
Question
One of the double bonds in phenanthrene,shown below,is much more reactive than the others.Which one is it? <strong>One of the double bonds in phenanthrene,shown below,is much more reactive than the others.Which one is it?  </strong> A) 1 B) 2 C) 3 D) 4 E) 5 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
E) 5
Question
Which of the following best describes the electronic nature of cyclooctatetraene? <strong>Which of the following best describes the electronic nature of cyclooctatetraene?  </strong> A) This compound is predicted to be aromatic. B) This compound is anti-aromatic and very unstable. C) This compound is non-planar and non-aromatic. D) Not all of the carbon atoms possess the <font face=symbol></font>-orbital required for conjugation. E) None of these are true. <div style=padding-top: 35px>

A) This compound is predicted to be aromatic.
B) This compound is anti-aromatic and very unstable.
C) This compound is non-planar and non-aromatic.
D) Not all of the carbon atoms possess the -orbital required for conjugation.
E) None of these are true.
Question
What would be the product of the following reaction? <strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs. <div style=padding-top: 35px>

A)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs. <div style=padding-top: 35px>
B)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs. <div style=padding-top: 35px>
C)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs. <div style=padding-top: 35px>
D)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs. <div style=padding-top: 35px>
E) No reaction occurs.
Question
What is the major product of the following reaction? <strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>

A)
<strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
B)
<strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
C)
<strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
D)
<strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction <div style=padding-top: 35px>
E) no reaction
Question
The infrared spectrum of a dimethylbenzene has a band at 738 cm-1.What is the most likely structure of the compound?

A) 1,2-dimethylbenzene
B) 1,3-dimethylbenzene
C) 1,4-dimethylbenzene
D) 1,5-dimethylbenzene
E) Not enough information to determine
Question
Which of the following statements are not true of benzene?

A) The carbon-carbon bond lengths alternated between single bonds and double bonds.
B) All carbons are sp2 hybridized.
C) The delocalized electrons form a circular pi-cloud above and below the ring.
D) It is especially stable according to heats of hydrogenation data.
E) None of the above.All of these statements are true.
Question
What is/are the product(s)in the following Friedel-Crafts Reaction? <strong>What is/are the product(s)in the following Friedel-Crafts Reaction?  </strong> A)   B)   C)   D) Both A and B. E) All of the above. <div style=padding-top: 35px>

A)
<strong>What is/are the product(s)in the following Friedel-Crafts Reaction?  </strong> A)   B)   C)   D) Both A and B. E) All of the above. <div style=padding-top: 35px>
B)
<strong>What is/are the product(s)in the following Friedel-Crafts Reaction?  </strong> A)   B)   C)   D) Both A and B. E) All of the above. <div style=padding-top: 35px>
C)
<strong>What is/are the product(s)in the following Friedel-Crafts Reaction?  </strong> A)   B)   C)   D) Both A and B. E) All of the above. <div style=padding-top: 35px>
D) Both A and B.
E) All of the above.
Question
Which of the following is not an allotrope of carbon?

A) Graphite
B) Diamond
C) Coal
D) C60
E) All are allotropes of carbon.
Question
If the heat of hydrogenation of the hypothetical 1,3,5-cyclohexatriene is -78.9 kcal/mol,but the heat of hydrogenation of benzene is -49.3 kcal/mol,what is the stabilization energy attributed to the resonance in benzene?

A) -49.3 kcal/mol + (-78.9 kcal/mol)= -128.2 kcal/mol
B) -49.3 kcal/mol - (-78.9 kcal/mol)= 29.6 kcal/mol
C) -49.3 kcal/mol
D) -78.9 kcal/mol
E) None of the above.
Question
What is/are the product(s)from the following reaction? <strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?

A)
<strong>Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
B)
<strong>Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
C)
<strong>Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
D)
<strong>Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
E) None of the above.
Question
Which of the following molecular orbitals corresponds to the 1 molecular orbital of benzene?

A)
<strong>Which of the following molecular orbitals corresponds to the <font face=symbol></font><sub>1</sub> molecular orbital of benzene?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
B)
<strong>Which of the following molecular orbitals corresponds to the <font face=symbol></font><sub>1</sub> molecular orbital of benzene?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
C)
<strong>Which of the following molecular orbitals corresponds to the <font face=symbol></font><sub>1</sub> molecular orbital of benzene?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
D)
<strong>Which of the following molecular orbitals corresponds to the <font face=symbol></font><sub>1</sub> molecular orbital of benzene?</strong> A)   B)   C)   D)   E) None of the above. <div style=padding-top: 35px>
E) None of the above.
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Deck 15: Benzene and Aromaticity: Electrophilic Aromatic Substitution
1
Which of the following carbocations would you expect to be most stable?

A)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following carbocations would you expect to be most stable?</strong> A)   B)   C)   D)   E)
2
How would you name the following? <strong>How would you name the following?  </strong> A) 3-chloro-5-methylphenol B) 3-hydroxy-5-chlorotoluene C) 1-chloro-3-hydroxy-5-methylbenzene D) Meta-methy-meta-hydroxytoluene E) 3-hydroxy-5-methylchlorobenzene

A) 3-chloro-5-methylphenol
B) 3-hydroxy-5-chlorotoluene
C) 1-chloro-3-hydroxy-5-methylbenzene
D) Meta-methy-meta-hydroxytoluene
E) 3-hydroxy-5-methylchlorobenzene
3-chloro-5-methylphenol
3
Which of the following would not be aromatic (i.e.,which would not be unusually stable)?

A)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following would not be aromatic (i.e.,which would not be unusually stable)?</strong> A)   B)   C)   D)   E)
4
Which of the following molecules would you predict to be aromatic?

A)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following molecules would you predict to be aromatic?</strong> A)   B)   C)   D)   E)
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5
What is the common name for the following compound? <strong>What is the common name for the following compound?  </strong> A) Toluene B) Anisole C) Aniline D) Phenol E) Cresol

A) Toluene
B) Anisole
C) Aniline
D) Phenol
E) Cresol
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6
The best experimental proof of aromaticity is

A) a pleasant odor.
B) infrared CH absorption frequency.
C) NMR chemical shifts.
D) presence of resonance structures.
E) presence of conjugation.
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7
Which of the following is not a resonance structure involved in electrophilic aromatic bromination?

A)
<strong>Which of the following is not a resonance structure involved in electrophilic aromatic bromination?</strong> A)   B)   C)   D)   E) All of these are valid resonance structures.
B)
<strong>Which of the following is not a resonance structure involved in electrophilic aromatic bromination?</strong> A)   B)   C)   D)   E) All of these are valid resonance structures.
C)
<strong>Which of the following is not a resonance structure involved in electrophilic aromatic bromination?</strong> A)   B)   C)   D)   E) All of these are valid resonance structures.
D)
<strong>Which of the following is not a resonance structure involved in electrophilic aromatic bromination?</strong> A)   B)   C)   D)   E) All of these are valid resonance structures.
E) All of these are valid resonance structures.
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8
What would be the expected product of the following reactions? <strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)

A)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
B)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
C)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
D)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
E)
<strong>What would be the expected product of the following reactions?  </strong> A)   <sup> </sup> B)   C)   D)   E)
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9
Which of the following would you expect to be aromatic?

A)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)
B)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)
C)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)
D)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)
E)
<strong>Which of the following would you expect to be aromatic?</strong> A)   B)   C)   D)   E)
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10
Which of the following reactions of aromatics is reversible?

A) Nitration
B) Bromination
C) F-C alkylation
D) Sulfonation
E) F-C acylation
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11
Which of the following reactions has an aromatic transition state with (4n + 2)electrons involved?

A)
<strong>Which of the following reactions has an aromatic transition state with (4n + 2)electrons involved?</strong> A)   B)   C)   D) Two of these. E) All of these.
B)
<strong>Which of the following reactions has an aromatic transition state with (4n + 2)electrons involved?</strong> A)   B)   C)   D) Two of these. E) All of these.
C)
<strong>Which of the following reactions has an aromatic transition state with (4n + 2)electrons involved?</strong> A)   B)   C)   D) Two of these. E) All of these.
D) Two of these.
E) All of these.
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12
What reagents are typically required to accomplish bromination of an aromatic ring?

A) Br2 + HBr
B) Br2 + heat
C) Br2 + light
D) Br2 + FeBr3
E) Br2 + H2SO4
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13
How many mononitrated (on the aromatic ring)derivatives of meta-xylene (= 1,3-dimethylbenzene)are possible? (Don't worry about how they might be made or which would be the major product.)

A) 1
B) 2
C) 3
D) 4
E) 5
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14
Which of the following would you expect to react fastest in an SN1 reaction (consider the mechanism)?

A)
<strong>Which of the following would you expect to react fastest in an S<sub>N</sub>1 reaction (consider the mechanism)?</strong> A)   B)   C)   D) All would react rapidly. E) None would react.
B)
<strong>Which of the following would you expect to react fastest in an S<sub>N</sub>1 reaction (consider the mechanism)?</strong> A)   B)   C)   D) All would react rapidly. E) None would react.
C)
<strong>Which of the following would you expect to react fastest in an S<sub>N</sub>1 reaction (consider the mechanism)?</strong> A)   B)   C)   D) All would react rapidly. E) None would react.
D) All would react rapidly.
E) None would react.
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15
What is/are the major product(s)in the following reaction? <strong>What is/are the major product(s)in the following reaction?  </strong> A)   B)   C)   D) Both A and C E) No Reaction

A)
<strong>What is/are the major product(s)in the following reaction?  </strong> A)   B)   C)   D) Both A and C E) No Reaction
B)
<strong>What is/are the major product(s)in the following reaction?  </strong> A)   B)   C)   D) Both A and C E) No Reaction
C)
<strong>What is/are the major product(s)in the following reaction?  </strong> A)   B)   C)   D) Both A and C E) No Reaction
D) Both A and C
E) No Reaction
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16
Which would be the best systematic name of vanillan,the primary flavoring ingredient in vanilla? <strong>Which would be the best systematic name of vanillan,the primary flavoring ingredient in vanilla?  </strong> A) 4-formyl-2-methoxyphenol B) 3-formyl-6-hydroxyanisole C) 4-hydroxy-3-methoxybenzaldehyde D) 5-formyl-2-hydroxyanisole E) 4-formyl-5-methoxyphenol

A) 4-formyl-2-methoxyphenol
B) 3-formyl-6-hydroxyanisole
C) 4-hydroxy-3-methoxybenzaldehyde
D) 5-formyl-2-hydroxyanisole
E) 4-formyl-5-methoxyphenol
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17
The reagents listed below all react readily with alkenes.Which one can react (slowly)irreversibly with an aromatic ring?

A) HBr + peroxides
B) CH3CO3H
C) HBr
D) H2/catalyst
E) H2O,H+
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18
One of the double bonds in phenanthrene,shown below,is much more reactive than the others.Which one is it? <strong>One of the double bonds in phenanthrene,shown below,is much more reactive than the others.Which one is it?  </strong> A) 1 B) 2 C) 3 D) 4 E) 5

A) 1
B) 2
C) 3
D) 4
E) 5
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19
Which of the following best describes the electronic nature of cyclooctatetraene? <strong>Which of the following best describes the electronic nature of cyclooctatetraene?  </strong> A) This compound is predicted to be aromatic. B) This compound is anti-aromatic and very unstable. C) This compound is non-planar and non-aromatic. D) Not all of the carbon atoms possess the <font face=symbol></font>-orbital required for conjugation. E) None of these are true.

A) This compound is predicted to be aromatic.
B) This compound is anti-aromatic and very unstable.
C) This compound is non-planar and non-aromatic.
D) Not all of the carbon atoms possess the -orbital required for conjugation.
E) None of these are true.
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20
What would be the product of the following reaction? <strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs.

A)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs.
B)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs.
C)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs.
D)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) No reaction occurs.
E) No reaction occurs.
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21
What is the major product of the following reaction? <strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction

A)
<strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction
B)
<strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction
C)
<strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction
D)
<strong>What is the major product of the following reaction?  </strong> A)   B)   C)   D)   E) no reaction
E) no reaction
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22
The infrared spectrum of a dimethylbenzene has a band at 738 cm-1.What is the most likely structure of the compound?

A) 1,2-dimethylbenzene
B) 1,3-dimethylbenzene
C) 1,4-dimethylbenzene
D) 1,5-dimethylbenzene
E) Not enough information to determine
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23
Which of the following statements are not true of benzene?

A) The carbon-carbon bond lengths alternated between single bonds and double bonds.
B) All carbons are sp2 hybridized.
C) The delocalized electrons form a circular pi-cloud above and below the ring.
D) It is especially stable according to heats of hydrogenation data.
E) None of the above.All of these statements are true.
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24
What is/are the product(s)in the following Friedel-Crafts Reaction? <strong>What is/are the product(s)in the following Friedel-Crafts Reaction?  </strong> A)   B)   C)   D) Both A and B. E) All of the above.

A)
<strong>What is/are the product(s)in the following Friedel-Crafts Reaction?  </strong> A)   B)   C)   D) Both A and B. E) All of the above.
B)
<strong>What is/are the product(s)in the following Friedel-Crafts Reaction?  </strong> A)   B)   C)   D) Both A and B. E) All of the above.
C)
<strong>What is/are the product(s)in the following Friedel-Crafts Reaction?  </strong> A)   B)   C)   D) Both A and B. E) All of the above.
D) Both A and B.
E) All of the above.
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25
Which of the following is not an allotrope of carbon?

A) Graphite
B) Diamond
C) Coal
D) C60
E) All are allotropes of carbon.
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26
If the heat of hydrogenation of the hypothetical 1,3,5-cyclohexatriene is -78.9 kcal/mol,but the heat of hydrogenation of benzene is -49.3 kcal/mol,what is the stabilization energy attributed to the resonance in benzene?

A) -49.3 kcal/mol + (-78.9 kcal/mol)= -128.2 kcal/mol
B) -49.3 kcal/mol - (-78.9 kcal/mol)= 29.6 kcal/mol
C) -49.3 kcal/mol
D) -78.9 kcal/mol
E) None of the above.
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27
What is/are the product(s)from the following reaction? <strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)

A)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)
B)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)
C)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)
D)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)
E)
<strong>What is/are the product(s)from the following reaction?  </strong> A)   B)   C)   D)   E)
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28
Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?

A)
<strong>Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?</strong> A)   B)   C)   D)   E) None of the above.
B)
<strong>Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?</strong> A)   B)   C)   D)   E) None of the above.
C)
<strong>Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?</strong> A)   B)   C)   D)   E) None of the above.
D)
<strong>Which of the following mechanisms best describes electrophilic aromatic substitution of benzene with bromine?</strong> A)   B)   C)   D)   E) None of the above.
E) None of the above.
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29
Which of the following molecular orbitals corresponds to the 1 molecular orbital of benzene?

A)
<strong>Which of the following molecular orbitals corresponds to the <font face=symbol></font><sub>1</sub> molecular orbital of benzene?</strong> A)   B)   C)   D)   E) None of the above.
B)
<strong>Which of the following molecular orbitals corresponds to the <font face=symbol></font><sub>1</sub> molecular orbital of benzene?</strong> A)   B)   C)   D)   E) None of the above.
C)
<strong>Which of the following molecular orbitals corresponds to the <font face=symbol></font><sub>1</sub> molecular orbital of benzene?</strong> A)   B)   C)   D)   E) None of the above.
D)
<strong>Which of the following molecular orbitals corresponds to the <font face=symbol></font><sub>1</sub> molecular orbital of benzene?</strong> A)   B)   C)   D)   E) None of the above.
E) None of the above.
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Unlock Deck
Unlock for access to all 29 flashcards in this deck.