Deck 21: Benzene and the Concept of Aromaticity

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Question
Which orbital contains the lone pair on the nitrogen atom of pyridine?

A) s
B) p
C) sp
D) sp2
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Question
Which orbital contains the lone pair on the nitrogen atom of pyrrole?

A) s
B) p
C) sp
D) sp2
Question
What is the hybridization of the oxygen atom of furan?

A) s
B) sp
C) sp2
D) sp3
Question
What is the correct assignment of the names of the following heterocycles? <strong>What is the correct assignment of the names of the following heterocycles?  </strong> A) 1 = pyrrole; 2 = thiophene; 3 = pyridine B) 1 = thiophene; 2 = furan; 3 = pyrrole C) 1 = pyridine; 2 = thiophene; 3 = furan D) 1 = pyridine; 2 = thiophene; 3 = pyrrole <div style=padding-top: 35px>

A) 1 = pyrrole; 2 = thiophene; 3 = pyridine
B) 1 = thiophene; 2 = furan; 3 = pyrrole
C) 1 = pyridine; 2 = thiophene; 3 = furan
D) 1 = pyridine; 2 = thiophene; 3 = pyrrole
Question
What is the correct assignment of the names of the following fused arenes? <strong>What is the correct assignment of the names of the following fused arenes?  </strong> A) 1 = naphthalene; 2 = anthracene; 3 = pyrene B) 1 = naphthalene; 2 = phenanthrene; 3 = coronene C) 1 = naphthalene; 2 = anthracene; 3 = benzo[a]pyrene D) 1 = anthracene; 2 = naphthalene; 3 = coronene <div style=padding-top: 35px>

A) 1 = naphthalene; 2 = anthracene; 3 = pyrene
B) 1 = naphthalene; 2 = phenanthrene; 3 = coronene
C) 1 = naphthalene; 2 = anthracene; 3 = benzo[a]pyrene
D) 1 = anthracene; 2 = naphthalene; 3 = coronene
Question
Which of the following statements is not true about the structure of benzene?

A) six atomic 2p-orbitals overlap to form six π-molecular orbitals
B) there are three bonding π-molecular orbitals and three π-antibonding molecular orbitals
C) the ground state electronic configuration of benzene has six electrons in three π-bonding molecular orbitals
D) the bonds alternate in length around the ring
Question
Which of the following is not one of Hückel's criteria for aromaticity?

A) The compound must be cyclic
B) The compound must have one p-orbital on each atom of a ring
C) The compound must be planar or nearly planar so that there is a continuous overlap of p orbitals
D) The compound must have a closed loop of six pi electrons
Question
Which orbitals contain the lone pairs on the nitrogen atoms labeled i and ii in the imidazole ring? <strong>Which orbitals contain the lone pairs on the nitrogen atoms labeled i and ii in the imidazole ring?  </strong> A) i = sp<sup>2;</sup>; ii = sp<sup>3</sup> B) i = p<sup>;</sup>; ii = sp<sup>3</sup> C) i = p<sup>;</sup>; ii = sp<sup>3</sup>. D) i = p<sup>;</sup>; ii = sp<sup>2</sup> <div style=padding-top: 35px>

A) i = sp2;; ii = sp3
B) i = p;; ii = sp3
C) i = p;; ii = sp3.
D) i = p;; ii = sp2
Question
Which of the following represents the energy levels of the molecular orbitals of benzene? <strong>Which of the following represents the energy levels of the molecular orbitals of benzene?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What is the approximate length of the carbon-carbon bonds in benzene?

A) 110 pm
B) 121 pm
C) 139 pm
D) 156 pm
Question
What is the hybridization of the nitrogen atom of pyridine?

A) s
B) sp
C) sp2
D) sp3
Question
Which of the following statements is not true about the structure of benzene?

A) the carbon-carbon bonds are all the same length
B) the structure rapidly transforms between two resonance contributors
C) the structure is an average of two resonance contributors
D) the ring of six carbon atoms is planar
Question
What is the correct assignment of the names of the following heterocycles? <strong>What is the correct assignment of the names of the following heterocycles?  </strong> A) 1 = pyrrole; 2 = thiophene; 3 = pyridine B) 1 = thiophene; 2 = furan; 3 = pyrrole C) 1 = furan; 2 = pyrrole; 3 = thiophene D) 1 = furan; 2 = thiophene; 3 = pyrrole <div style=padding-top: 35px>

A) 1 = pyrrole; 2 = thiophene; 3 = pyridine
B) 1 = thiophene; 2 = furan; 3 = pyrrole
C) 1 = furan; 2 = pyrrole; 3 = thiophene
D) 1 = furan; 2 = thiophene; 3 = pyrrole
Question
Which of the following compounds is aromatic?

A) ethane
B) cyclobutadiene
C) benzene
D) cyclooctatetraene
Question
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 2-nitro-6-carboxybromobenzene B) 2-bromo-1-nitro-4-benzoic acid C) 2-bromo-4-carboxynitrobenzene D) 3-bromo-4-nitrobenzoic acid <div style=padding-top: 35px>

A) 2-nitro-6-carboxybromobenzene
B) 2-bromo-1-nitro-4-benzoic acid
C) 2-bromo-4-carboxynitrobenzene
D) 3-bromo-4-nitrobenzoic acid
Question
Which is the correct assignment of the names of the following substituted benzenes? <strong>Which is the correct assignment of the names of the following substituted benzenes?  </strong> A) 1 = phenol; 2 = m-cresol; 3 = toluene B) 1 = m-cresol; 2 = resorcinol; 3 = m-xylene C) 1 = anisole; 2 = catechol; 3 = m-xylene D) 1 = m-cresol; 2 = anisole; 3 = cumene <div style=padding-top: 35px>

A) 1 = phenol; 2 = m-cresol; 3 = toluene
B) 1 = m-cresol; 2 = resorcinol; 3 = m-xylene
C) 1 = anisole; 2 = catechol; 3 = m-xylene
D) 1 = m-cresol; 2 = anisole; 3 = cumene
Question
What is the correct assignment of the names of the following substituted benzenes? <strong>What is the correct assignment of the names of the following substituted benzenes?  </strong> A) 1 = styrene; 2 = benzaldehyde; 3 = cumene B) 1 = anisole; 2 = benzaldehyde; 3 = toluene C) 1 = styrene; 2 = xylene; 3 = toluene D) 1 = aniline; 2 = phenol; 3 = cumene <div style=padding-top: 35px>

A) 1 = styrene; 2 = benzaldehyde; 3 = cumene
B) 1 = anisole; 2 = benzaldehyde; 3 = toluene
C) 1 = styrene; 2 = xylene; 3 = toluene
D) 1 = aniline; 2 = phenol; 3 = cumene
Question
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 1-bromo-2-fluoro-4-toluene B) 4-bromo-2-fluorotoluene C) 2-bromo-4-fluorophenol D) 4-bromo-2-fluoroxylene <div style=padding-top: 35px>

A) 1-bromo-2-fluoro-4-toluene
B) 4-bromo-2-fluorotoluene
C) 2-bromo-4-fluorophenol
D) 4-bromo-2-fluoroxylene
Question
What is the correct assignment of the names of the following substituted benzenes? <strong>What is the correct assignment of the names of the following substituted benzenes?  </strong> A) 1 = phenol; 2 = aniline; 3 = anisole B) 1 = benzaldehyde; 2 = anisole; 3 = toluene C) 1 = anisole; 2 = xylene; 3 = toluene D) 1 = anisole; 2 = aniline; 3 = toluene <div style=padding-top: 35px>

A) 1 = phenol; 2 = aniline; 3 = anisole
B) 1 = benzaldehyde; 2 = anisole; 3 = toluene
C) 1 = anisole; 2 = xylene; 3 = toluene
D) 1 = anisole; 2 = aniline; 3 = toluene
Question
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 2,4-dibromotoluene B) 2,4-dibromophenol C) 2,4-dibromohydroxybenzene D) 4,6-dibromophenol <div style=padding-top: 35px>

A) 2,4-dibromotoluene
B) 2,4-dibromophenol
C) 2,4-dibromohydroxybenzene
D) 4,6-dibromophenol
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following compounds is antiaromatic?

A) ethane
B) cyclobutadiene
C) benzene
D) cyclooctatetraene
Question
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 3 > 1 C) 3 > 2 > 1 D) 1 > 3 > 2 <div style=padding-top: 35px>

A) 1 > 2 > 3
B) 2 > 3 > 1
C) 3 > 2 > 1
D) 1 > 3 > 2
Question
What is the best choice of reagent to achieve the following reaction? <strong>What is the best choice of reagent to achieve the following reaction?  </strong> A) H<sub>2</sub>SO<sub>4</sub> B) NaOH, H<sub>2</sub>O C) K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>, H<sub>2</sub>SO<sub>4</sub> D) LiAlH<sub>4</sub> <div style=padding-top: 35px>

A) H2SO4
B) NaOH, H2O
C) K2Cr2O7, H2SO4
D) LiAlH4
Question
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 1 > 3 C) 3 > 2 > 1 D) 1 > 3 > 2 <div style=padding-top: 35px>

A) 1 > 2 > 3
B) 2 > 1 > 3
C) 3 > 2 > 1
D) 1 > 3 > 2
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following compounds undergoes heterolytic carbon-halogen bond cleavage to form a stable organic cation? <strong>Which of the following compounds undergoes heterolytic carbon-halogen bond cleavage to form a stable organic cation?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What is the best choice of reagent to achieve the following reaction? <strong>What is the best choice of reagent to achieve the following reaction?  </strong> A) H<sub>2</sub>SO<sub>4</sub> B) NaOH, H<sub>2</sub>O C) K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>, H<sub>2</sub>SO<sub>4</sub> D) H<sub>2</sub>/Pd <div style=padding-top: 35px>

A) H2SO4
B) NaOH, H2O
C) K2Cr2O7, H2SO4
D) H2/Pd
Question
Which of the following ions is aromatic? <strong>Which of the following ions is aromatic?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What is the best choice of reagent to achieve the following reaction? <strong>What is the best choice of reagent to achieve the following reaction?  </strong> A) Br<sub>2</sub>, CCl<sub>4</sub> B) HBr, H<sub>2</sub>O C) Br<sub>2</sub>, light D) NaBr <div style=padding-top: 35px>

A) Br2, CCl4
B) HBr, H2O
C) Br2, light
D) NaBr
Question
Which of the following molecules is the most acidic? <strong>Which of the following molecules is the most acidic?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 1 > 3 C) 3 > 2 > 1 D) 1 > 3 > 2 <div style=padding-top: 35px>

A) 1 > 2 > 3
B) 2 > 1 > 3
C) 3 > 2 > 1
D) 1 > 3 > 2
Question
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 3 > 1 C) 3 > 2 > 1 D) 2 > 1 > 3 <div style=padding-top: 35px>

A) 1 > 2 > 3
B) 2 > 3 > 1
C) 3 > 2 > 1
D) 2 > 1 > 3
Question
Which of the following represents the energy levels of the molecular orbitals of cyclopentadienyl anion? <strong>Which of the following represents the energy levels of the molecular orbitals of cyclopentadienyl anion?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following heterocycles is not aromatic? <strong>Which of the following heterocycles is not aromatic?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 3 > 1 C) 3 > 2 > 1 D) 1 > 3 > 2 <div style=padding-top: 35px>

A) 1 > 2 > 3
B) 2 > 3 > 1
C) 3 > 2 > 1
D) 1 > 3 > 2
Question
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following represents the energy levels of the molecular orbitals of cyclobutadiene? <strong>Which of the following represents the energy levels of the molecular orbitals of cyclobutadiene?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Which of the following is not true about [18]annulene? <strong>Which of the following is not true about [18]annulene?  </strong> A) [18]annulene is planar B) [18]annulene is aromatic C) [18]annulene gives one peak in the <sup>1</sup>H NMR spectrum D) [18]annulene has 18 pi bonds <div style=padding-top: 35px>

A) [18]annulene is planar
B) [18]annulene is aromatic
C) [18]annulene gives one peak in the 1H NMR spectrum
D) [18]annulene has 18 pi bonds
Question
Which of the following is not true about [the bridged [10]annulene shown below? <strong>Which of the following is not true about [the bridged [10]annulene shown below?  </strong> A) all of the carbon atoms of bridged [10]annulene are all in the same plane B) bridged [10]annulene is aromatic C) bridged [10]annulene undergoes substitution reactions similar to benzene D) bridged [10]annulene has 10 pi electrons <div style=padding-top: 35px>

A) all of the carbon atoms of bridged [10]annulene are all in the same plane
B) bridged [10]annulene is aromatic
C) bridged [10]annulene undergoes substitution reactions similar to benzene
D) bridged [10]annulene has 10 pi electrons
Question
How many p orbital electrons are present in cyclopentadienyl anion?

A) 4
B) 6
C) 7
D) 8
Question
The product of the following reaction would be 1-bromo-1-phenylethane. The product of the following reaction would be 1-bromo-1-phenylethane.  <div style=padding-top: 35px>
Question
What are the relative positions of the substituents in the following structure? <strong>What are the relative positions of the substituents in the following structure?  </strong> A) anti B) meta C) ortho D) para <div style=padding-top: 35px>

A) anti
B) meta
C) ortho
D) para
Question
What are the relative positions of the substituents in the following structure? <strong>What are the relative positions of the substituents in the following structure?  </strong> A) anti B) meta C) ortho D) para <div style=padding-top: 35px>

A) anti
B) meta
C) ortho
D) para
Question
How many p orbital electrons are present in furan?

A) 4
B) 6
C) 7
D) 8
Question
Phenols are stronger acids than alcohols because of the resonance stabilization of alkoxide ions.
Question
Furan has the structure shown below. Furan has the structure shown below.   The π orbitals in furan are shown below.  <div style=padding-top: 35px> The π orbitals in furan are shown below. Furan has the structure shown below.   The π orbitals in furan are shown below.  <div style=padding-top: 35px>
Question
The following compound should be name as 1-((1S, 3R)-3-methylcyclohexyl)benzene. The following compound should be name as 1-((1S, 3R)-3-methylcyclohexyl)benzene.  <div style=padding-top: 35px>
Question
Consider the following structures, Consider the following structures,   A B Structure A is more acidic than B.<div style=padding-top: 35px> A B
Structure A is more acidic than B.
Question
The product of the following reaction would be a dicarboxylic acid. The product of the following reaction would be a dicarboxylic acid.  <div style=padding-top: 35px>
Question
Which of the following is not true about cyclooctatetraene?

A) The planar conformation is antiaromatic
B) In the planar conformation there are two electrons in degenerate nonbonding pi orbitals.
C) In the tub conformation the pi system is not conjugated
D) The tub conformation is aromatic
Question
What are the relative positions of the substituents in the following structure? <strong>What are the relative positions of the substituents in the following structure?  </strong> A) anti B) meta C) ortho D) para <div style=padding-top: 35px>

A) anti
B) meta
C) ortho
D) para
Question
Which of the following is true about [10]annulene? <strong>Which of the following is true about [10]annulene?  </strong> A) [10]annulene is planar B) [10]annulene is nonaromatic C) [10]annulene undergoes addition reactions similar to simple alkenes D) [10]annulene has 10 pi electrons <div style=padding-top: 35px>

A) [10]annulene is planar
B) [10]annulene is nonaromatic
C) [10]annulene undergoes addition reactions similar to simple alkenes
D) [10]annulene has 10 pi electrons
Question
The following compound is named (Z)-2,3-diphenyl-2-hexene. The following compound is named (Z)-2,3-diphenyl-2-hexene.  <div style=padding-top: 35px>
Question
Which of the following does not undergo oxidation in the presence of H2CrO4? <strong>Which of the following does not undergo oxidation in the presence of H<sub>2</sub>CrO<sub>4</sub>?  </strong> A) 1 B) 2 C) 3 D) 4 <div style=padding-top: 35px>

A) 1
B) 2
C) 3
D) 4
Question
Consider the following structure. Consider the following structure.   The <sup>1</sup>H NMR spectrum of this compound −60°C shows a peak at 7.6 ppm, this would indicate aromaticity.<div style=padding-top: 35px> The 1H NMR spectrum of this compound −60°C shows a peak at 7.6 ppm, this would indicate aromaticity.
Question
What is the intermediate in the reaction of ethylbenzene with NBS in the presence of benzoyl peroxide to give 1-bromo-1-phenylethane?

A) Benzylic anion
B) Benzylic cation
C) Benzylic radical
D) Benzylic carbene
Question
Why are nitrophenols more acidic than phenols?
Question
Assuming that the sulfur atom is sp2-hybridized, there are _____ π-electrons in the sulfathiazole ring.
Question
The following compound could be produced by reaction of phenol with bromobenzene. The following compound could be produced by reaction of phenol with bromobenzene.  <div style=padding-top: 35px>
Question
Identify the most acidic compound.

A)
<strong>Identify the most acidic compound.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B)
<strong>Identify the most acidic compound.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C)
<strong>Identify the most acidic compound.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D)
<strong>Identify the most acidic compound.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Consider the following structure. Consider the following structure.   If named as an annulene, the name would be [ __ ] annulene.<div style=padding-top: 35px>
If named as an annulene, the name would be [ __ ] annulene.
Question
Consider the following general structure. Consider the following general structure.   Positions 1,4 and 2,6 and 3,5 are termed para, ortho, and meta, respectively.<div style=padding-top: 35px> Positions 1,4 and 2,6 and 3,5 are termed para, ortho, and meta, respectively.
Question
The ______ substituent is affected during the oxidation of 2-bromo-4-nitrotoulene using chromic acid.

A) methyl
B) nitro
C) bromo
D) hydroxy
Question
Which of the following compound is nonaromatic?

A)
<strong>Which of the following compound is nonaromatic?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B)
<strong>Which of the following compound is nonaromatic?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C)
<strong>Which of the following compound is nonaromatic?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D)
<strong>Which of the following compound is nonaromatic?</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
List all of the requirements of a molecule for it to be considered aromatic.
Question
Consider the following structure. Consider the following structure.   This structure contains ____ π electrons.<div style=padding-top: 35px>
This structure contains ____ π electrons.
Question
Provide a brief explanation of why the cyclopentadienyl anion (below) is aromatic. Your answer should identify the hybridization of each carbon atom and account for which electrons are in the pi system. Provide a brief explanation of why the cyclopentadienyl anion (below) is aromatic. Your answer should identify the hybridization of each carbon atom and account for which electrons are in the pi system.  <div style=padding-top: 35px>
Question
Identify the major product of the following reaction. ​ <strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>

A)
<strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B)
<strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C)
<strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D)
<strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
Provide a brief explanation of why furan (below) is aromatic. Your answer should identify the hybridization of the oxygen atom and account for which electrons are in the pi system. Provide a brief explanation of why furan (below) is aromatic. Your answer should identify the hybridization of the oxygen atom and account for which electrons are in the pi system.  <div style=padding-top: 35px>
Question
Using the Hückel criteria, the compound would be ______________.
Question
According to Hückel criteria, sulfathiazole is predicted to be ___________.
Question
Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound "A" by the process of esterification, using acetic anhydride. Identify compound "A".

A)
<strong>Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound A by the process of esterification, using acetic anhydride. Identify compound A.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
B)
<strong>Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound A by the process of esterification, using acetic anhydride. Identify compound A.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
C)
<strong>Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound A by the process of esterification, using acetic anhydride. Identify compound A.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
D)
<strong>Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound A by the process of esterification, using acetic anhydride. Identify compound A.</strong> A)   B)   C)   D)   <div style=padding-top: 35px>
Question
What is the chemical name of the following compound? ​ <strong>What is the chemical name of the following compound? ​  </strong> A) 2,3-dichloro-5,6-dicyano-1,4-benzoquinone B) 2,3-dichloro-5,6-dicyano-1,4-benzodione C) 5,6-dicyano-2,3-dichloro-1,4-benzodione D) 2,3-dicyano-5,6-dichloro-1,4-benzoquinone <div style=padding-top: 35px>

A) 2,3-dichloro-5,6-dicyano-1,4-benzoquinone
B) 2,3-dichloro-5,6-dicyano-1,4-benzodione
C) 5,6-dicyano-2,3-dichloro-1,4-benzodione
D) 2,3-dicyano-5,6-dichloro-1,4-benzoquinone
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Deck 21: Benzene and the Concept of Aromaticity
1
Which orbital contains the lone pair on the nitrogen atom of pyridine?

A) s
B) p
C) sp
D) sp2
sp2
2
Which orbital contains the lone pair on the nitrogen atom of pyrrole?

A) s
B) p
C) sp
D) sp2
p
3
What is the hybridization of the oxygen atom of furan?

A) s
B) sp
C) sp2
D) sp3
sp2
4
What is the correct assignment of the names of the following heterocycles? <strong>What is the correct assignment of the names of the following heterocycles?  </strong> A) 1 = pyrrole; 2 = thiophene; 3 = pyridine B) 1 = thiophene; 2 = furan; 3 = pyrrole C) 1 = pyridine; 2 = thiophene; 3 = furan D) 1 = pyridine; 2 = thiophene; 3 = pyrrole

A) 1 = pyrrole; 2 = thiophene; 3 = pyridine
B) 1 = thiophene; 2 = furan; 3 = pyrrole
C) 1 = pyridine; 2 = thiophene; 3 = furan
D) 1 = pyridine; 2 = thiophene; 3 = pyrrole
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5
What is the correct assignment of the names of the following fused arenes? <strong>What is the correct assignment of the names of the following fused arenes?  </strong> A) 1 = naphthalene; 2 = anthracene; 3 = pyrene B) 1 = naphthalene; 2 = phenanthrene; 3 = coronene C) 1 = naphthalene; 2 = anthracene; 3 = benzo[a]pyrene D) 1 = anthracene; 2 = naphthalene; 3 = coronene

A) 1 = naphthalene; 2 = anthracene; 3 = pyrene
B) 1 = naphthalene; 2 = phenanthrene; 3 = coronene
C) 1 = naphthalene; 2 = anthracene; 3 = benzo[a]pyrene
D) 1 = anthracene; 2 = naphthalene; 3 = coronene
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6
Which of the following statements is not true about the structure of benzene?

A) six atomic 2p-orbitals overlap to form six π-molecular orbitals
B) there are three bonding π-molecular orbitals and three π-antibonding molecular orbitals
C) the ground state electronic configuration of benzene has six electrons in three π-bonding molecular orbitals
D) the bonds alternate in length around the ring
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7
Which of the following is not one of Hückel's criteria for aromaticity?

A) The compound must be cyclic
B) The compound must have one p-orbital on each atom of a ring
C) The compound must be planar or nearly planar so that there is a continuous overlap of p orbitals
D) The compound must have a closed loop of six pi electrons
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8
Which orbitals contain the lone pairs on the nitrogen atoms labeled i and ii in the imidazole ring? <strong>Which orbitals contain the lone pairs on the nitrogen atoms labeled i and ii in the imidazole ring?  </strong> A) i = sp<sup>2;</sup>; ii = sp<sup>3</sup> B) i = p<sup>;</sup>; ii = sp<sup>3</sup> C) i = p<sup>;</sup>; ii = sp<sup>3</sup>. D) i = p<sup>;</sup>; ii = sp<sup>2</sup>

A) i = sp2;; ii = sp3
B) i = p;; ii = sp3
C) i = p;; ii = sp3.
D) i = p;; ii = sp2
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9
Which of the following represents the energy levels of the molecular orbitals of benzene? <strong>Which of the following represents the energy levels of the molecular orbitals of benzene?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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10
What is the approximate length of the carbon-carbon bonds in benzene?

A) 110 pm
B) 121 pm
C) 139 pm
D) 156 pm
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11
What is the hybridization of the nitrogen atom of pyridine?

A) s
B) sp
C) sp2
D) sp3
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12
Which of the following statements is not true about the structure of benzene?

A) the carbon-carbon bonds are all the same length
B) the structure rapidly transforms between two resonance contributors
C) the structure is an average of two resonance contributors
D) the ring of six carbon atoms is planar
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13
What is the correct assignment of the names of the following heterocycles? <strong>What is the correct assignment of the names of the following heterocycles?  </strong> A) 1 = pyrrole; 2 = thiophene; 3 = pyridine B) 1 = thiophene; 2 = furan; 3 = pyrrole C) 1 = furan; 2 = pyrrole; 3 = thiophene D) 1 = furan; 2 = thiophene; 3 = pyrrole

A) 1 = pyrrole; 2 = thiophene; 3 = pyridine
B) 1 = thiophene; 2 = furan; 3 = pyrrole
C) 1 = furan; 2 = pyrrole; 3 = thiophene
D) 1 = furan; 2 = thiophene; 3 = pyrrole
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14
Which of the following compounds is aromatic?

A) ethane
B) cyclobutadiene
C) benzene
D) cyclooctatetraene
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15
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 2-nitro-6-carboxybromobenzene B) 2-bromo-1-nitro-4-benzoic acid C) 2-bromo-4-carboxynitrobenzene D) 3-bromo-4-nitrobenzoic acid

A) 2-nitro-6-carboxybromobenzene
B) 2-bromo-1-nitro-4-benzoic acid
C) 2-bromo-4-carboxynitrobenzene
D) 3-bromo-4-nitrobenzoic acid
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16
Which is the correct assignment of the names of the following substituted benzenes? <strong>Which is the correct assignment of the names of the following substituted benzenes?  </strong> A) 1 = phenol; 2 = m-cresol; 3 = toluene B) 1 = m-cresol; 2 = resorcinol; 3 = m-xylene C) 1 = anisole; 2 = catechol; 3 = m-xylene D) 1 = m-cresol; 2 = anisole; 3 = cumene

A) 1 = phenol; 2 = m-cresol; 3 = toluene
B) 1 = m-cresol; 2 = resorcinol; 3 = m-xylene
C) 1 = anisole; 2 = catechol; 3 = m-xylene
D) 1 = m-cresol; 2 = anisole; 3 = cumene
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17
What is the correct assignment of the names of the following substituted benzenes? <strong>What is the correct assignment of the names of the following substituted benzenes?  </strong> A) 1 = styrene; 2 = benzaldehyde; 3 = cumene B) 1 = anisole; 2 = benzaldehyde; 3 = toluene C) 1 = styrene; 2 = xylene; 3 = toluene D) 1 = aniline; 2 = phenol; 3 = cumene

A) 1 = styrene; 2 = benzaldehyde; 3 = cumene
B) 1 = anisole; 2 = benzaldehyde; 3 = toluene
C) 1 = styrene; 2 = xylene; 3 = toluene
D) 1 = aniline; 2 = phenol; 3 = cumene
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18
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 1-bromo-2-fluoro-4-toluene B) 4-bromo-2-fluorotoluene C) 2-bromo-4-fluorophenol D) 4-bromo-2-fluoroxylene

A) 1-bromo-2-fluoro-4-toluene
B) 4-bromo-2-fluorotoluene
C) 2-bromo-4-fluorophenol
D) 4-bromo-2-fluoroxylene
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19
What is the correct assignment of the names of the following substituted benzenes? <strong>What is the correct assignment of the names of the following substituted benzenes?  </strong> A) 1 = phenol; 2 = aniline; 3 = anisole B) 1 = benzaldehyde; 2 = anisole; 3 = toluene C) 1 = anisole; 2 = xylene; 3 = toluene D) 1 = anisole; 2 = aniline; 3 = toluene

A) 1 = phenol; 2 = aniline; 3 = anisole
B) 1 = benzaldehyde; 2 = anisole; 3 = toluene
C) 1 = anisole; 2 = xylene; 3 = toluene
D) 1 = anisole; 2 = aniline; 3 = toluene
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20
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 2,4-dibromotoluene B) 2,4-dibromophenol C) 2,4-dibromohydroxybenzene D) 4,6-dibromophenol

A) 2,4-dibromotoluene
B) 2,4-dibromophenol
C) 2,4-dibromohydroxybenzene
D) 4,6-dibromophenol
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21
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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22
Which of the following compounds is antiaromatic?

A) ethane
B) cyclobutadiene
C) benzene
D) cyclooctatetraene
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23
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 3 > 1 C) 3 > 2 > 1 D) 1 > 3 > 2

A) 1 > 2 > 3
B) 2 > 3 > 1
C) 3 > 2 > 1
D) 1 > 3 > 2
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24
What is the best choice of reagent to achieve the following reaction? <strong>What is the best choice of reagent to achieve the following reaction?  </strong> A) H<sub>2</sub>SO<sub>4</sub> B) NaOH, H<sub>2</sub>O C) K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>, H<sub>2</sub>SO<sub>4</sub> D) LiAlH<sub>4</sub>

A) H2SO4
B) NaOH, H2O
C) K2Cr2O7, H2SO4
D) LiAlH4
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25
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 1 > 3 C) 3 > 2 > 1 D) 1 > 3 > 2

A) 1 > 2 > 3
B) 2 > 1 > 3
C) 3 > 2 > 1
D) 1 > 3 > 2
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26
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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27
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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28
Which of the following compounds undergoes heterolytic carbon-halogen bond cleavage to form a stable organic cation? <strong>Which of the following compounds undergoes heterolytic carbon-halogen bond cleavage to form a stable organic cation?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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29
What is the best choice of reagent to achieve the following reaction? <strong>What is the best choice of reagent to achieve the following reaction?  </strong> A) H<sub>2</sub>SO<sub>4</sub> B) NaOH, H<sub>2</sub>O C) K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>, H<sub>2</sub>SO<sub>4</sub> D) H<sub>2</sub>/Pd

A) H2SO4
B) NaOH, H2O
C) K2Cr2O7, H2SO4
D) H2/Pd
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30
Which of the following ions is aromatic? <strong>Which of the following ions is aromatic?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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31
What is the best choice of reagent to achieve the following reaction? <strong>What is the best choice of reagent to achieve the following reaction?  </strong> A) Br<sub>2</sub>, CCl<sub>4</sub> B) HBr, H<sub>2</sub>O C) Br<sub>2</sub>, light D) NaBr

A) Br2, CCl4
B) HBr, H2O
C) Br2, light
D) NaBr
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32
Which of the following molecules is the most acidic? <strong>Which of the following molecules is the most acidic?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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33
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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34
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 1 > 3 C) 3 > 2 > 1 D) 1 > 3 > 2

A) 1 > 2 > 3
B) 2 > 1 > 3
C) 3 > 2 > 1
D) 1 > 3 > 2
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35
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 3 > 1 C) 3 > 2 > 1 D) 2 > 1 > 3

A) 1 > 2 > 3
B) 2 > 3 > 1
C) 3 > 2 > 1
D) 2 > 1 > 3
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36
Which of the following represents the energy levels of the molecular orbitals of cyclopentadienyl anion? <strong>Which of the following represents the energy levels of the molecular orbitals of cyclopentadienyl anion?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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37
Which of the following heterocycles is not aromatic? <strong>Which of the following heterocycles is not aromatic?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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38
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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39
Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)? <strong>Which of the following has the compounds shown in the correct order of decreasing acidity (i.e., more acidic > less acidic)?  </strong> A) 1 > 2 > 3 B) 2 > 3 > 1 C) 3 > 2 > 1 D) 1 > 3 > 2

A) 1 > 2 > 3
B) 2 > 3 > 1
C) 3 > 2 > 1
D) 1 > 3 > 2
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40
What is the major organic product obtained from the following reaction? <strong>What is the major organic product obtained from the following reaction?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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41
Which of the following represents the energy levels of the molecular orbitals of cyclobutadiene? <strong>Which of the following represents the energy levels of the molecular orbitals of cyclobutadiene?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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42
Which of the following is not true about [18]annulene? <strong>Which of the following is not true about [18]annulene?  </strong> A) [18]annulene is planar B) [18]annulene is aromatic C) [18]annulene gives one peak in the <sup>1</sup>H NMR spectrum D) [18]annulene has 18 pi bonds

A) [18]annulene is planar
B) [18]annulene is aromatic
C) [18]annulene gives one peak in the 1H NMR spectrum
D) [18]annulene has 18 pi bonds
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43
Which of the following is not true about [the bridged [10]annulene shown below? <strong>Which of the following is not true about [the bridged [10]annulene shown below?  </strong> A) all of the carbon atoms of bridged [10]annulene are all in the same plane B) bridged [10]annulene is aromatic C) bridged [10]annulene undergoes substitution reactions similar to benzene D) bridged [10]annulene has 10 pi electrons

A) all of the carbon atoms of bridged [10]annulene are all in the same plane
B) bridged [10]annulene is aromatic
C) bridged [10]annulene undergoes substitution reactions similar to benzene
D) bridged [10]annulene has 10 pi electrons
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44
How many p orbital electrons are present in cyclopentadienyl anion?

A) 4
B) 6
C) 7
D) 8
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45
The product of the following reaction would be 1-bromo-1-phenylethane. The product of the following reaction would be 1-bromo-1-phenylethane.
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46
What are the relative positions of the substituents in the following structure? <strong>What are the relative positions of the substituents in the following structure?  </strong> A) anti B) meta C) ortho D) para

A) anti
B) meta
C) ortho
D) para
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47
What are the relative positions of the substituents in the following structure? <strong>What are the relative positions of the substituents in the following structure?  </strong> A) anti B) meta C) ortho D) para

A) anti
B) meta
C) ortho
D) para
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48
How many p orbital electrons are present in furan?

A) 4
B) 6
C) 7
D) 8
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49
Phenols are stronger acids than alcohols because of the resonance stabilization of alkoxide ions.
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50
Furan has the structure shown below. Furan has the structure shown below.   The π orbitals in furan are shown below.  The π orbitals in furan are shown below. Furan has the structure shown below.   The π orbitals in furan are shown below.
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51
The following compound should be name as 1-((1S, 3R)-3-methylcyclohexyl)benzene. The following compound should be name as 1-((1S, 3R)-3-methylcyclohexyl)benzene.
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52
Consider the following structures, Consider the following structures,   A B Structure A is more acidic than B. A B
Structure A is more acidic than B.
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53
The product of the following reaction would be a dicarboxylic acid. The product of the following reaction would be a dicarboxylic acid.
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54
Which of the following is not true about cyclooctatetraene?

A) The planar conformation is antiaromatic
B) In the planar conformation there are two electrons in degenerate nonbonding pi orbitals.
C) In the tub conformation the pi system is not conjugated
D) The tub conformation is aromatic
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55
What are the relative positions of the substituents in the following structure? <strong>What are the relative positions of the substituents in the following structure?  </strong> A) anti B) meta C) ortho D) para

A) anti
B) meta
C) ortho
D) para
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56
Which of the following is true about [10]annulene? <strong>Which of the following is true about [10]annulene?  </strong> A) [10]annulene is planar B) [10]annulene is nonaromatic C) [10]annulene undergoes addition reactions similar to simple alkenes D) [10]annulene has 10 pi electrons

A) [10]annulene is planar
B) [10]annulene is nonaromatic
C) [10]annulene undergoes addition reactions similar to simple alkenes
D) [10]annulene has 10 pi electrons
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57
The following compound is named (Z)-2,3-diphenyl-2-hexene. The following compound is named (Z)-2,3-diphenyl-2-hexene.
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58
Which of the following does not undergo oxidation in the presence of H2CrO4? <strong>Which of the following does not undergo oxidation in the presence of H<sub>2</sub>CrO<sub>4</sub>?  </strong> A) 1 B) 2 C) 3 D) 4

A) 1
B) 2
C) 3
D) 4
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59
Consider the following structure. Consider the following structure.   The <sup>1</sup>H NMR spectrum of this compound −60°C shows a peak at 7.6 ppm, this would indicate aromaticity. The 1H NMR spectrum of this compound −60°C shows a peak at 7.6 ppm, this would indicate aromaticity.
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60
What is the intermediate in the reaction of ethylbenzene with NBS in the presence of benzoyl peroxide to give 1-bromo-1-phenylethane?

A) Benzylic anion
B) Benzylic cation
C) Benzylic radical
D) Benzylic carbene
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61
Why are nitrophenols more acidic than phenols?
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62
Assuming that the sulfur atom is sp2-hybridized, there are _____ π-electrons in the sulfathiazole ring.
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63
The following compound could be produced by reaction of phenol with bromobenzene. The following compound could be produced by reaction of phenol with bromobenzene.
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64
Identify the most acidic compound.

A)
<strong>Identify the most acidic compound.</strong> A)   B)   C)   D)
B)
<strong>Identify the most acidic compound.</strong> A)   B)   C)   D)
C)
<strong>Identify the most acidic compound.</strong> A)   B)   C)   D)
D)
<strong>Identify the most acidic compound.</strong> A)   B)   C)   D)
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65
Consider the following structure. Consider the following structure.   If named as an annulene, the name would be [ __ ] annulene.
If named as an annulene, the name would be [ __ ] annulene.
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66
Consider the following general structure. Consider the following general structure.   Positions 1,4 and 2,6 and 3,5 are termed para, ortho, and meta, respectively. Positions 1,4 and 2,6 and 3,5 are termed para, ortho, and meta, respectively.
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67
The ______ substituent is affected during the oxidation of 2-bromo-4-nitrotoulene using chromic acid.

A) methyl
B) nitro
C) bromo
D) hydroxy
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68
Which of the following compound is nonaromatic?

A)
<strong>Which of the following compound is nonaromatic?</strong> A)   B)   C)   D)
B)
<strong>Which of the following compound is nonaromatic?</strong> A)   B)   C)   D)
C)
<strong>Which of the following compound is nonaromatic?</strong> A)   B)   C)   D)
D)
<strong>Which of the following compound is nonaromatic?</strong> A)   B)   C)   D)
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69
List all of the requirements of a molecule for it to be considered aromatic.
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70
Consider the following structure. Consider the following structure.   This structure contains ____ π electrons.
This structure contains ____ π electrons.
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71
Provide a brief explanation of why the cyclopentadienyl anion (below) is aromatic. Your answer should identify the hybridization of each carbon atom and account for which electrons are in the pi system. Provide a brief explanation of why the cyclopentadienyl anion (below) is aromatic. Your answer should identify the hybridization of each carbon atom and account for which electrons are in the pi system.
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72
Identify the major product of the following reaction. ​ <strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)

A)
<strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)
B)
<strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)
C)
<strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)
D)
<strong>Identify the major product of the following reaction. ​  </strong> A)   B)   C)   D)
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73
Provide a brief explanation of why furan (below) is aromatic. Your answer should identify the hybridization of the oxygen atom and account for which electrons are in the pi system. Provide a brief explanation of why furan (below) is aromatic. Your answer should identify the hybridization of the oxygen atom and account for which electrons are in the pi system.
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74
Using the Hückel criteria, the compound would be ______________.
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75
According to Hückel criteria, sulfathiazole is predicted to be ___________.
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76
Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound "A" by the process of esterification, using acetic anhydride. Identify compound "A".

A)
<strong>Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound A by the process of esterification, using acetic anhydride. Identify compound A.</strong> A)   B)   C)   D)
B)
<strong>Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound A by the process of esterification, using acetic anhydride. Identify compound A.</strong> A)   B)   C)   D)
C)
<strong>Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound A by the process of esterification, using acetic anhydride. Identify compound A.</strong> A)   B)   C)   D)
D)
<strong>Aspirin, also known as acetylsalicylic acid, is used to treat fever and inflammation. It is prepared from an unknown compound A by the process of esterification, using acetic anhydride. Identify compound A.</strong> A)   B)   C)   D)
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77
What is the chemical name of the following compound? ​ <strong>What is the chemical name of the following compound? ​  </strong> A) 2,3-dichloro-5,6-dicyano-1,4-benzoquinone B) 2,3-dichloro-5,6-dicyano-1,4-benzodione C) 5,6-dicyano-2,3-dichloro-1,4-benzodione D) 2,3-dicyano-5,6-dichloro-1,4-benzoquinone

A) 2,3-dichloro-5,6-dicyano-1,4-benzoquinone
B) 2,3-dichloro-5,6-dicyano-1,4-benzodione
C) 5,6-dicyano-2,3-dichloro-1,4-benzodione
D) 2,3-dicyano-5,6-dichloro-1,4-benzoquinone
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