Deck 19: Carboxylic Acids

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Question
Which of the following sets of reagents would accomplish the chemical transformation shown? <strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
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Question
What would be the major organic product of the following reaction? <strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which would be the best name of the following compound? <strong>Which would be the best name of the following compound?  </strong> A) 2-bromo-3-isopropylbutenoic acid B) (E)-2-bromo-3,4-dimethyl-2-pentenoic acid C) (E)-2-bromo-3-methyl-2-hexenoic acid D) (E)-2-bromo-3-methyl-2-pentenoic acid E) (Z)-2-bromo-3-methyl-2-pentenoic acid <div style=padding-top: 35px>

A) 2-bromo-3-isopropylbutenoic acid
B) (E)-2-bromo-3,4-dimethyl-2-pentenoic acid
C) (E)-2-bromo-3-methyl-2-hexenoic acid
D) (E)-2-bromo-3-methyl-2-pentenoic acid
E) (Z)-2-bromo-3-methyl-2-pentenoic acid
Question
What best accounts for the unusually high boiling points of carboxylic acids relative to other organic compounds of similar molecular weight?

A) The relatively large concentration of oxygen atoms.
B) The presence of intramolecular hydrogen bonding.
C) Carboxylic acids are mostly ionized and thus are mostly ionic compounds.
D) The presence of intermolecular hydrogen bonding.
E) Carboxylic acids do not have unusually high boiling points.
Question
What major product would result from the following reaction? <strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>

A)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What reagent(s)is (are)needed to complete the reaction shown? <strong>What reagent(s)is (are)needed to complete the reaction shown?  </strong> A) CH<sub>3</sub>CH<sub>2</sub>Br B) KMnO<sub>4</sub>/<sub> </sub><sup>-</sup>OH C) CH<sub>3</sub>CH<sub>2</sub>MgBr D) CH<sub>3</sub>Li E) CH<sub>3</sub>COCl <div style=padding-top: 35px>

A) CH3CH2Br
B) KMnO4/ -OH
C) CH3CH2MgBr
D) CH3Li
E) CH3COCl
Question
Rank the following in decreasing order of acidity (most acidic on left): <strong>Rank the following in decreasing order of acidity (most acidic on left):  </strong> A) X > Z > Y B) Y > X > Z C) Z > X > Y D) Z > Y > X E) X > Y > Z <div style=padding-top: 35px>

A) X > Z > Y
B) Y > X > Z
C) Z > X > Y
D) Z > Y > X
E) X > Y > Z
Question
Which,if any,of the reactions below would produce 2-methylpropanoic acid?

A)
<strong>Which,if any,of the reactions below would produce 2-methylpropanoic acid?</strong> A)   B)   C)   D) All of these reactions would produce the desired product. E) None of these reactions would produce the desired product. <div style=padding-top: 35px>
B)
<strong>Which,if any,of the reactions below would produce 2-methylpropanoic acid?</strong> A)   B)   C)   D) All of these reactions would produce the desired product. E) None of these reactions would produce the desired product. <div style=padding-top: 35px>
C)
<strong>Which,if any,of the reactions below would produce 2-methylpropanoic acid?</strong> A)   B)   C)   D) All of these reactions would produce the desired product. E) None of these reactions would produce the desired product. <div style=padding-top: 35px>
D) All of these reactions would produce the desired product.
E) None of these reactions would produce the desired product.
Question
What reagent(s)would accomplish the following conversion? <strong>What reagent(s)would accomplish the following conversion?  </strong> A) Br<sub>2</sub> B) PBr<sub>3</sub> C) Br<sub>2</sub>/light D) Br<sub>2</sub> + cat.PBr<sub>3</sub> E) PBr<sub>3 </sub>+ cat.Br<sub>2</sub> <div style=padding-top: 35px>

A) Br2
B) PBr3
C) Br2/light
D) Br2 + cat.PBr3
E) PBr3 + cat.Br2
Question
The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?

A)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
What would the common name of the following di-acid be? <strong>What would the common name of the following di-acid be?  </strong> A) Malonic acid B) Oxalic acid C) Succinic acid D) Adipic acid E) Glutaric acid <div style=padding-top: 35px>

A) Malonic acid
B) Oxalic acid
C) Succinic acid
D) Adipic acid
E) Glutaric acid
Question
Which would be the strongest acid of the following?

A) BrCH2CH2CO2H
B) ClCH2CH2CO2H
C) CH3CHClCO2H
D) CF3CO2H
E) CH3CHClCOCl
Question
The higher acidity of carboxylic acids compared to other functional groups is best explained by

A) hydrogen bonding.
B) electronegativity of oxygen.
C) water solubility.
D) resonance.
E) electronegativity of carbon.
Question
Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid? <strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D <div style=padding-top: 35px>

A)
<strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D <div style=padding-top: 35px>
B)
<strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D <div style=padding-top: 35px>
C)
<strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D <div style=padding-top: 35px>
D)
<strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D <div style=padding-top: 35px>
E) both B and D
Question
What would be the organic product of the following reaction? <strong>What would be the organic product of the following reaction?  </strong> A) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>H + CO<sub>2</sub> B) 2 CH<sub>3</sub>CO<sub>2</sub>H C)   D)   E) None of these are formed. <div style=padding-top: 35px>

A) CH3CH2CO2H + CO2
B) 2 CH3CO2H
C)
<strong>What would be the organic product of the following reaction?  </strong> A) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>H + CO<sub>2</sub> B) 2 CH<sub>3</sub>CO<sub>2</sub>H C)   D)   E) None of these are formed. <div style=padding-top: 35px>
D)
<strong>What would be the organic product of the following reaction?  </strong> A) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>H + CO<sub>2</sub> B) 2 CH<sub>3</sub>CO<sub>2</sub>H C)   D)   E) None of these are formed. <div style=padding-top: 35px>
E) None of these are formed.
Question
Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid? <strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B <div style=padding-top: 35px>

A)
<strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B <div style=padding-top: 35px>
B)
<strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B <div style=padding-top: 35px>
C)
<strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B <div style=padding-top: 35px>
D)
<strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B <div style=padding-top: 35px>
E) both A and B
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) none of these <div style=padding-top: 35px>

A)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) none of these <div style=padding-top: 35px>
B)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) none of these <div style=padding-top: 35px>
C)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) none of these <div style=padding-top: 35px>
D)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) none of these <div style=padding-top: 35px>
E) none of these
Question
What reagent is needed to complete the reaction shown? <strong>What reagent is needed to complete the reaction shown?  </strong> A) CH<sub>3</sub>Cl B) PCl<sub>3</sub> C) Cl<sub>2</sub> D) LiAlH<sub>4</sub> E) none of these <div style=padding-top: 35px>

A) CH3Cl
B) PCl3
C) Cl2
D) LiAlH4
E) none of these
Question
What reagent(s)would accomplish the following? <strong>What reagent(s)would accomplish the following?  </strong> A) Cl<sub>2</sub>,light B) Cl<sub>2</sub>,H<sub>2</sub>O C) SOCl<sub>2</sub> D) MgCl<sub>2</sub> E) aqueous HCl <div style=padding-top: 35px>

A) Cl2,light
B) Cl2,H2O
C) SOCl2
D) MgCl2
E) aqueous HCl
Question
What would be the name of the following? <strong>What would be the name of the following?  </strong> A) Malonic acid B) Propanoic acid C) Oxalic acid D) Succinic acid E) Butanedioic acid <div style=padding-top: 35px>

A) Malonic acid
B) Propanoic acid
C) Oxalic acid
D) Succinic acid
E) Butanedioic acid
Question
Rank the following in order of decreasing acidity (more acidic > less acidic): <strong>Rank the following in order of decreasing acidity (more acidic > less acidic):  </strong> A) II > III > I > IV > V B) IV > II > I > III > V C) II > IV > I > III > V D) V > III > I > II > IV E) II > IV > I > V > III <div style=padding-top: 35px>

A) II > III > I > IV > V
B) IV > II > I > III > V
C) II > IV > I > III > V
D) V > III > I > II > IV
E) II > IV > I > V > III
Question
Carboxylic acids have unusually high boiling points because:

A) they are significantly heavier than organic molecules with the same molecular weight.
B) they repel each other in the gas phase.
C) they strongly attract each other in the liquid phase.
D) they are usually solids,and solids are not volatile.
E) they exist mostly as ions (RCO2- + H+)and ionic materials are not volatile.
Question
Rank the following benzoic acids in order of decreasing acidity: <strong>Rank the following benzoic acids in order of decreasing acidity:  </strong> A) III > I > II B) I > III > II C) II > I > III D) I > II > III E) III > II > I <div style=padding-top: 35px>

A) III > I > II
B) I > III > II
C) II > I > III
D) I > II > III
E) III > II > I
Question
In the carboxylic acid dimer (below),which bond(s)has a strength of about 6-8 kcal/mol? <strong>In the carboxylic acid dimer (below),which bond(s)has a strength of about 6-8 kcal/mol?  </strong> A) Bond a B) Bond b C) Bond c D) Bond d E) Bond e <div style=padding-top: 35px>

A) Bond a
B) Bond b
C) Bond c
D) Bond d
E) Bond e
Question
Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?

A)
<strong>Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?</strong> A)   B)   C)   D)   E) All of the above are intermediates. <div style=padding-top: 35px>
B)
<strong>Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?</strong> A)   B)   C)   D)   E) All of the above are intermediates. <div style=padding-top: 35px>
C)
<strong>Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?</strong> A)   B)   C)   D)   E) All of the above are intermediates. <div style=padding-top: 35px>
D)
<strong>Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?</strong> A)   B)   C)   D)   E) All of the above are intermediates. <div style=padding-top: 35px>
E) All of the above are intermediates.
Question
Which compound best fits the following spectroscopic data? 1H NMR = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.13C NMR = 13.4,18.5,36.3,179.6 ppm.

A)
<strong>Which compound best fits the following spectroscopic data? <sup>1</sup>H NMR <font face=symbol></font> = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.<sup>13</sup>C NMR <font face=symbol></font> = 13.4,18.5,36.3,179.6 ppm.</strong> A)   B)   C)   D)   E) none of the above <div style=padding-top: 35px>
B)
<strong>Which compound best fits the following spectroscopic data? <sup>1</sup>H NMR <font face=symbol></font> = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.<sup>13</sup>C NMR <font face=symbol></font> = 13.4,18.5,36.3,179.6 ppm.</strong> A)   B)   C)   D)   E) none of the above <div style=padding-top: 35px>
C)
<strong>Which compound best fits the following spectroscopic data? <sup>1</sup>H NMR <font face=symbol></font> = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.<sup>13</sup>C NMR <font face=symbol></font> = 13.4,18.5,36.3,179.6 ppm.</strong> A)   B)   C)   D)   E) none of the above <div style=padding-top: 35px>
D)
<strong>Which compound best fits the following spectroscopic data? <sup>1</sup>H NMR <font face=symbol></font> = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.<sup>13</sup>C NMR <font face=symbol></font> = 13.4,18.5,36.3,179.6 ppm.</strong> A)   B)   C)   D)   E) none of the above <div style=padding-top: 35px>
E) none of the above
Question
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 2-hexyl-9-methyldecanoic acid B) 2-isononyloctanoic acid C) 1-methyl-9-carboxypentadecane D) 2-hexyldecanoic acid E) 14-methyl-7-carboxypentadecane <div style=padding-top: 35px>

A) 2-hexyl-9-methyldecanoic acid
B) 2-isononyloctanoic acid
C) 1-methyl-9-carboxypentadecane
D) 2-hexyldecanoic acid
E) 14-methyl-7-carboxypentadecane
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Deck 19: Carboxylic Acids
1
Which of the following sets of reagents would accomplish the chemical transformation shown? <strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)

A)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)
B)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)
C)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)
D)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)
E)
<strong>Which of the following sets of reagents would accomplish the chemical transformation shown?  </strong> A)   <sup> </sup> B)   C)   D)   E)
2
What would be the major organic product of the following reaction? <strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)

A)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)
B)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)
C)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)
D)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)
E)
<strong>What would be the major organic product of the following reaction?  </strong> A)   B)   C)   D)   E)
3
Which would be the best name of the following compound? <strong>Which would be the best name of the following compound?  </strong> A) 2-bromo-3-isopropylbutenoic acid B) (E)-2-bromo-3,4-dimethyl-2-pentenoic acid C) (E)-2-bromo-3-methyl-2-hexenoic acid D) (E)-2-bromo-3-methyl-2-pentenoic acid E) (Z)-2-bromo-3-methyl-2-pentenoic acid

A) 2-bromo-3-isopropylbutenoic acid
B) (E)-2-bromo-3,4-dimethyl-2-pentenoic acid
C) (E)-2-bromo-3-methyl-2-hexenoic acid
D) (E)-2-bromo-3-methyl-2-pentenoic acid
E) (Z)-2-bromo-3-methyl-2-pentenoic acid
(E)-2-bromo-3,4-dimethyl-2-pentenoic acid
4
What best accounts for the unusually high boiling points of carboxylic acids relative to other organic compounds of similar molecular weight?

A) The relatively large concentration of oxygen atoms.
B) The presence of intramolecular hydrogen bonding.
C) Carboxylic acids are mostly ionized and thus are mostly ionic compounds.
D) The presence of intermolecular hydrogen bonding.
E) Carboxylic acids do not have unusually high boiling points.
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5
What major product would result from the following reaction? <strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)

A)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)
B)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)
C)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)
D)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)
E)
<strong>What major product would result from the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E)
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6
What reagent(s)is (are)needed to complete the reaction shown? <strong>What reagent(s)is (are)needed to complete the reaction shown?  </strong> A) CH<sub>3</sub>CH<sub>2</sub>Br B) KMnO<sub>4</sub>/<sub> </sub><sup>-</sup>OH C) CH<sub>3</sub>CH<sub>2</sub>MgBr D) CH<sub>3</sub>Li E) CH<sub>3</sub>COCl

A) CH3CH2Br
B) KMnO4/ -OH
C) CH3CH2MgBr
D) CH3Li
E) CH3COCl
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7
Rank the following in decreasing order of acidity (most acidic on left): <strong>Rank the following in decreasing order of acidity (most acidic on left):  </strong> A) X > Z > Y B) Y > X > Z C) Z > X > Y D) Z > Y > X E) X > Y > Z

A) X > Z > Y
B) Y > X > Z
C) Z > X > Y
D) Z > Y > X
E) X > Y > Z
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8
Which,if any,of the reactions below would produce 2-methylpropanoic acid?

A)
<strong>Which,if any,of the reactions below would produce 2-methylpropanoic acid?</strong> A)   B)   C)   D) All of these reactions would produce the desired product. E) None of these reactions would produce the desired product.
B)
<strong>Which,if any,of the reactions below would produce 2-methylpropanoic acid?</strong> A)   B)   C)   D) All of these reactions would produce the desired product. E) None of these reactions would produce the desired product.
C)
<strong>Which,if any,of the reactions below would produce 2-methylpropanoic acid?</strong> A)   B)   C)   D) All of these reactions would produce the desired product. E) None of these reactions would produce the desired product.
D) All of these reactions would produce the desired product.
E) None of these reactions would produce the desired product.
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9
What reagent(s)would accomplish the following conversion? <strong>What reagent(s)would accomplish the following conversion?  </strong> A) Br<sub>2</sub> B) PBr<sub>3</sub> C) Br<sub>2</sub>/light D) Br<sub>2</sub> + cat.PBr<sub>3</sub> E) PBr<sub>3 </sub>+ cat.Br<sub>2</sub>

A) Br2
B) PBr3
C) Br2/light
D) Br2 + cat.PBr3
E) PBr3 + cat.Br2
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10
The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?

A)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)
B)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)
C)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)
D)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)
E)
<strong>The reaction of propanoic acid with lithium aluminum hydride,followed by water,would result in what product?</strong> A)   B)   C)   D)   E)
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11
What would the common name of the following di-acid be? <strong>What would the common name of the following di-acid be?  </strong> A) Malonic acid B) Oxalic acid C) Succinic acid D) Adipic acid E) Glutaric acid

A) Malonic acid
B) Oxalic acid
C) Succinic acid
D) Adipic acid
E) Glutaric acid
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12
Which would be the strongest acid of the following?

A) BrCH2CH2CO2H
B) ClCH2CH2CO2H
C) CH3CHClCO2H
D) CF3CO2H
E) CH3CHClCOCl
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13
The higher acidity of carboxylic acids compared to other functional groups is best explained by

A) hydrogen bonding.
B) electronegativity of oxygen.
C) water solubility.
D) resonance.
E) electronegativity of carbon.
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14
Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid? <strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D

A)
<strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D
B)
<strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D
C)
<strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D
D)
<strong>Which of the following sets of reagents would convert benzyl bromide to phenylethanoic acid?  </strong> A)   B)   C)   D)   E) both B and D
E) both B and D
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15
What would be the organic product of the following reaction? <strong>What would be the organic product of the following reaction?  </strong> A) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>H + CO<sub>2</sub> B) 2 CH<sub>3</sub>CO<sub>2</sub>H C)   D)   E) None of these are formed.

A) CH3CH2CO2H + CO2
B) 2 CH3CO2H
C)
<strong>What would be the organic product of the following reaction?  </strong> A) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>H + CO<sub>2</sub> B) 2 CH<sub>3</sub>CO<sub>2</sub>H C)   D)   E) None of these are formed.
D)
<strong>What would be the organic product of the following reaction?  </strong> A) CH<sub>3</sub>CH<sub>2</sub>CO<sub>2</sub>H + CO<sub>2</sub> B) 2 CH<sub>3</sub>CO<sub>2</sub>H C)   D)   E) None of these are formed.
E) None of these are formed.
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16
Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid? <strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B

A)
<strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B
B)
<strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B
C)
<strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B
D)
<strong>Several 2-arylpropanoic acids are used as analgesics (painkillers).Three of these [Ibuprofen (= Advil),Naproxen (= Aleve)and Ketoprofen (= Orudis KT)] are currently available in over-the-counter form.Which of the following sets of reagents would accomplish conversion of an ethyl aromatic to a 2-arylpropanoic acid?  </strong> A)   B)   C)   D)   E) both A and B
E) both A and B
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17
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) none of these

A)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) none of these
B)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) none of these
C)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) none of these
D)
<strong>What would be the product of the following reaction?  </strong> A)   <sup> </sup> B)   C)   D)   E) none of these
E) none of these
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18
What reagent is needed to complete the reaction shown? <strong>What reagent is needed to complete the reaction shown?  </strong> A) CH<sub>3</sub>Cl B) PCl<sub>3</sub> C) Cl<sub>2</sub> D) LiAlH<sub>4</sub> E) none of these

A) CH3Cl
B) PCl3
C) Cl2
D) LiAlH4
E) none of these
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19
What reagent(s)would accomplish the following? <strong>What reagent(s)would accomplish the following?  </strong> A) Cl<sub>2</sub>,light B) Cl<sub>2</sub>,H<sub>2</sub>O C) SOCl<sub>2</sub> D) MgCl<sub>2</sub> E) aqueous HCl

A) Cl2,light
B) Cl2,H2O
C) SOCl2
D) MgCl2
E) aqueous HCl
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20
What would be the name of the following? <strong>What would be the name of the following?  </strong> A) Malonic acid B) Propanoic acid C) Oxalic acid D) Succinic acid E) Butanedioic acid

A) Malonic acid
B) Propanoic acid
C) Oxalic acid
D) Succinic acid
E) Butanedioic acid
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21
Rank the following in order of decreasing acidity (more acidic > less acidic): <strong>Rank the following in order of decreasing acidity (more acidic > less acidic):  </strong> A) II > III > I > IV > V B) IV > II > I > III > V C) II > IV > I > III > V D) V > III > I > II > IV E) II > IV > I > V > III

A) II > III > I > IV > V
B) IV > II > I > III > V
C) II > IV > I > III > V
D) V > III > I > II > IV
E) II > IV > I > V > III
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22
Carboxylic acids have unusually high boiling points because:

A) they are significantly heavier than organic molecules with the same molecular weight.
B) they repel each other in the gas phase.
C) they strongly attract each other in the liquid phase.
D) they are usually solids,and solids are not volatile.
E) they exist mostly as ions (RCO2- + H+)and ionic materials are not volatile.
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23
Rank the following benzoic acids in order of decreasing acidity: <strong>Rank the following benzoic acids in order of decreasing acidity:  </strong> A) III > I > II B) I > III > II C) II > I > III D) I > II > III E) III > II > I

A) III > I > II
B) I > III > II
C) II > I > III
D) I > II > III
E) III > II > I
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24
In the carboxylic acid dimer (below),which bond(s)has a strength of about 6-8 kcal/mol? <strong>In the carboxylic acid dimer (below),which bond(s)has a strength of about 6-8 kcal/mol?  </strong> A) Bond a B) Bond b C) Bond c D) Bond d E) Bond e

A) Bond a
B) Bond b
C) Bond c
D) Bond d
E) Bond e
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25
Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?

A)
<strong>Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?</strong> A)   B)   C)   D)   E) All of the above are intermediates.
B)
<strong>Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?</strong> A)   B)   C)   D)   E) All of the above are intermediates.
C)
<strong>Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?</strong> A)   B)   C)   D)   E) All of the above are intermediates.
D)
<strong>Which of the following intermediates are not involved in the acid catalyzed esterification reaction of a carboxylic acid?</strong> A)   B)   C)   D)   E) All of the above are intermediates.
E) All of the above are intermediates.
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26
Which compound best fits the following spectroscopic data? 1H NMR = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.13C NMR = 13.4,18.5,36.3,179.6 ppm.

A)
<strong>Which compound best fits the following spectroscopic data? <sup>1</sup>H NMR <font face=symbol></font> = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.<sup>13</sup>C NMR <font face=symbol></font> = 13.4,18.5,36.3,179.6 ppm.</strong> A)   B)   C)   D)   E) none of the above
B)
<strong>Which compound best fits the following spectroscopic data? <sup>1</sup>H NMR <font face=symbol></font> = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.<sup>13</sup>C NMR <font face=symbol></font> = 13.4,18.5,36.3,179.6 ppm.</strong> A)   B)   C)   D)   E) none of the above
C)
<strong>Which compound best fits the following spectroscopic data? <sup>1</sup>H NMR <font face=symbol></font> = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.<sup>13</sup>C NMR <font face=symbol></font> = 13.4,18.5,36.3,179.6 ppm.</strong> A)   B)   C)   D)   E) none of the above
D)
<strong>Which compound best fits the following spectroscopic data? <sup>1</sup>H NMR <font face=symbol></font> = 1.00 (t,J=7.4 Hz,3H); 1.65 (sextet,J=7.5 Hz,2H); 2.31 (t,J=7.4 Hz,2H); and 11.68 (s,1H)ppm.<sup>13</sup>C NMR <font face=symbol></font> = 13.4,18.5,36.3,179.6 ppm.</strong> A)   B)   C)   D)   E) none of the above
E) none of the above
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27
What is the IUPAC name of the following compound? <strong>What is the IUPAC name of the following compound?  </strong> A) 2-hexyl-9-methyldecanoic acid B) 2-isononyloctanoic acid C) 1-methyl-9-carboxypentadecane D) 2-hexyldecanoic acid E) 14-methyl-7-carboxypentadecane

A) 2-hexyl-9-methyldecanoic acid
B) 2-isononyloctanoic acid
C) 1-methyl-9-carboxypentadecane
D) 2-hexyldecanoic acid
E) 14-methyl-7-carboxypentadecane
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