Deck 20: Carboxylic Acids and Their Derivatives
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Deck 20: Carboxylic Acids and Their Derivatives
1
What is the IUPAC name for the following compound? 
A) 2-methylpentanoic acid
B) 3-methylpentanoic acid
C) 2-methylhexanoic acid
D) 3-methylhexanoic acid
E) None of these

A) 2-methylpentanoic acid
B) 3-methylpentanoic acid
C) 2-methylhexanoic acid
D) 3-methylhexanoic acid
E) None of these
3-methylhexanoic acid
2
What is the IUPAC name for the following compound? 
A) 3-fluorobutanoic acid
B) 2-fluorobutanoic acid
C) β-fluorobutyric acid
D) α-fluorobutyric acid
E) none of these

A) 3-fluorobutanoic acid
B) 2-fluorobutanoic acid
C) β-fluorobutyric acid
D) α-fluorobutyric acid
E) none of these
3-fluorobutanoic acid
3
Which of the following is the strongest acid?

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


A) I
B) II
C) III
D) IV
E) V
II
4
Give the IUPAC name for oxalic acid.
A) ethanedioic acid
B) propanedioic acid
C) butanedioic acid
D) pentanedioic acid
E) benzoic acid
A) ethanedioic acid
B) propanedioic acid
C) butanedioic acid
D) pentanedioic acid
E) benzoic acid
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5
What is the IUPAC name for the following compound? 

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6
What is the common name for the following compound? 
A) 3-fluorobutanoic acid
B) 2-fluorobutanoic acid
C) β-fluorobutyric acid
D) α-fluorobutyric acid
E) none of these

A) 3-fluorobutanoic acid
B) 2-fluorobutanoic acid
C) β-fluorobutyric acid
D) α-fluorobutyric acid
E) none of these
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7
What is the correct structure for trichloroacetic acid?

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


A) I
B) II
C) III
D) IV
E) none of these
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8
Give the IUPAC name for malonic acid.
A) ethanedioic acid
B) propanedioic acid
C) butanedioic acid
D) pentanedioic acid
E) benzoic acid
A) ethanedioic acid
B) propanedioic acid
C) butanedioic acid
D) pentanedioic acid
E) benzoic acid
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9
Ethanoic acid is commonly known as ________.
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10
Which one of the following compounds has the highest boiling point?
A) butanoic acid
B) 1-butanol
C) 2-butanone
D) methoxyethane
E) butanal
A) butanoic acid
B) 1-butanol
C) 2-butanone
D) methoxyethane
E) butanal
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11
What is the IUPAC name for the following compound? 

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12
What is the IUPAC name for the following compound? 
A) 2,4-dimethylheptanedioic acid
B) 3,5-dimethylheptanedioic acid
C) 2,4-dimethylpentanedioic acid
D) 3,5-dimethylpentanedioic acid
E) 2,4-dimethylheptanoyl acid

A) 2,4-dimethylheptanedioic acid
B) 3,5-dimethylheptanedioic acid
C) 2,4-dimethylpentanedioic acid
D) 3,5-dimethylpentanedioic acid
E) 2,4-dimethylheptanoyl acid
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13
What is the IUPAC name for the following compound? 

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14
Which one of the following compounds has the highest boiling point?

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


A) I
B) II
C) III
D) IV
E) V
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15
Methanoic acid is commonly known as ________.
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16
Give the IUPAC name for glutaric acid.
A) ethanedioic acid
B) propanedioic acid
C) butanedioic acid
D) pentanedioic acid
E) benzoic acid
A) ethanedioic acid
B) propanedioic acid
C) butanedioic acid
D) pentanedioic acid
E) benzoic acid
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17
What is the IUPAC name for the following compound? 

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18
Provide the structure for 5-chloro-3-isopropyloctanoic acid.
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19
What is the correct structure for succinic acid.

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


A) I
B) II
C) III
D) IV
E) none of these
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20
Provide the structure for (3S,4S)-3-hydroxy-4-phenylnonanoic acid.
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21
Provide the reagents necessary to carry out the following conversion. 

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22
Predict the product for the following reaction.

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



A) I
B) II
C) III
D) IV
E) V
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23
Predict the product for the following reaction. 

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24
Predict the product for the following reaction. 

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25
Which one of the following compounds is the strongest acid?

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



A) I
B) II
C) III
D) IV
E) V
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26
Predict the product for the following reaction. 

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27
Predict the product for the following reaction. 
A) (CH3)2CHCH2COOH
B) (CH3)2CHCH2CH2COOH
C) (CH3)2CHCH2CN
D) (CH3)2CHCH2CH2CN
E) (CH3)2CHCH2OH

A) (CH3)2CHCH2COOH
B) (CH3)2CHCH2CH2COOH
C) (CH3)2CHCH2CN
D) (CH3)2CHCH2CH2CN
E) (CH3)2CHCH2OH
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28
Which one of the following is the strongest acid? Explain your choice.
A)2,3-dimethylheptanoic acid
B)3,3-dichlorohexanoic acid
C)4-bromo-3-iodohexanoic acid
D)4-bromo-3-chloroheptanoic acid
E)4-bromo-2-fluorohexanoic acid
A)2,3-dimethylheptanoic acid
B)3,3-dichlorohexanoic acid
C)4-bromo-3-iodohexanoic acid
D)4-bromo-3-chloroheptanoic acid
E)4-bromo-2-fluorohexanoic acid
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29
Predict the product for the following reaction.

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



A) I
B) II
C) III
D) IV
E) V
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30
Which of the following is the weakest acid?

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


A) I
B) II
C) III
D) IV
E) V
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31
Predict the product for the following reaction sequence.

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



A) I
B) II
C) III
D) IV
E) V
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32
Provide the reagents necessary to carry out the following conversion. 
A) 1. Mg/ether
2) CO2
3) H3O+
B) 1. NaOH
2) KMnO4/NaOH/H2O
3) H3O+
C) 1. NaCN
D) A and C
E) all of these

A) 1. Mg/ether
2) CO2
3) H3O+
B) 1. NaOH
2) KMnO4/NaOH/H2O
3) H3O+
C) 1. NaCN
D) A and C
E) all of these
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33
Predict the product for the following reaction.

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



A) I
B) II
C) III
D) IV
E) V
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34
Provide the reagents necessary to carry out the following conversion. 

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35
Which one of the following is the strongest acid?
A) benzoic acid
B) 4-nitrobenzoic acid
C) 4-ethylbenzoic acid
D) 4-chlorobenzoic acid
E) 4-hydroxybenzoic acid
A) benzoic acid
B) 4-nitrobenzoic acid
C) 4-ethylbenzoic acid
D) 4-chlorobenzoic acid
E) 4-hydroxybenzoic acid
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36
Which one of the following is the weakest acid?
A) benzoic acid
B) 4-nitrobenzoic acid
C) 4-ethylbenzoic acid
D) 4-chlorobenzoic acid
E) 4-hydroxybenzoic acid
A) benzoic acid
B) 4-nitrobenzoic acid
C) 4-ethylbenzoic acid
D) 4-chlorobenzoic acid
E) 4-hydroxybenzoic acid
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37
Which one of the following is the strongest acid?
A) 2,2-dichlorobutanoic acid
B) 2,3-dichlorobutanoic acid
C) 3,3-dichlorobutanoic acid
D) 3,4-dichlorobutanoic acid
E) 4,4-dichlorobutanoic acid
A) 2,2-dichlorobutanoic acid
B) 2,3-dichlorobutanoic acid
C) 3,3-dichlorobutanoic acid
D) 3,4-dichlorobutanoic acid
E) 4,4-dichlorobutanoic acid
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38
Which of the following reagent(s) can be used to carry out the following conversion? 
A) PCC/CH2Cl2
B) CO2 followed by H3O+
C) mCPBA
D) Na2Cr2O7/H2SO4/H2O
E) both A and D

A) PCC/CH2Cl2
B) CO2 followed by H3O+
C) mCPBA
D) Na2Cr2O7/H2SO4/H2O
E) both A and D
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39
Rank the following acids in decreasing (strongest to weakest) order of acidity. Explain your choice. 

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40
Rank the following acids in decreasing (strongest to weakest) order of acidity.

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


A) V > III > I > II > IV
B) II > I > III > V > IV
C) IV > III > I > II > V
D) IV > V > III > I > II
E) V > I > III > II > IV
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41
Provide the reagents necessary to carry out the following conversion. 

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42
Provide the structure for 4-ethylbenzoyl chloride.

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


A) I
B) II
C) III
D) IV
E) V
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43
Provide the reagents necessary to carry out the following conversion. 

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44
What is the common name for the following compound? 
A) ( -methylbutyryl chloride)
B) ( -methylbutyryl chloride)
C) ( -methylbutyryl chloride)
D) 2-methylbutanoyl chloride
E) 3-methylbutanoyl chloride

A) ( -methylbutyryl chloride)
B) ( -methylbutyryl chloride)
C) ( -methylbutyryl chloride)
D) 2-methylbutanoyl chloride
E) 3-methylbutanoyl chloride
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45
Provide the structure for cyclopentanecarbonyl chloride.
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46
What is the IUPAC name for the following compound? 
A) ( -methylvaleryl chloride)
B) 2-methylpentanoyl chloride
C) 3-methylhexanoyl chloride
D) 3-methylpentanoyl chloride
E) 2-methylhexanoyl chloride

A) ( -methylvaleryl chloride)
B) 2-methylpentanoyl chloride
C) 3-methylhexanoyl chloride
D) 3-methylpentanoyl chloride
E) 2-methylhexanoyl chloride
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47
What is the common name for the following compound? 
A) ( -bromobutyryl chloride)
B) ( -bromobutyryl chloride)
C) 1-bromobutanoyl chloride
D) 2-bromobutanoyl chloride
E) 2-bromopropanoyl chloride

A) ( -bromobutyryl chloride)
B) ( -bromobutyryl chloride)
C) 1-bromobutanoyl chloride
D) 2-bromobutanoyl chloride
E) 2-bromopropanoyl chloride
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48
Predict the product for the following reaction sequence. 
A) 2,2-dimethylpropanoic acid
B) 3,3-dimethyl-2-butanone
C) 2,2-dimethyl-1-propanol
D) 2,2-dimethylbutanoic acid
E) 2,2-dimethylethanoic acid

A) 2,2-dimethylpropanoic acid
B) 3,3-dimethyl-2-butanone
C) 2,2-dimethyl-1-propanol
D) 2,2-dimethylbutanoic acid
E) 2,2-dimethylethanoic acid
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49
What is the IUPAC name for the following compound? 
A) 3-ethyl-2,4-dimethylpentanoyl chloride
B) 4-ethyl-3,5-dimethylpentanoyl chloride
C) 3-ethyl-2,4-dimethylhexanoyl chloride
D) 4-ethyl-3,5-dimethylhexanoyl chloride
E) 3,4,5-trimethylhexanoyl chloride

A) 3-ethyl-2,4-dimethylpentanoyl chloride
B) 4-ethyl-3,5-dimethylpentanoyl chloride
C) 3-ethyl-2,4-dimethylhexanoyl chloride
D) 4-ethyl-3,5-dimethylhexanoyl chloride
E) 3,4,5-trimethylhexanoyl chloride
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50
Provide the reagents necessary to carry out the following conversion. 

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51
Provide the reagents necessary to carry out the following conversion. 

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52
What is the IUPAC name for the following compound? 
A) ( -bromobutyryl chloride)
B) ( -bromobutyryl chloride)
C) 1-bromobutanoyl chloride
D) 2-bromobutanoyl chloride
E) 2-bromopropanoyl chloride

A) ( -bromobutyryl chloride)
B) ( -bromobutyryl chloride)
C) 1-bromobutanoyl chloride
D) 2-bromobutanoyl chloride
E) 2-bromopropanoyl chloride
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53
Provide the structure for benzoyl chloride.
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54
Predict the product for the following reaction. 
A) 3-methyl-2-pentanone
B) 3-methyl -1-propanol
C) 2-methyl-1-butanol
D) 3-methyl-2-pentanol
E) none of these

A) 3-methyl-2-pentanone
B) 3-methyl -1-propanol
C) 2-methyl-1-butanol
D) 3-methyl-2-pentanol
E) none of these
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55
What is the common name for the following compound? 
A) ( -bromoacetyl bromide)
B) ( -bromoacetyl bromide)
C) 1-bromoethanoyl bromide
D) 2-bromoethanoyl bromide
E) 1,2-dibromoacetic acid

A) ( -bromoacetyl bromide)
B) ( -bromoacetyl bromide)
C) 1-bromoethanoyl bromide
D) 2-bromoethanoyl bromide
E) 1,2-dibromoacetic acid
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56
Provide the reagents necessary to carry out the following conversion. ![<strong>Provide the reagents necessary to carry out the following conversion. </strong> A) 1. LiAlH<sub>4</sub> 2) H<sub>2</sub>O B) NaBH<sub>4</sub>/CH<sub>3</sub>OH C) LiAl[OC(CH<sub>3</sub>)<sub>3</sub>]H D) BH<sub>3</sub>·THF E) C and D](https://storage.examlex.com/TB4454/11ea894b_ad39_5681_bba7_c102fd1ae36c_TB4454_00_TB4454_00.jpg)
A) 1. LiAlH4
2) H2O
B) NaBH4/CH3OH
C) LiAl[OC(CH3)3]H
D) BH3·THF
E) C and D
![<strong>Provide the reagents necessary to carry out the following conversion. </strong> A) 1. LiAlH<sub>4</sub> 2) H<sub>2</sub>O B) NaBH<sub>4</sub>/CH<sub>3</sub>OH C) LiAl[OC(CH<sub>3</sub>)<sub>3</sub>]H D) BH<sub>3</sub>·THF E) C and D](https://storage.examlex.com/TB4454/11ea894b_ad39_5681_bba7_c102fd1ae36c_TB4454_00_TB4454_00.jpg)
A) 1. LiAlH4
2) H2O
B) NaBH4/CH3OH
C) LiAl[OC(CH3)3]H
D) BH3·THF
E) C and D
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57
What is the IUPAC name for the following compound? 
A) ( -methylbutyryl chloride)
B) ( -methylbutyryl chloride)
C) ( -methylbutyryl chloride)
D) 2-methylbutanoyl chloride
E) 3-methylbutanoyl chloride

A) ( -methylbutyryl chloride)
B) ( -methylbutyryl chloride)
C) ( -methylbutyryl chloride)
D) 2-methylbutanoyl chloride
E) 3-methylbutanoyl chloride
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58
What is the IUPAC name for the following compound? 
A) bromoacetyl bromide
B) ( -bromoacetyl bromide)
C) 1-bromoethanoyl bromide
D) bromoethanoyl bromide
E) 1,2-dibromoacetic acid

A) bromoacetyl bromide
B) ( -bromoacetyl bromide)
C) 1-bromoethanoyl bromide
D) bromoethanoyl bromide
E) 1,2-dibromoacetic acid
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59
Provide the reagents necessary to carry out the following conversion. 

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60
Provide the reagents necessary to carry out the following conversion. ![<strong>Provide the reagents necessary to carry out the following conversion. </strong> A) 1. LiAlH<sub>4</sub> 2) H<sub>2</sub>O B) NaBH<sub>4</sub>/CH<sub>3</sub>OH C) LiAl[OC(CH<sub>3</sub>)<sub>3</sub>]H D) BH<sub>3</sub>·THF E) C and D](https://storage.examlex.com/TB4454/11ea894b_ad39_5682_bba7_0759c575b0d2_TB4454_00_TB4454_00.jpg)
A) 1. LiAlH4
2) H2O
B) NaBH4/CH3OH
C) LiAl[OC(CH3)3]H
D) BH3·THF
E) C and D
![<strong>Provide the reagents necessary to carry out the following conversion. </strong> A) 1. LiAlH<sub>4</sub> 2) H<sub>2</sub>O B) NaBH<sub>4</sub>/CH<sub>3</sub>OH C) LiAl[OC(CH<sub>3</sub>)<sub>3</sub>]H D) BH<sub>3</sub>·THF E) C and D](https://storage.examlex.com/TB4454/11ea894b_ad39_5682_bba7_0759c575b0d2_TB4454_00_TB4454_00.jpg)
A) 1. LiAlH4
2) H2O
B) NaBH4/CH3OH
C) LiAl[OC(CH3)3]H
D) BH3·THF
E) C and D
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61
What is the IUPAC name for the following compound? 
A) methanoic propanoic anhydride
B) formic propionic anhydride
C) ethanoic propionic anhydride
D) acetic butyric anhydride
E) butanoic ethanoic anhydride

A) methanoic propanoic anhydride
B) formic propionic anhydride
C) ethanoic propionic anhydride
D) acetic butyric anhydride
E) butanoic ethanoic anhydride
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62
What is the IUPAC name for the following compound? 
A) propanoic anhydride
B) butanoic anhydride
C) propionic anhydride
D) pentanoic anhydride
E) butyric anhydride

A) propanoic anhydride
B) butanoic anhydride
C) propionic anhydride
D) pentanoic anhydride
E) butyric anhydride
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63
Provide the structure for acetic formic anhydride.
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64
Provide the structure for benzoic ethanoic anhydride.
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65
What is the IUPAC name for the following compound? 

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66
What is the IUPAC name for the following compound? 

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67
What is the IUPAC name for the following compound? 
A) methanoic anhydride
B) ethanoic anhydride
C) acetic anhydride
D) formic anhydride
E) propanoic anhydride

A) methanoic anhydride
B) ethanoic anhydride
C) acetic anhydride
D) formic anhydride
E) propanoic anhydride
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68
What is the IUPAC name for the following compound? 
A) 2-methylbutyl 3-methylbutanoate
B) 3-methylbutyl 3-methylbutanoate
C) 2-methylbutyl isovalerate
D) 2-methylbutyl 2-methylbutanoate
E) isopentyl isovalerate

A) 2-methylbutyl 3-methylbutanoate
B) 3-methylbutyl 3-methylbutanoate
C) 2-methylbutyl isovalerate
D) 2-methylbutyl 2-methylbutanoate
E) isopentyl isovalerate
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69
Provide the structure for benzyl propionate.
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70
What is the common name for the following compound? 

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71
What is the common name for the following compound? 
A) propanoic anhydride
B) butanoic anhydride
C) propionic anhydride
D) pentanoic anhydride
E) butyric anhydride

A) propanoic anhydride
B) butanoic anhydride
C) propionic anhydride
D) pentanoic anhydride
E) butyric anhydride
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72
Provide the structure for N-methylcyclohexanecarboxamide.
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73
What is the common name for the following compound? 
A) methanoic anhydride
B) ethanoic anhydride
C) acetic anhydride
D) formic anhydride
E) propanoic anhydride

A) methanoic anhydride
B) ethanoic anhydride
C) acetic anhydride
D) formic anhydride
E) propanoic anhydride
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74
Provide the structure for N-phenyl-N-propyl-2,3-dimethylbutanamide?

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



A) I
B) II
C) III
D) IV
E) V
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75
What is the common name for the following compound? 
A) 2-methylbutyl acetate
B) 3-methylbutyl acetate
C) 2-methylbutyl methanoate
D) 3-methylbutyl methanoate
E) isopentyl formate

A) 2-methylbutyl acetate
B) 3-methylbutyl acetate
C) 2-methylbutyl methanoate
D) 3-methylbutyl methanoate
E) isopentyl formate
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76
What is the IUPAC name for the following compound? 
A) sec-butyl ethanoate
B) ethyl 3-methylpentanoate
C) 3-methylbutyl ethanoate
D) ethyl 3-methylbutanoate
E) none of these

A) sec-butyl ethanoate
B) ethyl 3-methylpentanoate
C) 3-methylbutyl ethanoate
D) ethyl 3-methylbutanoate
E) none of these
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77
What is the IUPAC name for the following compound? 
A) 2-methylbutyl acetate
B) 3-methylbutyl acetate
C) 2-methylbutyl methanoate
D) 3-methylbutyl methanoate
E) isopentyl formate

A) 2-methylbutyl acetate
B) 3-methylbutyl acetate
C) 2-methylbutyl methanoate
D) 3-methylbutyl methanoate
E) isopentyl formate
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78
What is the IUPAC name for the following compound? 

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79
What is the IUPAC name for the following compound? 

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80
What is the common name for the following compound? 
A) methanoic propanoic anhydride
B) formic propionic anhydride
C) ethanoic propionic anhydride
D) acetic butyric anhydride
E) butanoic ethanoic anhydride

A) methanoic propanoic anhydride
B) formic propionic anhydride
C) ethanoic propionic anhydride
D) acetic butyric anhydride
E) butanoic ethanoic anhydride
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