Deck 19: Carboxylic Acids and the Acidity of the O-H Bond

Full screen (f)
exit full mode
Question
What two groups make up the carboxylic acid group (RCOOH)?

A)Carbon dioxide and hydrogen
B)Carbonyl and hydroxyl
C)Carbon monoxide and hydroxyl
D)Carbonyl oxide and hydrogen
Use Space or
up arrow
down arrow
to flip the card.
Question
What is the common name of the following compound? <strong>What is the common name of the following compound?  </strong> A)a-Methylbutyric acid B)a-Propylpropionic acid C)a-Methylvaleric acid D)a-Methylcaproic acid <div style=padding-top: 35px>

A)a-Methylbutyric acid
B)a-Propylpropionic acid
C)a-Methylvaleric acid
D)a-Methylcaproic acid
Question
Arrange the following compounds in order of decreasing water solubility,putting the most soluble compound first. <strong>Arrange the following compounds in order of decreasing water solubility,putting the most soluble compound first.  </strong> A)I > II > III > IV B)I > IV > II > III C)I > II > IV > III D)IV > III > II > I <div style=padding-top: 35px>

A)I > II > III > IV
B)I > IV > II > III
C)I > II > IV > III
D)IV > III > II > I
Question
What is the common name of the following compound? <strong>What is the common name of the following compound?  </strong> A)a,b-Dimethoxyvaleric acid B)2,3-Dimethoxyvaleric acid C)2,3-Dimethoxycaproic acid D)a,b-Dimethoxycaproic acid <div style=padding-top: 35px>

A)a,b-Dimethoxyvaleric acid
B)2,3-Dimethoxyvaleric acid
C)2,3-Dimethoxycaproic acid
D)a,b-Dimethoxycaproic acid
Question
Which of the following is the most polar organic compound?

A)CH3CH2CH2CH3
B)CH3CH2CHO
C)CH3CH2CH2OH
D)CH3COOH
Question
Arrange the following compounds in order of increasing boiling point,putting the compound with the lowest boiling point first. <strong>Arrange the following compounds in order of increasing boiling point,putting the compound with the lowest boiling point first.  </strong> A)I < II < III < IV B)I < IV < II < III C)III < II < IV < I D)II < IV < I < III <div style=padding-top: 35px>

A)I < II < III < IV
B)I < IV < II < III
C)III < II < IV < I
D)II < IV < I < III
Question
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)2-sec-Butyl-4,4-dimethylnonanoic acid B)4,4-Dimethyl-2-isobutylnonanoic acid C)4,4-Dimethyl-2-sec-butylnonanoic acid D)2-Isobutyl-4,4-dimethylnonanoic acid <div style=padding-top: 35px>

A)2-sec-Butyl-4,4-dimethylnonanoic acid
B)4,4-Dimethyl-2-isobutylnonanoic acid
C)4,4-Dimethyl-2-sec-butylnonanoic acid
D)2-Isobutyl-4,4-dimethylnonanoic acid
Question
What two strong absorptions are characteristic of the IR spectrum of carboxylic acids?

A)A C=O absorption at 1710 cm-1 and a C-H absorption at 3000 cm-1.
B)A C=O absorption at 1710 cm-1 and an O-H absorption at 2500-3500 cm-1.
C)A C=O absorption at 1600 cm-1 and an O-H absorption at 2500-3000 cm-1.
D)A C-O absorption at 1500 cm-1 and an O-H absorption at 2500-3500 cm-1.
Question
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)3,4-Dimethylcyclohexanoic acid B)3,4-Dimethylcyclohexanecarboxylic acid C)4,5-Dimethylcyclohexanecarboxylic acid D)1,2-Dimethylcyclohexanecarboxylic acid <div style=padding-top: 35px>

A)3,4-Dimethylcyclohexanoic acid
B)3,4-Dimethylcyclohexanecarboxylic acid
C)4,5-Dimethylcyclohexanecarboxylic acid
D)1,2-Dimethylcyclohexanecarboxylic acid
Question
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)(E)-2-Hexenoic acid B)(Z)-2-Hexenoic acid C)(E)-4-Hexenoic acid D)(Z)-4-Hexenoic acid <div style=padding-top: 35px>

A)(E)-2-Hexenoic acid
B)(Z)-2-Hexenoic acid
C)(E)-4-Hexenoic acid
D)(Z)-4-Hexenoic acid
Question
Which of the following is the correct IUPAC name for the following structure? <strong>Which of the following is the correct IUPAC name for the following structure?  </strong> A)Potassium propanoate B)Butanoic potassium C)Potassium propanoic D)Potassium butanoate <div style=padding-top: 35px>

A)Potassium propanoate
B)Butanoic potassium
C)Potassium propanoic
D)Potassium butanoate
Question
Which of the following is the structure of oxalic acid? <strong>Which of the following is the structure of oxalic acid?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
What is the hybridization of the carbon atom in a carboxy group?

A)sp
B)sp2
C)sp3
D)p
Question
Why is the C-O single bond of a carboxylic acid shorter than the C-O single bond of an alcohol?

A)The carbon in the alcohol is sp2 hybridized and has a higher percent s-character that lengthens the C-O bond in the alcohol.
B)The carbon in the carboxylic acid is sp3 hybridized and has a lower percent s-character that shortens the C-O bond in the carboxylic acid.
C)The carbon in the carboxylic acid is sp hybridized and has a higher percent s-character that shortens the C-O bond in the carboxylic acid.
D)The carbon in the carboxylic acid is sp2 hybridized and has a higher percent s-character that shortens the C-O bond in the carboxylic acid.
Question
Arrange the following compounds in order of increasing water solubility,putting the least soluble compound first. <strong>Arrange the following compounds in order of increasing water solubility,putting the least soluble compound first.  </strong> A)I < II < III < IV B)II < I < III < IV C)I < III < II < IV D)IV < II < III < I <div style=padding-top: 35px>

A)I < II < III < IV
B)II < I < III < IV
C)I < III < II < IV
D)IV < II < III < I
Question
What is the common name of the following compound? <strong>What is the common name of the following compound?  </strong> A)b,b-Dimethyl-a-fluorobutyric acid B)a-Fluoro-b,b-dimethylbutyric acid C)a-Fluoro-b,b,b-trimethylpropionic acid D)a-Fluoro-b,b,b-trimethylbutyric acid <div style=padding-top: 35px>

A)b,b-Dimethyl-a-fluorobutyric acid
B)a-Fluoro-b,b-dimethylbutyric acid
C)a-Fluoro-b,b,b-trimethylpropionic acid
D)a-Fluoro-b,b,b-trimethylbutyric acid
Question
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)2-Methoxypentanoic acid B)2-Methoxybutanoic acid C)4-Methoxybutanoic acid D)4-Methoxypentanoic acid <div style=padding-top: 35px>

A)2-Methoxypentanoic acid
B)2-Methoxybutanoic acid
C)4-Methoxybutanoic acid
D)4-Methoxypentanoic acid
Question
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)4-Isopropyl-3-methylbutanoic acid B)2,4-Dimethylhexanoic acid C)3,5-Dimethylhexanoic acid D)3,5-Dimethy-1-hexanoic acid <div style=padding-top: 35px>

A)4-Isopropyl-3-methylbutanoic acid
B)2,4-Dimethylhexanoic acid
C)3,5-Dimethylhexanoic acid
D)3,5-Dimethy-1-hexanoic acid
Question
What is the common name of the following compound? <strong>What is the common name of the following compound?  </strong> A)Propanedioic acid B)1,3-Propanedicarboxylic acid C)Malonic acid D)Succinic acid <div style=padding-top: 35px>

A)Propanedioic acid
B)1,3-Propanedicarboxylic acid
C)Malonic acid
D)Succinic acid
Question
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)3,5,5-Trimethylcyclohexanecarboxylic acid B)3,3,5-Trimethylcyclohexanecarboxylic acid C)3,3,5-Trimethylcyclohexanoic acid D)3,5,5-Trimethylcyclohexanoic acid <div style=padding-top: 35px>

A)3,5,5-Trimethylcyclohexanecarboxylic acid
B)3,3,5-Trimethylcyclohexanecarboxylic acid
C)3,3,5-Trimethylcyclohexanoic acid
D)3,5,5-Trimethylcyclohexanoic acid
Question
Rank the following compounds in order of decreasing acidity,putting the most acidic first. <strong>Rank the following compounds in order of decreasing acidity,putting the most acidic first.  </strong> A)IV > III > I > II B)IV > II > I > III C)II > I > IV > III D)II > I > III > IV <div style=padding-top: 35px>

A)IV > III > I > II
B)IV > II > I > III
C)II > I > IV > III
D)II > I > III > IV
Question
What would happen if a mixture of benzoic acid and cyclohexanol dissolved in CH2Cl2 is treated with aqueous NaOH solution?

A)Benzoic acid would remain in the CH2Cl2 layer,and cyclohexanol would dissolve in the aqueous layer.
B)Benzoic acid would dissolve in the aqueous layer while cyclohexanol would remain in the CH2Cl2 layer.
C)The salt of benzoic acid would dissolve in the aqueous layer while cyclohexanol would remain in the CH2Cl2 layer.
D)The salt of benzoic acid would remain in the CH2Cl2 layer while cyclohexanol would dissolve in the aqueous layer.
Question
What would happen if a mixture of benzoic acid (C6H5COOH)and NaCl is added to a separatory funnel containing H2O and CH2Cl2?

A)The benzoic acid would dissolve in the water layer and the NaCl would dissolve in the organic layer.
B)The benzoic acid would dissolve in the organic layer and the NaCl would dissolve in the water layer.
C)Both benzoic acid and NaCl would dissolve in the organic layer.
D)Both benzoic acid and NaCl would dissolve in the water layer.
Question
Which of the following bases are strong enough to significantly deprotonate ethanol,CH3CH2OH (pKa = 16)?

A)NaOCH3
B)NaOH
C)NaH
D)NaOCH2CH3
Question
What is the overall charge of the amino acid,alanine,at pH = 2?

A)+ 1
B)- 1
C)No overall charge
D)+ 2
Question
What physical property and reaction type are used by extraction as useful techniques to separate and purify mixtures of compounds?

A)Physical property = solubility differences; reaction type = acid-base reaction
B)Physical property = boiling point; reaction type = acid-base reaction
C)Physical property = solubility differences; reaction type = oxidation-reduction
D)Physical property = density; reaction type = oxidation-reduction
Question
Where do the two noteworthy peaks of carboxylic acids appear in 1HNMR spectra?

A)Between 10 and 12 ppm for the OH proton and 2-2.5 ppm for the protons on the a carbon to the carboxy group.
B)Between 6 and 9 ppm for the OH proton and 2-2.5 ppm for the protons on the a carbon to the carboxy group.
C)Between 10 and 12 ppm for the OH proton and 1-1.5 ppm for the protons on the a carbon to the carboxy group.
D)Between 6 and 9 ppm for the OH proton and 1-1.5 ppm for the protons on the a carbon to the carboxy group.
Question
Rank the following compounds in order of increasing acidity,putting the least acidic first. <strong>Rank the following compounds in order of increasing acidity,putting the least acidic first.  </strong> A)I < II < III < IV B)III < II < I < IV C)IV < I < II < III D)I < IV < III < II <div style=padding-top: 35px>

A)I < II < III < IV
B)III < II < I < IV
C)IV < I < II < III
D)I < IV < III < II
Question
Rank the following compounds in order of increasing acidity,putting the least acidic first. <strong>Rank the following compounds in order of increasing acidity,putting the least acidic first.  </strong> A)III < II < IV < I B)III < IV < II < I C)I < IV < II < III D)I < II < III < IV <div style=padding-top: 35px>

A)III < II < IV < I
B)III < IV < II < I
C)I < IV < II < III
D)I < II < III < IV
Question
Why is pure acetic acid often called glacial acetic acid?

A)Because it freezes just below 0°C,forming white crystals
B)Because it freezes just below 100°C,forming white crystals
C)Because it freezes just below room temperature,forming white crystals
D)Because it freezes just above room temperature,forming white crystals
Question
In the presence of strong acids,which of the oxygen atoms on the carboxyl group is preferentially protonated and why?

A)Protonation occurs at the carbonyl oxygen because the resulting conjugate acid is stabilized by resonance.
B)Protonation occurs at the carbonyl oxygen because the resulting conjugate base is stabilized by the inductive effect.
C)Protonation occurs at the hydroxyl oxygen because the resulting conjugate acid is stabilized by resonance.
D)Protonation occurs at the hydroxyl oxygen because the resulting conjugate base is stabilized by the inductive effect.
Question
Rank the labeled protons (Ha-Hd)in order of increasing acidity,starting with the least acidic. <strong>Rank the labeled protons (H<sub>a</sub>-H<sub>d</sub>)in order of increasing acidity,starting with the least acidic.  </strong> A)Ha < Hb < Hc < Hd B)Hb < Hc < Ha < Hd C)Hd < Ha < Hc < Hb D)Hb < Hc < Hd < Ha <div style=padding-top: 35px>

A)Ha < Hb < Hc < Hd
B)Hb < Hc < Ha < Hd
C)Hd < Ha < Hc < Hb
D)Hb < Hc < Hd < Ha
Question
Which of the following reagents can accomplish the transformation below? <strong>Which of the following reagents can accomplish the transformation below?  </strong> A)PCC,CH<sub>2</sub>Cl<sub>2</sub> B)[1] LiAlH<sub>4</sub>,THF; [2] H<sub>2</sub>O C)[1] O<sub>3</sub>; [2] H<sub>2</sub>O D)K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>,H<sub>2</sub>SO<sub>4</sub>,H<sub>2</sub>O <div style=padding-top: 35px>

A)PCC,CH2Cl2
B)[1] LiAlH4,THF; [2] H2O
C)[1] O3; [2] H2O
D)K2Cr2O7,H2SO4,H2O
Question
Arrange the following compounds in order of increasing acidity,putting the least acidic first. <strong>Arrange the following compounds in order of increasing acidity,putting the least acidic first.  </strong> A)I < II < III < IV B)IV < III < II < I C)III < IV < II < I D)IV < II < III < I <div style=padding-top: 35px>

A)I < II < III < IV
B)IV < III < II < I
C)III < IV < II < I
D)IV < II < III < I
Question
What is the other product formed in the oxidation of the following terminal alkyne? <strong>What is the other product formed in the oxidation of the following terminal alkyne?  </strong> A)HCOOH B)HCOH C)CO<sub>2</sub> D)CO <div style=padding-top: 35px>

A)HCOOH
B)HCOH
C)CO2
D)CO
Question
Which of the following structures is the major contributor to the resonance hybrid of the phenoxide anion? <strong>Which of the following structures is the major contributor to the resonance hybrid of the phenoxide anion?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Rank the following compounds in order of decreasing acidity,putting the most acidic first. <strong>Rank the following compounds in order of decreasing acidity,putting the most acidic first.  </strong> A)IV > III > II > I B)IV > I > III > II C)I > II > III > IV D)IV > II > III > I <div style=padding-top: 35px>

A)IV > III > II > I
B)IV > I > III > II
C)I > II > III > IV
D)IV > II > III > I
Question
Which of the following cannot be the starting material for the following reaction? <strong>Which of the following cannot be the starting material for the following reaction?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Rank the following compounds in order of decreasing acidity,putting the most acidic first. <strong>Rank the following compounds in order of decreasing acidity,putting the most acidic first.  </strong> A)III > IV > I > II B)IV > III > I > II C)I > II > III > IV D)IV > III > II > I <div style=padding-top: 35px>

A)III > IV > I > II
B)IV > III > I > II
C)I > II > III > IV
D)IV > III > II > I
Question
Rank the following compounds in order of increasing acidity,putting the least acidic first. <strong>Rank the following compounds in order of increasing acidity,putting the least acidic first.  </strong> A)II < III < I < IV B)II < I < III < IV C)IV < III < I < II D)IV < I < II < III <div style=padding-top: 35px>

A)II < III < I < IV
B)II < I < III < IV
C)IV < III < I < II
D)IV < I < II < III
Question
Give the IUPAC name for the following compound. <strong>Give the IUPAC name for the following compound.  </strong> A)(E,R)-2-bromo-3-pentenoic acid B)(Z,R)-2-bromo-3-pentenoic acid C)(E,S)-2-bromo-3-pentenoic acid D)(Z,S)-2-bromo-3-pentenoic acid <div style=padding-top: 35px>

A)(E,R)-2-bromo-3-pentenoic acid
B)(Z,R)-2-bromo-3-pentenoic acid
C)(E,S)-2-bromo-3-pentenoic acid
D)(Z,S)-2-bromo-3-pentenoic acid
Question
What is the overall charge of the amino acid,alanine,at pH = 10?

A)+ 1
B)- 1
C)No overall charge
D)- 2
Question
As applied to the chemistry of amino acids,what is the definition for the isoelectric point?

A)The pH at which the amino acid exists primarily in its acidic form.
B)The pH at which the amino acid exists primarily in its basic form.
C)The pH at which the amino acid exists as a mixture of isomers.
D)The pH at which the amino acid exists primarily in its neutral form.
Question
What reagents are necessary to perform the following reaction? <strong>What reagents are necessary to perform the following reaction?  </strong> A)H<sub>2</sub>O,H<sup>+</sup> B)LiAlH<sub>4</sub>,H<sub>2</sub>O C)DIBAL-H,H<sub>2</sub>O D)CH<sub>3</sub>MgBr,H<sub>2</sub>O <div style=padding-top: 35px>

A)H2O,H+
B)LiAlH4,H2O
C)DIBAL-H,H2O
D)CH3MgBr,H2O
Question
Give the IUPAC name for the following compound. <strong>Give the IUPAC name for the following compound.  </strong> A)(E,R)-2-bromo-3-pentenoic acid B)(Z,R)-2-bromo-3-pentenoic acid C)(E,S)-2-bromo-3-pentenoic acid D)(Z,S)-2-bromo-3-pentenoic acid <div style=padding-top: 35px>

A)(E,R)-2-bromo-3-pentenoic acid
B)(Z,R)-2-bromo-3-pentenoic acid
C)(E,S)-2-bromo-3-pentenoic acid
D)(Z,S)-2-bromo-3-pentenoic acid
Question
What reagents are necessary to perform the following reaction? <strong>What reagents are necessary to perform the following reaction?  </strong> A)H<sub>2</sub>O,H<sup>+</sup> B)LiAlH<sub>4</sub>,H<sub>2</sub>O C)DIBAL-H,H<sub>2</sub>O D)CH<sub>3</sub>MgBr,H<sub>2</sub>O <div style=padding-top: 35px>

A)H2O,H+
B)LiAlH4,H2O
C)DIBAL-H,H2O
D)CH3MgBr,H2O
Question
Which of the following compounds is most basic? <strong>Which of the following compounds is most basic?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
What reagents are necessary to perform the following reaction? <strong>What reagents are necessary to perform the following reaction?  </strong> A)H<sub>2</sub>O,H<sup>+</sup> B)LiAlH<sub>4</sub>,H<sub>2</sub>O C)DIBAL-H,H<sub>2</sub>O D)CH<sub>3</sub>MgBr,H<sub>2</sub>O <div style=padding-top: 35px>

A)H2O,H+
B)LiAlH4,H2O
C)DIBAL-H,H2O
D)CH3MgBr,H2O
Question
Give the IUPAC name for the following compound. <strong>Give the IUPAC name for the following compound.  </strong> A)(E,R)-2-methyl-3-pentenenitrile B)(E,S)-2-methyl-3-pentenenitrile C)(Z,R)-2-methyl-3-pentenenitrile D)(Z,S)-2-methyl-3-pentenenitrile <div style=padding-top: 35px>

A)(E,R)-2-methyl-3-pentenenitrile
B)(E,S)-2-methyl-3-pentenenitrile
C)(Z,R)-2-methyl-3-pentenenitrile
D)(Z,S)-2-methyl-3-pentenenitrile
Question
Which of the following compounds is least basic? <strong>Which of the following compounds is least basic?  </strong> A)I B)II C)III D)IV <div style=padding-top: 35px>

A)I
B)II
C)III
D)IV
Question
Give the IUPAC name of the following compound. <strong>Give the IUPAC name of the following compound.  </strong> A)R-2-methylpentanenitrile B)S-2-methylpentanenitrile C)R-2-nitrilehexane D)S-2-nitrilehexane <div style=padding-top: 35px>

A)R-2-methylpentanenitrile
B)S-2-methylpentanenitrile
C)R-2-nitrilehexane
D)S-2-nitrilehexane
Question
What reagents are necessary to perform the following reaction? <strong>What reagents are necessary to perform the following reaction?  </strong> A)H<sub>2</sub>O,H<sup>+</sup> B)LiAlH<sub>4</sub>,H<sub>2</sub>O C)DIBAL-H,H<sub>2</sub>O D)CH<sub>3</sub>MgBr,H<sub>2</sub>O <div style=padding-top: 35px>

A)H2O,H+
B)LiAlH4,H2O
C)DIBAL-H,H2O
D)CH3MgBr,H2O
Question
What is the overall charge of the amino acid,alanine,at pH = 7?

A)+ 1
B)- 1
C)No overall charge
D)+ 2
Unlock Deck
Sign up to unlock the cards in this deck!
Unlock Deck
Unlock Deck
1/53
auto play flashcards
Play
simple tutorial
Full screen (f)
exit full mode
Deck 19: Carboxylic Acids and the Acidity of the O-H Bond
1
What two groups make up the carboxylic acid group (RCOOH)?

A)Carbon dioxide and hydrogen
B)Carbonyl and hydroxyl
C)Carbon monoxide and hydroxyl
D)Carbonyl oxide and hydrogen
Carbonyl and hydroxyl
2
What is the common name of the following compound? <strong>What is the common name of the following compound?  </strong> A)a-Methylbutyric acid B)a-Propylpropionic acid C)a-Methylvaleric acid D)a-Methylcaproic acid

A)a-Methylbutyric acid
B)a-Propylpropionic acid
C)a-Methylvaleric acid
D)a-Methylcaproic acid
a-Methylvaleric acid
3
Arrange the following compounds in order of decreasing water solubility,putting the most soluble compound first. <strong>Arrange the following compounds in order of decreasing water solubility,putting the most soluble compound first.  </strong> A)I > II > III > IV B)I > IV > II > III C)I > II > IV > III D)IV > III > II > I

A)I > II > III > IV
B)I > IV > II > III
C)I > II > IV > III
D)IV > III > II > I
I > II > IV > III
4
What is the common name of the following compound? <strong>What is the common name of the following compound?  </strong> A)a,b-Dimethoxyvaleric acid B)2,3-Dimethoxyvaleric acid C)2,3-Dimethoxycaproic acid D)a,b-Dimethoxycaproic acid

A)a,b-Dimethoxyvaleric acid
B)2,3-Dimethoxyvaleric acid
C)2,3-Dimethoxycaproic acid
D)a,b-Dimethoxycaproic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
5
Which of the following is the most polar organic compound?

A)CH3CH2CH2CH3
B)CH3CH2CHO
C)CH3CH2CH2OH
D)CH3COOH
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
6
Arrange the following compounds in order of increasing boiling point,putting the compound with the lowest boiling point first. <strong>Arrange the following compounds in order of increasing boiling point,putting the compound with the lowest boiling point first.  </strong> A)I < II < III < IV B)I < IV < II < III C)III < II < IV < I D)II < IV < I < III

A)I < II < III < IV
B)I < IV < II < III
C)III < II < IV < I
D)II < IV < I < III
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
7
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)2-sec-Butyl-4,4-dimethylnonanoic acid B)4,4-Dimethyl-2-isobutylnonanoic acid C)4,4-Dimethyl-2-sec-butylnonanoic acid D)2-Isobutyl-4,4-dimethylnonanoic acid

A)2-sec-Butyl-4,4-dimethylnonanoic acid
B)4,4-Dimethyl-2-isobutylnonanoic acid
C)4,4-Dimethyl-2-sec-butylnonanoic acid
D)2-Isobutyl-4,4-dimethylnonanoic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
8
What two strong absorptions are characteristic of the IR spectrum of carboxylic acids?

A)A C=O absorption at 1710 cm-1 and a C-H absorption at 3000 cm-1.
B)A C=O absorption at 1710 cm-1 and an O-H absorption at 2500-3500 cm-1.
C)A C=O absorption at 1600 cm-1 and an O-H absorption at 2500-3000 cm-1.
D)A C-O absorption at 1500 cm-1 and an O-H absorption at 2500-3500 cm-1.
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
9
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)3,4-Dimethylcyclohexanoic acid B)3,4-Dimethylcyclohexanecarboxylic acid C)4,5-Dimethylcyclohexanecarboxylic acid D)1,2-Dimethylcyclohexanecarboxylic acid

A)3,4-Dimethylcyclohexanoic acid
B)3,4-Dimethylcyclohexanecarboxylic acid
C)4,5-Dimethylcyclohexanecarboxylic acid
D)1,2-Dimethylcyclohexanecarboxylic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
10
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)(E)-2-Hexenoic acid B)(Z)-2-Hexenoic acid C)(E)-4-Hexenoic acid D)(Z)-4-Hexenoic acid

A)(E)-2-Hexenoic acid
B)(Z)-2-Hexenoic acid
C)(E)-4-Hexenoic acid
D)(Z)-4-Hexenoic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
11
Which of the following is the correct IUPAC name for the following structure? <strong>Which of the following is the correct IUPAC name for the following structure?  </strong> A)Potassium propanoate B)Butanoic potassium C)Potassium propanoic D)Potassium butanoate

A)Potassium propanoate
B)Butanoic potassium
C)Potassium propanoic
D)Potassium butanoate
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
12
Which of the following is the structure of oxalic acid? <strong>Which of the following is the structure of oxalic acid?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
13
What is the hybridization of the carbon atom in a carboxy group?

A)sp
B)sp2
C)sp3
D)p
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
14
Why is the C-O single bond of a carboxylic acid shorter than the C-O single bond of an alcohol?

A)The carbon in the alcohol is sp2 hybridized and has a higher percent s-character that lengthens the C-O bond in the alcohol.
B)The carbon in the carboxylic acid is sp3 hybridized and has a lower percent s-character that shortens the C-O bond in the carboxylic acid.
C)The carbon in the carboxylic acid is sp hybridized and has a higher percent s-character that shortens the C-O bond in the carboxylic acid.
D)The carbon in the carboxylic acid is sp2 hybridized and has a higher percent s-character that shortens the C-O bond in the carboxylic acid.
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
15
Arrange the following compounds in order of increasing water solubility,putting the least soluble compound first. <strong>Arrange the following compounds in order of increasing water solubility,putting the least soluble compound first.  </strong> A)I < II < III < IV B)II < I < III < IV C)I < III < II < IV D)IV < II < III < I

A)I < II < III < IV
B)II < I < III < IV
C)I < III < II < IV
D)IV < II < III < I
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
16
What is the common name of the following compound? <strong>What is the common name of the following compound?  </strong> A)b,b-Dimethyl-a-fluorobutyric acid B)a-Fluoro-b,b-dimethylbutyric acid C)a-Fluoro-b,b,b-trimethylpropionic acid D)a-Fluoro-b,b,b-trimethylbutyric acid

A)b,b-Dimethyl-a-fluorobutyric acid
B)a-Fluoro-b,b-dimethylbutyric acid
C)a-Fluoro-b,b,b-trimethylpropionic acid
D)a-Fluoro-b,b,b-trimethylbutyric acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
17
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)2-Methoxypentanoic acid B)2-Methoxybutanoic acid C)4-Methoxybutanoic acid D)4-Methoxypentanoic acid

A)2-Methoxypentanoic acid
B)2-Methoxybutanoic acid
C)4-Methoxybutanoic acid
D)4-Methoxypentanoic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
18
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)4-Isopropyl-3-methylbutanoic acid B)2,4-Dimethylhexanoic acid C)3,5-Dimethylhexanoic acid D)3,5-Dimethy-1-hexanoic acid

A)4-Isopropyl-3-methylbutanoic acid
B)2,4-Dimethylhexanoic acid
C)3,5-Dimethylhexanoic acid
D)3,5-Dimethy-1-hexanoic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
19
What is the common name of the following compound? <strong>What is the common name of the following compound?  </strong> A)Propanedioic acid B)1,3-Propanedicarboxylic acid C)Malonic acid D)Succinic acid

A)Propanedioic acid
B)1,3-Propanedicarboxylic acid
C)Malonic acid
D)Succinic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
20
What is the correct IUPAC name of the following compound? <strong>What is the correct IUPAC name of the following compound?  </strong> A)3,5,5-Trimethylcyclohexanecarboxylic acid B)3,3,5-Trimethylcyclohexanecarboxylic acid C)3,3,5-Trimethylcyclohexanoic acid D)3,5,5-Trimethylcyclohexanoic acid

A)3,5,5-Trimethylcyclohexanecarboxylic acid
B)3,3,5-Trimethylcyclohexanecarboxylic acid
C)3,3,5-Trimethylcyclohexanoic acid
D)3,5,5-Trimethylcyclohexanoic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
21
Rank the following compounds in order of decreasing acidity,putting the most acidic first. <strong>Rank the following compounds in order of decreasing acidity,putting the most acidic first.  </strong> A)IV > III > I > II B)IV > II > I > III C)II > I > IV > III D)II > I > III > IV

A)IV > III > I > II
B)IV > II > I > III
C)II > I > IV > III
D)II > I > III > IV
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
22
What would happen if a mixture of benzoic acid and cyclohexanol dissolved in CH2Cl2 is treated with aqueous NaOH solution?

A)Benzoic acid would remain in the CH2Cl2 layer,and cyclohexanol would dissolve in the aqueous layer.
B)Benzoic acid would dissolve in the aqueous layer while cyclohexanol would remain in the CH2Cl2 layer.
C)The salt of benzoic acid would dissolve in the aqueous layer while cyclohexanol would remain in the CH2Cl2 layer.
D)The salt of benzoic acid would remain in the CH2Cl2 layer while cyclohexanol would dissolve in the aqueous layer.
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
23
What would happen if a mixture of benzoic acid (C6H5COOH)and NaCl is added to a separatory funnel containing H2O and CH2Cl2?

A)The benzoic acid would dissolve in the water layer and the NaCl would dissolve in the organic layer.
B)The benzoic acid would dissolve in the organic layer and the NaCl would dissolve in the water layer.
C)Both benzoic acid and NaCl would dissolve in the organic layer.
D)Both benzoic acid and NaCl would dissolve in the water layer.
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
24
Which of the following bases are strong enough to significantly deprotonate ethanol,CH3CH2OH (pKa = 16)?

A)NaOCH3
B)NaOH
C)NaH
D)NaOCH2CH3
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
25
What is the overall charge of the amino acid,alanine,at pH = 2?

A)+ 1
B)- 1
C)No overall charge
D)+ 2
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
26
What physical property and reaction type are used by extraction as useful techniques to separate and purify mixtures of compounds?

A)Physical property = solubility differences; reaction type = acid-base reaction
B)Physical property = boiling point; reaction type = acid-base reaction
C)Physical property = solubility differences; reaction type = oxidation-reduction
D)Physical property = density; reaction type = oxidation-reduction
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
27
Where do the two noteworthy peaks of carboxylic acids appear in 1HNMR spectra?

A)Between 10 and 12 ppm for the OH proton and 2-2.5 ppm for the protons on the a carbon to the carboxy group.
B)Between 6 and 9 ppm for the OH proton and 2-2.5 ppm for the protons on the a carbon to the carboxy group.
C)Between 10 and 12 ppm for the OH proton and 1-1.5 ppm for the protons on the a carbon to the carboxy group.
D)Between 6 and 9 ppm for the OH proton and 1-1.5 ppm for the protons on the a carbon to the carboxy group.
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
28
Rank the following compounds in order of increasing acidity,putting the least acidic first. <strong>Rank the following compounds in order of increasing acidity,putting the least acidic first.  </strong> A)I < II < III < IV B)III < II < I < IV C)IV < I < II < III D)I < IV < III < II

A)I < II < III < IV
B)III < II < I < IV
C)IV < I < II < III
D)I < IV < III < II
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
29
Rank the following compounds in order of increasing acidity,putting the least acidic first. <strong>Rank the following compounds in order of increasing acidity,putting the least acidic first.  </strong> A)III < II < IV < I B)III < IV < II < I C)I < IV < II < III D)I < II < III < IV

A)III < II < IV < I
B)III < IV < II < I
C)I < IV < II < III
D)I < II < III < IV
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
30
Why is pure acetic acid often called glacial acetic acid?

A)Because it freezes just below 0°C,forming white crystals
B)Because it freezes just below 100°C,forming white crystals
C)Because it freezes just below room temperature,forming white crystals
D)Because it freezes just above room temperature,forming white crystals
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
31
In the presence of strong acids,which of the oxygen atoms on the carboxyl group is preferentially protonated and why?

A)Protonation occurs at the carbonyl oxygen because the resulting conjugate acid is stabilized by resonance.
B)Protonation occurs at the carbonyl oxygen because the resulting conjugate base is stabilized by the inductive effect.
C)Protonation occurs at the hydroxyl oxygen because the resulting conjugate acid is stabilized by resonance.
D)Protonation occurs at the hydroxyl oxygen because the resulting conjugate base is stabilized by the inductive effect.
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
32
Rank the labeled protons (Ha-Hd)in order of increasing acidity,starting with the least acidic. <strong>Rank the labeled protons (H<sub>a</sub>-H<sub>d</sub>)in order of increasing acidity,starting with the least acidic.  </strong> A)Ha < Hb < Hc < Hd B)Hb < Hc < Ha < Hd C)Hd < Ha < Hc < Hb D)Hb < Hc < Hd < Ha

A)Ha < Hb < Hc < Hd
B)Hb < Hc < Ha < Hd
C)Hd < Ha < Hc < Hb
D)Hb < Hc < Hd < Ha
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
33
Which of the following reagents can accomplish the transformation below? <strong>Which of the following reagents can accomplish the transformation below?  </strong> A)PCC,CH<sub>2</sub>Cl<sub>2</sub> B)[1] LiAlH<sub>4</sub>,THF; [2] H<sub>2</sub>O C)[1] O<sub>3</sub>; [2] H<sub>2</sub>O D)K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub>,H<sub>2</sub>SO<sub>4</sub>,H<sub>2</sub>O

A)PCC,CH2Cl2
B)[1] LiAlH4,THF; [2] H2O
C)[1] O3; [2] H2O
D)K2Cr2O7,H2SO4,H2O
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
34
Arrange the following compounds in order of increasing acidity,putting the least acidic first. <strong>Arrange the following compounds in order of increasing acidity,putting the least acidic first.  </strong> A)I < II < III < IV B)IV < III < II < I C)III < IV < II < I D)IV < II < III < I

A)I < II < III < IV
B)IV < III < II < I
C)III < IV < II < I
D)IV < II < III < I
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
35
What is the other product formed in the oxidation of the following terminal alkyne? <strong>What is the other product formed in the oxidation of the following terminal alkyne?  </strong> A)HCOOH B)HCOH C)CO<sub>2</sub> D)CO

A)HCOOH
B)HCOH
C)CO2
D)CO
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
36
Which of the following structures is the major contributor to the resonance hybrid of the phenoxide anion? <strong>Which of the following structures is the major contributor to the resonance hybrid of the phenoxide anion?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
37
Rank the following compounds in order of decreasing acidity,putting the most acidic first. <strong>Rank the following compounds in order of decreasing acidity,putting the most acidic first.  </strong> A)IV > III > II > I B)IV > I > III > II C)I > II > III > IV D)IV > II > III > I

A)IV > III > II > I
B)IV > I > III > II
C)I > II > III > IV
D)IV > II > III > I
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
38
Which of the following cannot be the starting material for the following reaction? <strong>Which of the following cannot be the starting material for the following reaction?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
39
Rank the following compounds in order of decreasing acidity,putting the most acidic first. <strong>Rank the following compounds in order of decreasing acidity,putting the most acidic first.  </strong> A)III > IV > I > II B)IV > III > I > II C)I > II > III > IV D)IV > III > II > I

A)III > IV > I > II
B)IV > III > I > II
C)I > II > III > IV
D)IV > III > II > I
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
40
Rank the following compounds in order of increasing acidity,putting the least acidic first. <strong>Rank the following compounds in order of increasing acidity,putting the least acidic first.  </strong> A)II < III < I < IV B)II < I < III < IV C)IV < III < I < II D)IV < I < II < III

A)II < III < I < IV
B)II < I < III < IV
C)IV < III < I < II
D)IV < I < II < III
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
41
Give the IUPAC name for the following compound. <strong>Give the IUPAC name for the following compound.  </strong> A)(E,R)-2-bromo-3-pentenoic acid B)(Z,R)-2-bromo-3-pentenoic acid C)(E,S)-2-bromo-3-pentenoic acid D)(Z,S)-2-bromo-3-pentenoic acid

A)(E,R)-2-bromo-3-pentenoic acid
B)(Z,R)-2-bromo-3-pentenoic acid
C)(E,S)-2-bromo-3-pentenoic acid
D)(Z,S)-2-bromo-3-pentenoic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
42
What is the overall charge of the amino acid,alanine,at pH = 10?

A)+ 1
B)- 1
C)No overall charge
D)- 2
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
43
As applied to the chemistry of amino acids,what is the definition for the isoelectric point?

A)The pH at which the amino acid exists primarily in its acidic form.
B)The pH at which the amino acid exists primarily in its basic form.
C)The pH at which the amino acid exists as a mixture of isomers.
D)The pH at which the amino acid exists primarily in its neutral form.
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
44
What reagents are necessary to perform the following reaction? <strong>What reagents are necessary to perform the following reaction?  </strong> A)H<sub>2</sub>O,H<sup>+</sup> B)LiAlH<sub>4</sub>,H<sub>2</sub>O C)DIBAL-H,H<sub>2</sub>O D)CH<sub>3</sub>MgBr,H<sub>2</sub>O

A)H2O,H+
B)LiAlH4,H2O
C)DIBAL-H,H2O
D)CH3MgBr,H2O
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
45
Give the IUPAC name for the following compound. <strong>Give the IUPAC name for the following compound.  </strong> A)(E,R)-2-bromo-3-pentenoic acid B)(Z,R)-2-bromo-3-pentenoic acid C)(E,S)-2-bromo-3-pentenoic acid D)(Z,S)-2-bromo-3-pentenoic acid

A)(E,R)-2-bromo-3-pentenoic acid
B)(Z,R)-2-bromo-3-pentenoic acid
C)(E,S)-2-bromo-3-pentenoic acid
D)(Z,S)-2-bromo-3-pentenoic acid
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
46
What reagents are necessary to perform the following reaction? <strong>What reagents are necessary to perform the following reaction?  </strong> A)H<sub>2</sub>O,H<sup>+</sup> B)LiAlH<sub>4</sub>,H<sub>2</sub>O C)DIBAL-H,H<sub>2</sub>O D)CH<sub>3</sub>MgBr,H<sub>2</sub>O

A)H2O,H+
B)LiAlH4,H2O
C)DIBAL-H,H2O
D)CH3MgBr,H2O
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
47
Which of the following compounds is most basic? <strong>Which of the following compounds is most basic?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
48
What reagents are necessary to perform the following reaction? <strong>What reagents are necessary to perform the following reaction?  </strong> A)H<sub>2</sub>O,H<sup>+</sup> B)LiAlH<sub>4</sub>,H<sub>2</sub>O C)DIBAL-H,H<sub>2</sub>O D)CH<sub>3</sub>MgBr,H<sub>2</sub>O

A)H2O,H+
B)LiAlH4,H2O
C)DIBAL-H,H2O
D)CH3MgBr,H2O
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
49
Give the IUPAC name for the following compound. <strong>Give the IUPAC name for the following compound.  </strong> A)(E,R)-2-methyl-3-pentenenitrile B)(E,S)-2-methyl-3-pentenenitrile C)(Z,R)-2-methyl-3-pentenenitrile D)(Z,S)-2-methyl-3-pentenenitrile

A)(E,R)-2-methyl-3-pentenenitrile
B)(E,S)-2-methyl-3-pentenenitrile
C)(Z,R)-2-methyl-3-pentenenitrile
D)(Z,S)-2-methyl-3-pentenenitrile
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
50
Which of the following compounds is least basic? <strong>Which of the following compounds is least basic?  </strong> A)I B)II C)III D)IV

A)I
B)II
C)III
D)IV
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
51
Give the IUPAC name of the following compound. <strong>Give the IUPAC name of the following compound.  </strong> A)R-2-methylpentanenitrile B)S-2-methylpentanenitrile C)R-2-nitrilehexane D)S-2-nitrilehexane

A)R-2-methylpentanenitrile
B)S-2-methylpentanenitrile
C)R-2-nitrilehexane
D)S-2-nitrilehexane
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
52
What reagents are necessary to perform the following reaction? <strong>What reagents are necessary to perform the following reaction?  </strong> A)H<sub>2</sub>O,H<sup>+</sup> B)LiAlH<sub>4</sub>,H<sub>2</sub>O C)DIBAL-H,H<sub>2</sub>O D)CH<sub>3</sub>MgBr,H<sub>2</sub>O

A)H2O,H+
B)LiAlH4,H2O
C)DIBAL-H,H2O
D)CH3MgBr,H2O
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
53
What is the overall charge of the amino acid,alanine,at pH = 7?

A)+ 1
B)- 1
C)No overall charge
D)+ 2
Unlock Deck
Unlock for access to all 53 flashcards in this deck.
Unlock Deck
k this deck
locked card icon
Unlock Deck
Unlock for access to all 53 flashcards in this deck.