Deck 8: Organic Reactions Hydrocarbons, Carboxlic Acids, Amines, and Related Compounds
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Deck 8: Organic Reactions Hydrocarbons, Carboxlic Acids, Amines, and Related Compounds
1
Which of the following statements is true about alkanes?
A) alkanes contain polar bonds
B) alkanes are attracted to one another by London forces
C) alkanes are polar molecules
D) alkanes are unsaturated hydrocarbons
A) alkanes contain polar bonds
B) alkanes are attracted to one another by London forces
C) alkanes are polar molecules
D) alkanes are unsaturated hydrocarbons
alkanes are attracted to one another by London forces
2
Hydocarbons are organic compounds that
A) contain carbon and hydrogen atoms only.
B) are soluble in water.
C) are polar molecules.
D) contain carbon, hydrogen, and halogen atoms.
A) contain carbon and hydrogen atoms only.
B) are soluble in water.
C) are polar molecules.
D) contain carbon, hydrogen, and halogen atoms.
contain carbon and hydrogen atoms only.
3
Which of the following molecules is an alkane?
A)
B)
C)
D)
A)

B)

C)

D)


4
Give the correct IUPAC name for the following molecule: 
A) 2-Ethylpentane
B) 3-Methylhexane
C) 3-Methylcycloheptane
D) 3-Methylheptane

A) 2-Ethylpentane
B) 3-Methylhexane
C) 3-Methylcycloheptane
D) 3-Methylheptane
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5
Give the correct IUPAC name for the following molecule: 
A) 3, 4-Dimethylpentane
B) 2,3-Dimethyl heptane
C) 2,3-Dimethylpentane
D) 1,1,2-Trimethylpentane

A) 3, 4-Dimethylpentane
B) 2,3-Dimethyl heptane
C) 2,3-Dimethylpentane
D) 1,1,2-Trimethylpentane
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6
Which of the following statements is true about nonane?
A) It is a polar molecule.
B) It dissolves in water.
C) It is a liquid at room temperature.
D) It contains one double bond.
A) It is a polar molecule.
B) It dissolves in water.
C) It is a liquid at room temperature.
D) It contains one double bond.
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7
Which of the following structures is a constitutional isomer of 2-Methylheptane?
A)
B)
C)
D)
A)

B)

C)

D)

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8
The name of the following compound is 
A) 2,2,4-trimethylpentane.
B) 1,1,1,3-tetramethylbutane.
C) 1,1,1,3,3-pentamethylpropane.
D) Both 1,1,1,3-tetramethylbutane and 1,1,1,3,3-pentamethylpropane are correct names.

A) 2,2,4-trimethylpentane.
B) 1,1,1,3-tetramethylbutane.
C) 1,1,1,3,3-pentamethylpropane.
D) Both 1,1,1,3-tetramethylbutane and 1,1,1,3,3-pentamethylpropane are correct names.
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9
Which of the following pairs of compounds represent constitutional isomers?
A) 2-methylpropane and Pentane
B) 2,2-dimethylbutane and 3-methylpentane
C) 2,2-dimethylpropane and 2-methylpentane
D) 2-methylbutane and 2-methylpropane
A) 2-methylpropane and Pentane
B) 2,2-dimethylbutane and 3-methylpentane
C) 2,2-dimethylpropane and 2-methylpentane
D) 2-methylbutane and 2-methylpropane
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10
The following is an example of what type of reaction? 
A) Hydration
B) Combustion
C) Hydrogeneation
D) Halogenation

A) Hydration
B) Combustion
C) Hydrogeneation
D) Halogenation
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11
The correct IUPAC name for the molecule below is ___. 
A) 1-pentene
B) 2,3-dimethyl-1-pentyne
C) 2,3,3-trimethyl-1-butyne
D) 2,3-dimethyl-1-heptene

A) 1-pentene
B) 2,3-dimethyl-1-pentyne
C) 2,3,3-trimethyl-1-butyne
D) 2,3-dimethyl-1-heptene
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12
Which of the following molecules represent trans- 2-Hexene?
A)
B)
C)
D)
A)

B)

C)

D)

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13
What is the major organic product of the following reaction? 
A) 1-propanol
B) 2-propanol
C) propanal
D) propanone

A) 1-propanol
B) 2-propanol
C) propanal
D) propanone
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14
Provide IUPAC name for the following molecule. 
A) 3-methyl-5-Hexene
B) 4-ethyl-1-pentene
C) 3-methyl-5-heptene
D) 4-methyl-1-hexene

A) 3-methyl-5-Hexene
B) 4-ethyl-1-pentene
C) 3-methyl-5-heptene
D) 4-methyl-1-hexene
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15
What is the major product of the reaction below? 
A)
B)
C)
D)

A)

B)

C)

D)

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16
Which of the following can participate in hydrogen bonding?
A) alcohols
B) carboxylic acids
C) primary amines
D) all of these choices
A) alcohols
B) carboxylic acids
C) primary amines
D) all of these choices
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17
Rank butane (CH3CH2CH2CH3), butanoic acid (CH3CH2CH2COOH), and pentane (CH3CH2CH2CH2CH3) in order of increasing boiling point. (From lowest to highest.)
A) butane < butanoic acid < pentane
B) butane < pentane < butanoic acid
C) butanoic acid < pentane < butane
D) pentane < butanoic acid < butane
A) butane < butanoic acid < pentane
B) butane < pentane < butanoic acid
C) butanoic acid < pentane < butane
D) pentane < butanoic acid < butane
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18
Carboxylic acids, when compared with other molecules of similar size,
A) have relatively lower melting points.
B) have relatively higher boiling points.
C) have a smaller number of hydrogen bonds.
D) have more nonpolar locations.
A) have relatively lower melting points.
B) have relatively higher boiling points.
C) have a smaller number of hydrogen bonds.
D) have more nonpolar locations.
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19
Give the IUPAC name of the following carboxylic acid? 
A) 4-propylnanoic acid
B) 3-octyl-butanoic acid
C) 4-butyl-3-methylheptanoic acid
D) 3-methyl-4-propyloctanoic acid

A) 4-propylnanoic acid
B) 3-octyl-butanoic acid
C) 4-butyl-3-methylheptanoic acid
D) 3-methyl-4-propyloctanoic acid
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20
What is the IUPAC name of the molecule below? 
A) octanoic acid
B) 6-ethyl-4-methylhexanoic acid
C) 4,6-dimethyloctanoic acid
D) 3,5-dimethyloctanoic acid

A) octanoic acid
B) 6-ethyl-4-methylhexanoic acid
C) 4,6-dimethyloctanoic acid
D) 3,5-dimethyloctanoic acid
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21
Provide the IUPAC name for the compound below. 
A) 2-methyl-5-heptanoic acid
B) 2-ethyl-5-methylhexanoic acid
C) 6-methyl-3-heptanoic acid
D) 6-methylheptanoic acid

A) 2-methyl-5-heptanoic acid
B) 2-ethyl-5-methylhexanoic acid
C) 6-methyl-3-heptanoic acid
D) 6-methylheptanoic acid
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22
The molecule responsible for the hot taste of chili peppers is capsaicin. Capsaicin is a phenol because it has
A) a double bond.
B) an amide within its structure.
C) a trans stereochemistry at its double bond.
D) an -OH attached to a benzene ring.
A) a double bond.
B) an amide within its structure.
C) a trans stereochemistry at its double bond.
D) an -OH attached to a benzene ring.
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23
The carboxylic acids share which characteristic with the phenols?
A) They have relatively high boiling points.
B) They are capable of forming hydrogen bonds.
C) They are weak acids.
D) All of these answer choices are correct.
A) They have relatively high boiling points.
B) They are capable of forming hydrogen bonds.
C) They are weak acids.
D) All of these answer choices are correct.
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24
The IUPAC name of the molecule below is 
A) hydroxyl -2,4-dichlorocyclohexene
B) 3,4-dichlorophenol
C) 2,4-dichlorophenol
D) 1,3-dichlorophenol

A) hydroxyl -2,4-dichlorocyclohexene
B) 3,4-dichlorophenol
C) 2,4-dichlorophenol
D) 1,3-dichlorophenol
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25
Phenol and toluene (structures shown below) have similar molecular weights.
Which of the following statements accounts for the higher boiling point of phenol (182 C) than that of toluene (111 C)?
A) Toluene is more soluble in water than phenol.
B) Phenol molecules are primarily attracted to one another by London forces.
C) Toluene has greater hydrogen bonding interactions than phenol.
D) Phenol molecules are primarily attracted to one another by hydrogen bonds.

A) Toluene is more soluble in water than phenol.
B) Phenol molecules are primarily attracted to one another by London forces.
C) Toluene has greater hydrogen bonding interactions than phenol.
D) Phenol molecules are primarily attracted to one another by hydrogen bonds.
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26
The carboxylic acids with less than 11 carbons are likely to have
A) lower vapor pressure than the larger carboxylic acids.
B) lower water solubility than larger carboxylic acids.
C) lower boiling points than the larger carboxylic acids.
D) the same chemical and physical properties as those with 11 to 20 carbons.
A) lower vapor pressure than the larger carboxylic acids.
B) lower water solubility than larger carboxylic acids.
C) lower boiling points than the larger carboxylic acids.
D) the same chemical and physical properties as those with 11 to 20 carbons.
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27
Which of the following produce acidic solutions in water?
A) phenols
B) 2º amines
C) carboxylic acids
D) both phenols and carboxylic acids
A) phenols
B) 2º amines
C) carboxylic acids
D) both phenols and carboxylic acids
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28
Which of the following lowers the pH when added to water?
A) ethyl alcohol
B) propanoic acid
C) methyl amine
D) methyl alcohol
A) ethyl alcohol
B) propanoic acid
C) methyl amine
D) methyl alcohol
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29
The chapter refers to physiological pH, which is approximately a
A) pH of 6.3.
B) pH of 7.
C) pH of 8.
D) pH of 10.
A) pH of 6.3.
B) pH of 7.
C) pH of 8.
D) pH of 10.
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30
Phenols are organic acids, as are carboxylic acids. The difference is that
A) the phenols have a Ka that is larger than the carboxylic acids.
B) the phenols are much stronger acids.
C) the carboxylic acids are significantly stronger.
D) the carboxylic acids are much larger than the phenols.
A) the phenols have a Ka that is larger than the carboxylic acids.
B) the phenols are much stronger acids.
C) the carboxylic acids are significantly stronger.
D) the carboxylic acids are much larger than the phenols.
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31
Both carboxylic acids and phenols react with strong bases to produce
A) the conjugate base of the carboxylic acid or phenol.
B) a stronger acid or phenol.
C) a complex with water.
D) gaseous products.
A) the conjugate base of the carboxylic acid or phenol.
B) a stronger acid or phenol.
C) a complex with water.
D) gaseous products.
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32
Provide the organic product formed when NaOH reacts with 3-bromophenol.
A) sodium 3-bromophenoxide
B) sodium phenoxide
C) 3-bromobenzoic acid
D) 3-bromobenzoate
A) sodium 3-bromophenoxide
B) sodium phenoxide
C) 3-bromobenzoic acid
D) 3-bromobenzoate
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33
Given: benzene, phenol, and sodium phenoxide. Rank these in order of increasing water solubility. (From lowest to highest.)
A) benzene < phenol < sodium phenoxide
B) phenol < benzene < sodium phenoxide
C) benzene < sodium phenoxide < phenol
D) sodium phenoxide < phenol < benzene
A) benzene < phenol < sodium phenoxide
B) phenol < benzene < sodium phenoxide
C) benzene < sodium phenoxide < phenol
D) sodium phenoxide < phenol < benzene
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34
The forces that hold one ester molecule to another are predominantly
A) hydrogen bonding.
B) dipole-dipole interactions and London forces.
C) ionic.
D) covalent.
A) hydrogen bonding.
B) dipole-dipole interactions and London forces.
C) ionic.
D) covalent.
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35
Carboxylic acids and alcohols can react under acidic conditions
A) to produce compounds that exist only under acidic conditions.
B) to produce esters with water being formed.
C) to produce phenols, if the appropriate hydrolyzing agents are present.
D) only if the carboxylic acid is an extremely strong acid.
A) to produce compounds that exist only under acidic conditions.
B) to produce esters with water being formed.
C) to produce phenols, if the appropriate hydrolyzing agents are present.
D) only if the carboxylic acid is an extremely strong acid.
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36
The organic product of the reaction between NaOH and 3-methylbutanoic acid is named
A) 3-methylbutane sodium.
B) 3-methylbutanoate.
C) methylbutanoate.
D) sodium 3-methylbutanoate.
A) 3-methylbutane sodium.
B) 3-methylbutanoate.
C) methylbutanoate.
D) sodium 3-methylbutanoate.
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37
The organic product formed when propanoic acid reacts with ethanol in the presence of an acid catalyst is called
A) ethyl propanoic acid.
B) ethylpropanoate.
C) propylethanoate.
D) propylethanoic acid.
A) ethyl propanoic acid.
B) ethylpropanoate.
C) propylethanoate.
D) propylethanoic acid.
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38
The reaction below is an example of what kind of reaction? 
A) neutralization
B) hydrolysis
C) esterification
D) saponification

A) neutralization
B) hydrolysis
C) esterification
D) saponification
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39
The missing product from the following reaction is 
A)
B)
C)
D)

A)

B)

C)

D)

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40
When the ester ethyl butanoate, CH3CH2CH2COOCH2CH3, is hydrolyzed under acidic conditions, which compounds are the products?
A) ethyl alcohol and butanoic acid
B) butanol and ethanoic (acetic acid)
C) ethyl alcohol and the butanoate ion
D) butanol and the ethanoate ion
A) ethyl alcohol and butanoic acid
B) butanol and ethanoic (acetic acid)
C) ethyl alcohol and the butanoate ion
D) butanol and the ethanoate ion
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41
When the ester ethyl butanoate, CH3CH2CH2COOCH2CH3, is hydrolyzed under basic conditions, which compounds are the products?
A) ethyl alcohol and butanoic acid
B) butanol and ethanoic (acetic) acid
C) ethyl alcohol and the butanoate ion
D) butanol and the ethanoate ion
A) ethyl alcohol and butanoic acid
B) butanol and ethanoic (acetic) acid
C) ethyl alcohol and the butanoate ion
D) butanol and the ethanoate ion
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42
Which raises the pH when added to water?
A) ethyl alcohol
B) propanoic acid
C) methyl amine
D) methyl alcohol
A) ethyl alcohol
B) propanoic acid
C) methyl amine
D) methyl alcohol
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43
The structure of amphetamine is shown.
Amphetamine is a ___ amine.
A) 1o
B) 2o
C) 3o
D) 4o

A) 1o
B) 2o
C) 3o
D) 4o
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44
The amide containing anti-flea drug Lufenuron is hydrophobic, therefore it dissolves easily in ___.
A) fatty tissue
B) aqueous solutions
C) hair
D) water
A) fatty tissue
B) aqueous solutions
C) hair
D) water
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45
To which class of compounds would a physiological stimulant most likely belong?
A) carboxylic acids
B) phenols
C) alcohols
D) amines
A) carboxylic acids
B) phenols
C) alcohols
D) amines
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46
Which compound is not an amine?
A)
B)
C)
D)
A)

B)

C)

D)

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47
This compound is mescaline, a hallucinogen.
Which of the following statements is true?
A) Mescaline is an amine.
B) Mescaline contains an alcohol group.
C) Mescaline is a carboxylic acid.
D) Mescaline is an amine and contains an alcohol group.

A) Mescaline is an amine.
B) Mescaline contains an alcohol group.
C) Mescaline is a carboxylic acid.
D) Mescaline is an amine and contains an alcohol group.
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48
What is the name of this compound? 
A) ethylmethyl-sec-butyl-ammonium
B) ethylmethylbutylammonium
C) N-ethyl-N-methyl-3-butamine
D) N-ethyl-N-methyl-2-butanamine

A) ethylmethyl-sec-butyl-ammonium
B) ethylmethylbutylammonium
C) N-ethyl-N-methyl-3-butamine
D) N-ethyl-N-methyl-2-butanamine
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49
Given the following amines:
These three amines all have the same formula weight. Rank them in order of increasing boiling point. (From lowest to highest.)
A) 1º < 2º < 3º
B) 2º < 1º < 3º
C) 3º < 2º < 1º
D) 3º < 1º < 2º

A) 1º < 2º < 3º
B) 2º < 1º < 3º
C) 3º < 2º < 1º
D) 3º < 1º < 2º
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50
Provide the IUPAC name for the following organic compound. 
A) N-Methyl-2-butamine
B) methylbutanamine
C) dimethypropyllamine
D) butylmethanamine

A) N-Methyl-2-butamine
B) methylbutanamine
C) dimethypropyllamine
D) butylmethanamine
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51
Provide the IUPAC name for the following organic compound. 
A) methylpentanamine
B) dimethylpentanamine
C) 2,N-Dimethyl-3-pentanamine
D) N-methyl-2-methylpentanamine

A) methylpentanamine
B) dimethylpentanamine
C) 2,N-Dimethyl-3-pentanamine
D) N-methyl-2-methylpentanamine
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52
What is the product if butanoic acid reacts with ammonia?
A) a secondary amine
B) the ammonium salt
C) a butane compound with a nitrogen attached to each carbon
D) a cyclic compound with one nitrogen and four carbons in the ring
A) a secondary amine
B) the ammonium salt
C) a butane compound with a nitrogen attached to each carbon
D) a cyclic compound with one nitrogen and four carbons in the ring
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53
Diproylamine and HBr react to produce
A) dipropylammonium bromide.
B) dipropyl bromide.
C) propylammonium bromide.
D) ammonium bromide.
A) dipropylammonium bromide.
B) dipropyl bromide.
C) propylammonium bromide.
D) ammonium bromide.
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54
Amine salts formed from amines are mainly used in the drug industry because
A) they are acidic and react with bases.
B) they do not have a strong, unpleasant odor as do amines.
C) they are weak acids.
D) they are more soluble in water and blood fluids than the amines.
A) they are acidic and react with bases.
B) they do not have a strong, unpleasant odor as do amines.
C) they are weak acids.
D) they are more soluble in water and blood fluids than the amines.
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55
Salts of quaternary (4º) ammonium salts
A) have low boiling points.
B) have high melting points.
C) have weak covalent bonds.
D) are liquids at room temperature.
A) have low boiling points.
B) have high melting points.
C) have weak covalent bonds.
D) are liquids at room temperature.
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56
An amine will be converted into its conjugate acid by
A) application of heat.
B) reaction with an oxidizing agent.
C) reaction with a strong acid.
D) reaction with a strong base.
A) application of heat.
B) reaction with an oxidizing agent.
C) reaction with a strong acid.
D) reaction with a strong base.
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57
Predict the organic product formed when heat is applied to the compound below: 
A)
B)
C)
D)

A)

B)

C)

D)

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58
The IUPAC name of the molecule below is 
A) N-methylbutanamide
B) methylbutyramide
C) methylbutylamide
D) N-methyl-1-butylamine

A) N-methylbutanamide
B) methylbutyramide
C) methylbutylamide
D) N-methyl-1-butylamine
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59
The products of the hydrolysis reaction below are 
A)
B)
C)
D)

A)

B)

C)

D)

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60
An amide can be identified by noting that
A) there is a nitrogen incorporated in the structure.
B) there is a nitrogen attached to an oxygen from a carbon.
C) all of the carbon chains attach to a nitrogen.
D) a nitrogen attaches to a carbonyl carbon.
A) there is a nitrogen incorporated in the structure.
B) there is a nitrogen attached to an oxygen from a carbon.
C) all of the carbon chains attach to a nitrogen.
D) a nitrogen attaches to a carbonyl carbon.
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61
The larger the carboxylic acid, the more hydrogen bonding occurs between molecules.
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62
The smell of rancid butter is due to the presence of butanoic acid.
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63
A common feature of carboxylic acids and phenols is that they contain an O-H group.
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64
When a carboxylic acid or phenol reacts with a strong base, one of the products is the conjugate base of the carboxylic acid or the phenol.
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65
Carboxylic acids have lower boiling points than esters of similar size.
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66
A 4º ammonium ion has four carbon atoms attached to a nitrogen atom causing it to have a 1+ charge.
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67
Water soluble amines form solutions with a pH that is greater than 7.
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68
Phenol forms a basic solution in water.
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69
Alcohols are not generally considered to be acids because they cannot donate a(n) ___ ion.
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70
Determine the major organic product of the following reaction:


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71
Determine the major organic product of the following reaction:


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72
Determine the major organic product of the following reaction:


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73
Generally, carboxylates are ___ in water if they contain fewer than 12 carbon atoms.
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74
A ___ amine is not capable of forming hydrogen bonds with a similar amine.
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75
A ____ amine is a ring compound in which at least one atom in the ring is nitrogen.
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76
Determine the major organic product of the following reaction:


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77
Determine the major organic product of the following reaction:


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