Deck 24: Organic Compounds

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Question
The compound shown below falls under the category of _____. <strong>The compound shown below falls under the category of _____.  </strong> A) ketones B) aldehydes C) carboxylic acids D) amides E) esters <div style=padding-top: 35px>

A) ketones
B) aldehydes
C) carboxylic acids
D) amides
E) esters
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Question
The compound shown below is an example of a(n) _____. <strong>The compound shown below is an example of a(n) _____.  </strong> A) ketone B) aldehyde C) carboxylic acid D) amide E) ester <div style=padding-top: 35px>

A) ketone
B) aldehyde
C) carboxylic acid
D) amide
E) ester
Question
The compound H2C=CH2\mathrm { H } _ { 2 } \mathrm { C } = \mathrm { CH } _ { 2 } falls under the category of _____.

A) arenes
B) alkenes
C) alkanes
D) amines
E) alkynes
Question
Alkanes have a general molecular formula CnH2n+2 where n is an integer.
Question
Hydrocarbons with the general formula CnH2n−2 are called _____.
Question
The compound shown below falls under the category of _____. <strong>The compound shown below falls under the category of _____.  </strong> A) ketones B) aldehydes C) carboxylic acids D) amides E) esters <div style=padding-top: 35px>

A) ketones
B) aldehydes
C) carboxylic acids
D) amides
E) esters
Question
State the major classes of organic compounds.
Question
The compound shown below falls under the category of _____. H3CCN\mathrm { H } _ { 3 } \mathrm { CC } \equiv \mathrm { N }

A) amides
B) amines
C) nitro compounds
D) nitriles
E) esters
Question
The compound shown below is an example of a(n) _____. <strong>The compound shown below is an example of a(n) _____.  </strong> A) amide B) amine C) nitro compound D) nitrile E) ester <div style=padding-top: 35px>

A) amide
B) amine
C) nitro compound
D) nitrile
E) ester
Question
The structural units that chemists use to classify organic compounds, and to predict their reactivities under a given set of conditions are called _____.
Question
The compound CH3CH2Cl\mathrm { CH } _ { 3 } \mathrm { CH } _ { 2 } \mathrm { Cl } is an example of a(n) _____.

A) aldehyde
B) alkyl halide
C) amine
D) arene
E) aryl halide
Question
The compound shown below falls under the category of _____. <strong>The compound shown below falls under the category of _____.  </strong> A) arenes B) alkenes C) alkanes D) amines E) alkynes <div style=padding-top: 35px>

A) arenes
B) alkenes
C) alkanes
D) amines
E) alkynes
Question
The compound shown below is an example of a(n) _____. <strong>The compound shown below is an example of a(n) _____.  </strong> A) ketone B) aldehyde C) carboxylic acid D) amide E) ester <div style=padding-top: 35px>

A) ketone
B) aldehyde
C) carboxylic acid
D) amide
E) ester
Question
The compound shown below falls under the category of _____. <strong>The compound shown below falls under the category of _____.  </strong> A) ketones B) aldehydes C) carboxylic acids D) amides E) esters <div style=padding-top: 35px>

A) ketones
B) aldehydes
C) carboxylic acids
D) amides
E) esters
Question
The compound CH3CH2OH is an example of a(n) _____.

A) phenol
B) ketone
C) aldehyde
D) alcohol
E) ether
Question
Alcohols, phenols, and ethers contain a carbonyl group (C=O).
Question
If the CH3 groups in dimethylbenzene, whose common name is xylene, are adjacent to each other, the compound is commonly called para-xylene.
Question
State the common nomenclature for aromatic ring substitutions with an example for each.
Question
The compound H3CH2COCH2CH3 falls under the category of _____.

A) phenols
B) ketones
C) aldehydes
D) alcohols
E) ethers
Question
The compound CH3CH3\mathrm { CH } _ { 3 } \mathrm { CH } _ { 3 } falls under the category of _____.

A) arenes
B) alkenes
C) alkanes
D) amines
E) alkynes
Question
_____ is the systematic name for formaldehyde.
Question
Electrophiles such as carbocations seek to gain electrons and thus have a strong tendency to react with nucleophiles.
Question
_____ is defined as the amount by which the plane of polarized light is rotated when the light is passed through a solution containing 1.0 g of solute per 1.0 mL of solvent in a tube 10.0 cm long.
Question
If the solution contains a single enantiomer of a chiral compound, the solute is said to be optically inactive.
Question
Differentiate between conformational and structural isomers.
Question
The eclipsed conformation is the most stable because it minimizes electrostatic repulsion between the hydrogen atoms on adjacent carbons.
Question
_____differ in the relative positions of substituents in a rigid molecule.
Question
_____ are molecules whose structures are mirror images but cannot be superimposed on one another in any orientation.
Question
A chiral solution that contains equal concentrations of a pair of enantiomers is called a(n) _____.
Question
A primary radical is more stable than a tertiary radical.
Question
Which of the following best defines conformational isomers?

A) They are the isomers that have the same molecular formula but differ in which atoms are bonded to one another.
B) They are the isomers whose molecules have the same connectivity but whose component atoms have different orientations in space.
C) They are the isomers whose structures are mirror images but cannot be superimposed on one another in any orientation.
D) They are the isomers whose three-dimensional structures differ because of rotation about a σ bond.
E) They are the isomers that differ in the relative positions of substituents in a rigid molecule.
Question
The carbon atom that is bonded to four different groups in most chiral organic molecules is called an asymmetric carbon atom.
Question
The reactivity of a molecule is affected by the degree of substitution of a carbon that is bonded to a functional group.
Question
Molecules that have the same connectivity but whose component atoms have different orientations in space are called _____.
Question
Which of the following best defines structural isomers?

A) They are the isomers that have the same molecular formula but differ in which atoms are bonded to one another.
B) They are the isomers whose molecules have the same connectivity but whose component atoms have different orientations in space.
C) They are the isomers whose structures are mirror images but cannot be superimposed on one another in any orientation.
D) They are the isomers whose three-dimensional structures differ because of rotation about a σ bond.
E) They are the isomers that differ in the relative positions of substituents in a rigid molecule.
Question
In the staggered conformation of ethane, the hydrogen atoms are positioned as far from one another as possible.
Question
The simplest alkane to have a conformational isomer is methane.
Question
Which of the following best defines enantiomers?

A) These are central atoms that are bonded to multiple groups of atoms.
B) These are molecules whose component atoms have different orientations in space.
C) These are molecules and their nonsuperimposable mirror images.
D) These are molecules in which the C-H bonds on adjacent carbon atoms lie in the same plane.
E) These are three-dimensional structures resulting from rotation about a σ bond.
Question
What are the two types of stereoisomers?
Question
Optical isomers have identical physical properties, although their chemical properties may differ in asymmetric environments.
Question
The oxidation state of carbon in carbon dioxide is _____.

A) -4
B) -2
C) 0
D) +2
E) +4
Question
Which of the following species is an electrophile?

A) BF3
B) NH2
C) CH4
D) C6H5OH
E) (CH3)4C
Question
How many valence electrons does a carbanion have?

A) Two
B) Four
C) Five
D) Six
E) Eight
Question
The reaction HCl + CH2=CH2 → CH3CH2Cl is an example of a(n) _____ reaction.

A) addition
B) rearrangement
C) substitution
D) redox
E) elimination
Question
The number of hydrogen atoms increases in going from the most oxidized to least oxidized compound.
Question
A(n) _____ carbon is bonded to only one other carbon and a functional group.
Question
A chemical reaction in which adjacent atoms are removed from a molecule, resulting in the formation of a multiple bond and a small molecule is called a(n) _____ reaction.
Question
A(n) _____ is a highly reactive species that has an unpaired valence electron.
Question
In nucleophilic substitution reactions, the nucleophile must have a greater affinity for the electropositive species than the original substituent.
Question
The reaction CH3Cl + OH → CH3OH + Cl is an example of a(n) _____ reaction.

A) addition
B) rearrangement
C) substitution
D) redox
E) elimination
Question
Differentiate between a carbanion and a carbocation.
Question
A(n) _____ carbon is bonded to three other carbons and a functional group.
Question
A(n) _____ carbon is bonded to two other carbons and a functional group.
Question
The π bonds of the multiple bond are stronger than the σ bond.
Question
Radical reactions are usually very selective because radicals are highly reactive.
Question
What are the three stages in radical chain reactions?
Question
A reaction in which the components of a species A-B are added to adjacent atoms across a carbon-carbon multiple bond is called a(n) _____ reaction.
Question
A chemical reaction in which one atom or a group of atoms in a substance is replaced by another atom or group of atoms from another substance is called a(n) _____ reaction.
Question
Which of the following is true of a carbocation?

A) It has a negatively charged carbon with eight valence electrons.
B) It is destabilized by groups that donate electrons.
C) A primary carbocation is more stable than a tertiary carbocation.
D) It is an electron-deficient species that needs electrons to complete its octet.
E) It does not react with nucleophiles.
Question
What are oxidation-reduction reactions?
Question
Alkenes and alkynes are most often prepared by substitution reactions.
Question
Which of the following organic compounds is prepared by a substitution reaction in which a nucleophilic alkoxide ion attacks the partially positively charged carbon atom of the polar C-X bond of an alkyl halide?

A) Ethers
B) Alcohols
C) Aldehydes
D) Ketones
E) Amides
Question
Alcohols can be prepared by reducing compounds that contain the carbonyl functional group.
Question
Which of the following is a characteristic of primary amines?

A) The nitrogen is bonded to three alkyl groups.
B) The nitrogen is bonded to two hydrogen atoms and one alkyl group.
C) The nitrogen is bonded to two hydrogen atoms and two alkyl groups.
D) The nitrogen is bonded to one hydrogen atom and two alkyl groups.
E) The nitrogen is bonded to three hydrogen atoms.
Question
Delocalization of π bonding over three atoms makes carboxylic acids and their derivatives more susceptible to nucleophilic attack than aldehydes and ketones with their single π bond.
Question
Which of the following methods is used to prepare alcohols?

A) They are prepared by reducing a carboxylic acid group.
B) They are prepared by adding water across a carbon-carbon double bond.
C) They are prepared by reacting a carboxylic acid derivative with a Grignard reagent.
D) They are prepared by reacting a Grignard reagent with CO2, followed by acidification.
E) They are prepared by the nucleophilic reaction of amines with more electrophilic carboxylic acid derivatives.
Question
The high reactivity of ethers makes them unsuitable as solvents for carrying out organic reactions.
Question
Which of the following is true of aldehydes and ketones?

A) They have an appreciable dipole moment because of the polar C=O bond.
B) They have lower boiling points than alkanes and alkenes of comparable molecular mass.
C) They are typically prepared by reducing alcohols.
D) In their reactions, the partially positively charged carbon atom of the carbonyl group is subject to an electrophilic attack.
E) In their reactions, the lone pairs of electrons on the oxygen atom of the carbonyl group allow a nucleophilic attack to occur.
Question
Which of the following methods is used to prepare ketones?

A) They are prepared by reducing a carboxylic acid group.
B) They are prepared by adding water across a carbon-carbon double bond.
C) They are prepared by reacting a carboxylic acid derivative with a Grignard reagent.
D) They are prepared by reacting an alcohol with a carboxylic acid in the presence of a catalytic amount of strong acid.
E) They are prepared by the nucleophilic reaction of amines with more electrophilic carboxylic acid derivatives.
Question
In the gas phase, the dipole moment of benzene is zero.
Question
Amines have the tendency to act as electrophiles.
Question
Which of the following best defines a dehydration reaction?

A) It is a reaction in which a -H of an arene is replaced by an electrophilic group.
B) It is a high-temperature decomposition reaction that can be used to form fibers of synthetic polymers.
C) It is a reaction that proceeds by eliminating the elements of water.
D) It is an electrochemical process in which an external voltage is applied to an electrolytic cell to drive a nonspontaneous reaction.
E) It is a catalytic reaction in which a catalyst is uniformly dispersed throughout the reactant mixture to form a solution.
Question
Which of the following methods is used to prepare esters?

A) They are prepared by adding water across a carbon-carbon double bond.
B) They are prepared by a nucleophilic substitution reaction of an alkyl halide using hydroxide.
C) They are prepared by reacting a Grignard reagent with CO2, followed by acidification.
D) They are prepared by the nucleophilic reaction of amines with more electrophilic carboxylic acid derivatives.
E) They are prepared by reacting an alcohol with a carboxylic acid in the presence of a catalytic amount of strong acid.
Question
Which of the following is true of alkanes?

A) Their boiling points decrease with increasing molecular mass.
B) Their melting points are insensitive to relatively small differences in structure.
C) They are easily attacked by nucleophiles and electrophiles.
D) Their reactions occur only under extreme conditions.
E) They are unaffected by catalytic cracking.
Question
Secondary and tertiary amines have higher boiling points than primary amines of comparable molecular mass.
Question
Amides are the least reactive of the carboxylic acid derivatives because amides participate in π bonding with the carbonyl group.
Question
Which of the following best defines a pyrolysis reaction?

A) It is a reaction in which a -H of an arene is replaced by an electrophilic group.
B) It is a high-temperature decomposition reaction that can be used to form fibers of synthetic polymers.
C) It is a reaction that proceeds by eliminating the elements of water.
D) It is an electrochemical process in which an external voltage is applied to an electrolytic cell to drive a nonspontaneous reaction.
E) It is a catalytic reaction in which a catalyst is uniformly dispersed throughout the reactant mixture to form a solution.
Question
Amines can react with virtually any electrophile, including the carbonyl carbon of an aldehyde, a ketone, or an ester.
Question
Which of the following is true of alcohols?

A) Their individual O-H bond dipoles cancel one another because of the electronegative oxygen atom.
B) They have lower boiling points than alkanes or alkenes of comparable molecular mass.
C) They are usually prepared by an electrophilic substitution reaction of an alkyl halide using hydroxide.
D) They are considered to be more acidic than phenols due to the presence an -OH functional group
E) They are weaker acids than water.
Question
Which of the following methods is used to prepare aldehydes?

A) They are prepared by reducing a carboxylic acid group.
B) They are prepared by adding water across a carbon-carbon double bond.
C) They are prepared by reacting a carboxylic acid derivative with a Grignard reagent.
D) They are prepared by reacting a Grignard reagent with CO2, followed by acidification.
E) They are prepared by the nucleophilic reaction of amines with more electrophilic carboxylic acid derivatives.
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Deck 24: Organic Compounds
1
The compound shown below falls under the category of _____. <strong>The compound shown below falls under the category of _____.  </strong> A) ketones B) aldehydes C) carboxylic acids D) amides E) esters

A) ketones
B) aldehydes
C) carboxylic acids
D) amides
E) esters
ketones
2
The compound shown below is an example of a(n) _____. <strong>The compound shown below is an example of a(n) _____.  </strong> A) ketone B) aldehyde C) carboxylic acid D) amide E) ester

A) ketone
B) aldehyde
C) carboxylic acid
D) amide
E) ester
carboxylic acid
3
The compound H2C=CH2\mathrm { H } _ { 2 } \mathrm { C } = \mathrm { CH } _ { 2 } falls under the category of _____.

A) arenes
B) alkenes
C) alkanes
D) amines
E) alkynes
alkenes
4
Alkanes have a general molecular formula CnH2n+2 where n is an integer.
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5
Hydrocarbons with the general formula CnH2n−2 are called _____.
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6
The compound shown below falls under the category of _____. <strong>The compound shown below falls under the category of _____.  </strong> A) ketones B) aldehydes C) carboxylic acids D) amides E) esters

A) ketones
B) aldehydes
C) carboxylic acids
D) amides
E) esters
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7
State the major classes of organic compounds.
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8
The compound shown below falls under the category of _____. H3CCN\mathrm { H } _ { 3 } \mathrm { CC } \equiv \mathrm { N }

A) amides
B) amines
C) nitro compounds
D) nitriles
E) esters
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9
The compound shown below is an example of a(n) _____. <strong>The compound shown below is an example of a(n) _____.  </strong> A) amide B) amine C) nitro compound D) nitrile E) ester

A) amide
B) amine
C) nitro compound
D) nitrile
E) ester
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10
The structural units that chemists use to classify organic compounds, and to predict their reactivities under a given set of conditions are called _____.
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11
The compound CH3CH2Cl\mathrm { CH } _ { 3 } \mathrm { CH } _ { 2 } \mathrm { Cl } is an example of a(n) _____.

A) aldehyde
B) alkyl halide
C) amine
D) arene
E) aryl halide
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12
The compound shown below falls under the category of _____. <strong>The compound shown below falls under the category of _____.  </strong> A) arenes B) alkenes C) alkanes D) amines E) alkynes

A) arenes
B) alkenes
C) alkanes
D) amines
E) alkynes
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13
The compound shown below is an example of a(n) _____. <strong>The compound shown below is an example of a(n) _____.  </strong> A) ketone B) aldehyde C) carboxylic acid D) amide E) ester

A) ketone
B) aldehyde
C) carboxylic acid
D) amide
E) ester
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14
The compound shown below falls under the category of _____. <strong>The compound shown below falls under the category of _____.  </strong> A) ketones B) aldehydes C) carboxylic acids D) amides E) esters

A) ketones
B) aldehydes
C) carboxylic acids
D) amides
E) esters
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15
The compound CH3CH2OH is an example of a(n) _____.

A) phenol
B) ketone
C) aldehyde
D) alcohol
E) ether
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16
Alcohols, phenols, and ethers contain a carbonyl group (C=O).
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17
If the CH3 groups in dimethylbenzene, whose common name is xylene, are adjacent to each other, the compound is commonly called para-xylene.
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18
State the common nomenclature for aromatic ring substitutions with an example for each.
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19
The compound H3CH2COCH2CH3 falls under the category of _____.

A) phenols
B) ketones
C) aldehydes
D) alcohols
E) ethers
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20
The compound CH3CH3\mathrm { CH } _ { 3 } \mathrm { CH } _ { 3 } falls under the category of _____.

A) arenes
B) alkenes
C) alkanes
D) amines
E) alkynes
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21
_____ is the systematic name for formaldehyde.
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22
Electrophiles such as carbocations seek to gain electrons and thus have a strong tendency to react with nucleophiles.
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23
_____ is defined as the amount by which the plane of polarized light is rotated when the light is passed through a solution containing 1.0 g of solute per 1.0 mL of solvent in a tube 10.0 cm long.
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24
If the solution contains a single enantiomer of a chiral compound, the solute is said to be optically inactive.
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25
Differentiate between conformational and structural isomers.
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26
The eclipsed conformation is the most stable because it minimizes electrostatic repulsion between the hydrogen atoms on adjacent carbons.
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27
_____differ in the relative positions of substituents in a rigid molecule.
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28
_____ are molecules whose structures are mirror images but cannot be superimposed on one another in any orientation.
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29
A chiral solution that contains equal concentrations of a pair of enantiomers is called a(n) _____.
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30
A primary radical is more stable than a tertiary radical.
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31
Which of the following best defines conformational isomers?

A) They are the isomers that have the same molecular formula but differ in which atoms are bonded to one another.
B) They are the isomers whose molecules have the same connectivity but whose component atoms have different orientations in space.
C) They are the isomers whose structures are mirror images but cannot be superimposed on one another in any orientation.
D) They are the isomers whose three-dimensional structures differ because of rotation about a σ bond.
E) They are the isomers that differ in the relative positions of substituents in a rigid molecule.
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32
The carbon atom that is bonded to four different groups in most chiral organic molecules is called an asymmetric carbon atom.
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33
The reactivity of a molecule is affected by the degree of substitution of a carbon that is bonded to a functional group.
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34
Molecules that have the same connectivity but whose component atoms have different orientations in space are called _____.
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35
Which of the following best defines structural isomers?

A) They are the isomers that have the same molecular formula but differ in which atoms are bonded to one another.
B) They are the isomers whose molecules have the same connectivity but whose component atoms have different orientations in space.
C) They are the isomers whose structures are mirror images but cannot be superimposed on one another in any orientation.
D) They are the isomers whose three-dimensional structures differ because of rotation about a σ bond.
E) They are the isomers that differ in the relative positions of substituents in a rigid molecule.
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36
In the staggered conformation of ethane, the hydrogen atoms are positioned as far from one another as possible.
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37
The simplest alkane to have a conformational isomer is methane.
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38
Which of the following best defines enantiomers?

A) These are central atoms that are bonded to multiple groups of atoms.
B) These are molecules whose component atoms have different orientations in space.
C) These are molecules and their nonsuperimposable mirror images.
D) These are molecules in which the C-H bonds on adjacent carbon atoms lie in the same plane.
E) These are three-dimensional structures resulting from rotation about a σ bond.
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39
What are the two types of stereoisomers?
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40
Optical isomers have identical physical properties, although their chemical properties may differ in asymmetric environments.
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41
The oxidation state of carbon in carbon dioxide is _____.

A) -4
B) -2
C) 0
D) +2
E) +4
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42
Which of the following species is an electrophile?

A) BF3
B) NH2
C) CH4
D) C6H5OH
E) (CH3)4C
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43
How many valence electrons does a carbanion have?

A) Two
B) Four
C) Five
D) Six
E) Eight
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44
The reaction HCl + CH2=CH2 → CH3CH2Cl is an example of a(n) _____ reaction.

A) addition
B) rearrangement
C) substitution
D) redox
E) elimination
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45
The number of hydrogen atoms increases in going from the most oxidized to least oxidized compound.
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46
A(n) _____ carbon is bonded to only one other carbon and a functional group.
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47
A chemical reaction in which adjacent atoms are removed from a molecule, resulting in the formation of a multiple bond and a small molecule is called a(n) _____ reaction.
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48
A(n) _____ is a highly reactive species that has an unpaired valence electron.
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49
In nucleophilic substitution reactions, the nucleophile must have a greater affinity for the electropositive species than the original substituent.
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50
The reaction CH3Cl + OH → CH3OH + Cl is an example of a(n) _____ reaction.

A) addition
B) rearrangement
C) substitution
D) redox
E) elimination
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51
Differentiate between a carbanion and a carbocation.
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52
A(n) _____ carbon is bonded to three other carbons and a functional group.
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53
A(n) _____ carbon is bonded to two other carbons and a functional group.
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54
The π bonds of the multiple bond are stronger than the σ bond.
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55
Radical reactions are usually very selective because radicals are highly reactive.
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56
What are the three stages in radical chain reactions?
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57
A reaction in which the components of a species A-B are added to adjacent atoms across a carbon-carbon multiple bond is called a(n) _____ reaction.
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58
A chemical reaction in which one atom or a group of atoms in a substance is replaced by another atom or group of atoms from another substance is called a(n) _____ reaction.
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59
Which of the following is true of a carbocation?

A) It has a negatively charged carbon with eight valence electrons.
B) It is destabilized by groups that donate electrons.
C) A primary carbocation is more stable than a tertiary carbocation.
D) It is an electron-deficient species that needs electrons to complete its octet.
E) It does not react with nucleophiles.
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60
What are oxidation-reduction reactions?
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61
Alkenes and alkynes are most often prepared by substitution reactions.
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62
Which of the following organic compounds is prepared by a substitution reaction in which a nucleophilic alkoxide ion attacks the partially positively charged carbon atom of the polar C-X bond of an alkyl halide?

A) Ethers
B) Alcohols
C) Aldehydes
D) Ketones
E) Amides
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63
Alcohols can be prepared by reducing compounds that contain the carbonyl functional group.
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64
Which of the following is a characteristic of primary amines?

A) The nitrogen is bonded to three alkyl groups.
B) The nitrogen is bonded to two hydrogen atoms and one alkyl group.
C) The nitrogen is bonded to two hydrogen atoms and two alkyl groups.
D) The nitrogen is bonded to one hydrogen atom and two alkyl groups.
E) The nitrogen is bonded to three hydrogen atoms.
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65
Delocalization of π bonding over three atoms makes carboxylic acids and their derivatives more susceptible to nucleophilic attack than aldehydes and ketones with their single π bond.
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66
Which of the following methods is used to prepare alcohols?

A) They are prepared by reducing a carboxylic acid group.
B) They are prepared by adding water across a carbon-carbon double bond.
C) They are prepared by reacting a carboxylic acid derivative with a Grignard reagent.
D) They are prepared by reacting a Grignard reagent with CO2, followed by acidification.
E) They are prepared by the nucleophilic reaction of amines with more electrophilic carboxylic acid derivatives.
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67
The high reactivity of ethers makes them unsuitable as solvents for carrying out organic reactions.
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68
Which of the following is true of aldehydes and ketones?

A) They have an appreciable dipole moment because of the polar C=O bond.
B) They have lower boiling points than alkanes and alkenes of comparable molecular mass.
C) They are typically prepared by reducing alcohols.
D) In their reactions, the partially positively charged carbon atom of the carbonyl group is subject to an electrophilic attack.
E) In their reactions, the lone pairs of electrons on the oxygen atom of the carbonyl group allow a nucleophilic attack to occur.
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69
Which of the following methods is used to prepare ketones?

A) They are prepared by reducing a carboxylic acid group.
B) They are prepared by adding water across a carbon-carbon double bond.
C) They are prepared by reacting a carboxylic acid derivative with a Grignard reagent.
D) They are prepared by reacting an alcohol with a carboxylic acid in the presence of a catalytic amount of strong acid.
E) They are prepared by the nucleophilic reaction of amines with more electrophilic carboxylic acid derivatives.
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70
In the gas phase, the dipole moment of benzene is zero.
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71
Amines have the tendency to act as electrophiles.
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72
Which of the following best defines a dehydration reaction?

A) It is a reaction in which a -H of an arene is replaced by an electrophilic group.
B) It is a high-temperature decomposition reaction that can be used to form fibers of synthetic polymers.
C) It is a reaction that proceeds by eliminating the elements of water.
D) It is an electrochemical process in which an external voltage is applied to an electrolytic cell to drive a nonspontaneous reaction.
E) It is a catalytic reaction in which a catalyst is uniformly dispersed throughout the reactant mixture to form a solution.
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73
Which of the following methods is used to prepare esters?

A) They are prepared by adding water across a carbon-carbon double bond.
B) They are prepared by a nucleophilic substitution reaction of an alkyl halide using hydroxide.
C) They are prepared by reacting a Grignard reagent with CO2, followed by acidification.
D) They are prepared by the nucleophilic reaction of amines with more electrophilic carboxylic acid derivatives.
E) They are prepared by reacting an alcohol with a carboxylic acid in the presence of a catalytic amount of strong acid.
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74
Which of the following is true of alkanes?

A) Their boiling points decrease with increasing molecular mass.
B) Their melting points are insensitive to relatively small differences in structure.
C) They are easily attacked by nucleophiles and electrophiles.
D) Their reactions occur only under extreme conditions.
E) They are unaffected by catalytic cracking.
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75
Secondary and tertiary amines have higher boiling points than primary amines of comparable molecular mass.
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76
Amides are the least reactive of the carboxylic acid derivatives because amides participate in π bonding with the carbonyl group.
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77
Which of the following best defines a pyrolysis reaction?

A) It is a reaction in which a -H of an arene is replaced by an electrophilic group.
B) It is a high-temperature decomposition reaction that can be used to form fibers of synthetic polymers.
C) It is a reaction that proceeds by eliminating the elements of water.
D) It is an electrochemical process in which an external voltage is applied to an electrolytic cell to drive a nonspontaneous reaction.
E) It is a catalytic reaction in which a catalyst is uniformly dispersed throughout the reactant mixture to form a solution.
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78
Amines can react with virtually any electrophile, including the carbonyl carbon of an aldehyde, a ketone, or an ester.
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79
Which of the following is true of alcohols?

A) Their individual O-H bond dipoles cancel one another because of the electronegative oxygen atom.
B) They have lower boiling points than alkanes or alkenes of comparable molecular mass.
C) They are usually prepared by an electrophilic substitution reaction of an alkyl halide using hydroxide.
D) They are considered to be more acidic than phenols due to the presence an -OH functional group
E) They are weaker acids than water.
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80
Which of the following methods is used to prepare aldehydes?

A) They are prepared by reducing a carboxylic acid group.
B) They are prepared by adding water across a carbon-carbon double bond.
C) They are prepared by reacting a carboxylic acid derivative with a Grignard reagent.
D) They are prepared by reacting a Grignard reagent with CO2, followed by acidification.
E) They are prepared by the nucleophilic reaction of amines with more electrophilic carboxylic acid derivatives.
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