Deck 3: Introduction to Organic Molecules and Functional Groups
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Deck 3: Introduction to Organic Molecules and Functional Groups
1
Which of the following is a tertiary amine? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
II
2
Which of the following molecules are aromatic hydrocarbons? 
A) I
B) II
C) III
D) I and III

A) I
B) II
C) III
D) I and III
I and III
3
Which of the following structures contains an amide? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
IV
4
Which of the following structures contains an alkene? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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5
Which of the following lists contains common heteroatoms found in organic molecules?
A) N, O, S, P, Cl
B) Na, O, S, P, Cl
C) Na, Mg, S, N, Cl
D) Na, Mg, O, N, Cl
A) N, O, S, P, Cl
B) Na, O, S, P, Cl
C) Na, Mg, S, N, Cl
D) Na, Mg, O, N, Cl
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6
Which of the following molecules are aliphatic hydrocarbons?
A) I, II, III
B) I and III
C) II, III, IV
D) II and IV
A) I, II, III
B) I and III
C) II, III, IV
D) II and IV
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7
Consider the molecule donepezil (used to treat Alzheimer's disease). Which of the following lists the correct functional groups present in donepezil? 
A) Amide, aromatic, ether, ketone.
B) Amide, aromatic, ester, ketone.
C) Amine, aromatic, ester, ketone.
D) Amine, aromatic, ether, ketone.

A) Amide, aromatic, ether, ketone.
B) Amide, aromatic, ester, ketone.
C) Amine, aromatic, ester, ketone.
D) Amine, aromatic, ether, ketone.
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8
Which of the following is a secondary alcohol? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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9
Rank the following compounds in order of increasing strength of intermolecular forces, putting the molecule with the weakest intermolecular force first. 
A) I < II < III
B) II < I < III
C) I < III < II
D) II < III < I

A) I < II < III
B) II < I < III
C) I < III < II
D) II < III < I
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10
Why do heteroatoms confer reactivity on a particular molecule?
A) Because they have lone pairs and create electron-rich sites on carbon.
B) Because they have lone pairs and create electron-deficient sites on carbon.
C) Because they are electronegative and act as electrophiles.
D) Because they are electropositive and act as nucleophiles.
A) Because they have lone pairs and create electron-rich sites on carbon.
B) Because they have lone pairs and create electron-deficient sites on carbon.
C) Because they are electronegative and act as electrophiles.
D) Because they are electropositive and act as nucleophiles.
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11
Which of the following correctly matches the molecules to the names of the functional groups? I.
CH3NH2
Amide
II)
CH3SCH3
Sulfide
III)
CH3CONH2
Amine
IV)
CH3CO2CH3
Ester
A) I and II
B) II and IV
C) III and IV
D) II and III
CH3NH2
Amide
II)
CH3SCH3
Sulfide
III)
CH3CONH2
Amine
IV)
CH3CO2CH3
Ester
A) I and II
B) II and IV
C) III and IV
D) II and III
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12
Which of the following statements best describes the relationship between the surface area of a molecule and the strength of the intermolecular forces?
A) The larger the surface area, the weaker the intermolecular force.
B) The larger the surface area, the stronger the intermolecular forces.
C) The smaller the surface area, the stronger the intermolecular forces.
D) There is no relationship between surface area and intermolecular forces.
A) The larger the surface area, the weaker the intermolecular force.
B) The larger the surface area, the stronger the intermolecular forces.
C) The smaller the surface area, the stronger the intermolecular forces.
D) There is no relationship between surface area and intermolecular forces.
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13
Which of the following structures contains a secondary amine? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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14
Consider the molecule atenolol (a blocker used to treat hypertension). Which of the following lists the correct functional groups present in atenolol? 
A) Primary alcohol, amide, primary amine, aromatic, ether.
B) Secondary alcohol, amide, secondary amine, aromatic, ether.
C) Secondary alcohol, amide, primary amine, aromatic, ether.
D) Secondary alcohol, amide, secondary amine, aromatic, ester.

A) Primary alcohol, amide, primary amine, aromatic, ether.
B) Secondary alcohol, amide, secondary amine, aromatic, ether.
C) Secondary alcohol, amide, primary amine, aromatic, ether.
D) Secondary alcohol, amide, secondary amine, aromatic, ester.
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15
Which of the following molecules contain the same functional groups?
A) I, II, III
B) I, II, IV
C) II, III, IV
D) I, III, IV
A) I, II, III
B) I, II, IV
C) II, III, IV
D) I, III, IV
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16
Which of the following correctly matches the molecules to the names of the functional groups? I.
CH3OCH3
Ether
II)
CH3CONH2
Amine
III)
CH3SH
Thiol
IV)
CH3CHO
Alcohol
A) I and II
B) II and III
C) III and IV
D) I and III
CH3OCH3
Ether
II)
CH3CONH2
Amine
III)
CH3SH
Thiol
IV)
CH3CHO
Alcohol
A) I and II
B) II and III
C) III and IV
D) I and III
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17
Why do bonds confer reactivity on a particular molecule?
A) Because bonds are difficult to break in chemical reactions.
B) Because bonds make a molecule an acid.
C) Because bonds are easily broken in chemical reactions.
D) Because bonds make a molecule an electrophile.
A) Because bonds are difficult to break in chemical reactions.
B) Because bonds make a molecule an acid.
C) Because bonds are easily broken in chemical reactions.
D) Because bonds make a molecule an electrophile.
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18
Which of the following correctly matches the molecules to the names of the functional groups? I.
CH3OH
Carboxylic acid
II)
CH3CO2CH3
Ester
III)
CH3COCH3
Ketone
IV)
H2CO
Alcohol
A) I and II
B) III and IV
C) II and III
D) II and IV
CH3OH
Carboxylic acid
II)
CH3CO2CH3
Ester
III)
CH3COCH3
Ketone
IV)
H2CO
Alcohol
A) I and II
B) III and IV
C) II and III
D) II and IV
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19
Which of the following structures contains a primary amine? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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20
Which of the following molecules contain the same functional groups?
A) I, II, IV
B) I, II, III
C) II, III, IV
D) I, III, IV
A) I, II, IV
B) I, II, III
C) II, III, IV
D) I, III, IV
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21
Which of the following compounds is expected to be H2O soluble? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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22
Which of the following compounds has the lowest boiling point? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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23
Rank the following compounds in order of increasing melting point, putting the compound with the least melting point first. 
A) II < I < III
B) I < III < II
C) I < II < III
D) III < II < I

A) II < I < III
B) I < III < II
C) I < II < III
D) III < II < I
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24
What molecular features are required for soap to properly dissolve grease and oil?
A) The molecule must be large.
B) The molecule must contain a polar head.
C) The molecule must contain a non-polar tail.
D) B and C are required.
A) The molecule must be large.
B) The molecule must contain a polar head.
C) The molecule must contain a non-polar tail.
D) B and C are required.
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25
Rank the following compounds in order of decreasing melting point, putting the compound with the highest melting point first. 
A) I > II > III
B) II > III > I
C) III > II > I
D) III > I > II

A) I > II > III
B) II > III > I
C) III > II > I
D) III > I > II
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26
Which of the following compounds has the highest boiling point? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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27
What intermolecular force is generally considered the strongest?
A) Hydrogen bonding
B) London dispersion forces
C) Covalent bonds
D) Dipole-dipole
A) Hydrogen bonding
B) London dispersion forces
C) Covalent bonds
D) Dipole-dipole
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28
Which of the following compounds has the highest boiling point? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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29
What is the strongest intermolecular force present in 1-propanol? 
A) Ion-ion
B) Hydrogen bonding
C) Dipole-dipole
D) Induced dipole-induced dipole

A) Ion-ion
B) Hydrogen bonding
C) Dipole-dipole
D) Induced dipole-induced dipole
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30
Which of the following alkanes is expected to have the highest melting point? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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31
Which of the following compounds has the highest boiling point? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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32
Which of the following compounds is expected to be the most soluble in H2O? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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33
Which of the following compounds has the highest boiling point? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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34
Which of the following statements about the solubility of organic compounds in H2O is true?
A) The non-polar part of a molecule that is not attracted to water is said to be hydrophilic.
B) The non-polar part of a molecule that is not attracted to water is said to be hydrophobic.
C) The polar part of a molecule that can hydrogen bond to water is said to be hydrophobic.
D) For an organic compound with one functional group that contains an O or N atom, the compound is water soluble only if it has 5 carbons.
A) The non-polar part of a molecule that is not attracted to water is said to be hydrophilic.
B) The non-polar part of a molecule that is not attracted to water is said to be hydrophobic.
C) The polar part of a molecule that can hydrogen bond to water is said to be hydrophobic.
D) For an organic compound with one functional group that contains an O or N atom, the compound is water soluble only if it has 5 carbons.
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35
Rank the following compounds in order of decreasing boiling point, putting the compound with the highest boiling point first. 
A) I > II > III > IV
B) III > IV > II > I
C) III > II > IV > I
D) I > IV > II > III

A) I > II > III > IV
B) III > IV > II > I
C) III > II > IV > I
D) I > IV > II > III
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36
What intermolecular force is generally considered the weakest?
A) Hydrogen bonding
B) London dispersion forces
C) Dipole-dipole
D) Ion-ion
A) Hydrogen bonding
B) London dispersion forces
C) Dipole-dipole
D) Ion-ion
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37
Which of the following intermolecular forces would not form between similar molecules of the structure below? 
A) London dispersion forces
B) Ion-ion
C) Hydrogen bonding
D) Dipole-dipole

A) London dispersion forces
B) Ion-ion
C) Hydrogen bonding
D) Dipole-dipole
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38
Which of the following compounds would be expected to be more soluble in hexane (C6H14)? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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39
Which of the following compounds is expected to be the least soluble in H2O? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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40
Which of the following compounds can form intermolecular hydrogen bonds with a molecule similar to itself? 
A) I
B) II
C) III
D) IV

A) I
B) II
C) III
D) IV
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41
The indicated carbon atom is: 
A) Electrophilic because it is electron-deficient.
B) Nucleophilic because it is electron-deficient.
C) Electrophilic because it is electron-rich.
D) Nucleophilic because it is electron-rich.

A) Electrophilic because it is electron-deficient.
B) Nucleophilic because it is electron-deficient.
C) Electrophilic because it is electron-rich.
D) Nucleophilic because it is electron-rich.
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42
Rank the following compounds in order of decreasing boiling point, putting the compound with the highest boiling point first. 
A) I > III > IV > II
B) IV > II > I > III
C) IV > I > II > III
D) I > IV > II > III

A) I > III > IV > II
B) IV > II > I > III
C) IV > I > II > III
D) I > IV > II > III
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43
The indicated bond is: 
A) Nucleophilic because it is electron-deficient.
B) Electrophilic because it is electron-rich.
C) Nucleophilic because it is electron-rich.
D) Electrophilic because it is electron-deficient.

A) Nucleophilic because it is electron-deficient.
B) Electrophilic because it is electron-rich.
C) Nucleophilic because it is electron-rich.
D) Electrophilic because it is electron-deficient.
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44
Which of the following list the correct functional groups found in aspartame, the artificial sweetener? 
A) Amine, aromatic, carboxylic acid, ether, ketone.
B) Amine, amide, aromatic, carboxylic acid, ester.
C) Amide, alcohol, aromatic, carboxylic acid, ether.
D) Amine, aromatic, carboxylic acid, ester, nitrile.

A) Amine, aromatic, carboxylic acid, ether, ketone.
B) Amine, amide, aromatic, carboxylic acid, ester.
C) Amide, alcohol, aromatic, carboxylic acid, ether.
D) Amine, aromatic, carboxylic acid, ester, nitrile.
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45
Which of the following statements about vitamin A, drawn below, are true? 
A) Vitamin A is soluble in H2O.
B) Vitamin A is insoluble in organic solvents.
C) Vitamin A contains an aromatic ring.
D) Vitamin A is insoluble in H2O.

A) Vitamin A is soluble in H2O.
B) Vitamin A is insoluble in organic solvents.
C) Vitamin A contains an aromatic ring.
D) Vitamin A is insoluble in H2O.
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46
Which of the following statements about vitamin C, drawn below, are true? 
A) Vitamin C is insoluble in H2O.
B) Vitamin C is soluble in H2O.
C) Vitamin C is an aliphatic hydrocarbon.
D) Vitamin C contains a ketone functional group.

A) Vitamin C is insoluble in H2O.
B) Vitamin C is soluble in H2O.
C) Vitamin C is an aliphatic hydrocarbon.
D) Vitamin C contains a ketone functional group.
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47
The indicated bond is: 
A) Nucleophilic because it is electron-deficient.
B) Electrophilic because it is electron-deficient.
C) Nucleophilic because it electron-rich.
D) Electrophilic because it is electron-rich.

A) Nucleophilic because it is electron-deficient.
B) Electrophilic because it is electron-deficient.
C) Nucleophilic because it electron-rich.
D) Electrophilic because it is electron-rich.
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48
Which of the following could most likely serve as an ionophore? 
A) I
B) II
C) III
D) IV

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