Deck 4: Carbon and the Molecular Diversity of Life

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Question
Which of the following people synthesized an organic compound, acetic acid, from inorganic substances that had been prepared directly from pure elements?

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
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Question
Which of the following people used this apparatus to study formation of organic compounds?
<strong>Which of the following people used this apparatus to study formation of organic compounds?  </strong> A)Stanley Miller B)Jakob Berzelius C)Friedrich Wohler D)Hermann Kolbe E)August Kekulé <div style=padding-top: 35px>

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
Question
One of the following people set up a closed system to mimic Earth's early atmosphere and discharged electrical sparks through it. A variety of organic compounds common in organisms were formed. Who did this?

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
Question
Organic chemistry is a science based on the study of

A)functional groups.
B)vital forces interacting with matter.
C)carbon compounds.
D)water and its interaction with other kinds of molecules.
E)inorganic compounds.
Question
<strong>  The two molecules shown in Figure 4.1 are best described as</strong> A)optical isomers. B)radioactive isotopes. C)structural isomers. D)nonradioactive isotopes. E)geometric isomers. <div style=padding-top: 35px>
The two molecules shown in Figure 4.1 are best described as

A)optical isomers.
B)radioactive isotopes.
C)structural isomers.
D)nonradioactive isotopes.
E)geometric isomers.
Question
How many structural isomers are possible for a substance having the molecular formula C₄H₁₀?

A)1
B)2
C)4
D)3
E)11
Question
Which of the following people's synthesis of this compound from inorganic starting materials provided evidence against vitalism?
<strong>Which of the following people's synthesis of this compound from inorganic starting materials provided evidence against vitalism?  </strong> A)Stanley Miller B)Jakob Berzelius C)Friedrich Wohler D)Hermann Kolbe E)August Kekulé <div style=padding-top: 35px>

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
Question
Which of the following people's synthesis of this compound from inorganic starting materials provided evidence against vitalism?
<strong>Which of the following people's synthesis of this compound from inorganic starting materials provided evidence against vitalism?  </strong> A)Stanley Miller B)Jakob Berzelius C)Friedrich Wohler D)Hermann Kolbe E)August Kekulé <div style=padding-top: 35px>

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
Question
How many electron pairs does carbon share in order to complete its valence shell?

A)1
B)2
C)3
D)4
E)8
Question
One of the following people was the first to suggest that organic compounds, those found in living organisms, were distinctly different from inorganic compounds found in the nonliving world. Though this suggestion is now known to be incorrect, it stimulated important research into organic compounds. Who suggested this?

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
Question
<strong>  The two molecules shown in Figure 4.3 are best described as</strong> A)enantiomers. B)radioactive isotopes. C)structural isomers. D)nonisotopic isomers. E)geometric isomers. <div style=padding-top: 35px>
The two molecules shown in Figure 4.3 are best described as

A)enantiomers.
B)radioactive isotopes.
C)structural isomers.
D)nonisotopic isomers.
E)geometric isomers.
Question
Why are hydrocarbons insoluble in water?

A)The majority of their bonds are polar covalent carbon-to-hydrogen linkages.
B)The majority of their bonds are nonpolar covalent carbon-to-hydrogen linkages.
C)They are hydrophilic.
D)They exhibit considerable molecular complexity and diversity.
E)They are lighter than water.
Question
Which of the following statements best describes the carbon atoms present in all organic molecules?

A)They were incorporated into organic molecules by plants.
B)They were processed into sugars through photosynthesis.
C)They are ultimately derived from carbon dioxide.
D)Only A and C are correct.
E)A, B, and C are correct.
Question
<strong>  Shown here in Figure 4.2 are the structures of glucose and fructose. These two molecules differ in the</strong> A)number of carbon, hydrogen, and oxygen atoms. B)types of carbon, hydrogen, and oxygen atoms. C)arrangement of carbon, hydrogen, and oxygen atoms. D)number of oxygen atoms joined to carbon atoms by double covalent bonds. E)answers A, B, and C <div style=padding-top: 35px>
Shown here in Figure 4.2 are the structures of glucose and fructose. These two molecules differ in the

A)number of carbon, hydrogen, and oxygen atoms.
B)types of carbon, hydrogen, and oxygen atoms.
C)arrangement of carbon, hydrogen, and oxygen atoms.
D)number of oxygen atoms joined to carbon atoms by double covalent bonds.
E)answers A, B, and C
Question
The experimental approach taken in current biological investigations presumes that

A)simple organic compounds can be synthesized in the laboratory from inorganic precursors, but complex organic compounds like carbohydrates and proteins can only be synthesized by living organisms.
B)a life force ultimately controls the activities of living organisms and this life force cannot be studied by physical or chemical methods.
C)although a life force, or vitalism, exists in living organisms, this life force cannot be studied by physical or chemical methods.
D)living organisms are composed of the same elements present in nonliving things, plus a few special trace elements found only in living organisms or their products.
E)living organisms can be understood in terms of the same physical and chemical laws that can be used to explain all natural phenomena.
Question
Early 19th-century scientists believed that living organisms differed from nonliving things as a result of possessing a "life force" that could create organic molecules from inorganic matter. The term given to this belief is

A)organic synthesis.
B)vitalism.
C)mechanism.
D)organic evolution.
E)inorganic synthesis.
Question
Which of the following statements correctly describes geometric isomers?

A)They have variations in arrangement around a double bond.
B)They have an asymmetric carbon that makes them mirror images.
C)They have the same chemical properties.
D)They have different molecular formulas.
E)Their atoms and bonds are arranged in different sequences.
Question
Shown here in Figure 4.2 are the structures of glucose and fructose. These two molecules are

A)geometric isotopes.
B)enantiomers.
C)geometric isomers.
D)structural isomers.
E)nonisotopic isomers.
Question
A carbon atom is most likely to form what kind of bond(s)with other atoms?

A)ionic
B)hydrogen
C)covalent
D)A and B only
E)A, B, and C
Question
Which of the following people was the first to synthesize an organic compound, urea, from inorganic starting materials?

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
Question
Which is the best description of a carbonyl group?

A)an oxygen joined to a carbon by a single covalent bond
B)a nitrogen and two hydrogens joined to a carbon by covalent bonds
C)a carbon joined to two hydrogens by single covalent bonds
D)a sulfur and a hydrogen joined to a carbon by covalent bonds
E)a carbon atom joined to an oxygen by a double covalent bond
Question
Which of the following contains nitrogen in addition to carbon, oxygen, and hydrogen?

A)an alcohol such as ethanol
B)a monosaccharide such as glucose
C)a steroid such as testosterone
D)an amino acid such as glycine
E)a hydrocarbon such as benzene
Question
Research indicates that Albuterol, a drug used to relax bronchial muscles, improving airflow and thus offering relief from asthma, consists only of one enantiomer, the R-form. Why is it important for this drug to consist of only one enantiomeric form, rather than a mixture of enantiomers?

A)Different enantiomers may have different or opposite physiological effects.
B)It is impossible to synthesize mixtures of enantiomers.
C)It is much less expensive to synthesize one enantiomer at a time.
D)Albuterol is an example of a compound for which only one enantiomer exists.
E)Only the R-form of Albuterol has been studied; until more information is available, physicians prefer to use the pure R-form.
Question
The following questions refer to the structures shown in Figure 4.5.
A.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures <div style=padding-top: 35px>

B.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures <div style=padding-top: 35px>

C.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures <div style=padding-top: 35px>

D.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures <div style=padding-top: 35px>

E.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures <div style=padding-top: 35px>


-In which of the structures are the atoms bonded by ionic bonds?

A)A
B)B
C)C
D)C, D, and E only
E)none of the structures
Question
Which functional groups can act as acids?

A)amine and sulfhydryl
B)carbonyl and carboxyl
C)carboxyl and phosphate
D)hydroxyl and aldehyde
E)ketone and amino
Question
Which two functional groups are always found in amino acids?

A)ketone and aldehyde
B)carbonyl and carboxyl
C)carboxyl and amino
D)phosphate and sulfhydryl
E)hydroxyl and aldehyde
Question
Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.

A) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule. <div style=padding-top: 35px>
B) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule. <div style=padding-top: 35px>
C) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule. <div style=padding-top: 35px>
D) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule. <div style=padding-top: 35px>
E) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule. <div style=padding-top: 35px>
F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule.
Question
Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?

A) <strong>Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?</strong> A)   B)   C)   D)   E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄. <div style=padding-top: 35px>
B) <strong>Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?</strong> A)   B)   C)   D)   E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄. <div style=padding-top: 35px>
C) <strong>Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?</strong> A)   B)   C)   D)   E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄. <div style=padding-top: 35px>
D) <strong>Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?</strong> A)   B)   C)   D)   E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄. <div style=padding-top: 35px>
E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄.
Question
Research indicates that Ibuprofen, a drug used to relieve inflammation and pain, is a mixture of two enantiomers; that is, molecules that

A)have identical three-dimensional shapes.
B)are mirror images of one another.
C)lack an asymmetric carbon.
D)differ in the location of their double bonds.
E)differ in their electrical charge.
Question
A carbon skeleton is covalently bonded to both an amino group and a carboxyl group. When placed in water it

A)would function only as an acid because of the carboxyl group.
B)would function only as a base because of the amino group.
C)would function as neither an acid nor a base.
D)would function as both an acid and a base.
E)is impossible to determine how it would function.
Question
The following questions refer to the structures shown in Figure 4.5.
A.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E <div style=padding-top: 35px>

B.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E <div style=padding-top: 35px>

C.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E <div style=padding-top: 35px>

D.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E <div style=padding-top: 35px>

E.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E <div style=padding-top: 35px>


-Which of the structures is an impossible covalently bonded molecule?

A)A
B)B
C)C
D)D
E)E
Question
Thalidomide and L-dopa, shown below, are examples of pharmaceutical drugs that occur as enantiomers, or molecules that <strong>Thalidomide and L-dopa, shown below, are examples of pharmaceutical drugs that occur as enantiomers, or molecules that  </strong> A)have identical three-dimensional shapes. B)are mirror images of one another. C)lack an asymmetric carbon. D)differ in the location of their double bonds. E)differ in their electrical charge. <div style=padding-top: 35px>

A)have identical three-dimensional shapes.
B)are mirror images of one another.
C)lack an asymmetric carbon.
D)differ in the location of their double bonds.
E)differ in their electrical charge.
Question
Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?

A) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
Which of the following is a False statement concerning amino groups?

A)They are basic in pH.
B)They are found in amino acids.
C)They contain nitrogen.
D)They are nonpolar.
E)They are components of urea.
Question
Amino acids are acids because they always possess which functional group?

A)amino
B)carbonyl
C)carboxyl
D)sulfhydryl
E)aldehyde
Question
Figure 4.4 <strong>Figure 4.4   What is the name of the functional group shown in Figure 4.4?</strong> A)carbonyl B)ketone C)aldehyde D)carboxyl E)hydroxyl <div style=padding-top: 35px>
What is the name of the functional group shown in Figure 4.4?

A)carbonyl
B)ketone
C)aldehyde
D)carboxyl
E)hydroxyl
Question
A chemist wishes to make an organic molecule less acidic. Which of the following functional groups should be added to the molecule in order to do so?

A)carboxyl
B)sulfhydryl
C)hydroxyl
D)amino
E)phosphate
Question
Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?

A) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
B) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
C) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
D) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
E) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)   <div style=padding-top: 35px>
Question
The following questions refer to the structures shown in Figure 4.5.
A.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures <div style=padding-top: 35px>

B.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures <div style=padding-top: 35px>

C.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures <div style=padding-top: 35px>

D.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures <div style=padding-top: 35px>

E.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures <div style=padding-top: 35px>


-Which of the structures contain(s)a carboxyl functional group?

A)A
B)B
C)C
D)C and E
E)none of the structures
Question
A compound contains hydroxyl groups as its predominant functional group. Which of the following statements is True concerning this compound?

A)It lacks an asymmetric carbon, and it is probably a fat or lipid.
B)It should dissolve in water.
C)It should dissolve in a nonpolar solvent.
D)It won't form hydrogen bonds with water.
E)It is hydrophobic.
Question
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule can increase the concentration of hydrogen ions in a solution and is therefore an organic acid?<div style=padding-top: 35px>
Which molecule can increase the concentration of hydrogen ions in a solution and is therefore an organic acid?
Question
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a basic functional group that can accept H+ and become positively charged?<div style=padding-top: 35px>
Which is a basic functional group that can accept H+ and become positively charged?
Question
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule contains a carboxyl group?<div style=padding-top: 35px>
Which molecule contains a carboxyl group?
Question
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule is an alcohol?<div style=padding-top: 35px>
Which molecule is an alcohol?
Question
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is an acidic functional group that can dissociate and release H+ into a solution?<div style=padding-top: 35px>
Which is an acidic functional group that can dissociate and release H+ into a solution?
Question
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule contains a sulfhydryl functional group?<div style=padding-top: 35px>
Which molecule contains a sulfhydryl functional group?
Question
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a functional group that helps stabilize proteins by forming covalent cross-links within or between protein molecules?<div style=padding-top: 35px>
Which is a functional group that helps stabilize proteins by forming covalent cross-links within or between protein molecules?
Question
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule is an organic phosphate?<div style=padding-top: 35px>
Which molecule is an organic phosphate?
Question
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is an amino functional group?<div style=padding-top: 35px>
Which is an amino functional group?
Question
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a carbonyl functional group?<div style=padding-top: 35px>
Which is a carbonyl functional group?
Question
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule can function as a base?<div style=padding-top: 35px>
Which molecule can function as a base?
Question
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule has a carbonyl functional group in the form of a ketone?<div style=padding-top: 35px>
Which molecule has a carbonyl functional group in the form of a ketone?
Question
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule is water soluble because it has a hydroxyl functional group?<div style=padding-top: 35px>
Which molecule is water soluble because it has a hydroxyl functional group?
Question
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule functions to transfer energy between organic molecules?<div style=padding-top: 35px>
Which molecule functions to transfer energy between organic molecules?
Question
The following questions refer to the molecules shown in Figure 4.7.
A.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A <div style=padding-top: 35px>

B.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A <div style=padding-top: 35px>

C.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A <div style=padding-top: 35px>

D.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A <div style=padding-top: 35px>

E.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A <div style=padding-top: 35px>


-Which molecules contain a carbonyl group?

A)A and B
B)B and C
C)C and D
D)D and E
E)E and A
Question
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule has a carbonyl functional group in the form of an aldehyde?<div style=padding-top: 35px>
Which molecule has a carbonyl functional group in the form of an aldehyde?
Question
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule is a thiol?<div style=padding-top: 35px>
Which molecule is a thiol?
Question
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule contains an amino functional group, but is not an amino acid?<div style=padding-top: 35px>
Which molecule contains an amino functional group, but is not an amino acid?
Question
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a carboxyl functional group?<div style=padding-top: 35px>
Which is a carboxyl functional group?
Question
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a hydroxyl functional group?<div style=padding-top: 35px>
Which is a hydroxyl functional group?
Question
The following questions refer to the molecules shown in Figure 4.8.
A.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H? <div style=padding-top: 35px>

B.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H? <div style=padding-top: 35px>

C.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H? <div style=padding-top: 35px>

D.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H? <div style=padding-top: 35px>

E.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H? <div style=padding-top: 35px>


-Which of the following hydrocarbons has a double bond in its carbon skeleton?

A)C?H?
B)C?H?
C)CH?
D)C?H?
E)C?H?
Question
The following questions refer to the molecules shown in Figure 4.8.
A.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons. <div style=padding-top: 35px>

B.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons. <div style=padding-top: 35px>

C.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons. <div style=padding-top: 35px>

D.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons. <div style=padding-top: 35px>

E.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons. <div style=padding-top: 35px>


-Organic chemistry is currently defined as

A)the study of compounds made only by living cells.
B)the study of carbon compounds.
C)the study of vital forces.
D)the study of natural (as opposed to synthetic)compounds.
E)the study of hydrocarbons.
Question
Which action could produce a carbonyl group?

A)the replacement of the OH of a carboxyl group with hydrogen
B)the addition of a thiol to a hydroxyl
C)the addition of a hydroxyl to a phosphate
D)the replacement of the nitrogen of an amine with oxygen
E)the addition of a sulfhydryl to a carboxyl
Question
Which functional group is not present in this molecule?
<strong>Which functional group is not present in this molecule?  </strong> A)carboxyl B)sulfhydryl C)hydroxyl D)amino <div style=padding-top: 35px>

A)carboxyl
B)sulfhydryl
C)hydroxyl
D)amino
Question
Choose the term that correctly describes the relationship between these two sugar molecules: <strong>Choose the term that correctly describes the relationship between these two sugar molecules:  </strong> A)structural isomers B)geometric isomers C)enantiomers D)isotopes <div style=padding-top: 35px>

A)structural isomers
B)geometric isomers
C)enantiomers
D)isotopes
Question
The following questions refer to the molecules shown in Figure 4.8.
A.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule. <div style=padding-top: 35px>

B.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule. <div style=padding-top: 35px>

C.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule. <div style=padding-top: 35px>

D.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule. <div style=padding-top: 35px>

E.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule. <div style=padding-top: 35px>


-Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?

A)Testosterone and estradiol are structural isomers but have the same molecular formula.
B)Testosterone and estradiol are geometric isomers but have the same molecular formula.
C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton.
D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings.
E)Testosterone and estradiol are enantiomers of the same organic molecule.
Question
The following questions refer to the molecules shown in Figure 4.8.
A.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids. <div style=padding-top: 35px>

B.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids. <div style=padding-top: 35px>

C.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids. <div style=padding-top: 35px>

D.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids. <div style=padding-top: 35px>

E.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids. <div style=padding-top: 35px>


-Testosterone and estradiol are

A)nucleic acids.
B)carbohydrates.
C)proteins.
D)phospholipids.
E)steroids.
Question
Which chemical group is most likely to be responsible for an organic molecule behaving as a base?

A)hydroxyl
B)carbonyl
C)carboxyl
D)amino
E)phosphate
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Deck 4: Carbon and the Molecular Diversity of Life
1
Which of the following people synthesized an organic compound, acetic acid, from inorganic substances that had been prepared directly from pure elements?

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
D
2
Which of the following people used this apparatus to study formation of organic compounds?
<strong>Which of the following people used this apparatus to study formation of organic compounds?  </strong> A)Stanley Miller B)Jakob Berzelius C)Friedrich Wohler D)Hermann Kolbe E)August Kekulé

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
A
3
One of the following people set up a closed system to mimic Earth's early atmosphere and discharged electrical sparks through it. A variety of organic compounds common in organisms were formed. Who did this?

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
A
4
Organic chemistry is a science based on the study of

A)functional groups.
B)vital forces interacting with matter.
C)carbon compounds.
D)water and its interaction with other kinds of molecules.
E)inorganic compounds.
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5
<strong>  The two molecules shown in Figure 4.1 are best described as</strong> A)optical isomers. B)radioactive isotopes. C)structural isomers. D)nonradioactive isotopes. E)geometric isomers.
The two molecules shown in Figure 4.1 are best described as

A)optical isomers.
B)radioactive isotopes.
C)structural isomers.
D)nonradioactive isotopes.
E)geometric isomers.
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6
How many structural isomers are possible for a substance having the molecular formula C₄H₁₀?

A)1
B)2
C)4
D)3
E)11
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7
Which of the following people's synthesis of this compound from inorganic starting materials provided evidence against vitalism?
<strong>Which of the following people's synthesis of this compound from inorganic starting materials provided evidence against vitalism?  </strong> A)Stanley Miller B)Jakob Berzelius C)Friedrich Wohler D)Hermann Kolbe E)August Kekulé

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
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8
Which of the following people's synthesis of this compound from inorganic starting materials provided evidence against vitalism?
<strong>Which of the following people's synthesis of this compound from inorganic starting materials provided evidence against vitalism?  </strong> A)Stanley Miller B)Jakob Berzelius C)Friedrich Wohler D)Hermann Kolbe E)August Kekulé

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
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9
How many electron pairs does carbon share in order to complete its valence shell?

A)1
B)2
C)3
D)4
E)8
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10
One of the following people was the first to suggest that organic compounds, those found in living organisms, were distinctly different from inorganic compounds found in the nonliving world. Though this suggestion is now known to be incorrect, it stimulated important research into organic compounds. Who suggested this?

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
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11
<strong>  The two molecules shown in Figure 4.3 are best described as</strong> A)enantiomers. B)radioactive isotopes. C)structural isomers. D)nonisotopic isomers. E)geometric isomers.
The two molecules shown in Figure 4.3 are best described as

A)enantiomers.
B)radioactive isotopes.
C)structural isomers.
D)nonisotopic isomers.
E)geometric isomers.
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12
Why are hydrocarbons insoluble in water?

A)The majority of their bonds are polar covalent carbon-to-hydrogen linkages.
B)The majority of their bonds are nonpolar covalent carbon-to-hydrogen linkages.
C)They are hydrophilic.
D)They exhibit considerable molecular complexity and diversity.
E)They are lighter than water.
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13
Which of the following statements best describes the carbon atoms present in all organic molecules?

A)They were incorporated into organic molecules by plants.
B)They were processed into sugars through photosynthesis.
C)They are ultimately derived from carbon dioxide.
D)Only A and C are correct.
E)A, B, and C are correct.
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14
<strong>  Shown here in Figure 4.2 are the structures of glucose and fructose. These two molecules differ in the</strong> A)number of carbon, hydrogen, and oxygen atoms. B)types of carbon, hydrogen, and oxygen atoms. C)arrangement of carbon, hydrogen, and oxygen atoms. D)number of oxygen atoms joined to carbon atoms by double covalent bonds. E)answers A, B, and C
Shown here in Figure 4.2 are the structures of glucose and fructose. These two molecules differ in the

A)number of carbon, hydrogen, and oxygen atoms.
B)types of carbon, hydrogen, and oxygen atoms.
C)arrangement of carbon, hydrogen, and oxygen atoms.
D)number of oxygen atoms joined to carbon atoms by double covalent bonds.
E)answers A, B, and C
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15
The experimental approach taken in current biological investigations presumes that

A)simple organic compounds can be synthesized in the laboratory from inorganic precursors, but complex organic compounds like carbohydrates and proteins can only be synthesized by living organisms.
B)a life force ultimately controls the activities of living organisms and this life force cannot be studied by physical or chemical methods.
C)although a life force, or vitalism, exists in living organisms, this life force cannot be studied by physical or chemical methods.
D)living organisms are composed of the same elements present in nonliving things, plus a few special trace elements found only in living organisms or their products.
E)living organisms can be understood in terms of the same physical and chemical laws that can be used to explain all natural phenomena.
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16
Early 19th-century scientists believed that living organisms differed from nonliving things as a result of possessing a "life force" that could create organic molecules from inorganic matter. The term given to this belief is

A)organic synthesis.
B)vitalism.
C)mechanism.
D)organic evolution.
E)inorganic synthesis.
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17
Which of the following statements correctly describes geometric isomers?

A)They have variations in arrangement around a double bond.
B)They have an asymmetric carbon that makes them mirror images.
C)They have the same chemical properties.
D)They have different molecular formulas.
E)Their atoms and bonds are arranged in different sequences.
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18
Shown here in Figure 4.2 are the structures of glucose and fructose. These two molecules are

A)geometric isotopes.
B)enantiomers.
C)geometric isomers.
D)structural isomers.
E)nonisotopic isomers.
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19
A carbon atom is most likely to form what kind of bond(s)with other atoms?

A)ionic
B)hydrogen
C)covalent
D)A and B only
E)A, B, and C
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20
Which of the following people was the first to synthesize an organic compound, urea, from inorganic starting materials?

A)Stanley Miller
B)Jakob Berzelius
C)Friedrich Wohler
D)Hermann Kolbe
E)August Kekulé
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21
Which is the best description of a carbonyl group?

A)an oxygen joined to a carbon by a single covalent bond
B)a nitrogen and two hydrogens joined to a carbon by covalent bonds
C)a carbon joined to two hydrogens by single covalent bonds
D)a sulfur and a hydrogen joined to a carbon by covalent bonds
E)a carbon atom joined to an oxygen by a double covalent bond
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22
Which of the following contains nitrogen in addition to carbon, oxygen, and hydrogen?

A)an alcohol such as ethanol
B)a monosaccharide such as glucose
C)a steroid such as testosterone
D)an amino acid such as glycine
E)a hydrocarbon such as benzene
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23
Research indicates that Albuterol, a drug used to relax bronchial muscles, improving airflow and thus offering relief from asthma, consists only of one enantiomer, the R-form. Why is it important for this drug to consist of only one enantiomeric form, rather than a mixture of enantiomers?

A)Different enantiomers may have different or opposite physiological effects.
B)It is impossible to synthesize mixtures of enantiomers.
C)It is much less expensive to synthesize one enantiomer at a time.
D)Albuterol is an example of a compound for which only one enantiomer exists.
E)Only the R-form of Albuterol has been studied; until more information is available, physicians prefer to use the pure R-form.
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24
The following questions refer to the structures shown in Figure 4.5.
A.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures

B.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures

C.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures

D.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures

E.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -In which of the structures are the atoms bonded by ionic bonds?</strong> A)A B)B C)C D)C, D, and E only E)none of the structures


-In which of the structures are the atoms bonded by ionic bonds?

A)A
B)B
C)C
D)C, D, and E only
E)none of the structures
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25
Which functional groups can act as acids?

A)amine and sulfhydryl
B)carbonyl and carboxyl
C)carboxyl and phosphate
D)hydroxyl and aldehyde
E)ketone and amino
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26
Which two functional groups are always found in amino acids?

A)ketone and aldehyde
B)carbonyl and carboxyl
C)carboxyl and amino
D)phosphate and sulfhydryl
E)hydroxyl and aldehyde
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27
Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.

A) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule.
B) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule.
C) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule.
D) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule.
E) <strong>Three or four of the pairs of structures shown below depict enantiomers (enantiomeric forms)of the same molecule. Which pair, if any, are NOT enantiomers of a single molecule? If each of the pairs depicts enantiomers, choose answer F.</strong> A)   B)   C)   D)   E)   F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule.
F)Both illustrations in each of the other answer choices depict enantiomers of the same molecule.
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28
Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?

A) <strong>Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?</strong> A)   B)   C)   D)   E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄.
B) <strong>Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?</strong> A)   B)   C)   D)   E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄.
C) <strong>Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?</strong> A)   B)   C)   D)   E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄.
D) <strong>Three or four of the following illustrations depict different structural isomers of the organic compound with molecular formula C₆H₁₄. For clarity, only the carbon skeletons are shown; hydrogen atoms that would be attached to the carbons have been omitted. Which one, if any, is NOT a structural isomer of this compound?</strong> A)   B)   C)   D)   E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄.
E)Each of the illustrations in the other answer choices depicts a structural isomer of the compound with molecular formula C₆H₁₄.
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29
Research indicates that Ibuprofen, a drug used to relieve inflammation and pain, is a mixture of two enantiomers; that is, molecules that

A)have identical three-dimensional shapes.
B)are mirror images of one another.
C)lack an asymmetric carbon.
D)differ in the location of their double bonds.
E)differ in their electrical charge.
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30
A carbon skeleton is covalently bonded to both an amino group and a carboxyl group. When placed in water it

A)would function only as an acid because of the carboxyl group.
B)would function only as a base because of the amino group.
C)would function as neither an acid nor a base.
D)would function as both an acid and a base.
E)is impossible to determine how it would function.
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31
The following questions refer to the structures shown in Figure 4.5.
A.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E

B.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E

C.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E

D.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E

E.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures is an impossible covalently bonded molecule?</strong> A)A B)B C)C D)D E)E


-Which of the structures is an impossible covalently bonded molecule?

A)A
B)B
C)C
D)D
E)E
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32
Thalidomide and L-dopa, shown below, are examples of pharmaceutical drugs that occur as enantiomers, or molecules that <strong>Thalidomide and L-dopa, shown below, are examples of pharmaceutical drugs that occur as enantiomers, or molecules that  </strong> A)have identical three-dimensional shapes. B)are mirror images of one another. C)lack an asymmetric carbon. D)differ in the location of their double bonds. E)differ in their electrical charge.

A)have identical three-dimensional shapes.
B)are mirror images of one another.
C)lack an asymmetric carbon.
D)differ in the location of their double bonds.
E)differ in their electrical charge.
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33
Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?

A) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the pairs of molecular structures shown below depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
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34
Which of the following is a False statement concerning amino groups?

A)They are basic in pH.
B)They are found in amino acids.
C)They contain nitrogen.
D)They are nonpolar.
E)They are components of urea.
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35
Amino acids are acids because they always possess which functional group?

A)amino
B)carbonyl
C)carboxyl
D)sulfhydryl
E)aldehyde
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36
Figure 4.4 <strong>Figure 4.4   What is the name of the functional group shown in Figure 4.4?</strong> A)carbonyl B)ketone C)aldehyde D)carboxyl E)hydroxyl
What is the name of the functional group shown in Figure 4.4?

A)carbonyl
B)ketone
C)aldehyde
D)carboxyl
E)hydroxyl
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37
A chemist wishes to make an organic molecule less acidic. Which of the following functional groups should be added to the molecule in order to do so?

A)carboxyl
B)sulfhydryl
C)hydroxyl
D)amino
E)phosphate
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38
Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?

A) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
B) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
C) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
D) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
E) <strong>Which of the pairs of molecular structures shown below do NOT depict enantiomers (enantiomeric forms)of the same molecule?</strong> A)   B)   C)   D)   E)
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39
The following questions refer to the structures shown in Figure 4.5.
A.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures

B.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures

C.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures

D.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures

E.
<strong>The following questions refer to the structures shown in Figure 4.5. A.    B.    C.    D.    E.     -Which of the structures contain(s)a carboxyl functional group?</strong> A)A B)B C)C D)C and E E)none of the structures


-Which of the structures contain(s)a carboxyl functional group?

A)A
B)B
C)C
D)C and E
E)none of the structures
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40
A compound contains hydroxyl groups as its predominant functional group. Which of the following statements is True concerning this compound?

A)It lacks an asymmetric carbon, and it is probably a fat or lipid.
B)It should dissolve in water.
C)It should dissolve in a nonpolar solvent.
D)It won't form hydrogen bonds with water.
E)It is hydrophobic.
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41
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule can increase the concentration of hydrogen ions in a solution and is therefore an organic acid?
Which molecule can increase the concentration of hydrogen ions in a solution and is therefore an organic acid?
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42
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a basic functional group that can accept H+ and become positively charged?
Which is a basic functional group that can accept H+ and become positively charged?
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43
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule contains a carboxyl group?
Which molecule contains a carboxyl group?
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44
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule is an alcohol?
Which molecule is an alcohol?
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45
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is an acidic functional group that can dissociate and release H+ into a solution?
Which is an acidic functional group that can dissociate and release H+ into a solution?
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46
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule contains a sulfhydryl functional group?
Which molecule contains a sulfhydryl functional group?
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47
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a functional group that helps stabilize proteins by forming covalent cross-links within or between protein molecules?
Which is a functional group that helps stabilize proteins by forming covalent cross-links within or between protein molecules?
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48
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule is an organic phosphate?
Which molecule is an organic phosphate?
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49
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is an amino functional group?
Which is an amino functional group?
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50
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a carbonyl functional group?
Which is a carbonyl functional group?
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51
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule can function as a base?
Which molecule can function as a base?
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52
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule has a carbonyl functional group in the form of a ketone?
Which molecule has a carbonyl functional group in the form of a ketone?
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53
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule is water soluble because it has a hydroxyl functional group?
Which molecule is water soluble because it has a hydroxyl functional group?
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54
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule functions to transfer energy between organic molecules?
Which molecule functions to transfer energy between organic molecules?
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55
The following questions refer to the molecules shown in Figure 4.7.
A.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A

B.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A

C.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A

D.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A

E.
<strong>The following questions refer to the molecules shown in Figure 4.7. A.    B.    C.    D.    E.     -Which molecules contain a carbonyl group?</strong> A)A and B B)B and C C)C and D D)D and E E)E and A


-Which molecules contain a carbonyl group?

A)A and B
B)B and C
C)C and D
D)D and E
E)E and A
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56
The following questions refer to the molecules shown in Figure 4.7.
The following questions refer to the molecules shown in Figure 4.7.   Which molecule has a carbonyl functional group in the form of an aldehyde?
Which molecule has a carbonyl functional group in the form of an aldehyde?
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57
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule is a thiol?
Which molecule is a thiol?
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58
The following questions refer to the molecules shown in Figure 4.8.
The following questions refer to the molecules shown in Figure 4.8.   Which molecule contains an amino functional group, but is not an amino acid?
Which molecule contains an amino functional group, but is not an amino acid?
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59
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a carboxyl functional group?
Which is a carboxyl functional group?
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60
The following questions refer to the functional groups shown in Figure 4.6.
The following questions refer to the functional groups shown in Figure 4.6.   Which is a hydroxyl functional group?
Which is a hydroxyl functional group?
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61
The following questions refer to the molecules shown in Figure 4.8.
A.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H?

B.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H?

C.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H?

D.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H?

E.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Which of the following hydrocarbons has a double bond in its carbon skeleton?</strong> A)C?H? B)C?H? C)CH? D)C?H? E)C?H?


-Which of the following hydrocarbons has a double bond in its carbon skeleton?

A)C?H?
B)C?H?
C)CH?
D)C?H?
E)C?H?
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62
The following questions refer to the molecules shown in Figure 4.8.
A.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons.

B.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons.

C.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons.

D.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons.

E.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Organic chemistry is currently defined as</strong> A)the study of compounds made only by living cells. B)the study of carbon compounds. C)the study of vital forces. D)the study of natural (as opposed to synthetic)compounds. E)the study of hydrocarbons.


-Organic chemistry is currently defined as

A)the study of compounds made only by living cells.
B)the study of carbon compounds.
C)the study of vital forces.
D)the study of natural (as opposed to synthetic)compounds.
E)the study of hydrocarbons.
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63
Which action could produce a carbonyl group?

A)the replacement of the OH of a carboxyl group with hydrogen
B)the addition of a thiol to a hydroxyl
C)the addition of a hydroxyl to a phosphate
D)the replacement of the nitrogen of an amine with oxygen
E)the addition of a sulfhydryl to a carboxyl
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64
Which functional group is not present in this molecule?
<strong>Which functional group is not present in this molecule?  </strong> A)carboxyl B)sulfhydryl C)hydroxyl D)amino

A)carboxyl
B)sulfhydryl
C)hydroxyl
D)amino
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65
Choose the term that correctly describes the relationship between these two sugar molecules: <strong>Choose the term that correctly describes the relationship between these two sugar molecules:  </strong> A)structural isomers B)geometric isomers C)enantiomers D)isotopes

A)structural isomers
B)geometric isomers
C)enantiomers
D)isotopes
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66
The following questions refer to the molecules shown in Figure 4.8.
A.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule.

B.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule.

C.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule.

D.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule.

E.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?</strong> A)Testosterone and estradiol are structural isomers but have the same molecular formula. B)Testosterone and estradiol are geometric isomers but have the same molecular formula. C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton. D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings. E)Testosterone and estradiol are enantiomers of the same organic molecule.


-Testosterone and estradiol are male and female sex hormones, respectively, in many vertebrates. In what way(s)do these molecules differ from each other?

A)Testosterone and estradiol are structural isomers but have the same molecular formula.
B)Testosterone and estradiol are geometric isomers but have the same molecular formula.
C)Testosterone and estradiol have different functional groups attached to the same carbon skeleton.
D)Testosterone and estradiol have distinctly different chemical structures, with one including four fused rings of carbon atoms, while the other has three rings.
E)Testosterone and estradiol are enantiomers of the same organic molecule.
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67
The following questions refer to the molecules shown in Figure 4.8.
A.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids.

B.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids.

C.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids.

D.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids.

E.
<strong>The following questions refer to the molecules shown in Figure 4.8. A.    B.    C.    D.    E.     -Testosterone and estradiol are</strong> A)nucleic acids. B)carbohydrates. C)proteins. D)phospholipids. E)steroids.


-Testosterone and estradiol are

A)nucleic acids.
B)carbohydrates.
C)proteins.
D)phospholipids.
E)steroids.
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68
Which chemical group is most likely to be responsible for an organic molecule behaving as a base?

A)hydroxyl
B)carbonyl
C)carboxyl
D)amino
E)phosphate
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Unlock for access to all 68 flashcards in this deck.