Ch15 Organic Compounds And The Atomic Test Bank + Answers - Chemistry Molecular Nature 8e Complete Test Bank by Martin Silberberg. DOCX document preview.
Chapter 15 Test Bank
Organic Compounds and the Atomic Properties of Carbon
1. Select the correct name for the following compound.
A. 1,1,3-triethyl-2-methylbutane
B. 1,1-diethyl-2,3-dimethylpentane
C. 2,4-diethyl-3-methylhexane
D. 3-ethyl-4,5-dimethylheptane
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Easy
Gradable: automatic
Subtopic: Alkanes
Topic: Organic Molecules
2. Select the correct name for the following compound.
A. 2-isopropyl-2,3,4-trimethylbutane
B. 2-isopropyl-2,3-dimethylpentane
C. 2,3,3,4-tetramethylhexane
D. 1,1,2,2,3-pentamethylpentane
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Easy
Gradable: automatic
Subtopic: Alkanes
Topic: Organic Molecules
3. Select the correct name for the following compound.
A. 1,2-diethyl-1-methyl-3-propyl-4-isobutylhexane
B. 1,6,6-trimethyl-1,2,4-triethyl-3-propylhexane
C. 1,1,6-trimethyl-3,5,6-triethyl-4-propylhexane
D. 4,6-diethyl-2,7-dimethyl-5-propylnonane
E. 3,5-diethyl-1,1,6-trimethyl-4-propyloctane
Bloom's: 3. Apply
Difficulty: Easy
Gradable: automatic
Subtopic: Alkanes
Topic: Organic Molecules
4. Select the correct name for the following compound.
A. 2,4,5-tripropylheptane
B. 6-methyl-3,4-dipropylnonane
C. 4-ethyl-5,7-dipropyloctane
D. 5-ethyl-2,4-dipropyloctane
E. 4-ethyl-7-methyl-5-propyldecane
Bloom's: 3. Apply
Difficulty: Easy
Gradable: automatic
Subtopic: Alkanes
Topic: Organic Molecules
5. Select the correct name for the following compound.
A. ortho-dipropylcyclopentylhexane
B. 2,3-dipropylcyclopentylhexane
C. 2-hexyl-1,5-dipropylcyclopentane
D. 1-hexyl-2,3-dipropylcyclopentane
E. 1,2-dipropyl-3-hexylcyclopentane
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkanes
Topic: Organic Molecules
6. Select the correct name for the following compound.
A. ortho-ethylheptylcyclopentane
B. meta-ethylheptylcyclopentane
C. 1-ethyl-2-heptylcyclopentane
D. ethylcyclopentylheptane
E. ortho-ethylheptylbenzene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkanes
Topic: Organic Molecules
7. Select the correct name for the following compound.
A. 1-ethyl-3-methylcyclohexane
B. 1-methyl-5-ethylcyclohexane
C. meta-ethylmethylcyclohexane
D. meta-ethylmethylbenzene
E. 3-ethyltoluene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkanes
Topic: Organic Molecules
8. Select the correct name for the following compound.
A. cis-2-methyl-4-heptene
B. trans-2-methyl-4-heptene
C. cis-6-methyl-3-heptene
D. trans-6-methyl-3-heptene
E. cis-2-methyl-3-heptene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
9. Select the correct name for the following compound.
A. cis-3-ethyl-2,6-dimethyl-6-propyl-4-nonene
B. trans-3-ethyl-2,6-dimethyl-6-propyl-4-nonene
C. cis-7-ethyl-4,8-dimethyl-4-propyl-5-nonene
D. trans-7-ethyl-4,8-dimethyl-4-propyl-5-nonene
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
10. Select the correct name for the following compound.
A. cis-2-methyl-2,3-dipropyl-4-octene
B. cis-7-methyl-6,7-dipropyl-4-octene
C. cis-4,4-dimethyl-5-propyl-6-decene
D. trans-7,7-dimethyl-6-propyl-4-decene
E. cis-7,7-dimethyl-6-propyl-4-decene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
11. Select the correct name for the following compound.
A. cis-2,3-dimethyl-4-hexene
B. trans-2,3-dimethyl-4-hexene
C. cis-4,5-dimethyl-2-hexene
D. trans-4,5-dimethyl-2-hexene
E. trans-4,5-dimethyl-2-heptene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
12. Select the correct name for the following compound.
A. cis-2,5-diethyl-6-methyl-3-nonene
B. 2,5-diethyl-6-methyl-3-nonene
C. cis-4,6-diethyl-3-methyl-6-nonene
D. 4,6-diethyl-3-methyl-6-nonene
E. trans-2,5-diethyl-6-methyl-3-nonene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
13. Select the correct name for the following compound.
A. 2-ethyl-3-pentene
B. 4-ethyl-2-pentene
C. 3-methyl-4-hexene
D. 4-methyl-2-hexene
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
14. Select the correct name for the following compound.
A. 1,1-diethyl-3-butyl-3-hexene
B. 5-butyl-3-ethyl-5-octene
C. 4-butyl-6-ethyl-3-octene
D. 3-ethyl-5-propyl-5-nonene
E. 4-butyl-6-ethyl-3,4-octene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
15. Select the correct name for the following compound.
A. 1-butyl-4-pentyl-3-propylcyclohexene
B. 1-butyl-4-pentyl-5-propylcyclohexene
C. 2-butyl-5-pentyl-6-propylcyclohexene
D. 4-butyl-1-pentyl-2-propylcyclohexene
E. 1-butyl-4-pentyl-3-propylbenzene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
16. Select the correct name for the following compound.
A. 1,1-dimethyl-1-cylcopentyl-2-pentane
B. 1,1-dimethyl-2-hexene-cyclopentane
C. 2-cyclopentyl-2-methyl-3-hexene
D. 5,5-dimethyl-5-cyclopentyl-3-pentane
E. 5,5-dimethyl-5-cyclopentyl-3-pentene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
17. Select the correct name for the following compound.
A. 2-ethyl-4-propylcycloheptene
B. 3-ethyl-5-propylcycloheptene
C. 6-ethyl-4-propylcycloheptene
D. 7-ethyl-5-propylcycloheptene
E. 3-ethyl-5-propylcyclohexene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkenes
Topic: Organic Molecules
18. Select the correct name for the following compound.
A. 4-ethyl-1,1,5-trimethyl-2-heptyne
B. 4,5-diethyl-1,1-dimethyl-2-heptyne
C. 5-ethyl-2,6-dimethyl-3-octene
D. 3-ethyl-3,7-dimethyl-5-octyne
E. 5-ethyl-2,6-dimethyl-3-octyne
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkynes
Topic: Organic Molecules
19. Select the correct name for the following compound.
A. 5-butyl-4,4-dimethyl-3-propyl-1-heptene
B. 5-ethyl-4-4-dimethyl-3-propyl-1-nonyne
C. 5-ethyl-6-6-dimethyl-7-propyl-8-nonyne
D. 4,6-diethyl-5-5-dimethyl-4-decyne
E. 5-ethyl-4-4-dimethyl-3-propyl-1-nonene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkynes
Topic: Organic Molecules
20. Select the correct name for the following compound.
A. 4-4-diethyl-2-pentyne
B. 2,2-diethyl-3-pentyne
C. 2-ethyl-2-methyl-4-hexyne
D. 4-ethyl-4-methyl-2-hexyne
E. 2-ethyl-2-methyl-4-hexene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkynes
Topic: Organic Molecules
21. Select the correct name for the following compound.
A. 2,5-dimethyl-3-octyne-6-cyclobutane
B. 4-cyclobutyl-1-isopropyl-3-methyl-1-hexyne
C. 3-cyclobutyl-4,7-dimethyl-5-octyne
D. 6-cyclobutyl-2,5-dimethyl-3-octyne
E. 3-cyclobutyl-4,7-dimethyl-5-octene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Alkynes
Topic: Organic Molecules
22. Select the correct name for the following compound.
A. meta-chloroethylcyclohexene
B. 1-chloro-5-ethylcyclohexene
C. meta-chloroethylbenzene
D. 1-chloro-5-ethylbenzene
E. 1-chloro-3-ethylcyclohexane
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Aromatic Molecules
Topic: Organic Molecules
23. Select the correct name for the following compound.
A. 1-chloro-2-ethyl-3-propylcyclohexane
B. 1-chloro-2-ethyl-3-propylcyclohexene
C. 1-chloro-ortho-ethylpropylbenzene
D. 1-chloro-meta-ethylpropylbenzene
E. 1-chloro-2-ethyl-3-propylbenzene
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Aromatic Molecules
Topic: Organic Molecules
24. Select the correct name for the following compound.
A. ortho-butylethylbenzene
B. meta-butylethylbenzene
C. para-butylethylbenzene
D. 1-butyl-2-ethylcyclohexene
E. 1-butyl-2-ethylcyclohexane
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Aromatic Molecules
Topic: Organic Molecules
25. Select the correct name for the following compound.
A. ortho-dibromobenzene
B. meta-dibromobenzene
C. para-dibromobenzene
D. 1,4-dibromocyclohexene
E. 1,4-dibromocyclohexane
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Aromatic Molecules
Topic: Organic Molecules
26. Select the correct name for the following compound.
A. para-bromochloro-2-ethylbenzene
B. 4-bromo-1-chloro-2-ethylbenzene
C. 5-bromo-2-chloro-1-ethylbenzene
D. 1-bromo-4-chloro-3-ethylcyclohexene
E. 4-bromo-1-chloro-2-ethylcyclohexane
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Aromatic Molecules
Topic: Organic Molecules
27. Select the correct name for the following compound.
A. 3,4-diethyl-4-methyl-2-butanol
B. 2,3-diethyl-4-pentanol
C. 3,4-diethyl-2-pentanol
D. 3-ethyl-4-methyl-2-hexanol
E. 3-ethyl-4-methyl-2-hexanal
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
28. What is the molecular formula of the compound 2,3-dimethyl-4-cyclopentyl-5-ethyldecane?
A. C16H34
B. C17H34
C. C18H36
D. C19H38
E. C20H40
Accessibility: Keyboard Navigation
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Representing Organic Molecules (Structural Formulas)
Topic: Organic Molecules
29. What is the difference between 1-butyne and 1-butene?
A. 1 carbon atom
B. 1 carbon atom and 2 hydrogen atoms
C. 2 hydrogen atoms
D. 4 hydrogen atoms
E. 1 carbon atom and 4 hydrogen atoms
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Medium
Gradable: automatic
Subtopic: Representing Organic Molecules (Structural Formulas)
Topic: Organic Molecules
30. Select the correct name for the following compound.
A. 3-ethyl-2,3-dimethyl-1-propanol
B. 2,3,4-trimethyl-1-butanol
C. 2,3-dimethyl-1-pentanol
D. 3,4-dimethyl-5-pentanol
E. 2,3-dimethyl-1-pentanal
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
31. Which compound, if any, will be optically active?
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Isomerism (Constitutional isomers and Stereoisomers)
Topic: Organic Molecules
32. Which compound, if any, will not be optically active?
A. A
B. B
C. C
D. D
E. They are all optically active.
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Isomerism (Constitutional isomers and Stereoisomers)
Topic: Organic Molecules
33. Excluding cyclic compounds, how many possible isomers exist for C4H8?
A. 2
B. 4
C. 5
D. 6
E. 7
Accessibility: Keyboard Navigation
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Isomerism (Constitutional isomers and Stereoisomers)
Topic: Organic Molecules
34. Including cyclic compounds, how many possible isomers exist for C4H8?
A. 2
B. 4
C. 5
D. 6
E. 7
Accessibility: Keyboard Navigation
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Isomerism (Constitutional isomers and Stereoisomers)
Topic: Organic Molecules
35. Which of the following features do cyclohexene and 3-methyl-1-pentyne have in common?
A. same physical properties
B. same chemical properties
C. same boiling point
D. same molecular weight
E. same number of double bonds
Accessibility: Keyboard Navigation
Bloom's: 4. Analyze
Difficulty: Medium
Gradable: automatic
Subtopic: Representing Organic Molecules (Structural Formulas)
Topic: Organic Molecules
36. Select the correct type for the following reaction.
CH3CH2CH2CH2OH + HBr → CH3CH2CH2CH2Br + H2O
A. Dehydration
B. Dehydroxylation
C. Addition
D. Elimination
E. Substitution
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
37. Alcohols undergo a variety of reactions. Which one of the following reactions is not undergone by the alcohol functional group?
A. Substitution
B. Addition
C. Dehydration
D. oxidation to form a ketone
E. oxidation to form an aldehyde or a carboxylic acid
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
38. Benzene will react with chloromethane in the presence of a catalyst to produce toluene and hydrogen chloride. Select the correct reaction type for the process.
A. addition
B. elimination
C. substitution
D. oxidation
E. reduction
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
39. Select the correct reaction type for the following process.
A. addition
B. elimination
C. substitution
D. oxidation
E. reduction
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
40. The reaction of bromine with an alkene such as cyclopentene is a good laboratory test for the presence of a double bond in a compound. What type of reaction is it?
A. addition
B. elimination
C. substitution
D. displacement
E. reduction
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
41. 2-chloro-2,3-dimethylbutane will react with potassium hydroxide dissolved in alcohol to produce 2,3-dimethyl-2-butene. What type of reaction is this?
A. addition
B. elimination
C. substitution
D. oxidation
E. displacement
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
42. Select the correct type for the following reaction.
A. addition
B. elimination
C. substitution
D. oxidation
E. dehydrogenation
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
43. Select the correct type for the following reaction.
A. addition
B. elimination
C. carbonylation
D. dehydration
E. oxidation
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
44. Select the correct type for the following reaction.
b
A. addition
B. elimination
C. substitution
D. oxidation
E. reduction
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
45. Identify the functional group circled.
A. aldehyde
B. ketone
C. alcohol
D. ester
E. carboxylic acid
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
46. Vanillin is a flavoring agent which occurs naturally in the vanilla bean, the seed of an orchid.
Identify the functional group circled.
A. aldehyde
B. ketone
C. alcohol
D. carboxylic acid
E. carbonyl
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
47. One source of a musky odor in perfumes is civetone, a compound extracted from the scent gland of the civet cat. Identify the functional group circled.
A. aldehyde
B. ketone
C. alcohol
D. carboxylic acid
E. oxide
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
48. Aspirin is an effective and widely used pain reliever. Identify the functional group circled.
A. aldehyde
B. ketone
C. ester
D. carboxylic acid
E. carbonyl
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
49. Enflurane is an effective gaseous anesthetic with relatively low flammability. Identify the functional group circled.
A. aldehyde
B. ketone
C. ester
D. ether
E. alcohol
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
50. Anethole, a derivative of anise, is used in flavoring and as perfume in soap and toothpaste. Identify the functional group circled.
A. aldehyde
B. ketone
C. alcohol
D. ester
E. ether
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
51. Glycerin is used in cosmetics as a moisturizer. Identify the functional group circled.
A. carboxylic acid
B. alcohol
C. ester
D. ether
E. aldehyde
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
52. Glucose is an important sugar in a person's metabolic cycle. Identify the functional group circled.
A. aldehyde
B. ketone
C. alcohol
D. ester
E. carboxylic acid
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
53. Testosterone is a male hormone. Identify the functional group circled.
A. aldehyde
B. ketone
C. alcohol
D. ester
E. carboxyl
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
54. The compound shown below is responsible for the odor in rancid butter. Identify the functional group circled.
A. aldehyde
B. ketone
C. alcohol
D. carboxylic acid
E. carbonyl
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
55. Benzocaine is from a family of chemicals that are good local anesthetics. Identify the functional group circled.
A. aldehyde
B. ketone
C. ester
D. carboxylic acid
E. carbonyl
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
56. Putrescine is produced during the decay and protein breakdown of meats and is responsible for some of the odor found in them. Identify the functional group circled.
A. aldehyde
B. ketone
C. amide
D. nitrile
E. amine
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
57. Serotonin transmits nerve impulses through the body. Identify the functional group circled.
A. aldehyde
B. alcohol
C. amide
D. amine
E. nitride
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
58. Acetaminophen is a widely used and an effective pain reliever. Identify the functional group circled.
A. aldehyde
B. alcohol
C. amide
D. amine
E. carbonyl
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
59. Urea carries waste nitrogen from the body in urine. Identify the functional group circled.
A. aldehyde
B. alcohol
C. carboxyl
D. amine
E. amide
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
60. The millipede ejects the compound shown below to protect itself from its enemies. Identify the functional group circled.
A. nitrile
B. alcohol
C. amide
D. amine
E. nitro
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
61. Amygdalin (Laetrile) was once touted for its potential anticancer activity. However, the claims were never scientifically verified. Identify the functional group circled.
A. carbonite
B. ether
C. amide
D. amine
E. nitrile
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
62. Which one of the following classes of organic compound does not contain the carbonyl (C=O) group?
A. aldehydes
B. carboxylic acids
C. ketones
D. alcohols
E. esters
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
63. Identify the principal organic product of the reaction between butane and chlorine.
A. CH3Cl
B. CH3CH2Cl
C. CH3CHClCH3
D. CH3CH2CHClCH3
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
64. Identify the principal organic product when benzyl chloride reacts with aqueous sodium hydroxide.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
65. Identify the two principal products of the reaction between ammonia and ethyl propionate.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Hard
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
66. Identify the products of the following reaction.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Hard
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
67. Identify the products for the reaction between cycloheptene and bromine.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
68. Identify the products of the reaction of 3-octene with chlorine.
A.
B.
C.
D.
E.
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
69. Identify the products of the reaction between 2-bromopentane and potassium ethoxide.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Hard
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
70. Identify the principal organic products for the following reaction.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Hard
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
71. Identify the organic product when cyclohexanol reacts with excess potassium dichromate in the presence of sulfuric acid.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
72. Identify the organic product when 3-cylcobutyl-1-propanol reacts with excess potassium dichromate in sulfuric acid.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Hard
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
73. Identify the organic product for the reaction of 2-pentanol with sulfuric acid.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
74. Identify the organic product when cyclopentanol reacts with sulfuric acid.
A. A
B. B
C. C
D. D
E. None of these choices are correct.
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
75. One characteristic of the monomers that form condensation polymers that is not common in monomers which form addition polymers is
A. the presence of pi bonds.
B. the presence of two functional groups.
C. the presence of alkyl side chains.
D. the ability to form free radicals.
E. the presence of sulfur atoms.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Polymers
Topic: Organic Molecules
76. Which of the following polymers is a condensation polymer?
A. Polystyrene
B. Teflon®
C. polyvinylchloride
D. polypropylene
E. Dacron®
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Polymers
Topic: Organic Molecules
77. Nylon-type compounds are prepared by the reaction of
A. a diol with a diacid.
B. an alcohol with a diacid.
C. a diamine with a diacid.
D. an amine with a diacid.
E. a diamine with an acid.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Polymers
Topic: Organic Molecules
78. Dacron is a ___________ compound and is produced by a __________ reaction.
A. polyamide; addition
B. polyamide; condensation
C. polyester; addition
D. polyester; condensation
E. polyene; addition
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Polymers
Topic: Organic Molecules
79. The most abundant organic chemical on earth is
A. glycogen.
B. starch.
C. cellulose.
D. glucose.
E. carbonate.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Biological Molecules (Biochemistry)
Topic: Organic Molecules
80. Each amino acid has two functional groups in common and one of 20 other groups attached to the α-carbon. The two functional groups are
A. carboxyl and amine.
B. ester and amine.
C. carboxyl and amide.
D. alcohol and amine.
E. carboxyl and peptide.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Biological Molecules (Biochemistry)
Topic: Organic Molecules
81. Helical and sheet-like segments in proteins arise from
A. disulfide bridges.
B. salt bridges.
C. crosslinking via covalent bonds.
D. dispersion forces within the protein's interior.
E. hydrogen bonding.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Biological Molecules (Biochemistry)
Topic: Organic Molecules
82. The protein amino acid sequence, the RNA base sequence, and the DNA base sequence are interrelated. Which of the following descriptions is correct?
A. The RNA base sequence determines the DNA base sequence which, in turn, determines the protein amino acid sequence.
B. The DNA base sequence determines the RNA base sequence which, in turn, determines the protein amino acid sequence.
C. The DNA base sequence determines the protein amino acid sequence which, in turn, determines the RNA base sequence.
D. The RNA base sequence determines the protein amino acid sequence which, in turn, determines the DNA base sequence.
E. None of these choices are correct.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Biological Molecules (Biochemistry)
Topic: Organic Molecules
83. Because organic compounds are associated with living organisms, their properties are governed by fundamentally different chemical principles from those of inorganic compounds.
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Trends in Chemical Reactivity
Topic: Chemical Periodicity
84. Ethane (C2H6) is much more reactive than disilane (Si2H6).
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Medium
Gradable: automatic
Subtopic: Trends in Chemical Reactivity
Topic: Chemical Periodicity
85. The carbon atoms in a molecule of cyclohexane lie in the same plane.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Representing Organic Molecules (Structural Formulas)
Topic: Organic Molecules
86. All the atoms in a molecule of benzene lie in the same plane.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Representing Organic Molecules (Structural Formulas)
Topic: Organic Molecules
87. Both alkenes and alkynes exhibit geometric (cis/trans) isomerism.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Isomerism (Constitutional isomers and Stereoisomers)
Topic: Organic Molecules
88. Because of delocalization, all the carbon-carbon bond lengths in 1,3-cyclopentadiene are identical.
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Medium
Gradable: automatic
Subtopic: Representing Organic Molecules (Structural Formulas)
Topic: Organic Molecules
89. As a result of delocalization of the pi-electrons, all the carbon-carbon bonds in benzene are identical.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Representing Organic Molecules (Structural Formulas)
Topic: Organic Molecules
90. A characteristic reaction of alkanes is addition.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
91. A characteristic reaction of alkenes is addition.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
92. A characteristic reaction of haloalkanes is substitution.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
93. All alcohols are capable of hydrogen bonding.
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Medium
Gradable: automatic
Subtopic: Types of Intermolecular Forces
Topic: Intermolecular Forces
94. All ketone molecules are capable of hydrogen bonding to other ketone molecules.
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Medium
Gradable: automatic
Subtopic: Intermolecular Forces
Subtopic: Types of Intermolecular Forces
95. Carboxylic acids are weak acids.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
96. Secondary amines have the general formula RNH2.
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Biological Molecules (Biochemistry)
Topic: Organic Molecules
97. Esters can be formed by the dehydration-condensation of a carboxylic acid and an alcohol.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Organic Reactions
Topic: Organic Molecules
98. Addition polymers are mostly made from monomers with carbon-carbon double bonds.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Polymers
Topic: Organic Molecules
99. Condensation polymers are formed by free radical addition reactions.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Polymers
Topic: Organic Molecules
100. Both nylons and proteins are polyamides.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Polymers
Topic: Organic Molecules
101. Amino acids in solution can undergo an internal acid-base reaction.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Biological Molecules (Biochemistry)
Topic: Organic Molecules
102. The backbone of protein molecules consists of repeating N–C–C–O units.
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Medium
Gradable: automatic
Subtopic: Biological Molecules (Biochemistry)
Topic: Organic Molecules
103. Which of the following is likely to be an aromatic compound?
A. C6H5Cl
B. C6H12
C. C2H4Cl2
D. C2H2
E. C4H8
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Medium
Gradable: automatic
Subtopic: Aromatic Molecules
Topic: Organic Molecules
104. Which of the formulas in the answers represents the alcohol parent of the ester below?
A. CH3 - CH2 - CH2 - OH
B. CH3 - CH2 - OH
C. CH3 - COOH
D. CH3 - CH2 - COOH
E. None of these choices are correct
Bloom's: 3. Apply
Difficulty: Medium
Gradable: automatic
Subtopic: Classes of Organic Molecules (Functional Groups)
Topic: Organic Molecules
105. Which of the following is not a constitutional isomer of CH3CH2COOH?
A. CH3CH2COOCH3
B. CH3COOCH3
C. CH3COCH2OH
D. HOCH=CHOCH3
E. CH3CH(OH)CHO
Accessibility: Keyboard Navigation
Bloom's: 2. Understand
Difficulty: Medium
Gradable: automatic
Subtopic: Isomerism (Constitutional isomers and Stereoisomers)
Topic: Organic Molecules
106. Tartaric acid, shown below, is a dihydroxycarboxylic acid. How many chiral centers does it possess?
A. 0
B. 1
C. 2
D. 3
E. 4
Bloom's: 2. Understand
Difficulty: Easy
Gradable: automatic
Subtopic: Isomerism (Constitutional isomers and Stereoisomers)
Topic: Organic Molecules
107. What is the general formula for alkynes?
A. CnH2n+2
B. C2nH2n
C. CnH2n-2
D. CnHn-2
E. CnH2n
Accessibility: Keyboard Navigation
Bloom's: 1. Remember
Difficulty: Easy
Gradable: automatic
Subtopic: Alkynes
Topic: Organic Molecules
Category # of Questions
Accessibility: Keyboard Navigation 39
Bloom's: 1. Remember 25
Bloom's: 2. Understand 37
Bloom's: 3. Apply 44
Bloom's: 4. Analyze 1
Difficulty: Easy 44
Difficulty: Hard 5
Difficulty: Medium 57
Difficulty: Medium 1
Gradable: automatic 107
Subtopic: Alkanes 7
Subtopic: Alkenes 10
Subtopic: Alkynes 5
Subtopic: Aromatic Molecules 6
Subtopic: Biological Molecules (Biochemistry) 7
Subtopic: Classes of Organic Molecules (Functional Groups) 22
Subtopic: Intermolecular Forces 1
Subtopic: Isomerism (Constitutional isomers and Stereoisomers) 7
Subtopic: Organic Reactions 25
Subtopic: Polymers 7
Subtopic: Representing Organic Molecules (Structural Formulas) 7
Subtopic: Trends in Chemical Reactivity 2
Subtopic: Types of Intermolecular Forces 2
Topic: Chemical Periodicity 2
Topic: Intermolecular Forces 1
Topic: Organic Molecules 103
Document Information
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Chemistry Molecular Nature 8e Complete Test Bank
By Martin Silberberg
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