Organic Chemistry Maxwell presented by Macmillan Learnin- Classify the pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. H3C H CH3 H3C. CI CI H H3C Compound 1 Compound 2 The compounds are enantiomers identical diastereomers constitutional isomers O not isomeric The correct IUPAC names are: O Compound 1: (2S,3R)-2,3-dichlorobutane Compound 2: (2R,3S)-2,3-dichlorobutane O Compound 1: (2R,3R)-2,3-dichlorobutane, Compound 2: (2R,35)-2,3-dichlorobutane Compound 1: (2S,35)-2,3-dichlorobutane, Compound 2: (2R,3R)-2,3-dichlorobutane O Compound 1: (2R,3S)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane Ill
Organic Chemistry Maxwell presented by Macmillan Learnin- Classify the pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. H3C H CH3 H3C. CI CI H H3C Compound 1 Compound 2 The compounds are enantiomers identical diastereomers constitutional isomers O not isomeric The correct IUPAC names are: O Compound 1: (2S,3R)-2,3-dichlorobutane Compound 2: (2R,3S)-2,3-dichlorobutane O Compound 1: (2R,3R)-2,3-dichlorobutane, Compound 2: (2R,35)-2,3-dichlorobutane Compound 1: (2S,35)-2,3-dichlorobutane, Compound 2: (2R,3R)-2,3-dichlorobutane O Compound 1: (2R,3S)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane Ill
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![Organic Chemistry
Maxwell
presented by Macmillan Learning
Classify the pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric.
Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each.
H3C
H
CH3
H3C.
CI.
CI
H3C
Compound 1
Compound 2
The compounds are
O enantiomers
O identical
O diastereomers
O constitutional isomers
O not isomeric
The correct IUPAC names are:
O Compound 1: (2S,3R)-2,3-dichlorobutane Compound 2: (2R,3S)-2,3-dichlorobutane
O Compound 1: (2R,3R)-2,3-dichlorobutane, Compound 2: (2R,3S)-2,3-dichlorobutane
O Compound 1: (2S,3S)-2,3-dichlorobutane, Compound 2: (2R,3R)-2,3-dichlorobutane
O Compound 1: (2R,3S)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane
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Transcribed Image Text:Organic Chemistry
Maxwell
presented by Macmillan Learning
Classify the pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric.
Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each.
H3C
H
CH3
H3C.
CI.
CI
H3C
Compound 1
Compound 2
The compounds are
O enantiomers
O identical
O diastereomers
O constitutional isomers
O not isomeric
The correct IUPAC names are:
O Compound 1: (2S,3R)-2,3-dichlorobutane Compound 2: (2R,3S)-2,3-dichlorobutane
O Compound 1: (2R,3R)-2,3-dichlorobutane, Compound 2: (2R,3S)-2,3-dichlorobutane
O Compound 1: (2S,3S)-2,3-dichlorobutane, Compound 2: (2R,3R)-2,3-dichlorobutane
O Compound 1: (2R,3S)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane
48°F Light ra
F5
F6
PrtScn
Home
End
PgUp
F7
F8
F9
PgDc
F10
F11
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