Select the proper IUPAC name for the compound, including the (R) or (S) designation where appropriate. The best name of the compound is: (meso)-2,3-dijodobutane O (2R 3R)-2,3-diiodobutane O (2R,3S)-2,3-dijodobutane O (25,3R)-2,3-diiodobutane H₂C O 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. Compound 1 HD H The correct IUPAC names are. Compound 2 НІ CI The compounds are Onot isomeric O identical O diastereomers O constitutional isomers Oenantiomers O Compound 1: (2R,3S)-2,3-dichlorobutane, Compound 2: (2S, 3R)-2,3-dichlorobutane O Compound 1: (2R, 3R)-2,3-dichlorobutane, O Compound 1: (2S,3S)-2,3-dichlorobutane, O Compound 1: (2S,3R)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane Compound 2: (2R, 3R)-2,3-dichlorobutane Compound 2: (2R,3S)-2,3-dichlorobutane

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter10: Alcohols
Section: Chapter Questions
Problem 10.33P: Two diastereomeric sets of enantiomers, A/B and C/D, exist for 3-bromo-2-butanol. When enantiomer A...
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Solve correctly please, need both parts with some explanation also
Select the proper IUPAC name for the compound, including the (R) or (S) designation where appropriate.
The best name of the compound is:
(meso)-2,3-dijodobutane
(2R 3R)-2,3-dijodobutane
(2R,3S)-2,3-diiodobutane
O (2S,3R)-2,3-diiodobutane
O
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.
Compound 1
Compound 2
H
==
H
НІ
The correct IUPAC names are.
are.
CI
The compounds are
not isomeric
identical
O diastereomers
constitutional isomers
Oenantiomers
ming
O Compound 1: (2R, 3S)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane
O Compound 1: (2R, 3R)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane
O Compound 1: (2S,3S)-2,3-dichlorobutane, Compound 2: (2R, 3R)-2,3-dichlorobutane
O Compound 1: (2S,3R)-2,3-dichlorobutane,
Compound 2: (2R, 3S)-2,3-dichlorobutane
Transcribed Image Text:Select the proper IUPAC name for the compound, including the (R) or (S) designation where appropriate. The best name of the compound is: (meso)-2,3-dijodobutane (2R 3R)-2,3-dijodobutane (2R,3S)-2,3-diiodobutane O (2S,3R)-2,3-diiodobutane O 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. Compound 1 Compound 2 H == H НІ The correct IUPAC names are. are. CI The compounds are not isomeric identical O diastereomers constitutional isomers Oenantiomers ming O Compound 1: (2R, 3S)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane O Compound 1: (2R, 3R)-2,3-dichlorobutane, Compound 2: (2S,3R)-2,3-dichlorobutane O Compound 1: (2S,3S)-2,3-dichlorobutane, Compound 2: (2R, 3R)-2,3-dichlorobutane O Compound 1: (2S,3R)-2,3-dichlorobutane, Compound 2: (2R, 3S)-2,3-dichlorobutane
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