compound I compound II Il Classify the pair of compounds. They are enantiomers. diastereomers. constitutional isomers. the same compound. not isomeric. ect the correct IUPAC name, including the correct (R) or (S) designation, for each compound. compound 1: (25,3R)-2,3-dichlorobutane; compound 11: (25,3R)-2,3-dichlorobutane compound 1: (2R,3R)-2,3-dichlorobutane; compound II: (2R 3R)-2,3-dichlorobutane compound 1: (25,35)-2,3-dichlorobutane; compound II: (25,3S)-2,3-dichlorobutane compound 1: (25,35)-2,3-dichlorobutane; compound II: (2R,3R)-2,3-dichlorobutane

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Chapter1: Chemical Foundations
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Consider the pair of compounds.
Classify the pair of compounds. They are
compound II
compound I
O enantiomers
chandomes
O diastereomers.
O constitutional isomers
O the same compound.
O not isomeric.
111
OIIIIII
Select the correct IUPAC name, including the correct (R) or (S) designation, for each compound.
compound II: (2R 3R)-2,3-dichlorobutane
compound II: (25,35)-2,3-dichlorobutane
compound
II: (2R,3R)-2,3-dichlorobutane
O compound 1: (25,3R)-2,3-dichlorobutane; compound II: (25,3R)-2,3-dichlorobutane
O compound 1: (2R,3R)-2,3-dichlorobutane;
O compound 1: (25,35)-2,3-dichlorobutane;
O compound I: (25,35)-2,3-dichlorobutane;
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
H
Olli...
***
НЕ
The correct IUPAC names are.
Compound 2
CI
НІ
CI
The compounds are
Onot isomeric
identical
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, 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:Consider the pair of compounds. Classify the pair of compounds. They are compound II compound I O enantiomers chandomes O diastereomers. O constitutional isomers O the same compound. O not isomeric. 111 OIIIIII Select the correct IUPAC name, including the correct (R) or (S) designation, for each compound. compound II: (2R 3R)-2,3-dichlorobutane compound II: (25,35)-2,3-dichlorobutane compound II: (2R,3R)-2,3-dichlorobutane O compound 1: (25,3R)-2,3-dichlorobutane; compound II: (25,3R)-2,3-dichlorobutane O compound 1: (2R,3R)-2,3-dichlorobutane; O compound 1: (25,35)-2,3-dichlorobutane; O compound I: (25,35)-2,3-dichlorobutane; 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 H Olli... *** НЕ The correct IUPAC names are. Compound 2 CI НІ CI The compounds are Onot isomeric identical 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, 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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