4. What is the relationship (resonance structures, constitutional isomers, conformational isomers, enantiomers, meso compounds, diastereomers, or none of these) between the pair of structures below? а. b. с. 5. Circle the most stable conformer of (S)-3,3-dimethyl-2-hexanol. H H CH3 CH3 H3C (CH2)2CH3 CH3 CH3 H3C(H2C)2CH3 H3C(H2C)2 H3C(H2C)2 H3C. „CH2CH3 -CH3 OH HO CH3 ČH2CH3 H3C H H,C HO, H но. ČH3 CH3 6. Circle the compound(s) that is/are optically active (a chiral molecule). (CH2)3CH3 H. HO CH3 H,

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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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What is the relationship (resonance structures, constitutional isomers, conformational isomers, enantiomers, meso
compounds, diastereomers, or none of these) between the pair of structures below?
4.
а.
b.
C.
CI
5. Circle the most stable conformer of (S)-3,3-dimethyl-2-hexanol.
H
CH3
CH3
H
CH3
(CH2)2CH3
H3C(H2C)2CH3
H3C(H2C)2
CH3
H3C
H3C(H2C)2
H3C
CH2CH3
CH3
H3C
OH
H
OH
H
HO,
HO
CH3
H
H,C
CH3
ČH2CH3
CH3
6. Circle the compound(s) that is/are optically active (a chiral molecule).
(CH2)3CH3
H.
HO
ČH3
:11 1.
Transcribed Image Text:What is the relationship (resonance structures, constitutional isomers, conformational isomers, enantiomers, meso compounds, diastereomers, or none of these) between the pair of structures below? 4. а. b. C. CI 5. Circle the most stable conformer of (S)-3,3-dimethyl-2-hexanol. H CH3 CH3 H CH3 (CH2)2CH3 H3C(H2C)2CH3 H3C(H2C)2 CH3 H3C H3C(H2C)2 H3C CH2CH3 CH3 H3C OH H OH H HO, HO CH3 H H,C CH3 ČH2CH3 CH3 6. Circle the compound(s) that is/are optically active (a chiral molecule). (CH2)3CH3 H. HO ČH3 :11 1.
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