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,

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,

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter7: Cycloalkanes

Section: Chapter Questions

Problem 12CTQ: Fill in the blanks: cis-1,3-Dimethylcyclohexane has two different chair conformations: one withboth...

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1. Rank the following conformers of the isomers of 1-ethyl-2,4-dimethylcyclohexane from most to least stable. JI. B. C. E D.
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