4. What is the relationship (resonance structures, constitutional isomers, conformational isomers, enantiomers, meso com
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4. What is the relationship (resonance structures, constitutional isomers, conformational isomers, enantiomers, meso com
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? a. b. C. CI 110 5. Circle the most stable conformer of (S)-3,3-dimethyl-2-hexanol. H H H3C(H2C)2CH3 CH3 (CH2)2CH3 CH3 H3C(H2C2y CH3 H2C(H2C)2 -CH₃ H3C H3C. CH2CH3 H3C -CH3 OH OH H HO OH H ОН CH3 H H3C CH3 CH2CH3 CH3 CH3 6. Circle the compound(s) that is/are optically active (a chiral molecule). (CH2)3CH3 H H mo Q НО H CH3 Claulu it conierufalse" Talanteifhef 11 urinat rue or false hybrid letters will be
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