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- Which structure is the enantiomer of the original molecule? F H3C- original structure H F H3C- H3C- H3C- CH3 H A В ID2) Draw the molecule that corresponds to (3R,5R,6R)-5-cyclopropyl-6-ethyl-3-iodo-1-methylcyclohex-1-ene.Translate the Fischer projection to a wedge-and-hashed bond structure in a zig-zag chain. Be sure each stereocenter clearly shows one wedged bond, one hashed bond and two in-plane bonds. Select Draw Rings More Erase H |||| с Q2 Q H HO HO HO -OH -H -H -H CH₂OH H O
- 4. Label each of pair of compounds as: identical, enantiomers, diastereomers, or constitutional isomers. Write your label in the box provided below each pair. Br CH3 CH2CH3 НО Но- H- H -CI H- -CI Br ČH2CH3 CH3 CI Br BrLabel each asymmetrical carbon in the compound below as R or S. H3C HHO H CH₂OH HO ОНСWhich of the following are meso compounds? CH3 CH3 CH3 CH3 CH H- CI H CI -H CI- H CI- -CI H- -H H- H H- -H H -H H- -H H- -CI -H H H -CI H- -H CH3 CH3 CH3 CH3 CH3 D E A B
- Label each asymmetric carbon in the compound below as R or S. Br H₂C I H₂C CH₂CH₂Cl CHOof the following represents the enantiomer of the following compound? Br CI A Br Br Ω!!!, CI BrIdentify. SN1 CI SN1 SN1 Br "|||| CH3CH₂O Na CH3CH₂OH Br SN2 H3C `ONa+ DMSO SN2 t-BuOK t-BuOH SN2 E1 E1 E1 major product E2 E2 E2
- Instructions: Label each pair of molecules below as enantiomers, diastereomers, constitutional isomers, or identical. H3C H. OH H3C ОН HO-- H CH,OH НО CH2OH CO,H H HO- HO CH3 H2OC CH3 HO,C HO,C--. CO,H CO,H н Он H НОСI CHO ОНС CH2OH Н Он НО Н н ОННО Н H;C CH3 H3C" H H Cl H3C CI Br Br. H;C^ H3C Br Br CI CH3 CH3 H H3C H H;C Cl0 || CH,-O-C-(CH2)2 – CH3 O || CH-O - C - (CH2), – (CH = CH – CH2)2 – (CH2)3 – CH3 O || CH,- O-C-(CH2)8 – CH3 - 3 KOHTranslate the given theoretical conformer from the wedge-and-dash drawing into its Newman projection. H. Clm IF Br ОН Answer Bank Cl Но Br I