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- Consider the molecules shown here. Assign the R/S configuration to each chiral center.Assign (R) or (S) configuration to each chiral center in the molecules below. Then indicate if the molecules are identical, constitutional isomers, enantiomers, or diastereomers. F F ОН VS. OHd Copy the following structures into your notebook and determine the absolute configuration of each chiral center: H3CH₂C F Cl H H MIC1 CH3 ||| BI H₂CH₂C H H I ||||| CH₂CH₂CH3 "III COOH H OH OH
- Please indicate which of the molecules in the attached image are chiral.d) Molecular relationships; identify whether the compounds in each group are const. isomers, conformers, enantiomers, diastereomers, identical, meso or none of the above. ОН ОН H3C Br H3C LF H Br CH3 HO CI Br Br CI NH NHHow many carbon atoms in this remdesivir are considered chiral? Please circle each one.
- What chair structure corresponds to the highest energy conformation of trans-1,4-dichlorocyclohexane (shown on left)? CI CI CI CI CI CI CI .CI CI A C D CI B O O O OPayal1) For each pair of structures, determine if they are identical (I), resonance forms (RF), structural isomers (S), conformers (C), enantiomers (E), diastereomers (D), or None (N). b) F H OCH 3 H3CO H F Om Ω d) f) CI CI LL www LL CH3 H CI CH H H H H3C CI CH3
- 1) For each pair of structures, determine if they are identical (I), resonance forms (RF), structural isomers (S), conformers (C), enantiomers (E), diastereomers (D), or None (N). Om d) P f) CI CI CH3 H CI CH H H H H3C CI CH3How many chiral centers are in the molecule shown below? O HNIdentify the configurations (R or S) of the chiral centers in the molecules below OH