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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 IDPropose a chemical structure for the name below. Make sure to clearly define the stereochemistry where applicable: (R)-4-methyl-4-phenylcyclohex-2-en-1-one A B C DWhat is true about the relationship between the following compounds? CH3 CH3 CH; CH; CH3 CH3 A В O All three are stereoisomers of each other. OA and B are the same compound while C is a stereoisomer. All three are the same compound. A and B are the same while C is a conformer, all of the same compound . O A and C are the same while B is a stereoisomer.
- Identify enantiomers. F A CI H CI ex H H B and D B CIH CI A and C F B and D, A and C H A and B, A and D, B and C, C and D CI CL B and D, A and B, A and D, B and C, C and D H H H CL F D HCL A H H F HH H H CIBe sure to answer all parts. i i Finish drawing the last possible stereoisomer of CH3CCHOHCHOHCCH3 and indicate which are enantiomers, diastereomers, or meso compounds. H H A CH3 OH HO OH -CH3 Enantiomers? A and B A and C A and D B and C HO B and D C and D none of the above C- -CH3 B H H -CH3 HO H Diastereomers? A and B A and C A and D B and C C B and D -CH3 H OH -CH3 C and D none of the above finish structure ... Meso? D A and B A and C A and D B and C B and D C and D none of the aboveWhich of the following pairs are constitutional isomers? ClCH2CH2CH2CH3 and CH3CH2CH2CH2Cl H2NCH2CH=CHCOOH and HOOCCH=CH(H2N)CH2 CH3CH(OH)CH2CH3 and CH3CH2(HO)CHCH3 CH3CH=CHCH2OH and CH3CH=CHOCH3 CH3OCH2CH2CH2CH3 and CH3OCH2CH2CH2OCH3
- Indicate whether the pair of structures shown represent stereoisomers, constitutional isomers, different conformations of the same compound, or the same conformation of a compound viewed from a different perspective. Note that cis, trans isomers are an example of stereoisomers. CH3 H3C- H3C Cl OH CI CH3 stereoisomers OH same conformation Submit Answer Retry Entire Group 2 more gro stereoisomers constitutional isomers different conformations same conformation2 Draw all stereoisomers for the following molecules; indicate the stereochemica interrelationships (enantiomer, diastereomer, or meso) for all its possible pairs. 4) H;C CH3 Но CH3 OH CI CI Но OHIdentify the stereochemical configuration of this compound. SH CH3 O R S
- Which molecule below is an enantiomer of the molecule drawn here? OH OH HO OH H 'H H H OH OH OH HO 'H H OH HO H HClassify the following pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. H ÷ ||I The correct IUPAC names are: || J k CI same compound enantiomers diastereomers constitutional isomers not isomeric Compound I: (2R, 3R)-2,3-dichloropentane, Compound II: (2R, 3S)-2,3-dichloropentane Compound I: (2S, 3S)-2,3-dichloropentane, Compound II: (2S, 3S)-2,3-dichloropentane Compound I: (2S, 3R)-2,3-dichloropentane, Compound II: (2S, 3R)-2,3-dichloropentane Compound I: (2R, 3R)-2,3-dichloropentane, Compound II: (2R, 3R)-2,3-dichloropentaneWhich is the most stable chair conformer of the following compound? E 1 -NH Y = || IZ -NH E ||| -NH IV NH