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- H- CO₂H CH3 F Select the appropriate stereochemical designation based on the Fischer projection shown above.I and II are: H H Br O constitutional isomers. O enantiomers. O identical. diastereomers. O not isomeric. H- Br -CH₂CH3 ∙H CH3 ||Which of the following pairs of stereoisomers are related as enantiomers? a) A & B; C&D b) A& C; B&D c) A&D; B&C d) C&D; B&C
- What is the relationship between the following molecules? OCH H3C H,CO O constitutional isomers O same molecule O conformational isomers enantiomersThe image shows Fischer projections for the structures of four isomers of a ketopentose. CH₂OH CH₂OH CH₂OH ПА пс C=O D HOEC H HOECH CH,OH A C=O H➡ COH но-с-н CH₂OH Which of the structures are stereoisomers of B? B Which of the structures are diastereomers of D? C=O HOI-C-H HOI-C-H CH₂OH с 000 ΤΑ B HO D CH₂OH O Which of the structures are enantiomers of C? H HI COH D CH₂OHDetermine the absolute configuration of the following compounds anc draw the structure (Fischer projection) of the other enantiomer. F CH3 CN HO I`CH2NH2 H Br "CH3 CI H A В SH OH H3C" CH3 ČH2OH -C三CH ČH3 E HOOC D
- Draw the Fischer Projectionents ncements IS Student urces C Syllabus mation CC Bookstore CC Library C-Tutoring mvas Support omputer Labs campus Tutoring ervices mportant Dates Student Help ny F2 C-2 Question 20 CH,OH H H OH Oanomers O enantiomers Classify the structures: O epimers O diasteriomers Question 21 H F3 O + OH OH F4 CH₂OH Search F5 H H OH OH F6 % [Choose ] H ОН F7 F8NH2 N CH2 CH2 The stereochemistry around this chiral carbon is: O cannot be determined. O Rand S OR OS
- Which of the following is an enantiomer of the compound shown below? CH3 HC CI H O CH3 H--C1 H H C1-|-CH3 I H Cl H--H CH3 A and B It does not have an enantiomer.4. What is the relationship between the following pairs of molecules? Are they "identical", "enantiomers", or "diastereomers"? H CI OH ‚OH CI ClH ´OH ОН OH OH OH H. H ´OH, ОН ОН4. Classify each pair of compounds as either enantiomers, diastereomers, identical, constitutional isomers, or not isomers. x HO OH NH OH H. H HN HO Me H HO n-Pr Me -OH