Draw the enantiomer of the molecule shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable.
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- erences) Draw a structural formula of the SR configuration of the compound shown below. CH3 S NR HO Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only If a group is achiral, do not use wedged or hashed bonds on it. ood2 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 OHSerine is a naturally-occuring amino acid shown below. Draw the two possible enantiomers of the molecule. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. H₂N, HO H O OH
- Assign R and S configurations to the chirality centres of the compounds below: O₂N ... OH ||||| 15 IC/ CI CH₂OH NHCOCHCI₂ HO₂C NH₂ H H H3C HO CH38. Identify the stereochemical relationship between the structural pairs shown below as (A) identical structures that are not meso; (B) identical structures that ARE meso; (C) structures that are enantiomers; or (D) structures that are diastereomers. a) b) H3C c) CH3 Br H. CH3 Br Br CH3 H. CI Holl H Cill Cl- CH3 Br H. CI CH3 HO. H. H3C Cl H3C- H- H. CH3 Cl a) b) c) 9. Identify the stereochemical relationship between the structural pairs shown below as (A) identical structures that are not meso; (B) identical structures that ARE meso; (C) structures that are enantiomers; or (D) structures that are diastereomers. a) b) c) CH2CH3 NH2 HO CH3 H3C. CH3 Cl HO H;C CH2CH3 F. F H;C. CI H H,N -CH3 CH3 NH2 H3C Br H2N C1 H3C CH3 CH3 H;CH,C- Cl F H. H Br CH,CH3 CH3 a) b) c)of al Authenticatior X T McGraw-Hill Connect X 6 Question 19- Lab 3H X A app.101edu.co the enantiomer of the molecule shown below. Use a dash edge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. но
- Draw all possible constitutional isomers and stereoisomers for acompound of molecular formula C6H12 having a cyclobutane ring andtwo methyl groups as substituents. Label each compound as chiral orachiral.H₂C -CH₂3 H 11 СН3- CH₂ Criven Structures give the relationship of given molecules Cat Enantiomerg (b) Diastereomers (c) Constitutional isomery (d) same molecule GIVE EXPLAINED HANDWRITTEN AnbwerQ3:- Draw and specify as R or S the enantiomers (if any) of: (a) 3-bromohexane (d) 1,3-dichloropentane
- Construct models of 1,2-dibromocyclopentaneand draw all the possible stereoisomers. Label each chirality centre with an*,andan Ror S. Indicate clearly which pairs are relatedasenantiomers and which as diastereoisomersor meso.H3C Cl \ / C=C / \ H2N I (R)-enantiomer (Z) isomer (S)-enantiomer (E) isomer meso compoundIdentify if the following pairs of compounds are identical, enantiomers, diastereomers or constitutional isomers. * ОН CN and H;C uNCN INCN H3C H. C HO, (ii) and O (1) Identical; (ii) Enantiomers O (1) Enantiomers; (ii) Diastereomers O (1) Enantiomers; (ii) Enantiomers O (1) Identical; (ii) Identical