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- b) a) b) Identify the functional group for each organic compound below and give the IUPAC name the compound. 0 CH3CH₂CH₂CH₂C-O-CH₂CH3 CH3-C=CH2 CH₂ CH3 mature Functional group_ Name: Functional group_ Name:Draw all stable isomers of C4H9Cl. Be sure to label cis/trans isomers on rings, Z/E isomers on double bonds as well as R/S on chiral centers1. Which of the following is a chiral molecule? Encircle the substituents that make it chiral. H c=c=CCH3 'CO2OH (A) CH2OH CO2H H (B) (C) CH3 CH3 (D) poddns
- 0 (1 CH₂-C-CI AICI>Draw all possible stereoisomers of the following compound (there are four of them). You need to consider both the chiral carbon and the double bond CH;CH=CHCH(CI)CH32. Identify the type of stereoisomerism in each of the following molecules and draw the stereoisomer pair. (a) CH;CH=CHCOH (b) CgH;CH2CH(NH2)CH3
- Draw a structural formula of the S configuration of the compound shown below. • Use the wedge /hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. • Ifa group is achiral, do not use wedged or hashed bonds on it. CH3 CH3 CH;CHCHCN CH,CH,CH,CHCH,CH, CH2NH2 Draw a structural formula of the RS configuration of the compound shown below. 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. ÇI5) For the following: a) Draw the "flat" line structure of the following (be sure to indicate stereochemistry) Br OH b) Draw both chair conformations of the following compound. Indicate which form is the most stable H3C°3) Draw the most stable conformation of (2Z, 4E)-2,4-hexadiene.