[References] Draw a tetrahedral representation of (R)-3-chloro-1-pentene. • 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.
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- [References] Write a structural formula for the lowest-molecular-weight chiral compound that contains C and H, contains only one functional group, and is an alkane. • 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. • Alkene or alkyne groups are not considered to be functional groups for this purpose. H - + O. √n Sn [1 [F ChemDoodleDraw a structural formula of the SS configuration of the compound shown below. CH₂F . 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. . HO₂C *** S Y ChemDoodle[References] Draw a structural formula of the RS configuration of the compound shown below. OH CH2NH2 R S CN • 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. -81 / II... #[ ] در
- Draw a structural formula of the S configuration of the compound shown below. NH₂ HO₂CCH₂CHCO₂H aspartic acid . . . 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.Draw the mirror image of this molecule. COOH H₂N-CH CH3 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. . Include H atoms at chiral centers only. • Use the "flat" representation of rings in your drawing. 3 / QQ **** C opy aste []} ?Draw a structural formula of the SR configuration of the compound shown below. HO CH3 S -NHCH3 R H3C ephedrine • 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. * #[ ] در ?
- Draw a structural formula for trans-1-bromo-3-isopropylcyclobutane. • Show stereochemistry only if given in the name. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it. • In cases where there is more than one answer, just draw one.[Review Topics) [References) Draw a structural formula of the R configuration of the compound shown below. CH3 HOCH,CH,CH,CHCHCH3 CH3 • 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. (eDraw a structural formula of the S configuration of the compound shown below. CH₂CI [Referer • 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. n ? ChemDoodle
- Draw a formula for the lowest molecular weight compound that contains C, H, and possibly O, N or 5, is a chiral compound, contains ONLY one functional group, and is a sulfide. 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. Alkene or alkyne groups are considered to be functional groups. 98 4 - /IP ChemDoodleDraw a tetrahedral representation of the (2S,3R) enantiomer of 2,3-dibromopentane. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • Show stereochemistry in a meso compound. **8 MAVIL On [] ? Ⓡ ChemDoodle(Review Topics] [References] Draw a structural formula of the SR configuration of the compound shown below. CH2SH • 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. opy