References Mailings Review View Help Layout b 13 ^些,, … Emphasis n12 A A Aa v Heading 1 ab x, x A 2 A- , 三三三三三 Paragraph Styles Font For each of the following, indicate whether it is in the R or the S configuration: (a) HO HO (a) CH3 CH2C1 cr CH2CH3 ČNH2 121

Why must enantiomers be converted to diastereomers before separation processes such as crystallization?

Please answer this correctly and quickly

Given the following compounds and boiling points: Determine the IMFs Order the compounds from weakest to strongest IMFs, and Pentane (C5H12)                                     36°C Methane (CH4)                                     -164°C Sodium n-butoxide (C4H9NaO)      +260°C Hydrogen dioxide (H2O)                   100°C

Draw the skeletal (line-bond) structure for (S)-2- isopropylheptanoic acid. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. I I 1 I I I 0 I 1 I 1 1 I I I U 1 1 1 I 0 1 1 1 U 1 I I Drawing I 1 I I I I I U I I I 1 3 1 3 1 I I i I 1 I I