tps:/blackboard.udmercy.edu/bbcswebdav/pid-1029221- 1. Retrosynthetic Analysis Of Your What... C University of Detroit Mercy Project 2 CHM 2270, Fall 2017 Name: Write your name on the back of the last page you use. Substance: Draw your substance here. 1. Identify all chiral centers in your substance and assign R-or S- designations. (10 pt.) Retrosynthetic analysis of your compound: What is a possible precursor? reagents you need to obtain your product when using this precursor? In a drawing, show the synthetic steps that lead from the precursor to your compound. 2. What are the (10 pt.) 3. Use curved arrows properlyl (10 pt.) Using your precursor, show mechanisms and products of a Markovnikov and an anti- Markovnikov addition. Use the proper reagents to make both happen. 4. (10 pt.) 5. Based on the materials obtained through Markovnikov and anti-Markovnikov additions to the precursor, discuss stereochemical aspects. That means: Enantiomers? Diastereomers? Regioisomers? E. g, Markovnikov addition yields the (7)-enantiomer, while Indicate the proper orientation of substituents by drawing structures with wedges and dashes where necessary . Are the compounds chiral or achiral, why is that? (10 pt.)