12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal...
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) но: +Hy0 ное
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) 10-M 13. Provide a synthesis for the target molecule shown. (18 pts) он TM SM он NC. SM TM
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) Hot 13. Provide a synthesis for the target molecule shown. (18 pts) OH OH SM TM Oн NC. SM TM
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) 13. Provide a synthesis for the target molecule shown. (18 pts) NC OH SM CH TM SM Bonus: (10 pts) Starting from Benzene and using reagents that we have discussed in class, design a synthesis for the Target molecule (TM). HONHO
10 12. Provide a eurved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) ot sh 13. Provide a synthesis for the target molecule shown. (18 pts) SM TM Он NC SM TM
showing the conversion of the aldehyde to the cycle ketal 12. Provide a curved arrow mechan product. (6 pts) 13. Provide a synthesis for the target molecule shown. (18 pts) оно SM TM
provide a curved arrow mechanism for the conversion of Pentanol-2 or 2-pentanol to 2-bromopentane in presence of HBr. Draw all structures including all intermediate for full credit.
7. Provide a curved arrow mechanism and predict the product for the following SN2 reactions. (9 pts) Br H2N a) O Na b) C Cl NaCN c) 7. Provide a curved arrow mechanism and predict the product for the following SN2 reactions. (9 pts) Br H2N a) O Na b) C Cl NaCN c)
Show the curved-arrow mechanism for the first step, and the structure of the cyclic intermediate formed, when cyclopentene in treated with KMnO4. A Lewis structure for the permanganate ion is provided below in the hint. Make sure to show all non-bonding electron pairs and formal charges where necessary. Omit K. Curved-Arrow Step Cyclic Intermediate
Using the curved-arrow formalism, provide a mechanism that accounts for the following transformation. (5 pts) 1. OH НА OH 2. Using the curved-arrow formalism, provide a mechanism that accounts for the following transformation. (10 pts) H3O но C) OH