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Mechanism of the reaction is :
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) 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) 10-M 13. Provide a synthesis for the target molecule shown. (18 pts) он TM SM он NC. SM TM
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
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts)
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) но: +Hy0 ное
13.) Provide a synthesis for the target molecule shown. (18 pts)product. (6 pts) Bonus: (10 pts) Starting from Benzene and using reagents that we have discussed in class, design a synthesis for the Target molecule (TM) 13. Provide a synthesis for the target molecule shown. (18 pts) go alcohol aketone OH СОН M 얘 SM omgBr =sin 1-2 OH => KongBros Naz6.2010 H2SO4, H2O & H300 q Etmaira H20 어 #C=, 2° alcohol, aldehyde 20 TM o o #C77, Ketore...
provide a synthesis for the target molecule shown. н" TM SM Bonus: (10 pts) Starting from Benzene and using reagents that we have discussed in class, design a sy molecule (TM).
CH3 SM TM Bonus: (10 pts) Starting from Benzene and using reagents that we have discussed in class, design a synthesis for the Target molecule (TM). На C NH2 но. ? ОН TM SM
5. Each transformation shown below requires at least two steps. provide the reagent/conditions for each transformation. 6. Predict the products from the birch reduction shown below. Bonus: Prodvide a synthesis for the target molecule using benzene 5. Each transformation shown below requires at least two steps. Provide the reagents/conditions for each transformation. (20 pts) Reagents ? Reagents A-2 COM Reagents D-? Reagents B-? Reagents C-2 6. Predict the products from the Birch reductions shown below. (3 pts) ON N NH,...