Free Response Section 10. Provide the products formed when the cyclic acetal shown is hydrolyzed with...
Free Response Section 10. Provide the products formed when the cyclic acetal shown is hydrolyzed with curved arrow mechanism to show how the acetal breaks down into the produce acetal shown is hydrolyzed with acid. You must provide a H30+ heat oh 11. Provide the mechanisms for the reactions shown. (30 pts)
Free Response Section 10. Provide the products formed when the cyclic acetal shown is hydrolyzed with acid. You must provide a curved arrow mechanism to show how the acetal breaks down into the products. (6 pts) : H0+ To: heat
Free Response Section 10. Provide the products formed when the cyclic acetal shown is hydrolyzed with acid. You must po curved arrow mechanism to show how the acetal breaks down into the products. (p) Н,0* To: . heat 11. Provide the mechanisms for the reactions shown. (30 pts) CH2CO3H Baeyer-Villiger Oxidation
Free Response Section Provide the products formed when the cyclic dostal shown is hydrolyzed with acid. You must provide a curved arrow mechanism to show how the asetal breaks down into the products. ( pes) H,0* heat 11. Provide the mechanisms for the reactions shown. (30 pts) CH,COH Baeyer-Villiger Oxidation Enamine formation
provide the products formed when the cyclic acetal shown is hydrolized with acid. Provide a curved arrow mechanism to show how the acetyl breaks down into the products HO LaH 1. LAHA 2. HO
Free Response Section 10. Provide the products formed when they wished with c ompris curved er mechanism to show how the table des into the prote ) H,00 11. Provide the mechanisms for the reactions shown. (30 pts) CH.CO Bacyer-Villiger Oxidation
16.72 What products are formed when each acetal is hydrolyzed with water and sulfuric acid? OCH2CH3 a. CH3CH2-C-CH2CH3 OCH2CH3 b. CH20- LOCH3 ГОСНЫ
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) 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