Free Response Section 10. Provide the products formed when they wished with c ompris curved er...
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
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 curved arrow mechanism to show how the acetal breaks down into the products. (6 pts) H30* heat
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
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
CHEM 241 Assignment 6
2. Provide the structure of the major products A, B, and C formed in each of the synthesis routes below. OH EINH Croz, H2SO A Hicat. B H, (-H20) 2) H30* В B ~ Br. 1 с LE A H30C b) H O V 2EOH cat (H20) 1) Hg(OAC). THE 2) NBH OAC - OCCH c) 1) POCI Me DMF - 2) NaHCO, (aq) Ph, P=CHCOMe - A Pdic. H C No Mg в с но...
7. Shown below are the major product formed and the proposed mechanism when 1- methylcyclohexanol reacts with 85% H3PO4 at 150 °C. Name all curved arrows shown in each step as either "lone pair to bond" or "bond to long pair". Specify the atom that donates/accepts the lone pair. [1 Mark] Step 1 -H O ro-H + Ho + H2O H H Commons Kagamo Step 2 + H2O Step 3 = + H,PO. H HAPO Zaitsev product 6. Given below...
Section 4Mechanisms (40 pts) Choose te of the three reacties c provide the reaction products Fosa show the who H30* HNO H2SO4 1" reaction: A B C (underline your choice - 1 pt) Structure of product (3 pts) Reaction mechanism (include all lone pairs, formal charges, and electr HAJOZ H₂SO,