ОН HCI (catalytic) 03 THF 65 °C mol. sieves
show the mechanism + H20 HCI (catalytic) THF mol. sieves 25 °C
CICI CH3CH2OH 25 °C MT2 Mastery 1 Predict the Product HCI (catalytic) om ". i THF/H20 65 °C MT2 Mastery 5 Provide the structure of the charged intermediate from the second step of the mechanism that leads to these products? HN KNH2 NO2 NO2 NH3 (liquid) -38 °C MT2 Mastery 6 Provide the structure of first intermediate of the mechanism that leads to this products?
Please help me with the product LOH HCI (catalytic) THF 65 °C mol. sieves MT2 Master 1 0 Type here to search
Predict the Product. (5 pts each; 20 pts TOTAL) Provide the stable organic product(s) that would result for each reaction below. Label the product formed in highest yield as “major" and include stereochemistry whenever appropriate. H20 (1 equiv.) HCI (catalytic) OH THF 65°C MgBr (2 equiv) 1-hydroxybutan-2-one Et20 25 °C Br2 (1 equiv.) benzene 80 °C UV light 2. NaOH H2O - THE 50 °C PCC 3. CH2Cl2 (1 equiv.) HCI (catalytic) benzaldehyde THF 65 °C mol. sieves
OH r. Он reagent(s) Br OEt S. reagent(s) Br Он K2Cr2O7 (excess) H2SO4, H20 Он но 1. PhLi, Et O 2. HCI, H2O 3. SOCI2, EtN 4. NaOAc u. н 1. Mg (1 eq), Et2O V. Br 2. (1 eq) -сно 3. HCI, Н,О W. 1. NaBH,, MeOН, 0° С 2. PBra THF 3. LIAID4, THF 4. HCI, H20
How would this react? OH HCI (cat) THF 65 degree
B-H (1 equiv.) MT2R QZ THF 25 °C H2O2 NaOH/HO
1. NaBH4, CH3OH eo 2. HCI, H20 1. NaBH4 (1 eq.), CH3OH 2. HCI, H2O os Ο 1. NaBH(OCH3)3, (1 eq.), CH3OH 2. HCI, H2O & 1. LIAIH4 (1 eq.), THF 2. HCI, H20
PREDICT THE PRODUCTS ORGANIC CHEMISTRY!! Cl2 (1 equiv) THF تن 1. C0 2. CHI, THF 1. BHCyz, THF 2. NaOH, H2O2 HBr ( 1 eg .1 د ,( د ,CH2N2 .2 Br