Please help me with the product LOH HCI (catalytic) THF 65 °C mol. sieves MT2 Master 1 0 Type here to search
show the mechanism + H20 HCI (catalytic) THF mol. sieves 25 °C
H20 (1 equiv.) HCI (catalytic) ОН THF 65 °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?
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
How would this react? OH HCI (cat) THF 65 degree
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. _0H HCI (catalytic) THE 65 °C mol. sieves Enter Full Screen CH2ONa (1 equiv.) 3-bromo-1,1,1-trifluoroacetone CHOH 25 °C - H (1 equiv.) THF 25 °C H2O2 NaOH/HO NaCN (2 equiv.) DMSO 100 °C NO,
mark the relationship as either same, enantiomers or diastereomers ОН он 64. ОН ОН 65. ОН он нотон 66. Он CIH H.,CI CIH HCI CI, H HCI сі CICI 70. СІ CIH нсі «я» , , мур- CIH 15 CHE CH3 HCI СІН СІ Η Η. бо | т 16. Тат
mark structures as either same, enantiomers or diastrereomers ОН он 64. ОН 65. ОН он нотон 66. Он нс СІ, н 70. сі CIH нсі «я» , . •9% CIH 74. ОН Сн, несі HCI CIH CI H. е Р . CITH CHз 16. ат т CI
220 °C que Pd(PPhz), K2CO3 THF, 65 °C, 18 h Pd(PPh 3). Cul EtsN, THF, reflux Pd(PPhz)4, Cul EtsN, THF, it HETIPS (excess) Product A Product B (excess) TBAF TBAF = tetrabutylammonium fluoride Product C