Please help me with the product LOH HCI (catalytic) THF 65 °C mol. sieves MT2 Master...
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?
H20 (1 equiv.) HCI (catalytic) ОН THF 65 °C
provide the structure of the first intermediate of the mechanism
that leads to the product above
X 0 Spectroscopy Unknown Pre-tect x G 1-hydroxybutan-2-one Google + C o app.tophat.com/e/170799/assigned reanic Chemistoclecture with MMD (SD201 MT2 Mastery 4 - Image HCI (catalytic) CH3CH2OH mol. sieves 78 °C MT2 Mastery 4 Provide the structure of first intermediate of the mechanism that leads to this products? 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
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,
Please help me show the arrow
mechanism of the following reaction. thank you
CHO 1) NaH8, THF, o CHO 2 TSNN NaOAC THF H20, 80 Me o 3) DIBAL C e O Bn te) 2
CHO 1) NaH8, THF, o CHO 2 TSNN NaOAC THF H20, 80 Me o 3) DIBAL C e O Bn te) 2
can you help me with a detailed mechanism for number 7
HONOME cat. H SO, Dean-Stark trap PhBr - PhVO SOCIE HN 2 NEL 1) LDA, -78 °C CO Me 2) HPn (give a reactant and a reagent) (sterochem. can be neglected; elim. product (alkene) also okay) 1) Ph Br 2) HCIH,0 molecular sieves (dehydrating agent) OME 1) NaOME 2) Mel 3) LiOH 4) HCI (quench) 5) heat
Hi, could you please help me identify these organic chemistry
reactions throughout? Thanks!
c. H2, PIO2 MaOH OTBS a. Buli, THF b. DMP d. AcOH, H20 CH2Ch Me 50 C 20 + O Me Me MeO оме g. TPAP, NMO h. NaCIO2 e TBAF, TH OTBS 0 Me Me Nal2PO Me2C-CH(Me) Mel Me Hz0z. K2003 OTBS HIH Me Me O BocN BocN 24 25 . TMSCHN2 i TMSCI, LHMOS THF LACOH, Hz。 Me Me Me Me CH3CN 100 °C Me...