Can you Show and Explain the Mechanism for a Kiliani-Fisher Synthesis D-Gly ceraldehycle Hi 1H lH OH 0 H 0-(-)-Ery throse D-Gly ceraldehycle Hi 1H lH OH 0 H 0-(-)-Ery throse
7. Show the mechanism for the following Acid Catalyzed Fisher Esterification | H obrang OH НО- H20
Hi Can you guys show the detailed mechanism and explanation please. Thanks in advance. TBHP R OD OH VO(acac), or
hi would someone please explain the mechanism behind this 2. What is the product after all the steps show below? 1. Br,/H,0 1. NaCN 2. NaH 2. NH4Cl (aq) OH CN OH + enantiomer + enantiomer + enantiomer + enantiomer
Jacobsen's Ligand/Catalyst Mechanism Can I get help with a detailed mechanism for synthesis of the Jacobsen's ligand and it's formation of the Jacobsen's catalyst о он " Y YH 2 equiv K2CO3/Abs EtOH EN NE V HN NH3 Ⓡocco, HO OH reflux, 40 min I C002 reflux, ao min toon hot -OH HO! V Ho- 1. Mn(OA).4H 0 Air, Ethanol, Reflux,-1h 2. LICI, Reflux, 30 min OH HO
7. Show a detailed step-wise mechanism for the following reaction. H,OH,O+ 0 HẠCHẮC CN. (excess) H,CHC OH NH4+
Organic Chemistry question partial step of a synthesis. Can someone explain the mechanism? Thank you. c) NaOH, H2O O O HCI, H20 d) Heat cyclobutyl methyl ketone
Hi can someone show me the mechanism of A for enol/keto reaction of an alkyne? I'm having trouble visualizing where the elements are added to the triple bond or how it breaks down to a double bond. 11.14 Reaction with H,O, H,SO, and H3SO, adds the oxygen to the more substituted carbon. Reaction with [1] R,BH, [2] H,O2, OH adds the oxygen to the less substituted carbon Н2о Forms a ketone. H20 is added with the O atom on the...
can you show me the mechanism and the products. thank you 1 eq HSO, OH + NH, heat NaOH ОН ОН heat TEA
can you please explain these reactions BH3/THE H₂O2 OH HD Peroxide +H Br
Show FULL arrow pushing mechanism for this reaction, and explain it step by step. Reagent used was c) K2CO3, MeOH, room temp., 1 h (quant.). (please disregard BOTH arrows on s11, as this only one step of a multi-step synthesis) Label all chiral centers on s12 and draw its enantiomer ОН OH C Y і 0 (97 : 3) Л s11 Л s12