can you show me how each reagent affects the starting material to get the product ОН...
can you please show how eaxh reagent affects the starting material to get to the product 1. EtMgBr, Et20 2. HBO NH a) NaOH b) 1-bromopropane c) HCI, H2O, A d) NaOH, H20 H₂N ONa ONa 1. DIBAL-H, -78 °C ОMe Et 2. MeOH, HCI Оме
can you show me how each reagent affects the starting material , I undertand that the NaCN,DMF adds the CN where the br is at but dont understand what the H2so4 ,h20 does Meo Meo YB 1) NaCN, DMF 2) H2SO4, H2O, A. Meo ОMe
can you please draw how each of these reagents affects the starting material for both these questions OET ОН с 1. 1,2-ethanediol, HCI 2. EtMgBr (xs), Et,0 3. HCI, НО него. от LiAIH, ло, . - НО. ОН
Devise a 3-step synthesis of the product from the starting material shown. 1. reagent 1 2.reagent 2 3. reagent 3 Select reagent 1: Select reagent 2: HOCH,CH,OH, cal. H CH,CHỌ, cai. HÀ KMnO H.Pd NaOH 0,H,O, Zn NaBH, LAH LAIH CH,CH,OH,H,O, neat Select reagent 3: H.Pd H,O, H, NaBH KMnO, NAOH In line Wrap textBreak text
Complete the reactions by giving what is missing. This can be either the starting material, reagent(s) or product. 1. Br, FeBrz 2.Mg 3. CO 4.H20 HRYY ort 1. Mg 2. O 3. HO 4. K CrO, H2SO4 5. Ph3PCH 1. m-CPBA 2. CHỊCH MgBr 3. H2O
Can someone help me solve these box questions? 01-Fill in the boxes with the product of the following reactions. Draw only the predominate regioisomer and indicate the stereochemistry where appropriate. If a racemic mixture is formed. you may indicate this using a wavy line or mark the chiral center with an asterisk (*), and write racemic in the box. RT 1) Н,CrO, 2) SOCI OH но 3) MeOH NH он H2Cro OMe Ан,сго, OH 1) NaOH 2) Мео Br OMe...
19. (Spts total) Match the reagents with the product if the starting material is: Reagent Product Br Br, HO I) RCO H 2) H,O Br он КМпО. NaOH, cold HBr, ROOR A X Он ) Hg(OAc)p.H;O X2) NaBH Br 1) BHy THF 2) H2O2, NaOH "Вг F. он Н.Pt "Вг G. он ) O 2) DMS "ОН Он HBr X OH Br2
012- Synthesis question A-L. Show how the starting material can be converted to the product through any of the reactions you have learned in O.Chem-I and O.Chem-I1. Show all the reagents you need and indicate the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism question, only the reactions. If a racemic mixture is formed indicate the chiral center/s with an ASTERISK( and write racemic next to the structure. All carbon atoms should come...
How do you get salbutamol as a product from 2-Butene as a starting material? Show the synthesis and explain each reaction.
4. Complete the reactions below by supplying the reactant, reagent or product. (*pts each OH b H,0,HCI Heat O it CI d. (excess) 1. LAIH 2. H2O -CHCH PPh; 3 Name: f. 1. CHACHIMBI 2. H,0 1. LAIH 2. HO h. CuLi(CH 3)2 i. 1. LDA (1 equiv) 2. CHỊCH,C 5