Which of the following sequences of reactions (from those shown below) would yield the desired product...
Draw the major product for the following reactions. -OH 2. Draw the major product for the following reactions. 1) TSCI 2) NaOEt, Heat 3) O; 4) DMS 1) NBS, heat (I cq.) 2) NaNH, DMSO 3) KMnO4 (aq) NaOH, cold 4) NaOCI, acetic acid 1) O 2) H,0 3)NI, H, 150, 100 atm 1) RBH 2) H.O, NaOH 3) NBS, heat (I eq) 1) KMnO heat 2) Na, NH, CH OH 3) Bry, light (I eq) 1) NBS, light 2)...
Provide the major product(s) for the following reactions: Show Stereochemistry when necessary (9 points total) HBr (1 equivalent) HBr (2 equivalents) Br2 Brz (1 equivalent) CH,CI, (2 equivalents) CH,CI, HO 1) disyamylborane HgSo., H2SO4 2) H0, NaOH, H2O Bonus: Provide the major product(s) for the following reactions: Show Stereochemistry when necessary (4 points total) 1) NaNH, (1) NaNH, 2) (CH),CHCH,Br 2) (CH),CHCH,Br 3) H, 3) L, NH, Lindlar's catalyst 1) NaNH, 2) EtBr 3) Hz, Pd/C 1) NaNH, 2) EtBr...
What is the correct sequence of reactions that can achieve the following multistep transformation? List in the correct order. (No spaces nor commas in between letters) eg: GAKJO ☺ > REAGENTS A Br2 B TosCl, pyr CHOH SO, cat DO Na 1 MeBr 2. EtBr 3. NaNH 1 eq E 1. OsO4 2. NaHSO3 F NaNHExcess GHO H NBS, hv I HBr ROOR L HBr M NaOtBu N NaOEt O NaoMe PETOH, H+ Cat Q NaCN RH, Lindlar's SH, Pt...
4. Draw the structures of the compounds formed in the following synthetic schemes. Br2 (CH3)2CHCH2CH3 UV NaOEt HBr C ROOR 1. Br2 E KOTBU ETOH 2. NaNH2(xs) 3. Нао light a. OH CHCH3 TsCl -сHа HBr B ROOR Кови A На C NaCECH 1. BH E 2. H2O2 NaOH F base Lindlars catalyst b. Br NaOMe HBr A ROOR 1. Br2 с 2. NANH2(xs) 3. H2O KOtBu В (CH3)2CCH2CH3 D MeOH с. Br2 NaOMe HBr c NaC CHD На (CH3)3CH...
For each of the following reactions, provide the product with proper stereochemistry if applicable. In addition, draw the arrow-pushing mechanism for the reaction. 1. CH HCI 2. CH HBr ROOR 3. CH, Н,0 H, SO 4. CH3 1. Hg(OA), 2. NaBH + 5. CH, 1. BH, THF 2. HO, NaOH
what is the correct sequence of reactions that can acheieve the followong multipstep transformation. please list the correct order (no spaces nor commas in between letter) eg: GAKJO. please use words and illustrations to fully explain. Synthesis 2 Answered What is the correct sequence of reactions that can achieve the following multistep transformation? List in the correct order. (No spaces nor commas in between letters) eg: GAKJO BMIDW Incorrect CHONSO DI MERAH, El.OO.2. SO QUIN RH, Lda SHP TIO, DES...
Question 23 Predict the final product for the series of reactions shown below. 1. Bra, H2O 2. Nah ?? 3. CH 0 con Cloon Question 24 Predict the final product for the two reaction sequence shown below. 1. HBr ~ 2. OC(CH). n 2. 0-C(CH3)3, 22 Ocichols Question 25 Which of the structures below contain an E-alkene? (choose all correct answers) Br HO 0 Br
1. PREDICT THE PRODUCT: Provide the structure of the major product expected from the following reactions or reaction sequences. Make sure you account for any regio- and/or stereochemistry! (24 pts.) H2O 1. Hg(OAC), CH, OH 2. NaBH H2SO4 H20 1) BH-THF 2) H202, KOH HBr Bry, H2O HBr ROOR 1. BH3-THF 2. H2O2, NaOH H20, H2SO4 1. NaNH2 H2 H-CEC-CH2 CH2 CH3 2. CH CH Br Lindlar cat 1. Sia BH-THF 2. H2O2, H2O
Specify the reagent you would use in each step of the following synthesis: step 1 step 2 step 2 Reagents Available a. LIAIHA f. PBr3 b. H2SO4 c. HCI d. HBO e. SOC2 k. CH3CH MgBr g. Dess-Martin periodinane (DMP) I. CH.MgBr (phenylmagnesium bromide) h. Nah m. (CH3)2CHMgBr 1. NaOH n. Croz J. CH3MgBr Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2 Submit Answer Retry Entire Group 9 more group...
Propose an efficient synthesis for the transformation below. Enter the appropriate number of letter from the reagent list handout Step 1 Step 2 Step 3 OH Alkyl Halides (X = CI, Br or 1) and Acyl chlorides: Assume Allig 15 present, if needed CIP CU CH3X X CI E A B EE Ketones. Aldehydes and Epoxides: Assume "then H20" is included if a protonation step is needed F A A K 0 MN Р Grignard, Wittig and Organocuprate Reagents: Assume...