We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
Please write neatly. 3. Show the products formed in the tollowing reactions draw two enols 1) Mg. Et O 2) CO2 3) H:O NHz Jo .OTo. 쁘. pyridne CI NH Ci CI 0 SOCl OH heat NH 1) CH3MgBr excess CH, CH, -OCH,C 2) H2O COOMe LIAIH OH Ci 0 3. Show the products formed in the tollowing reactions draw two enols 1) Mg. Et O 2) CO2 3) H:O NHz Jo .OTo. 쁘. pyridne CI NH Ci CI 0...
predict the product please!!!!! H₂SO4 HO a) 5) c) d) NHL Но OH NHz OH H₂ Sou a) NOH C) WOH (D) 1, CME CH, OH cone mel equivalent 2. Hot @ b) via vien HU d) HO c) OH H OM DH 1) NaOH 2) b) c) +H2O +NaBr hal D) +thorNaBr +120 + Na Br 120 + No Br is CA che con lans all ole ola "OʻNG
Draw the arrows for the 7-step mechanism in formation of the mixed acetal shown. Map CH,OH OH mi # + HO ht Mixed ACETAL HEMIACETAL click to edit H. 0 Step он H Step w HỘ One H Two HⓇ H H 16 Step 3. Step HÖCH3 Step + H H Five Four Step 6 Draw the arrows for the 7-step mechanism for hydrolysis of an acetal to a carbonyl. Map . H2O Hö: H,O L; E i + CH,CH,OH...
COLUMNA 0 NO2 19 COLUMN B O + OH OH A) HAN AICI: 1) ch 2 BHA 3) H,09 B) YN B 1) My C) ОН 2) 2)CO2 3) H30 4) CH3OH D) 3) E) 0 OH H 1)DBAL-H 2)Ph PCH2 3) mCPBA 1) SOCI2 2CH.NH. pyridine 3) excess LAHA 4)H,0* F) 0 O 4) OH o G) excess HB H) 5) 1) 6) H30* Δ. Mglk J) 7) OH 0 2 1,0 hp question completion Status: Н. 6) Н...
Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: OH SOCI2 pyridine M + SO2 + HCI + 802 + HCI Part 1 out of 3 HO H a + O HO осі" O HOCI O SO2 OHCI НОСІ finish structure ... draw structure ... HCI 3 attempts left Check my work Next part
1. SOCI2 2. CH3NH2 3. LiAIHA 4. H20* O glo OH O H Br
what would the mechanism be for these NH2 NaB (CN) Hz CH,OH solvent OCH3 Reductive I-2 NaB (CN) HZ H2N CH,OH solvent
ta 2.0 L. O .O. HC-CC- 24 d. HC OH 1 2 CH,CHỊU. 2.H,0 c. CH CH 1. SOCH OH 2. LIAHOT-Bus CH,CHE 1. SOCI OH 2 CH CHO Php C ake h. CH CH, NaBH CH,CH, OH 1. AH,THE 2 HOHO I CHOCHEM 1. CH CH CH.CH 3. SO.
1. NBS 2. Mg, ether 3. 4. H2Cr04 5. SOCI2 6. CH CH OH Work out the synthesis on a separate sheet of paper, and then draw the structure of the final organic product. The 'H- and 'SC-NMR spectra for an unknown compound with molecular formula C H1402 are shown below. Deduce a structural formula for this compound. 1H-NMR 13 C-NMR 0.92 (d, 6H) 1.52 (m, 2H) 1.70 (m, 1H) 2.09 (s, 3H) 4.10 (t, 2H) 171.15 63.12 37.31 25.05...
6. CH3 Br CCI 7. CH3 Br CH, OH 8. CHE 1. MCPBA 2. CH,OH, H* 9. CH Oso,,H,O, 10. Na, NH 0