In Class Assignment 11-14-2019 Complete the following assignments on your own paper. 1. Show the reaction...
Complete the following problems on your own paper. Rewrite the problem. Draw the answer to the following reactions. 1. NaCr O 1. CO2 2. Н,о. Mg Br 1. NaCN 2. H20 Br 1. LIAIH 2. H0 HO 1. Mg 2. CO2 3. Hy0 4. CH,CH2CH CH2OH, H2SOcatalytic amount) Br 1. Na2Cr O7, H2SO H20 2. SOCh 3. (CH2CH2CH22CuLi 1. SOC 2, CH,CH2OH он
Methyl vinylketone was subjected to Reaction 1, worked-up, and then Reaction 1. Following the work-up, the following NMR data was obtained. The overall molecular weight has increased by 80. Propose reagents for Reaction 1. and then Reaction 2 1 CH -2- -1- -1- 6 7 5 4 3 1 2 PPM A. H.CLI, Et20.0°C B. HCMgBr. Et 0.0°C E. Me Culi, EVO,0 °C F. MeZnCI. Et 0,25 °C C. Hz. Pd/C, ETOH, 25 °C G. NaBH. ETOH, 25 °C D....
ICA 11-21-2019 (CA Derivatives) Complete the following problems on your own paper. Rewrite the problem 1. Draw the answer to the following reactions, o Nacion 1. NaCN -Br 2 H₂O 1. LAIH 2. H,0 1. Mg 2. CO 4. CH CH CH.CH,OH, H2SO (catalytic amount) 3. HO Br 1. Na2Cr20, H SO4 H20 2. SOCI 3. (CHỊCH,CH, CALI 1. SOCI 2, CH.CH OH 0 OH
fill in the missing products or read chains for the following reaction scheme Give the IUPAC name of the following compound Indicate which letter below would be best prepared using the Williams eat her synthesis then show the starting material you would use to prepare them all kill you choose alkyl halide and alcohol 15 pes Fill in the missing products or reagents for the following reaction scheme. 1.) Hg(OA), (CH),CHOH 2.) NaBH, HB MgBr 1.) THF + 2.)1,0 Give...
80 & NH 10 OH 11 12 og NH, Reaction 7: Reaction 8: Reaction 9: Reaction 10: Reaction 11: Reaction 12: Below is a list of reagents that will be used for the following question (reactions 7-12). L. 1.CH,Br 2. Ho P. Hz, Pd M. NaBH CHOH N 1 KCN 2. LAIH 3. H20 o. Brz o OH Q. NaOH, Br S. NH T. NHS U. 1. CHgMgBr 2. HO, mild H. NaĚH CN R. 1, KCN 2. HCI 3....
2. Draw, in the provided spaces/ boxes, the major organic products of the following transformations. Be sure to indicate appropriate stereochemistry. If the reaction generates enantiomers, draw one and write tenantiomer' 1. Cl2, H20 2. NaOH На Pd/C 1.Hg(OAc)2 CH,OH 2. NABH 1. CH CO H 2. Hао* Н,с" HC @) 1. ВНа, THF 2. H202, NaOH Br2 CH2CI2 (E)-5-methylhept-3-ene MeOH conc'd H3PO4 ОН Br NAOCH3
FALL 2019 QUIZNIO 1 Draw the MAJOR organic products of each reaction and indicate stereochemistry where necessary (4 points SOCIE нанд tok OMSO HCI (2 e) 2 SYNTHESIS: How would you prepare compound 1 from cyclopentanol? You may use any other organic reagents of inorganic reagents you wish but you must start with cyclopentanol. The desired product for each reaction must be the MAJOR PRODUCT. Give the reactants, conditions (where appropriate and products of each synthetic step but NO MECHANISMS....
3. Please provide the major product for each of the following. * CHCI + KF —- H2O HCI CH+ CHOH CH30 NH + H20 HCI Cougat, » excess .COH CASCO OH 1.50C 2.2 CH NH og= HOME LO + NH, — excess + CH3OH HCI O excess 4. For each of the following, please provide the reagents: CNH2 NHCH IN OH 2. Provide the products for each of the following reactions: 1. (CH3)2Culi 2. EtOH - Å 1 CUM CULI...
1) Reactions. Provide the major product for each reaction sequence, account for stereochemistry 1) PCC, CHCI 2) Bry, acetic acid 3) KOBU, A 4) NaOEI, ETOH, P CO- 5) H30 workup 6) THF, H.COPPA HC CH2 O e .cat. Pd(OAc) cat. PPh. DMF, EIN 2) LDA, THF. -78 °C 3) Chichen H3O* workup 4) NaBH, EtOH, then H3O+ workup 5) cat. TSOH, benzaldehyde (c) L AL SUO TESTE TO 1) cat. H2SO4. A лон 2) O3, CH, Cl, then (CH),...
Could you please answer questions 2-5 2. Complete the following reactions by writing the missing reagents or products (8 points) CrO; но" PBry CH,CH,CH.CH.CH-OH 3. Find the best synthetic method for the following coverstion (8 points) (CHCHCH OH CH),CHCH,BE - S (CH, CHCH MgBr (CHỊ) CHCHACH-CO-H (CH),CHCH.CH.CH OH 4. Draw a multistep synthetic route to accomplish the following transformation (8 points) 3. Draw the structure of the starting material that would be needed in the following reactions (8 points) HOCH...