5) Complete the following synthesis by filling in all of the blanks marked by the letters....
please help in all sections asap!! Provide the reagents necessary to carry out the following conversion. CCH3 Choose the correct reagents for step 1. CH3CH2Cl / AICI Cl2 / AICI Bry/ FeBry CH3CCI / AICI: Choose the correct reagents for step 2. NON CH3CH2C / AICI Cl2 / AICI Bry/FeBry o CH,CCI/ AICI Predict the major product for the following reaction. CI/AICI: ОН ОН ОН 0 none of these Provide the reagents necessary to carry out the following conversion. Choose...
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List of Reagents -N:C:N- KMnO4, H2SO4 8 00 (CH3),COCOCOC(CH3)3 Ag(NH3)2+, 120 Fe, HCI KMnO4, NaOH, H2O, cold AlCl3 Bra (excess), NaOH (excess), H20 Brz, Fe Br2, H20 Br2, H2O, H3O+ Br2, hy Br2, NaOH (excess), H2O Br2, P Buli CF3CO,H CH;=0 Formaldehyde оо CH3COCCH o CH_CC1, pyridine H2, Lindlar's catalyst H2.Pd/C H2, Pa/C, high pressure H, Raney-Ni HANNH HENNH, KOH, (HOCH2CH2)20, heat H2O H20, H2SO4,...
Part A Complete the following reaction by filling in the necessary reagents. OH он о 1. CO2, NaOH 2. HCI 1. CH2OH 2. HCI 1. KMnO4, HO 2. HCI 1. CH3COCI, AICI, 2. Zn(Hg), HCI
Please help me with this synthesis problem. Provide the structure or reagent needed to complete this synthesis. You will only use each answer once but you will NOT use all of answers. CN NH2 OH OH CN вв. c DD CUCN LOK NaCN THF, O C DMSO,.. KMnO OH cat. Oso H202 H2SO4 then H 16) O PPTS, Na(CN)BH, PPTS, Na(CN)BH 21) PBry H2SO4 FeBry SOCI mCPBA 25) MOCI MOBI NaONO HCI Mecl Swern AICI 33) MOCI NH2 AICH then...
10. Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B and then C, and then D, your answer would be: ABCD. ? CH3CI H2 HNO3 H2SO4 AICI Pd-C H2SO4 heat offen AICI A B С D E Cl2 H-Br...
Constants 1 Periodic Ta Part A Complete the following reaction by filling in the necessary reagents. OH OH 0 1. CO2, NaOH 2. HCI 1. CH3OH 2. HCI 1. KMnO4, HO 2. HCI 1. CH3COCI, AICI 2. Zn(Hg), HCI Submit Request Answer
Choose the correct reagents for each step to accomplish the following synthesis in good chemical yield. Write the letter from each box in the spaces below. Choose the correct reagents for each step to accomplish the following synthesis in good chemical yield Write the letter from each box in the spaces below CH3 Rxn 1 Rxn 2 02 Rxn 3 Rxn 4 a. NBS, hv b. HBr c. Br2, FeBr3 AICl3 AlCI3 i. HCI, Zn(Hg) CH2N2 then H3O* Rxn 1...
please help in all sections asap!! Which of the following reactions would produce isopropylbenzene as the major product? ОН AICI: H2SO4 H2SO4 AICI3 IV I all of these Predict the product for the following reaction fuming H2SO4 SO3H Predict the structure of the major product for the following reaction Which of the following compounds will not undergo nucleophilic aromatic substitution? 1-chloro-2,4-dinitrobenzene 1-bromo-4-nitrobenzene O-chloronitrobenzene m-chloronitrobenzene p-chloronitrobenzene Choose the correct sequence of reagents for the following transformation. 2) 3 . NH2 2)...
are these correct? if not, can you explain? thanks! Synthesis Reactions: Draw the major products for the following reactions (need not show any byproducts). (3 points each, 21 points) Note: For Diels-Alder reactions, be sure to show relative stereochemistry, if appropriate. atz CH3 1111 CH₂ (be sure to specify the CN product stereochemistry) CN CH2-CH₂-CH₃ SO3, H2SO4 + a. ILICN 30개 Br OCHz AICI: (show monosub. only) - CH₂ CH CH₃ OCH3 H₂ - CH₂ - CH₂ CH₂ - CH₂...
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...