Be sure to answer all parts. Synthesize the following compound from benzene. Use a diazonium salt...
Be sure to answer all parts. Devise a synthesis of the following compound from benzene. You may use any other organic or inorganic reagents. Draw the intermediates and select the correct reagent for each step of the reaction sequence. HO Br Br2, FeBr3 PBr HBr NaBr draw structure NaNO, HCI; [2] HBF HNO3, H,SO ) NaNO, HCI; [2] H2O draw structure. NANO, HCI; [2] HBF HNO3, H,SO J NaNO;, HCI; [2] H,O NO; draw structure H.O HgSO2, H,0 I DIBAL-H;...
o GO 34. Aryl diazonium ions are formed from anilines reacted with: A. HNO, B. HNO3, H2SO4 C. H2NNH, KOH D. NaNO, HCI 35. Starting with phthalic anhydride, which other reagents are needed for the Gabriel amine synthesis?: ? A. NH3, A/KOH, 1-pentyl-Br /H2NNH2 NH2 B. KOH, NH3 /LDA, 1-pentanol /NaOH C. NBS, Br, A/HCI, pentanamide / NaNO2, HCI D. NH3, HCI / NaH, 1-penty-CI/ KCN 36. Select the final product for the multi-step sequence indicated below: NHACCI EICI NaNO2...
Be sure to answer all parts. Draw the epoxide and organometallic reagent needed to synthesize the following alcohol. Indicate stereochemistry where appropriate. CH, OH Epoxide: edit structure ... Organometallic reagent: edit structure ...
51. Make the following compound from the starting reagent. Show all the steps, reagents involved and the intermediate products. a. 7 بل mynd OH b. Synthesize the following molecule from benzene via a diazonium salt. Show all the reagents and the intermediate products. COOH OH c. Synthesize the following amine from the given alkyl halide in good yield. Show all the intermediates and reagents. CHE
Be sure to answer all parts. What reagents are needed to convert acetophenone (CH,COCH3) into the following compound? More than one step is required. NHCH,CH,CH.CH CE Part 1 out of 2 draw structure Select the correct reagent X. O Br2 O Br2, CH,COOH 2 attempts left Check my work Next part
Be sure to answer all parts. What reagents are needed to convert acetophenone (CH,COCH3) into the following compound? More than one step is required. NHCH,CH,CH.CH CE Part 1 out of 2 draw structure Select the correct reagent X. O Br2 O Br2, CH,COOH 2 attempts left Check my work Next part
Select the reagents you would use to synthesize the compound below from benzene. (More than one step is required. If no third step is needed, choose (none).) Reagents Available f. KMnO4, H20 g. H2, Pd/C h. SO3, H2SO4 i. NaOH, H2O a. Br2, FeBr3 b. Cl2, FeCl 0 d. CH3CI, AICl3 Br e. CH3COCI, AICl3 N-bromosuccinimide (NBS) ball & stick labels Step 1: Step 2 Step 3
Hi, if you can answer all of the following questions, I will definitely thumbs up! 1. For the above picture, E is incorrect (the double bond w/ NH). Please select the correct option and also write the rest of the synthesis with reagents. 2. I put just Fe, HCl and it marked it wrong. I'm not sure if Fe, HCl is wrong or if there is just another answer I also need to select. Please select which reagent/reagents are correct!...
Homework 9: Alpha Be sure to answer all parts. Report Synthesize (2)-hept-5-en-2-one from ethyl acetoacetate (CH,COCH Co,Et) and the given starting material. Sol Br Guided (z)-hept-5-en-2-one Draw four organic reaction intermediates, and seleet the single best set of reaction steps. reagents for each of CHCoCH2CO2Et [1] NaOEt, [2] HC-CCH2Br [1 HCL, [21 HC CCH2Br O I1 Mg, 12] HC CCH2Br draw structure 0 H2 (2 equiv), Pd-C H2 (2 equiv), Pd c mCPBA H,SO4 11,0+,a HOCH CH,OH, TSOH LIAIH KMno,...
DOME 4. What will be the best way to synthesize the following compound starting from benzene? the o ů na A. 1) CH3CH2CI, AICI3; 2) Cl2, FeCl3 B. 1) CH2=CH2, HF; 2) Cl2, FeCl3; ovods and to none C. 1) CH3CO-O-COCH3, AICI3; 2) Cl2, FeCl3; 3) Zn, HCI; D. 1) CH3CO-O-COCH3, AICI3; 2) Zn, HCI; 3) Cl2, FeCl3; E. none of the above EVE. none droedsw abruogo Oriollot to 8 Smund og tengsmont to 5. What set of reagents will...