5. Show how the following compound can be synthesized from Benzene (may require 2-3 steps) 5....
5. Determine the order of reagents to transform benzene to the product shown. Choose one: A. CH.COCI, AICI.; LiAlH.; CH.CH COCI, AICI B. CH.COCI, AICI.; HCI, Zn(Hg); CH.CH.COCI, AICI, C. CH.CH.CI, AICI.; CH.CH.COCI, AICI: D. CH.CH COCI, AICI.; CH.COCI, AICI; ► HCI, Zn(Hg) E. CH.CH.COCI, AICI; CH.CH.CI, AICI: 6. Determine the product for each step in the following synthetic sequence: HNO, H,SO2 Step 1 Bry FeBry Step 2 H CI, Fe Step 3
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...
show how the following compound can be synthesized from Benzene (may require 2-3 steps) c) c) L
How many siginals in 13 C-NMR spectrum are expected from this compound? tay 10 5 8 11 ود 1) (CH3)2Culi 2) H30 What is the major product of the reaction? را O OH C ОН HNO, H2SO4 CH BINOZ Which of the following is the correct intermediate for the above reaction? Br 28 NOZ Br NO2 Br NOZ BI NO CH3 Br -& NO2 What is the best method to synthesize the above compound? Brz HNO3 CH3CI FeBra Haso. AICI:...
show how the following compound could be synthesized from benzene.. p-methylbenzonitre m-chlorobenzaldehyde m-methylnitrobenzene Review Constants CH, CH, AICI CHE HNO H2SO4 ON CH CO, HAI AICICUCI high pressure HAN CH, Ha Parc ON NEC CH NaNO, HI 0°C NEN CUCEN СТ NEN m-Chlorobenzaldehyde Complete the scheme by dragging the labels to the appropriate targets. Note: not all labels will be used. CO, HCI AICI/Cuci high pressure Cl2 Focis CHCI AICI Сн, CH m-Methylnitrobenzene Complete the scheme by dragging the labels...
15.-19. Starting with benzene, match each sequence of reagents (separated by commas) to a major product. Answers may be repeated. Assume any necessary workup. 15 AICI, Bro/FeBr Br 16. 6 /AlCI3, Zn/HC, HNO3/H2S04, H2/Pd, NaNO2/HCI/O C, CuBr b. /AlCl3, Br2/FeBr3, N2Ha/KOH/heat C. Br Br 18. /AlCl3, HS(CH2)2SH/H+, H2/Ni, H2S04, Br2/FeBr3, H2O/heat d. 19. /AICls, HNO:/H S04, H2/Pd, Bra/FeBr3, NaNO/HCI/o'C, H3PO2 e.not a.-d
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)...
please help in all sections!! Provide the reagents necessary to carry out the following conversion. Choose the correct reagents for step 1. AICI AICI CI CH3CI/ AICI3 CH3CI/ FeCl Choose the correct reagents for step 2 Zn(Hg), HCI A Zn(Hg), H2SO Zn, HCI A Mg(Hg), HCI A Predict the major product for the following reaction. B Feble 11 11 IV V E2 > Identify the electrophile in the bromination of benzene. Br Br2 Br-Br-Fe-Br Br FeBr2 FeBr3 Br 11 11...
10. How can p-aminobenzoic acid (a sunscreen) be synthesized from benzene? (Note that sometimes more than one isomer will be obtained, which is fine as long as the desired isomer is one of the major products.) several steps HOOC NH2 A)) 1.CH3CI, AİCİ3 3.KMnO4 . CH CI, AICl 4.KMnO 4. Sn, HCI 2. IINO, H2SO4 )1. HNO3, H2SO4 2. Sn, HCI C) 1. HNO, HSO42. CHCI, AIC D) 1. CHCl, AlCl KMO 4.KMnO 4. Sn, HCI 3. Sn, HCI 3....
Practice Problem 22.68b Starting with benzene, show how you would prepare the following compound: NH2 NH2 cl 1) HNO3, H2SO4 2)? Compound A Cla 3)? 4) ? 5) H30* Choose from the following list of reagents: A B с D Fe, H3O+ CuCN LDA H30+ E F G H NaOH, heat NaOEt/EtOH H20 HCI, Zn[Hg), heat J K L CO2 NaNH2, NH3 [H] NaBH3CN NaNO2 HCI