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organic chemistry Question 15 Choose correct reagent(s) for the conversion below Aniline to Phenol a) NaNO2,...
Choose correct reagent(s) for the conversion below Aniline to Phenol a) H3PO2 O A. b) H307, heat a) NaNO2, HCI, 0°C b) CuBr B. c) H307, heat a) NaNO2, HCI, 0°C b) H3PO2 0 H30. heat a) NaNO2. HCI, 0°C b) H3PO2 D. c) Cuzo, Cu(NO3)2, H20 a) NaNO2. HCI, 0°C E b) H307 heat
organic chemistry Question 5 Choose correct reagent(s) for the conversion below Benzene ---> Propylbenzene a) propanoyl chloride with (1) AlCl3 and (2) H20 ОА. b) H2NNH2, HO", heat a) propyl chloride / AlCl3 OB. b) H2, Pd/C oc. (propyl)2CULI OD. bromopropane / AlBr3 OE. chloropropane / AlCl3
Choose correct reagent(s) for the conversion below: Benzene to Aniline NH3 A. a) HNO3 7 H2504 B. b) Sn/HCI a) NH2 / HO, H20 OC. b) HCI D.NH2/0H a) NO 2, OH E. b) HCI 30 d
provide the reagents necessary to carry out the following conversion. Testbank, Question 095 Provide the reagents necessary to carry out the following conversion. OOH NH2 Br Br Choose the correct reagents for step 1. xs Br2 / FeBr3 NaNO2/ HCI / < 5°C OH3PO2 KMnO4/ NaOH / H20 CH3CI / AICI: Huden/shared/assignment/test/aalistiuni?idmasnmt2593399 #N10170 Choose the correct reagents for step 2. NaNO2 / HCI / < 5°C xs Br2 / FeBr3 H3PO2 O KMnO4 / NaOH / H2O CH3CI / AICI:...
Choose correct reagent(s) for the conversion below Br ? a) propanoyl chloride with (1) AlCl3 and (2) H20 b) NBS a) propanoyl chloride with (1) AlCl3 and (2) H20 B. b) Br2 / heat or light a) propyl bromide / AlCl3 с. b) Br2/ heat or light a) Br2 / FeBr3 b) (propyD2Cuu c) Br2 / light or heat E a) propyl bromide / AICI: b) NBS MacBook Air
organic chemistry Question 6 Choose the final, major product for the following reactions. cyclohexanol reacts with: a) PC13/ pyridine b) гон c) HBr / heat d) tert-butoxide e) BH3 / THE f) OH, H202, H20 1. bromocyclohexanol O2. cyclohexane 3. cyclohexene 4. cyclohexanol
help! chemistry predict the products and mechanism! the Product. Provide the stable organic product(s) for the reactions below. predict the Pro 1. Mgº, CH,CH,OCH,CH 2. CO (9) 3. H,O, HCI MgBr (X) 2. H,0,HCI 1. K Cr2O, H,SO, H,0 2. CH, MgBr (1 eq.) 3. H2O, HCI 1. Mgº, CH,CH,OCHCH 2. H20, HCI echanism. The following Grignard reaction has been observed to yield products A and B. MgCI THF-70 C 2. HCI, H20 0. Org. Chem. 1980, 45, 4952-4954. https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b01430)...
organic chemistry Question 17 Choose the correct name Br O2N OA. 1-bromo-2-cyclohexyl-5-nitrobenzene O B. o-bromo-cyclohexyl-p-bromo-nitro benzene 2-bromo-1-cyclohexyl-4-nitrobenzene Op. 1-cyclohexyl-2-bromo-4-nitrobenzene 3-bromo-5-cyclohexylbenzenenitro O E.
QUESTION 9 Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially. A. Ph3PMeBr, KotBu, PhMe, 25 °C B. CuBr, 0 °C C. Cu20, Cu(NO3)2, H20, 0 °C D. CuCN, 0 °C E. SO3, H2SO4, 100 °C F. Cl2, FeCl3, THF, 65 °C G. Br2, FeBr3,...
Part 9 out of 11 6 Choose the most appropriate reagent(s) for the conversion of 1-butanol to butanal. PCC CH2Cl2 points COH Cl2 FeCl3 OH reagent(s) Trayers) points A NaOH,H,O, heat B PCC, CH.CH C 1.0 ) LAIH, diethyl ether 2. S(CH) e Na Cr»0», H,804, H,0 13 Design a synthesis of 2-cyclohexenone from 2-methylcyclopentanone. points Part 1: Choose the best option for the precursor to the target molecule. i i Part 2 out of 10 Choose the best option...