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Choose correct reagent(s) for the conversion below: Benzene to Aniline NH3 A. a) HNO3 7 H2504...
Choose correct reagent(s) for the conversion below Aniline to Phenol a) H3PO2 O A. b) H307,...
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 15 Choose correct reagent(s) for the conversion below Aniline to Phenol a) NaNO2,...
organic chemistry
Question 15 Choose correct reagent(s) for the conversion below Aniline to Phenol a) NaNO2, HCI, 0°C b) H3PO2 OA. c) Cu20, Cu(NO3)2, H20 a) NaNO2, HCI, O°C b) H3PO2 ОВ. c) H307, heat a) H3PO2 O c. b) H307, heat a) NaNO2, HCI, 0°C OD. b) H307, heat a) NaNO2, HCI, 0°C b) CUBE OE. c) H307, heat
organic chemistry Question 5 Choose correct reagent(s) for the conversion below Benzene ---> Propylbenzene a) propanoyl...
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 Br ? a) propanoyl chloride with (1) AlCl3 and...
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
Choose the most appropriate reagent(s) for the conversion of 2-methyl-1-propanol to 2-methyl-1-tosyloxypropane. CH3 -CH3 reagent(s) I...
Choose the most appropriate reagent(s) for the conversion of 2-methyl-1-propanol to 2-methyl-1-tosyloxypropane. CH3 -CH3 reagent(s) I A 101, Et @ 1,80, H20 C SO3, HCI OSO E TSOH, CH,OH Next part
what would be the reagent? Part 7 out of 8 Choose the most appropriate reagent(s) for...
what would be the reagent?
Part 7 out of 8 Choose the most appropriate reagent(s) for the conversion of the cis-epoxide intermediate to the target molecule. H2, Lindar catalyst CH3CO3H OH reagent(s) HOH A H,O, H,SO H,O, HBO CH,0 D 1.03 2. CH_SCH @ H20, HCI 2 attempts left 2 atempts et Check my work Next part
What are the correct conditions? What are the steps? 02V A.) 1.) H2504, HNO3 2.) H2,...
What are the correct conditions? What are the steps?
02V A.) 1.) H2504, HNO3 2.) H2, Pd 3.) ACCI, AICI3 4.) NaNO2, HCI 5.) CuCN B.) 1.) ACCI, AICI; 2.) H2504, HNO3 3.) Hą, Pd 4.) NaNO2, HCI 5.) CuCN C.) 1.) H2SO4, HNO3 2.) ACCI, AICI; 3.) H2, Pd 4.) NaNO2, HCl 5.) CUCN D.) All of the Above E.) None of the Above
Choose the incorrect statement Aniline undergoes Friedel-Crafts reactions. OA B. Using (1) HCI, H20, heat and...
Choose the incorrect statement Aniline undergoes Friedel-Crafts reactions. OA B. Using (1) HCI, H20, heat and (2) HO-to remove (deprotect) the acetyl group back to amino group, The amino group on aniline can be protected by acetylation step. Halogenation of benzene with a strong activating substitutent does not require FeBrz. D. Friedel-Crafts acylations will not occur if there is a meta-director already on the benzene ring. E. 000 30 М.
Choose the most appropriate reagent(s) for the conversion of the amide to the amine target molecule....
Choose the most appropriate reagent(s) for the conversion of the amide to the amine target molecule. SOCI2 Ph OH Ph CI HN Ph N reagent(s) I- I- A H2, Pd B NaBH4, CH3OH © NaNH2, NHz 1. LiAIH4 2. H*, H20 E NH2NH2, KOH
o GO 34. Aryl diazonium ions are formed from anilines reacted with: A. HNO, B. HNO3,...
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...
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 15 Choose correct reagent(s) for the conversion below Aniline to Phenol a) NaNO2, HCI, 0°C b) H3PO2 OA. c) Cu20, Cu(NO3)2, H20 a) NaNO2, HCI, O°C b) H3PO2 ОВ. c) H307, heat a) H3PO2 O c. b) H307, heat a) NaNO2, HCI, 0°C OD. b) H307, heat a) NaNO2, HCI, 0°C b) CUBE OE. c) 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 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
Choose the most appropriate reagent(s) for the conversion of 2-methyl-1-propanol to 2-methyl-1-tosyloxypropane. CH3 -CH3 reagent(s) I A 101, Et @ 1,80, H20 C SO3, HCI OSO E TSOH, CH,OH Next part
what would be the reagent?
Part 7 out of 8 Choose the most appropriate reagent(s) for the conversion of the cis-epoxide intermediate to the target molecule. H2, Lindar catalyst CH3CO3H OH reagent(s) HOH A H,O, H,SO H,O, HBO CH,0 D 1.03 2. CH_SCH @ H20, HCI 2 attempts left 2 atempts et Check my work Next part
What are the correct conditions? What are the steps?
02V A.) 1.) H2504, HNO3 2.) H2, Pd 3.) ACCI, AICI3 4.) NaNO2, HCI 5.) CuCN B.) 1.) ACCI, AICI; 2.) H2504, HNO3 3.) Hą, Pd 4.) NaNO2, HCI 5.) CuCN C.) 1.) H2SO4, HNO3 2.) ACCI, AICI; 3.) H2, Pd 4.) NaNO2, HCl 5.) CUCN D.) All of the Above E.) None of the Above
Choose the incorrect statement Aniline undergoes Friedel-Crafts reactions. OA B. Using (1) HCI, H20, heat and (2) HO-to remove (deprotect) the acetyl group back to amino group, The amino group on aniline can be protected by acetylation step. Halogenation of benzene with a strong activating substitutent does not require FeBrz. D. Friedel-Crafts acylations will not occur if there is a meta-director already on the benzene ring. E. 000 30 М.
Choose the most appropriate reagent(s) for the conversion of the amide to the amine target molecule. SOCI2 Ph OH Ph CI HN Ph N reagent(s) I- I- A H2, Pd B NaBH4, CH3OH © NaNH2, NHz 1. LiAIH4 2. H*, H20 E NH2NH2, KOH
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...
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