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- H₂N NH NH₂ COOH Arginine O A, B- heterocyclic aromatic amines, C - 1° aliphatic amine OA - 1º aliphatic amine, B - 2º aliphatic amine, C - 1° aliphatic amine A - 2º aromatic amine, B - heterocyclic aromatic amine, C - 3° aliphatic amine A - 3º aromatic amine, B - heterocyclic aromatic amine, C - 1° aliphatic amine O A - 3º aliphatic amine, B - heterocyclic aromatic amine, C - 1° aliphatic amine1) Listen 4 Select the two molecules that could be used to make the imine shown, JDHDMC Select 2 correct answer(s) H2N. HN H2NChoose the set of letters corresponding to the BEST answer. WXY can be produced from cyclopentanamine and CH31 most basic amine most H₂O-soluble least basic amine -NH₂ ZAB CDE [Choose ] [Choose ] [Choose ] [Choose ] FGH -NH₂ IJK
- Draw the organic product(s) for each of the following reactions. If there is more than one product likely indicate the major. Be sure and show any stereochemistry.The following three derivatives of succinimide are anticonvulsants and have found use in the treatment of epilepsy, particularly petit mal seizures. Ph Ph `N' `N' ČH3 ČH3 Methsuximide Ethosuximide Phensuximide Following is a synthesis of phensuximide. CN Ph CN Ph CN 1. NaOH, H2O 2. HC, Н20 NaOEt KCN Ph-CHO cOOEt H cOOEt NC COOEt 3. Нeat Ethyl cyanoacetate (A) (B) Benzaldehyde Ph Ph Ph CH;NH2 НООС СООН Et0oC COOEt `N' (C) (D) ČH3 Phensuximide Methsuximide is formed by a similar pathway to that shown for phensuximide. Draw the structure of the compound that reacts with ethyl cyanoacetate in the synthesis of methsuximide.eq Teq Oran Classify each of the following amines as primary, secondary or tertiary. CH₂CH3 CH₂CH₂NCH₂CH3 CH3 CH3CHNCH3 CH3 ₂₂ CH3 Submit Answer Retry Entire Group 11: 5 more group attempts remaining this question. ENG 9:53 6/2/20
- The following amine is a amine. NH2 CHCH-CH-CH, O tertiary O quaternary O primary O secondary No new datta to save Last checke DELL OFWhich are viable ways to prepare the amine shown? || H NH + N ZI N NaBH3CN NaBH3CN A. Method I only B. Method II only C. Both methods are viable. D. Neither method is viable.3. If the compound shown is subjected to reaction conditions that will hydrolyze amides one of two products shown will form faster. Which one, A or B? Explain your choice. * for H H3N. HCI -ОН + 'N H2 H20 A B
- An imine is hydrolyzed under acidic conditions. NH H20 + NH3 (18-20) Draw the complete mechanism for the hydrolysis reaction above.Draw the products formed when each of the amides is treated with water and HCl. H HCI H₂O Reaction A Select Draw Templates More Erase C 0 N H clWhich of the following is a secondary amide? A B A NH₂ RÅN-CH₂ Cannot be determined B Å R .: CH3 CH3 C