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A: As per question guidelines I have solved 5 parts.
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A: Option C) is the correct answer. Because,
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Q: What is the CORRECT product A for the following reaction? i. Mg, Et,0 Br ii. CO, iii. H,O" i. LIAH,…
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Q: Which of the following is the major product of the reaction below: OH Br. OH Br Br₂, H₂O Br major…
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Q: Identify the major product produced from this series of reactions. HO, SOCI, NH, HO HO. NH A B O 1.…
A: Option C is current option.
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A: its option - C Since trimethyl amine is a good base it will abstract the proton from carboxylic acid…
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- Fill in the blanks in the following reaction scheme. OH 1) MCPBA NaNH, 1) NaOH 2) H₂O+ 1) TMS-Cl in TEA CI OH Major Product 1)Trimethylsilyl chloride Triethylamine3C Complete the reactions below. MgBr 1. G 2. H₂O/H* OH SOCI₂/Py H (2 ισοδ) NaCECNa H₂/Pd (περίσσεια) K1. Oxazolines (five membered ring with N and O shown below) are an important functional group in organic chemistry because they can be used to help facilitate catalytic, enantioselective reactions during the synthesis of important pharmaceutical molecules. One way to make oxazolines is through the ring expansion of N-acylaziridines. Me Ph Nal Acetone Ph An N-Acylaziridine An oxazoline a. This reaction utilizes nucleophilic substitution reactions to get from the aziridine to the oxazoline. Provide a complete arrow pushing mechanism for this transformation. You do not have to draw it while talking. You can have the mechanism already drawn out and simply talk through the steps. If you choose to use ChemDraw, be sure it is very clear where your arrows are pointing. You may also draw it by hand (paper or tablet) and screenshare an image of your work while explaining what happens. You must talk through each step of your mechanism and use proper terms such as nucleophile and electrophile. b.…
- 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.Which hydrogen is removed by base in this elimination reaction? На. На На о нь Hc Hd Hb Ha Br He C Hd Hc Hd Hdfollowing reactions. a. HO b. HO OH OH NH₂ NH₂ H₂SO4 H₂O + 1. LIAIH4 2. H* workup Imine Formation trace acid
- Br OH 45°C +HO a higher temperature favors elimination + H₂O + Br 47% 53% Br OH 100 °C + HO¯ + + H₂O + Br 29% 71%Answer the following questions based on the information provided. (a) Sildenafil (Viagra) is used to treat erectile dysfunction (impotence; inability to get or keep an erection) in men. Sildenafil (Revatio) is used to improve the ability to exercise in adults with pulmonary arterial hypertension. One of the key step of Sildenafil synthesis is shown below. OEt O OEt O i) Amine HO CHO ii) H20 washing to remove the HCI residue CI N. i) What's the structure of Amine reagent? Amine structure ii) Why does not carboxyl acid react with amine? iii) Draw the mechanism of the reaction.Which choice does not produce 2-propanol? OH (2-propanol) 1) LIAIH, Et,0 2) H20 H. 1) MeMgBr. Et,O H. 2) H20 H30* NaBH, EIOH
- 2 +OH- 2 OH (route IV)Choose the most appropriate reagent(s) for the conversion of the ketone to the primary amine intermediate. OH NH2 Na Cr207 HSO4 HO reagent (s) N(CH3 H2, Pd B) NABH4, CH3CH,OH NANH2, NH3 1. LIAIH, 2. H, H20Question 2 Select an acceptable name for the compound below. N' N,N.2-tributyl-3-phenyl-1-propanone 2-benzyl-N, N-dibutylhexanamide N,N,2-tributyl-3-phenylpropanamide 2-benzyl-N,N-dibutyl-1-hexanone A Moving to another question will save this response.