Paragraph Predict the main product of each of the following reactions: CH;CH2OH (a) 1-bromopropane + NaOCH2CH3; CH3OH (b) 2-bromo-2-methylbutane + NaOCH3
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- Amantadine is effective in preventing infections caused by the influenza A virus and in treating established illnesses. It is thought to block a late stage in the assembly of the virus. Amantadine is synthesized by treating 1-bromoadamantane with acetonitrile in sulfuric acid to give N-adamantylacetamide, which is then converted to amantadine. CH,C=N in H,SO, Br NHCCH3 NH2 1-Bromoadamantane Amantadine (a) Propose a mechanism for the transformation in Step 1. (b) Describe experimental conditions to bring about Step 2.но на но Ex099 Which of the following is the product(s) of the following reaction? (1) NaBH, -? (2) H₂O* CH₂R (A)RCH₂CO₂H (B)RCH₂CHO (C)RCH₂CH₂OH (D)RCH₂CH₂NH₂ (E)no answer Ans: (B) Dy to E) A Ex003 WH A) 3860What is the expected major product for the following reaction sequence? OH OH + enantiometr 01 00 0 || OIV OV OsO4 (cat.) NMO 애 OH + enantiomer 11 OH + enantiomer ||| IV مة HO OH
- 1 D D eq M eq [References] Draw a structural formula for the major organic product of the reaction shown below. &. (02)00 CH₂ CuLi CH3CH₂0 2 ether • You do not have to consider stereochemistry. + ? H30+10 ll atit VPN * +964 771 368 9066 قبل ۲۰ دقيقة rcise 23-6 it Yourself ormulate a mechanism for the following reaction. 1. CH,CH-O-Na*, CH,CH OH 2. H, HO co.CH,CH3 + CH,CO,CH,CH3 -Co.CH,CH, COOCH2CH3 Diethyl 1,2-benzenedicarboxylate (Diethyl phthalate) 60-80%Nitriles, R–=C≡N, undergo a hydrolysis reaction when heated with aqueous acid. What is the structure of the compound produced by hydrolysis of propanenitrile, CH3CH2C≡N, if it has IR absorptions from 2500–3100 cm-1 and at 1710 cm-1, and has M+=74?
- Naturally occurring compounds called terpenoids, which we'll discuss in Section 27-5, are biosynthesized by a pathway that involves loss of CO2 from 3-phosphomevalonate 5-diphosphate to yield isopentenyl diphosphate. Use curved arrows to show the mechanism of this reaction.Acidcatalyzed dehydration of 3hydroxy3phenylcyclohexanone leads to an unsaturated ketone. What possible structures are there for the product? At what position in the ER spectrum would you expect each to absorb? If the actual product has an absorption at 1670 cm-1, what is its structure?When pent-1-ene is treated with mercury(II) acetate in methanol and the resulting product is reacted with NaBH4, what is the primary organic compound which results? 1-ethoxypentane 1-methoxypentane 3-ethoxypentane 2-ethoxypentane 2-methoxypentane
- My C mentProblemID=192850292 A&P II Mast o ethyl butanoate ▼ PSY Connect Part A Pears Bb 1574 b Ansv G great H₂C NN Course Home pt My [ chem in career H 12D EXP CONT Predict the major organic product formed when the compound shown below undergoes a reaction with LiAlH4. Interactive 3D display mode CH3 Chen Chen Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Ter * I ο phys G phys N Olo CI H3C H3C 07 ↔X + :0: OH Dimethylaminopyridine (DMAP) is often used as a catalyst in esterification reactions. A basic solvent such as triethylamine is used to react with the liberated proton from the alcohol group. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions CI NMe₂ N(CH₂CH3)3 CH3 6--10-- NMe2Identify the major organic product of the following reactions: а) - OH H30* Нeat b) || CH3—с-о-он c) 1, NABH4 2. H30*