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- 5.Synthesis. Make the following products from a suitable cyclic alkene starting material. Look at the functional group PATTERN present in the molecule, including stereochemistry. CH3 ОН ОН CH3Use the E2 mechanism to explain why when I is mixed with sodium ethoxide (NaOEt) in ethanol, the major product is III, but when II is mixed with sodium ethoxide in ethanol, the major product is IV. H3C CH3 H3C CH3 ..CI CI CH3 I CH3 || H3C. CH3 H3C CH3 E ||| CH3 CH3 IV SANHelp me please
- Choose reagents to convert 2-cyclohexenone to the following compounds. Syntheses may require several steps. Use letters from the table to list reagents in the order used (first at the left). Reagents 1. Li(CH3)2Cu 2. H30* 1. Li(CeHs)2Cu 2. H30* 1. Li(CH2=CH)2Cu 2. H3O* a b. 1. NaBH, CH2l2 / Zn(Cu) / ether (CgHs)3P*-CH2 2. H,O* NH3 / KOH 1. CH3M9B / dry ether 2 H30* H2 over Pd/C H2NNH2 / KOH h HN(CH3)2 KMNO4 / H30* CH3 b) Submit Answer Try Another Verslon 1 item attempt remainingGive one example of elimination reaction (E2) type. Show the reactants materials and the product. Draw the reaction mechanism?b).. .. Under each potential product of this E2 elimination, write "major product," "minor product," or "not formed." Me Br H Me Me OH Me Ph Ph H Me H Et Me Me Me Ph Ph Me Me Et
- 1. Assign E or Z to the following alkenes. If the alkene does not have stereochemistry, write "NONE". H CI H3C SH T. H CI, ОН H3CH2C НО D D EN C(CH3)3 CH3 Me H Et N' 'N' C=C H3C Et Me what Columbus sought in the 'Indies' - Piperine CH2OH Br (H3C);C, H3C HOH, CH,CF, H3C Br HOH2C НО H the spice Columbus found (Capsaicin) HO. Muscalure Bombykol (the sex attaractant for the male silkworm) (the sex attaractant for the common housefly) OH .CO2H the "heart healthy" part of olive oil a 'less healthy' trans fatty acid from trans fat3) Draw the structures of the major organic product(s) for the following reactions. HI in CH₂Cl₂ 3 excess Cl₂ in H₂O H₂SO4 in H₂O (Two products) Br-Cl in THF 1) BH3 2) alkaline H₂O₂ OSO4 + HOOHDescribe a sequence of reactions by which 2-hexyne can be prepared from acetylene while minimizing the number of steps required. O 1. NANH2; 2. CH3CH2CH2Br; 3. NaNH2; 4. CH3B1 O 1. NANH2: 2. CH3Br; 3. CH3CH2CH2B1; O 1. NANH2; CH3Br; 3. NANH2; 4. CH3CH2CH2B O A or B O A or C
- b Use curved arrows to show the mechanism of the step below. If more than one resonance form of the product is possible, show the most stable form. Arrow-pushing Instructions ^^C↔X™ H to HI.... H3CSOCl2 (thionyl chloride) converts alcohols into alkyl chlorides. Explain How ?Q2. When (CH3CH2)3CBR is added to CH3OH at room temperature, the major product is (CH30)C(CH2CH3)3 and a minor product is CH3CH3DC(CH2CH3)2. Propose a mechanism for the product that is formed by the substitution reaction. Use curved arrows to show the movement of electrons.