Which is the most efficient synthesis of (Z)-3-hexene? n-BuLi HC=CH n-BuLi Br H2, Lindlar n-BuLi n-BuLi Br Na, NH3 HC=CH n-BuLi HCỊCH Bri n-BuLi H2, Lindlar n-BuLi HC=CH H₂, Lindlar n-BuLi Br
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- Which stereoisomer of 3,4-dimethyl-3-hexene forms (3S,4S)-3,4-dimethylhexane and (3R,4R)-3,4-dimethylhexane when it reacts with H2, Pd/C?The expected product from the addition of HCl to CH3–CH2–CH=CH2 is? CH3-CH2-CH2-CH2CI CH3-CH2-CHCI-CH3 CH3-CHCI-CH=CH2 CH3-CH2-CCI=CH2Draw the alkene that would react with the reagent given to account for the product formed. ? + + H₂O **** H₂S04 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. CH3 CH3 CHCCH3 | | OH CH3 +1
- 8. Determine the product of the reaction. CH3-CH-CH-OH + HCI ČH3 a) CH,-CH-CH3 b) CH;-CH-CH3 CI CH3 CI c) CH3-C-CH2-OH d) CH3-CH-CH;-CI CH3Which represents an efficient synthetic route to go from an alkane to an alkene? O elimination with NaNH2, followed by a water workup O anti-Markovnikov hydrohalogenation, followed by elimination O radical bromination, followed by elimination O hydration, followed by elimination O hydration, followed by ozonolysis of the double bondDraw the major organic product(s) for the following reactions, including stereochemistry when appropriate
- What are the reagents used to convert 2-butyne to C4H8? What are the products when that C4H8 is mixed with OsO4, and H2O (the formula will be C4H10O2 racemic)? What is the product when C4H8 is mixed with RCO3H, and H2O (the formula will be C4H10O2 meso)?Take 1-methylcyclohexene as the alkene and treat it with the reagent.What reagent/reagents is/are necessary to transform the starting molecule into the desired product? ?. CH,CH•CHỔH CH3CH
- B-Instructions: What reagent and/or catalysts are necessary to bring about each conversion? Br 1. CH-CH=CH-CH3 + CH;-CH CH-CH, CH CH 2. CH3-C=CH2 CH,C CH, HO. 3. CH, CH; 4. CH, C=CH, + CH, - C - CH, Br Brorganic chemistry 6) Aniline NH₂ is best prepared byDraw the organic products formed when cyclopentene is treated with each reagent. With some reagents, no reaction occurs. a.H2 + Pd-C b.H2 + Lindlar catalyst c.Na, NH3 d.CH3CO3H e.[1] CH3CO3H; [2] H2O, HO− f.[1]OsO4 + NMO; [2] NaHSO3, H2O g.KMnO4, H2O, HO− h.[1] LiAlH4; [2] H2O i. [1] O3; [2] CH3SCH3 j.(CH3)3COOH, Ti[OCH(CH3)2]4, (−)-DET k.mCPBA l.Product in (k); then [1] LiAlH4; [2] H2O