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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- What is the organic product formed in the following reaction? C6H5-CH=CH-C-C6H5 ÷ (CH3CH2)2NH O C6H-CH-CH-C-C6H5 (CH3CH2)2N || III CH-CH, CH- (CH3CH2)2N -CH OH IV O-N(CH2CH3)2 C6H3-CH=CH-C-CH¸ CH-CH=CH-C-CHS (CH3CH₁₂N Select one: A. IV B. II OC. III D. I F1 10: - F2 80 F3 000 000 FADraw the structure for an alkene that gives the following reaction product. 1. Hg(OАc)2, Н2О ? -CHCH3 2. NABH4 ОН Ignore alkene stereochemistry. You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one. Visited opy aste ChemDoodle8. 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 CH3
- Which 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 bondB-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 BrWhich reaction would yield cyclopentanol? سیدگی (A) (B) -d (C) (D) 1. LiAlH4 2. H+ 1. NaBH4 2. H+ 1. BHg:THF 2. H2O2, NaOH OSO4
- To which category does the following reaction belong? -CH₂CH₂CI+ OH7 elimination O substitution reduction O addition 米* -CH=CH₂ + Cr 2 ✓Which of the following reaction conditions would result in Markovnikov addition to an alkene? O[1] BH3; [2] H₂O2/HO™ Cl2 HBr, ROOR CH3OH, H₂SO4Draw 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