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- Complete the following reaction: CH3-C≡CH + NaNH2 =Please advise: is model of the (E) 2-bromo-2-butene has its priority numbers of each substituent labeled correctly. I also, belive this is a E-isomer. JustinDraw structures corresponding to the following names: (a) 3, 3-Dimethyl-4-octyne (b) 3-Ethyl-5-methyl-1, 6, 8-decatriyne (c) 2, 2, 5, 5-Tetramethyl-3-hexyne (d) 3, 4-Dimethylcyclodecyne (e) 3, 5-Heptadien-1-yne (f) 3-Chloro-4, 4-dimethyl-1-nonen-6-yne (g) 3-sec-Butyl-1-heptyne (h) 5-tert-Buty1-2-methyl-3-octyne
- 1. When you add H-Br in a terninal alkene, the product has the rule od Markovnikov? 2. The type pf intermetary thag forms when we add HgSO4/H2SO4/H2O in an alkyl is? Please solve my both questions.thank you.KMnO4, warm, conc'd reacts with hept-1-ene to yield __________. CO2, hex-1-ene CO2, hexanoic acid Formic acid, pentanoic acid Ethanoic acid, pentanal Formic acid, hexanoneWhen (CH3CH2)3CBr is added to CH3OH at room temperature, the product is(CH3O)C(CH2CH3)3. Propose a mechanism(s) for the reactions leading to theseproducts and use curved arrows to show the movement of electrons.
- Which of the following statement/s is/are false about the reaction of 3-methylhex-3-ene with H3O+?Indicate si/re faces of carbons in double bond highlighted in blue, and explain why?As a rule, axial alcohols oxidize somewhat faster than equatorial alcohols. Which would you expect to oxidize faster, cis-4-tert-butylcyclo-hexanol or trans-4-tert-butylcyclohexanol? Draw the more stable chair conformation of each molecule.
- What alkene is the major product formed from attached alkyl halide in an E1reaction?Cyclohexene plus 1) Hg(OAc)2, H2O; 2) NaBH4; yields __________. HO2CCH2CH2CH2CH2CO2H a cyclic diketone cyclohexyne cyclohexanol OHCCH2CH2CH2CH2CHOA chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under thesame conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C.Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structuresof A, B, and C; give equations for their formation; and explain the stereospecificity of these reactions