of 20 Draw the structure of the major organic product(s) for the following reaction between an acetylenic anion and an alkyl halide. (The reaction stoichiometry is 1:1.) Na C C-CH3 -Br G Draw the major organic product or products for the reaction. Select Draw Templates More Erase /c H Q2Q
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- raw the structure of the organic product formed when the given compounds undergo the three-step reaction equence indicated. Br 1. NaOC₂H5, C₂H5OH 2. NaOH, H₂O 3. H3O+, heat Select Draw Templates More 2 S C H ODraw the structure of the organic product that is formed when the compound shown below is treated with the following reagents: 1) TsCl, pyridine; 2) NaCN. Interactive 3D display mode H₂Cl OH Draw the molecule on the canyas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single beShow reaekson and don't use hend raiting and step by step solutions please
- app.101edu.co Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. esc F1 CH3CH2CH2OH H2SO4 (cat), heat ☀ F2 80 F3 OH a F4 W Q F5 Atoms and P Draw or ta MacBook A C F61. aq. NaOH reflux NaCI H20 OH 2. HI a = Proton transfer d = Radical chain addition g = E2 Elimination b = Lewis acid/base e = Electrophilic addition h = SN1 Nucleophilic substitution C = Radical chain substitution f = E1 Elimination i = SN2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. Submit Answer Retry Entire Group 9 more group attempts remainingI got this question wrong on my exam and I don't understand why. Could you please explain?
- 人,。 1. CH,OH Br Br2 HBr ÓCH, 2. CH2 LiT a = Proton transfer d = Radical chain addition g = E2 Elimination b = Lewis acid/base e = Electrophilic addition SN1 Nucleophilic substitution h = C = Radical chain substitution f = E1 Elimination i = SN2 Nucleophilic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2. Submit Answer Retry Entire Group 9 more group attempts remainingThe given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Reduction Rearrangement reaction Acid O || R₁-C-O-R₂ Meeting in "General"HW9 #5
- What is the full mechanism for the oxidation of cyclododecanol through NaOCI; EtOAc/H2O, Bu4NBr, HCI-cat ? Please include all arrows and formal charges.1. Na OEt 2. CH;OH Br Br2 HBr ÓCH a = Proton transfer d = Radical chain addition g = E2 Elimination h = SN1 Nucleophilic substitution i= Sy2 Nucleophilic substitution b = Lewis acid/base e = Electrophilic addition c = Radical chain substitution f=El Elimination Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 1. 2.Content 54°F Clear * X app.101edu.co Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts. F1 Aktiv Chemistry. @ 2 CH3CO2H Draw SN1 Product F2 # 3 DII X OSN2/SN1 Reactions Fl: X G Which alkyl bromide i X F3 $ ▬ F4 % 5 J F5 A 6 Question 8 of 22 â 6 F6 & G whats a stro 7 Please select a c F7 O PrtScn 8