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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- Classify each of the following organic reactions. reaction Hör H₂O 1) Hg(OAc)₂, H₂O aveau Br OH OH type of reaction (check all that apply) Odihydroxylation addition hydrogenation Dhalogenation halohydrin formation. subtraction halogenation hydrogenation addition halohydrin formation inhalation Odihydroxylation addition hydrogenation oxyhydration halogenationShow reaekson and don't use hend raiting and step by step solutions pleaseRank the compounds in order of reactivity toward nitration with HNO3: benzene 2-methylfuran thiophene Most reactive Least reactive Answer Bank 3-methylthiophene
- Rank the following esters from most reactive to least reactive in the first slow step of a nucleophilic acyl substitution reaction (formation of the tetrahedral intermediate): Rank the same esters from most reactive to least reactive in the second slow step of a nucleophilic acyl substitution reaction (collapse of the tetrahedral intermediate).LOH NaOH `N' (S) H20 'N' ČI This nucleophilic substitution occurs with rearrangement. Draw curved arrows to show the movement of electrons in the following step of the reaction mechanism. Arrow-pushing Instructions OH :OH N. H.EtOH 1. + NaQEt [Review Topics] [References] NaCl HOEL 2. Br Acetone + Nal a = Proton transfer b = Lewis acid/base C c = Radical chain substitution d = Electrophilic addition e E1 Elimination f = E2 Elimination + NaBr g= SN1 Nucleophilic substitution h = 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.
- 1. 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 remaining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 remainingWhat is the mechanism to get from the reactant to the products
- 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.Show the organic product formed when 4-methylpentanal is heated with sodium methoxide in methanol as solvent. Show the steps in the mechanism as reactant is converted to final product. show appropriate arrow pushing and any charges,and draw a box around the final product.Pyridine reacts with hydroxide by nucleophilic aromatic substitution. Complete the mechanism by drawing curved arrows, the structure of the charged intermediate, and the structure of the major uncharged product. All non-bonding electrons must be shown, including those associated with charges. Step 1: Draw curved arrows. Select Draw Templates More ||||||||||| C H H 1 0: 3 C cl N 0 : a: Q2Q Step 3: Draw the uncharged product. Chloride ion is pre-drawn for your convenience. Select Draw Templates More ||||||||||| CH cl N O Erase : CI Erase Q2 Q Step 2: Draw the charged intermediate. Draw curved arrows to form the product. Select Draw Templates More ||||||||||| CH cl N G E 0 Erase Q2Q