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- What is the strongest nucleophile in this list? B OH D A B U D9. Complete Reactions. Provide only the major product for E2&SN2 reactions. E1/SN1 provide all possible products. NaOH Br provide mechanism CI Provide mechanism + CI NaOCH 3 KCNClassify the following reaction as an Sn1, Sn2, E1, E1cB, E2 reaction. Can you show me the leaving group and explain how to find a leaving group? And how to identify the other reactions?
- Predict the major product of the reaction and draw it in the space provided. + HN. NPh NaBH3CN MeOH/ACOH11. Determine whether each reaction occurs by an SN2, SN1, E1, and/or E2 reaction. Provide a detailed mechanism with curved arrows and the major product(s). OMs Br Br OH мон OH NaSH DMF NaOH H₂O, heat LDA DMF NaOH H₂O, heat HBr H, H₂O heatThe nucleophile approaches from the opposite side of the carbon with the leaving group in which reaction mechanism? O E2 O SN1 O SN2 O SN1 and SN2
- O In this step alkyne anion is alting and it is attacking cecting acting as 4 electrophile a Pla وعك Ho as a nucleophile on the genen molecule, which is Br pom 산 2-Bromo propane (26105 576 honros он 2Draw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND BOND-BREAKING STEPS. SHOW ALL INTERMEDIATES. 1) NaOH 2) H3O* H3C H3C HO3. Which of the following are nucleophiles? 1 CH3NH2 2 CH3O 3 H3CC=CH
- Answer the question below the reaction. ta The reaction above proceeds through which type of mechanism? SN2 SN1 E1 E2 OH + Excess NH4C1 H₂SO4 + H₂OPlease explain the steps from the reactant to product. Are they SN1/SN2/E1 or E2 reactions, good or bad leaving groups.7Which nuclophile tend to favor conjugate addition to an alpha, b'eta-unsaturated carbonyl CH3CH2)3 Nna Br CH,Li D LIATHY CH,CH20 13.