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- Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compounds below with base.Draw the major organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. H :O: Ha I -0 H-O :O: :0: о-н oIdentify compounds A and B from the following reaction sequence LINH lig MeO 0 (Ozone) MeOH Me₂S B
- The pKa of hydroxyl a on the compound is 7.15, while the pKa of hydroxyl b is 9.3. What key resonance structure explains that difference?Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base.For following substituted benzenes: [1] C6H5Br; [2] C6H5CN; [3] C6H5OCOCH3: Does the substituent activate or deactivate the benzene ring inelectrophilic aromatic substitution?
- Provide a detailed electron pushing mechanism describing the following conversion HCI MeOH Br2 NaOH O:Which nitrogen atom in the structure below is most nucleophilic? Please explain by discussing the electron density around each nitrogen atom. Show at least three resonance structures of the compound. N.Show how the enamine below can be synthesized. Then draw the resonance structure(s) for the enamine. 그
- Q. Explain why Azole undergoes electrophilic substitution at position 2Complete the mechanism for the base-catalyzed opening of the epoxide below by adding any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. -CH3 -CHз Нзс—ӧ: :0-CH3 :ÖH НзС—0:A. Draw all significant resonance structures of each compound below, using appropriate arrows, and then indicate the most significant contributor (multiple structures may be equal in significance). Briefly explain your reasoning in each case. O: (a). H-O: (b).
