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- 8. (8) Circle the most acidic compound from each set below. Then, list the structural influence(s) th best explains your answer. structural influences: Resonance, atom size, electronegativity, hybridization, and inductive effect. CI NH2 но. OH A) B)H-Br The above reaction involves heterolytic bond breakage of HBr. a) Encircle the nucleophile(s) and electrophile(s) and explain why. (4 points) b) Give the mechanism of the reaction by: i) Drawing the appropriate arrows to track the flow of electrons. (3 points) ii) Showing the species formed after bond breakage and bond formation with appropriate charges. (3 points) c) Predict the final products. (2 points) SUBMIT YOUR SOLUTION. +Which side of the equilibrium is favored in this acid/base rxn? pka of product: 6.9
- 8. (8) Circle the most acidic compound from each set below. Then, list the structural influence(s) that best explains your answer. structural influences: Resonance, atom size, electronegativity, hybridization, and inductive effect. CI HO. NH2 HO A) B)Queation 13. Please draw the major product and mechanism of the following reaction. (6 points) Br DMSO `O` Na*
- Select the best answer for the product of the reaction below. TOEt 1.) NaOEt (1 equiv.) 2.) Br 3.) NaOEt (1 equiv.) 4.) Br 5.) H2SO4, H2O, Boil a.) OH b.) d.) a.) c.) O تو e.) C.) OHUsing ChemDraw Draw a mechanism of a reversible reaction of acetophenone and strong acid (H-A) to form a protonated acetophenone and a weak base. Draw all the electron pairs of the molecules and the arrows.H₂C H₂C لیے CH–COOH +CH,CH(CH,)NH, H₂C heat 2 Reaction D Select Draw Rings More Erase / |||||| CON H COOH +CH,CH(CH,)NH₂ CH3 Draw the amide formed when isopropylamine (CH₂CH(CH3)NH₂) (CH3CH(CH3)NH₂) is heated with each carboxylic acid. Include all hydrogen atoms. heat G Q2Q
- (5 points) What hydrolysis products are formed when the following compound is treated with aqueous acid? No reaction is an acceptable answer. CH3 H3C- H20, H+Finished A-C need help with the remaining D-ISummarize the relationship between pKa and acid strength by completing the following sentences: a. The higher the pKa of an acid, the stronger or weaker the acid. b. The lower the pKa of an acid, the stronger or weaker the acid.