9. Draw the products of each of the following acid-base reactions. Use curved arrows to depict the mechanism. (12 pts) (a) K+ (b) Θ Nat (c) NH (d) NaOH + K+ OH
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- 6. Consider the following acid/base reaction. OH a) Show an arrow pushing mechanism. b) Calculate Keq. H CNA -0Draw the arrow-pushing mechanism of the following reactions on blank A4 printer papers, then scan it (or take photo) and submit to Canvas for extra credits. (1) + HC1 (2) H+ مه H₂O OH (3) Br CH3OH (4) (5) Br OH HO H₂O A H, H₂O A OCH 3Consider the reaction below. If the concentration of the nucleophile is doubled, the rate of the reaction will If the concentration of the alkyl halide is doubled, the rate of the reaction will H₂O x CI OH (c) double, not change (d) triple, triple (a) not change, double(b) double, double (e) not change, not change
- What is shown below is an interesting way of making lactone B from lactone A. The reaction takes place when A is treated with sodium hydride, a strong base, which deprotonates the OH group. Draw a curved arrow mechanism which explains how B is formed. The reaction takes place in multiple steps. Show all curved arrows, relevant lone pairs, and formal charges. (7 p) OH H = A Br NaH H [strong base] H Bgive arrow pushing mechanismDetermine the major product of the reaction shown in the box د b C A B C NaBH CH₂OH Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. d D OH OH B ON OH C b D
- Hello, I do not understand these questions and I am stuck. May I get help please please?? Question: Draw the curved arrow mechanism for the following reactionsDraw the mechanism for each of the following reaction. Show all steps in the reaction, the intermediates formed at each step, and use curved arrows to track the flow of electrons.I need help please
- Draw the correct products for the following reaction. (1)Cl, NaOH (Э)но"Modify the given carbon skeleton to draw the structure of stearolic acid: H,C OH Edit Drawing Identify the reagents (1-7) you would use to convert stearolic acid into (A) oleic acid and (B) elaidic acid: stearolic acid A B Oieic acid Elaide acid 1) HBr (2 eq.) 2) H2, Lindlar's catalyst 3) O3 followed by H20 4) H2, Pt 5) Na, NH3 (1) 6) HCI(1 еq.) 7) H2SO4, H20, H&SO4 Reagent A Reagent B i i46. The Strength of Nucleophile: Which one is the strongest nucleophile? OH (B) 0-CH, -CH, (D) O (C) O (A) O (D) O (B)