I got this question wrong on my exam, I now understand that a or b woul dwork, but I can't figure out whihc would work better and why. Could you please explain why either Zn(Hg), HCl or H2, Pd-C works better than the other for this reaction? O Because it stabilizes the intermediate cationIncorrectQuestion 330 / 2 ptsWhat is the best choice of reagent to bring about thefollowing transformation?O Zn (Hg), HCIH2, Pd-CO NH3, NaOHO [1] LiAlH4; [2] H2OIncorrectQuestion 340 / 2 pts

Clemenson Reduction: Mechanism: First the oxygen will be protonated and Zn attacks on the carbonyl…

O Because it stabilizes the intermediate cation Incorrect Question 33 0 / 2 pts What is the best choice of reagent to bring about the following transformation? O Zn (Hg), HCI H2, Pd-C O NH3, NaOH O [1] LiAlH4; [2] H2O Incorrect Question 34 0 / 2 pts

O Because it stabilizes the intermediate cation Incorrect Question 33 0 / 2 pts What is the best choice of reagent to bring about the following transformation? O Zn (Hg), HCI H2, Pd-C O NH3, NaOH O [1] LiAlH4; [2] H2O Incorrect Question 34 0 / 2 pts

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Similar questions

For the reaction given below, draw a mechanism (curved arrows) and then predict which side of the reaction is favoured under equilibrium conditions. Include lone pairs and formal charges. Predict which side of the reaction is favored under equilibrium conditions, and explain your choice. a. the reactants are favored, because the negative charge on the electronegative oxygen atom is more stable (making it the stronger base). b. the products are favored, because the negative charge on the electronegative oxygen atom is more stable (making it the weaker base). c. the products are favored, because the negative charge on the large sulfur atom is more stable (making it the weaker base). d. the reactants are favored, because the negative charge on the large sulfur atom is more stable (making it the stronger base).
Just problem number 2 please. Thanks
Question (Organic Chemistry) Consider molecules A–D. Does the arrow pushing in each structure leadto an acceptable resonance form? If so, explain why it is acceptable or unacceptable? What are the rules and logic? If so, draw it and carefully explain your answer and provide explanations for why each structure leds to an acceptable or unacceptable resonance form. Why is the arrow pushing acceptable or unacceptable in each individual case? Explain you answer with many details, logic, and in a step-by-step fashion.
осх (Intermediate) Reactant ķ H H: Tip: Only add curved arrows in this sketcher 1
12
Step 4b: Add curved arrows to show ethoxide deprotonating the most acidic proton. Select Draw Rings More Erase / | c H0 H H :0 : H H H H
The first step should be proton transfer. As I included in my work and the second step I think should be nucleophilic attack but I don't know how to continue on from there. Please but problem as a list of reactions
ile EtOH View Policies Show Attempt History Identify the major and minor product(s) that are expected for the following reaction. Select all that apply. Br NaOH ?
Just Q2
The reaction below is at equilibrium. Explain why the reaction is at equilibrium. Your answer must reference the specific pKa values from our pKa table. Drawing the curved arrow mechanism can also help your answer but is not necessary. OH NaO NaOH
Click on a basic (nucleophilic) atom. HH | | H-C-C=C₂ | H H H H-CI:
I think answer is C... explanation?