Show work. don't give Ai generated solution This is a Brønsted-Lowry acid-base reaction. Draw structures for all the products, showing any non-zero formal charges in each one. Make sure your reaction isbalanced.Note for advanced students: Draw only the most stable resonance structure for each product.:0:+LiOHCH-CH-C-OHClick and drag to start drawing astructure.

Answered: Image /qna-images/answer/53dd547f-b6c1-43cc-bc49-328cdad0d9c6.jpg

Answered: This is a Brønsted-Lowry acid-base…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 35E

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Add curved arrows to the reactants in this reaction. A double-barbed curved arrow is used to represent the movement of a pair of electrons. Draw curved arrows. : 0: si H : OH :: H―0: H
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6. Rank the indicated a-H's from most to least acidic (most acidic= 1). Be sure to explain your rankings for each by drawing significant resonance structures for the conjugate base and commenting on any other factors that contribute to your rankings. H H H H. A B Cmpd Rank Resonance Structures Reasoning A В
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This structure has a lower pKa than usual because he conjugate base of the structure has unusual stability. Using the provided resonance structures, draw the curved electron- pushing arrows to show the deprotonation step. Then, draw the curved electron-pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond-breaking and bond-making steps. H H:O H. H H H H. H H H Select to Add Arrows NaH .H H H Na Ⓒ Na Ⓒ H Problem 4 of 21 Please sel
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Phosphorus trichloride (PCl3) can be used to convert carboxylic acids into acid chlorides. The mechanism for the reaction is shown but the curved arrows and the formal charges on the respective atoms have been left out. a. Draw the missing curved arrows for each step. b. Add any missing formal charges
Use the information in the pk, table below to determine which side of the equilibrium is favored for each of the reactions in the second table. acid pk, acid PK CHA CHÍNH, 36 CH₂SH OH 9 50 45 CH2=CH2 19 15.9 CH₂OH 15.7 10.3 .OH 10.0 4.8 он OH CH₂OH₂ -2.2 -7.2 снон, + i + OH + CH4 Equilibrium Equation CH₂OH + io OH CH3NH + CH2=CH2 CH3NH₂ + он + + H₁₂-C CH2=CH 0 O Left Favored Equal Right Favored о 0 0
осх (Intermediate) Reactant ķ H H: Tip: Only add curved arrows in this sketcher 1
See image below
Be sure to answer all parts. 9. Draw one resonance structure for each of the conjugate bases formed by removal of the labeled protons (H2, Hp, and H) in cyclohexane-1,3-dione. Rank these protons in order of increasing acidity and explain the order you chose. 10 points Ha H. еВook Print cyclohexane-1,3-dione References Part 1 out of 3 Draw one resonance structure for each of the conjugate bases formed by removal of the labeled protons (H2, Hp, and H) in cyclohexane-1,3-dione. Don't forget to include lone pairs in each structure. draw structure ... draw structure ... draw structure .. Ha removed Нь removed H. removed
Draw curved arrows to indicate the movement of electrons in the following reaction. H но: -C-CI HO-C :Cl: -- H Arrow-pushing Instructions H H HỌ: H----C-CI HO-C----H :CI: H

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