10. Nitric acid and nitrous acid are both acids that you would not want to spill on your feet.But one is much more acidic than the other and would do real damage. Draw themolecular structures of each of these and explain - based on what you learned in thismodule - why nitric acid (pKa =-1.35) is much more acidic than nitrous acid (pKa = 3.15).

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Answered: 10. Nitric acid and nitrous acid are…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter5: Resonance

Section: Chapter Questions

Problem 13E: Complete each Lewis structure, draw all important resonance structures, predict a value for thebond...

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Consider the following reactions and choose the correct structures from the pool of choices below. If the reaction is not feasible, you may choose No Reaction. CLA OH LET POOL OF CHOICES: acidic KMnO4, heat Br₂, H₂O OH Br RIS PDT2 Br PIE COOH The correct structure for PDT1 is CLA PDT1 OH Br KUL OH Br and that of PDT2 is choose your answer... R
You are planning to carry out a reaction that produces protons. The reaction will be buffered at pH = 10.5. Would it be better to use a protonated methylamine/methylamine buffer or a protonated ethylamine/ethylamine buffer? (pKa of protonated methylamine = 10.7; pKa of protonated ethylamine = 11.0)
Acetic acid can also react as a very weak base (pKb = 20). Two different sites on acetic acid might become protonated to give the conjugate acid. Draw both of these possible conjugate acids, and explain (resonance) why the correct one is more stable. Calculate the pKa of this conjugate acid.
2) -OH phenylacetic acid K₂ = 5.2 x10-5 + propionic acid pK, = 4.87 Using the information above, draw the products of the reaction and determine if the reaction is reactant- or product-favored. Briefly elaborate on how the equilibrium was determined. H3C H3C OH OH
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(CQ10) Hello! Please help me answer this one. Please refer to the given picture/s below for the questions. Please read the instructions and directions very carefully. Double and triple check your answers, previous tutors got it wrong. NOTE: Type only your answers. Please do not handwritten your answers. Make sure your formulas, solutions and answers' format are all correct.
Draw the structure of the product of the reaction between the compound shown below and H2SO4.
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eq eq M M M ereg 2req 2req 2req X 2req J F3 $ 4 R C V [Review Topics] [References] Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. 4x Include all valence lone pairs in your answer. • For structures having different hydrogens of comparable acidity, assume that the reaction occurs at the less-substituted carbon. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. ✓✓99.81 O 0- F4 . % 5 T G B F5 *** ^ 6 Cengage Learning Cengage Technical Support Y ChemDoodle H N F6 & N& 7 U O J F7 + [ ] در M 8 PrtScn K F8 9 Home O 83°F Sunny F9 L ) 0 End F10 P Previous C PgUp F11 9 ? Next Save and Exit 9:38 AM 7/18/2022 PgDn F12 0 Ins D Back
Phenol (hydroxybenzene) behaves as a weak acid. a) Write out the equilibrium equation for its partial dissociation in water. b) Write out the expression for the acid dissociation constant, Ka. d) Draw the conjugate base of phenol and show how it is stabilised by resonance. e) Compare and explain the acidity of phenol (p = 9.9) with that of: cyclohexanol (pk = 16.0) 3-fluorophenol (pK₁ = 9.3) 4-acetylphenol (pK, = 8.1)
1.

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