Give the clear handwritten answer..give the answer given below questions 4.8-pyridinium ion(PK, -5.2)acetylacetone(pK₂ =9)PConjugate base of acetylacetone deprotonated acetyla cepyridineBdeprotonatedacetylacetoneCBConjugate acid of pyridine pyridinium ionof the two acidic species in the above equilibrium, the weaker acid is acetyl acetoneof the two basic species in the above equilibrium, the more stable/weaker base is deprotonated acetylacutonAs written, the above equilibrium is favored in the forword (right) direction.

Answered: Image /qna-images/answer/376ad8eb-c8eb-4b63-805c-412cf123e206.jpg

deprotonated acetylacetone CR pyridinium ion (pK, -5.2) acetylacetone (pK₂ =9) A Conjugate base of acetylacetone deprotonated acetyla o pyridine B Conjugate acid of pyridine puridinium ion of the two acidic species in the above equilibrium, the weaker acid is acetyl acetone of the two basic species in the above equilibrium, the more stable/weaker base is deprotonated acetylacuto As written, the above equilibrium is favored in the forword (right) direction.

deprotonated acetylacetone CR pyridinium ion (pK, -5.2) acetylacetone (pK₂ =9) A Conjugate base of acetylacetone deprotonated acetyla o pyridine B Conjugate acid of pyridine puridinium ion of the two acidic species in the above equilibrium, the weaker acid is acetyl acetone of the two basic species in the above equilibrium, the more stable/weaker base is deprotonated acetylacuto As written, the above equilibrium is favored in the forword (right) direction.

Chemistry: Principles and Practice

3rd Edition

ISBN:9780534420123

Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer

Publisher:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer

Chapter15: Solutions Of Acids And Bases

Section: Chapter Questions

Problem 15.116QE

See similar textbooks

Similar questions

(Q8) The Ka of formic acid is 1.8 x 10-4, the Ka of hydrofluoric acid is 6.4 x 10-4 and the K, of hypobromous acid is 2.8 x 10-9. Which of the following statements is true? O Hypobromous acid is a base The weakest conjugate base is fluoride O Hydrofluoric acid is a strong acid O The weakest conjugate base is hypobromite O The weakest conjugate base is formate
Given that Ka for acetic acid is 1.8 * 10-5 and that for hypochlorous acid is 3.0 * 10-8, which is the stronger acid?
Shown below is the equilibrium between phenol and phenolate. pKa = 10.00 Phenol 01H Phenolate The pKa of phenol is 10.00. At what pH is phenol 85% ionized? Type your answer...
7:07 Acid CsH,NH* CH3CO₂H The approximate pKa values of several acids are given in the table below. In which of the following acid-base reactions will both the forward and reverse reactions be equally favored? NH₂+ HCN C6H5OH HCO3 CH3NH3* Question 1 of 11 H₂O CH3OH -pka 5 5 9 9 10 10 11 16 16 A) NH4+ (aq) + CN¯(aq) = NH3(aq) + HCN (aq) Submit B) CH3NH3(aq) + CH3CO₂ (aq) = CH3NH₂(aq) + CH3CO₂H(aq) C) C5H5NH*(aq) + HO¯(aq) = C₁H5N(aq) + H₂O (1) Tap here or pull up for additional resources
For each value of Ka, calculate the corresponding value of pKa. Which compound is the stronger acid? Q.) chloroacetic acid, Ka = 1.38 X 10-3
Acid Conjugate base Acid H2CO3 HCO3 Base Strength Strength Increases Increases H2PO4 HPO,- (1) The acid with the smallest value of Ka is (A) H2CO3 (B) H2PO4 (1) The acid with the largest value of pKa is (A) H2CO3 (B) H2PO4
Question 3 What must be the minimum concentration of cyanoacetic acid in 1.00L buffer solution of a pH 2.07 cyanoacetic acid/sodium cyanoacetate buffer if the pH changes by 0.20 units when 0.072 moles HCl are added? Click here for the table of lonization Constants of Weak Acids.
Sulfonic acids are the "organic versions" of sulfuric acid: they are really acidic, but are more soluble in organic solvents, making them better suited for organic acid/base reactions. Sulfonic acids have pka values from 0 down to -15! a) Which of the following sulfonic acids is the strongest? ofor H3C-S-OH F3C-S-OH -S-OH F3C- A B b) In ONE WORD, name the effect (not the property) that causes the acidity difference across this series of sulfonic acids c) Draw the acid/base reaction between the weakest of the pictured acids and triethylamine (NET3). Include curved arrows to show the electron-flow
The correct order of increasing the acidity for the following molecules is: 1,3-Diketone > carboxylic acid > alcohol > ketone > amide (the weakest) Carboxylic acid >1,3-diketone > ketone > alcohol > nitrile (the weakest) 1,3-Diketone > 1,3-diester > alcohol > ketone > amide (the weakest) الأنتنامى 1,3-Diketone > ketone > alcohol > 1,3-diester > amide (the weakest) Carboxylic acid >1,3-diketone > nitrile > alcohol > ketone (the weakest)
(a) Given that Ka for acetic acid is 1.8 x 10-5 and that forhypochlorous acid is 3.0 x 10-8, which is the stronger acid?(b) Which is the stronger base, the acetate ion or the hypochloriteion? (c) Calculate Kb values for CH3COO- and ClO-.
Rank the benzoic acid derivatives 1-6 from weakest to strongest acid
Consider two acids: HCO,H (formic acid, pk,- 3.8) and CgH;C0,H (benzoic acid, pK, = 4.2). Which acid has the larger K,? Select the single best answer. a formic acid benzoic acid