please help and explain thanks! Rank the following organic acids in order of acidity, from strongest to weakest. (Hint: consider how resonance and electronegativity will influence the stability of the conjugate base.)Rank from strongest to weakest. To rank items as equivalent, overlap them.ResetHelp|||3|H,C -S- OH|3|H,CонH,CNH,H,Cон

Given acids: We have to arrange them in order of acidity from the strongest to the weakest.

Answered: Rank the following organic acids in…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter2: Polar Covalent Bonds; Acids And Bases

Section2.SE: Something Extra

Problem 47AP

See similar textbooks

Similar questions

Did you first add the H2O(l) on the right side of the equaton and then added the 2HO- on the left side and multiplied CIO2 on the left side by 2?
What is a weak acid? Arrange the following acids in aqueous solution in order of increasing acid strength NH4+ , H2SO4 , CH3CO2H Explain your reasoning
Write the reaction as proton-transfer reactions. Label which reactant is the acid and which is the base, which product is the conjugate base of the original acid, and which is the conjugate acid of the original base. In addition, write Lewis structures for each reactant and product and use curved arrows to show the flow of electrons in each reaction.
What is the conjugate base of H2O?
4. THE ANSWERS ON THE QUESTIONS MUST BE SIMILAR TO THE FOLLOWING: a. X(OH)2(s) ⇌ X2+(aq) + 2OH-(aq) ; Ksp = [X2+][OH−]2; Ksp = (s)(2s)2 b. s = 3.1 x 10–4 M c. Ksp = 1.2 x 10–10SHOW THE COMPLETE SOLUTION CLEARLY.
What is the conjugate base of [Fe (H2O)6]^3+ (aq) ?
Write the products of these reactions. Use single or double arrows as appropriate. When you are done, label the acid and base on the left side and the conjugate acid (CA) and conjugate base (CB) on the right side. (a) PO43- + CH3NH3+ (b) H2O + H2SO4
What are the names of these structures? Write its arrangement by increasing acidity
Write the equilibrium-constant expressions and obtain numerical values for each constant in the basic dissociation of aniline, C6H5NH2. the acidic dissociation of hypochlorous acid, HClO.
Acid-Base Equilibria Many factors contribute to the acidity of organic compounds. Electronegativity, resonance, induction, hybridization, aromaticity, and atomic size, all play a role. In the following comparisons, you are asked to identify the factor(s) that would be most important to analyze when predicting relative acidity, and then to predict the trend in acidity and pKa values. For each of the following pairs of compounds answer the following two multiple-choice questions. 1. What factor(s) are the most important to consider when predicting the relative acidity of the two compounds? a. Electronegativity of the atom possessing the hydrogen. b. Resonance stabilization of the anionic conjugate base. c. Inductive stabilization of the anionic conjugate base. d. Hybridization of the atom possessing the hydrogen. e. The atomic size of the atom possessing the hydrogen.
16-27 Guanidine, p/Ca 13.6, is a very strong base, almost as basic as hydroxide ion. NH NH2+ II II H2N—C—NH2 + H2O H2N—C—NH2 + OH" Guanidine Guanidinium ion pKb = 13.6 Complete the Lewis structure for guanidine, showing all valence electrons. The remarkable basicity of guanidine is attributed to the fact that the positive charge on the guanidinium ion is delocalized by resonance over the three nitrogen atoms. This delocalization increases the stability of the guanidinium ion relative to the ammonium ion or substituted ammonium ions. Draw three equivalent contributing structures for the guanidinium ion and show by the use of curved arrows how these three contributors are related. Propose an explanation for the fact that protonation occurs on the C=NH nitrogen rather than on one of the —NH., nitrogens. (Hint: Consider the resonance stabilization of the structure formed by protonation on a —NH., nitrogen compared with the resonance stabilization of the structure formed by protonation on the =NH nitrogen.) Predict the N—C—N bond angles in the hybrid. Which is the stronger acid, the ammonium ion or the guanidinium ion?
Which base is weaker, the one that has kb 4.0 x 10-10, or the one that has kb 4.4 x 10-4 ?

SEE MORE QUESTIONS

Recommended textbooks for you

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

Chemistry: The Molecular Science

Chemistry

ISBN:

9781285199047

Author:

John W. Moore, Conrad L. Stanitski

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

Chemistry: The Molecular Science

Chemistry

ISBN:

9781285199047

Author:

John W. Moore, Conrad L. Stanitski

Publisher:

Cengage Learning

Introduction to General, Organic and Biochemistry

Chemistry

ISBN:

9781285869759

Author:

Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS