Rank the compounds in each group in order of increasing acidity.ÇIBr.COOH„COOHCOOHа.COOHCOOHCOOHCHCF3LOHHOHOHOHOHOb.d.CHO,NBrO,NO,N`NO2Rank the compounds in each group in order of increasing basicity.NH2NH2NH2a. NH3-NH2-NH2c.O,NCH3b.d. CgHgNH2 (C,H5)2NH-NH2N.HHC.

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Chemistry

9th Edition

ISBN:9781133611097

Author:Steven S. Zumdahl

Publisher:Steven S. Zumdahl

Chapter14: Acids And Bases

Section: Chapter Questions

Problem 86E: Use Table 14.3 to help order the following acids from strongest to weakest HNO3,H2O,NH4+,C5H5NH+

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The following reactions illustrate Brnsted acid-base behavior. Complete each equation. a.HI(aq)+?H3O+(aq)+I(aq) b.NH3(l)+?NH4++NH2 c.H2C2O4(aq)+H2O(l)?+HC2O4(aq) d.H2N2O2(aq)+H2O(l)H3O+(aq)+? e.?+H2O(l)H3O+(aq)+CO32(aq)
Consider the following four solutions: (1) apple juice, pH 3.8, (2) pickle juice, pH 3.5, (3) carbonated beverage, pH 3.0, and (4) drinking water, pH 7.2. a. Which solution has the highest [H3O+]? b. Which solution has the highest [OH]? c. List the solutions in order of increasing acidity. d. List the solutions in order of decreasing basicity.
What is the conjugate acid of each of the following? What is the conjugate base of each?. (a) OH-. (b) H2O. (c) HCO3-. (d) NH3. (e) HSO4-. (f) H2O2. (g) HS-. (h) H5N2+
Trimethylamine, (CH3)3N, reacts readily with diborane, B2H6. The diborane dissociates to two BH3 fragments, each of which can react with trimethylamine to form a complex, (CH3)3N:BH3. Write an equation for this reaction and interpret it in terms of Lewis acid-base theory.
Use Table 14.3 to help order the following acids from strongest to weakest HNO3,H2O,NH4+,C5H5NH+
What is the conjugate acid of each of the following? What is the conjugate base of each?. (a) H2S. (b) H2 PO4-. (c) PH3. (d) HS-. (e) HSO3-. (f) H3O2+. (g) H4N2. (h) CH3OH
The butylammonium ion, C4H9NH3+, has a Ka of 2.3 1011. C4H9NH3+(aq) + H2O() H3O+(aq) + C4H9NH2(aq) a) Calculate Kb for the conjugate base, C4H9NH2 (butyl amine). b) Place the butylammonium ion and its conjugate base in Table 16.2. Name an acid weaker than C4H9NH3+ and a base stronger than C4H9NH3. c) What is the pH of a 0.015M solution of butylammonium chloride?
Salicylic acid, HOC6H4CO2H, and its derivatives have been used as pain relievers for a long time. Salicylic acid occurs in small amounts in the leaves, bark, and roots of some vegetation (most notably historically in the bark of the willow tree). Extracts of these plants have been used as medications for centuries. The acid was first isolated in the laboratory in 1838. (a) Bath functional groups of salicylic acid ionize in water, with Ka=1.0103 for the—CO2H group and 4.201013 for the -OH group. What is the pH of a saturated solution of the acid (solubility = 1.8 g/L).. (b) Aspirin was discovered as a result of efforts to produce a derivative of salicylic acid that would not be irritating to the stomach lining. Aspirin is acetylsalicylic acid, CH3CO2C6H4CO2H. The -CO2H functional group is still present, but its acidity is reduced, Ka=3.0104. What is the pH of a solution of aspirin with the same concentration as a saturated solution of salicylic acid (See Part a). (c) Under some conditions, aspirin reacts with water and forms a solution of salicylic acid and acetic acid: CH3CO2C6H4CO2H(aq)+H2O(l)HOC6H4CO2H(aq)+CH3CO2H(aq) i. Which of the acids, salicylic acid or acetic acid, produces more hydronium ions in such a solution? ii. What are the concentrations of molecules and ions in a solution produced by the hydrolysis of 0.50 g of aspirin dissolved in enough water to give 75 mL of solution?

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Rank the compounds in each group in order of increasing acidity. CI Br .COOH .COOH .COOH а. C. СООН COOH СООН CH5 CF3 LOH LOH LOH OH LOH HO b. d. CH, O,N Br O,N O,N `NO2