None Which bases are strong enough to deprotonate the acid, CH3OH, so that the equilibrium favors the products? Check all that apply.Note: Reference the pK values for selected organic molecules table for more information.✓ CH3COO• NaNH,□ H₂ONone of the above✗

To determine which bases are strong enough to deprotonate methanol (CH3OH) such that the equilibrium…

Answered: Which bases are strong enough to…

Chemistry: The Molecular Science

5th Edition

ISBN:9781285199047

Author:John W. Moore, Conrad L. Stanitski

Publisher:John W. Moore, Conrad L. Stanitski

Chapter14: Acids And Bases

Section: Chapter Questions

Problem 133QRT

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4. Explain using equilibrium principles, how the Carbonic Acid/Bicarbonate system regulates breathing. carbonie anhydrase co, + H,0S H,co,S HCO, + H* carbon dioxide + carbonic acid bicarbonate + water hydrogen lon
Will acetylene react with sodium hydride according to the following equation to form a salt and hydrogen, H,? Using pK, values given in Table 4.1, calculate K for this equilibrium. HC=CH + Na H- HC=C Na+ + H, Acetylene Sodium Sodium Hydrogen hydride acetylide
Alcohols are weak organic acids, pKa 15–18. The pKa of ethanol, CH3CH2OH, is 15.9. Write equations for the equilibrium reactions of ethanol with each base. Which equilibria lie considerably toward the right? Which lie considerably toward the left? Q.) NaOH
Disulfides are compounds that have S¬ S bonds, like peroxides have O¬ O bonds. Thiols are organic compounds that have the general formula R¬ SH, where R is a generic hydrocarbon. The SH- ion is the sulfur counterpart of hydroxide, OH-. Two thiols can react to make a disulfide, R¬ S¬ S¬ R. If you wanted to convert a disulfide to two thiols, should you add a reducing agent or oxidizing agent to the solution?
Oxacarbazepine ( C15H12N2O) is used to treat epilepsy. What would happen to the equilibrium of oxacarbazepine in water when more oxacarbazepine is added to the system? a.) Ratef < Rateb and the equilibrium would shift to reactants (to the left) b.) Ratef > Rateb and the equilibrium would shift to reactants (to the left) c.) Ratef < Rateb and the equilibrium would shift to products (to the right) d.) Ratef > Rateb and the equilibrium would shift to products (to the right)
Consider this equation again: H2CO3 (aq) + H2O (l) double arrows HCO3- (aq) + H3O (aq) Ka of carbonic acid = 4.5 X 10-7 This reaction favors the products This reaction favors the reactants Neither the reactants or products are favored.
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its sodium salt, C¢HsCOO`Na*, is quite soluble in water. In which of the following Benzoic acid, C6H5COOH (pK = 4.19), is only slightly soluble in water, solutions will benzoic acid dissolve more readily than in pure water? O Ba(HCO3)2 O HF O Ca(OH)2 O NazPO4 O HNO2
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What is the pH of an aqueous solution containing 0.50 mol L–1 ethanoic acid, 0.30 mol L–1 sodium ethanoate, and 0.10 mol L–1 HCl? [The pKa of ethanoic acid is 4.75.]
Alcohols are weak organic acids, pKa 15–18. The pKa of ethanol, CH3CH2OH, is 15.9. Write equations for the equilibrium reactions of ethanol with each base. Which equilibria lie considerably toward the right? Which lie considerably toward the left? Q.) NaHCO3

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Which bases are strong enough to deprotonate the acid, CH3OH, so that the equilibrium favors the products? Check all that apply. Note: Reference the pK values for selected organic molecules table for more information. ✓ CH3COO • NaNH, □ H₂O None of the above ✗