For the following acid–base pairs, (iv) calculate Keq;
(e)
For the following acid–base pairs, (iv) calculate Keq;
(e)
Given that the indicated pKa values correspond to the acid dissociation reactions shown, calculate the ratio of acid to conjugate base for the reactions shown.
(a)
Using pKa values, calculate an approximate Keq value for the following substitution reaction.
At what pH is the concentration of a compound, with a pKa = 4.6, 10 times greater in its basic form than in its acidic form?
At what pH does 80% of the acid exist in its acidic form?
The pKa of a protonated alcohol is about -2.5, and the pKa of an alcohol is about 15. Therefore, as long as the pH of the solution is greater than _______ and less than _______, more than 50% of 2-propanol (the product of the reaction on p. 244) will be in its neutral, nonprotonated form.
The pKa of protonated acetone is about –7.5 and the pKa of protonated hydroxylamine is 6.0.
a. In a reaction with hydroxylamine at pH 4.5 (Figure 16.2), what fraction of acetone is present in its acidic, protonated form?
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The pKa of acetic acid in water is 4.76. What effect will a decrease in the polarity of the solvent have on the pKa? Why?
Calculate the equilibrium constant for the acid–base reaction between the reactants in each of the following pairs:
c. CH3NH2 + H2O
d. CH3N+H3 + H2O
Which reaction in Problem 23 has the smallest equilibrium constant?
Given that pH + pOH = 14 and that the concentration of water in a solution of water is 55.5 M, show that the pKa of water is 15.7. (Hint: pOH=−log [HO−])
For each of the following compounds, draw the form that predominates at pH = 3, pH = 6, pH = 10, and pH = 14:
b. CH3CH2N+H3 (pKa = 11.0)
A naturally occurring amino acid such as alanine has a group that is a carboxylic acid and a group that is a protonated amine. The pKa values of the two groups are shown.
c. Draw the structure of alanine in a solution at physiological pH (pH 7.4).
For each of the following compounds (here shown in their acidic forms), write the form that predominates in a solution with a pH = 5.5:
a. CH3COOH(pKa = 4.76)
b. CH3CH2N+H3 (pKa = 11.0)
At what pH is the concentration of a compound, with a pKa = 8.4, 100 times greater in its acidic form than in its basic form? At what pH is 50% of a compound, with a pKa = 7.3, in its basic form?