EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
10th Edition
ISBN: 9781259636875
Author: Carey
Publisher: MCGRAW HILL BOOK COMPANY
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Chapter 27, Problem 22P

(a) The two most acidic hydrogens of uracil have p K a 's of 9.5 and 14.2 , respectively. Match these p K a 's with the hydrogens in the structural formula and provide structures for the stable resonance contributors of the monoanion and the dianion.

Chapter 27, Problem 22P, (a) The two most acidic hydrogens of uracil have pKa's of 9.5 and 14.2, respectively. Match these

(b) The p K a of the conjugate acid of triethylamine is 10.4 . Is triethylamine a strong enough base to convert uracil to its monoanion? To its dianion.

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(a) The two most acidic hydrogens of uracil have pKa’s of 9.5 and 14.2, respectively. Match these pKa’s with the hydrogens in the structural formula and provide structures for the most stable resonance contributors of the monoanion and the dianion.(b) The pKa of the conjugate acid of triethylamine is 10.4. Is triethylamine a strong enough base to convert uracil to its monoanion? To its dianion?
Isoerythrogenic acid, C18H26O2, is a acetylic fatty acid that turns vivid vle on exposure to UV light. On Catalytic hydrogenation over a palladium catalyst, five molar equivalents of hydrogen are absorbed, and stearic acid
The pKa values of the carboxylic acid groups of oxaloacetic acid are 2.22 and 3.98. a. Which carboxyl group is the stronger acid? b. The amount of hydrate present in an aqueous solution of oxaloacetic acid depends on the pH of the solution: 95% at pH 0, 81% at pH 1.3, 35% at pH 3.1, 13% at pH 4.7, 6% at pH 6.7, and 6% at pH 12.7. Explain this pH dependence.
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