Draw the mechanism showing the Brønsted acid/base reaction between propanoic acid and methylamine. Label the acid, base, conjugate base, and conjugate acid. Show all curved arrows, lone pairs and nonzero formal charges. HO, CH;NH, methylamine propanoic acid pKa = 4.9 Mechanism:
Draw the mechanism showing the Brønsted acid/base reaction between propanoic acid and methylamine. Label the acid, base, conjugate base, and conjugate acid. Show all curved arrows, lone pairs and nonzero formal charges. HO, CH;NH, methylamine propanoic acid pKa = 4.9 Mechanism:
Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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
Transcribed Image Text:Draw the mechanism showing the Brønsted acid/base reaction between propanoic acid and
methylamine. Label the acid, base, conjugate base, and conjugate acid. Show all curved
arrows, lone pairs and nonzero formal charges.
HO.
CH;NH2
methylamine
propanoic acid
pKa = 4.9
Mechanism:
uerm lo noits adi ol maie
Using the pKa information provided/pKa tables (table appended to the end of this document),
determine whether the starting reagents (propanoic acid and methyl amine) or products
would be favored at equilibrium (no math needed!).
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