First point is correct.
Conjugate base of first molecule is resonance stabilized, so it is more acidic.
One should remember that lower the value of pKa more it will be acidic. And also that higher the stability of conjugate base, the molecule is more acidic.
Conjugate base means remaining molecule after removing acidic hydrogen, more stability of conjugate base more it is acidic.
See below how it's conjugate base is resonance stabilized.
Hope it helps you.
9.(4 points) Which choice correctly explains the pka values below? OH тон pka = 4.20 pka...
Which of the following statements best explains the decreased acidic nature of carbonic acid compared to other carboxylic acids? OH carboxylic acid HO OH carbonic acid A. The extra hydroxyl group on the carbonic acid is an electron donating group, dampening the acidity of the molecule. B. The carbonyl group is an electron withdrawing group, increasing acidity of the OH through resonance. C. The carboxylate anion is stabilized by hyperconjugation and is a weak base, so the conjugate acid is...