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OH pka 3.1 pKa 4.5 HO -OH pka 5.8 depicts the structure of citric acid with the corresponding pka values for each of the thre
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Answer #1

Part a.

The carboxylic acid at the top of the structure is attached to the carbon where the electronegative oxygen atom is directly attached, due to which the corresponding proton can be readily donated, i.e. most acidic.

Part b.

One of the carboxylic acids is near to the OH group attached to central carbon-atom, hence they each can form hydrogen bonding, as a result, the corresponding proton is comparatively acidic (less pKa, i.e. 4.5) than the one which is oriented far (more pKa, i.e. 5.8) from it.

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