Using only the information in the pKₐ table below, write an estimated pKₐ value for each labeled H in the two structures below. For example, if the pKₐ value of the H labeled **a** has an estimated value of 50, write 50 in the first box of the answer table and so on.There are two chemical structures depicted with labeled hydrogen atoms (H):1. The first structure is a cyclohexane ring with two oxygen atoms. The hydrogens are labeled: - **H a** attached to a carbon with a hydroxyl group. - **H b** attached to a carbon adjacent to an ester group.2. The second structure is a cyclopentanone ring with an aldehyde group. The hydrogen atoms are labeled: - **H c** attached to the carbon of the aldehyde group. - **H d** attached to a carbon on the opposite side of the ring from **H c**.To the right, there is a table listing acids and their corresponding pKₐ values:| Acid | pKₐ ||-----------|-----|| CH₄ | 50 || NH₃ | 35 || HC≡CH | 25 || CH₃C(=O)CH₃ | 19 || H₂O | 16 || CH₃C≡N | 15 |Below the labeled hydrogens (H a, H b, H c, H d), there's an answer box where the estimated pKₐ values for each labeled hydrogen are to be filled in based on the provided pKₐ table. ### Chemical Structures and pKa Values#### Chemical StructuresThe image displays a series of chemical structures with labeled hydrogen atoms:- The structure labeled "a" features an oxygen atom with lone pairs.- Another structure, labeled "c," has an "H" attached to an oxygen atom connected to a ring structure.- The structure labeled "d" shows an "H" attached to a nitrogen atom, which is part of a chain.#### pKa TableAlongside the structures, a table lists various chemical species and their corresponding pKa values:| Compound | pKa ||------------------|-----|| HC≡CH | 25 || CH₃C(=O)CH₃ | 19 || H₂O | 16 || CH₃C(=O)NH₂ | 15 || NH₄⁺ | 9 || CH₃C(=O)OH | 5 || H₃O⁺ | -2 |This table provides the acidity levels (pKa values) of various compounds, offering insight into their chemical behavior in different environments.

Acidity is defined as the ability of a molecule to release protons. If a compound easily donates proton it is highly acidic.it depends on the stability of the conjugate base.Acidity is inversely related to pKa. This means more acidic compound will have a lower pKa.