Identify the base(s) that can deprotonate CH3COOH (pKa=4.756). The conjugate acid products produced from the deprotonation of CH3COOH and their pka values are given in parentheses. Check all that apply. ### Evaluation of Acids and Their Conjugate BasesWhen determining the strength of an acid, the \( pK_a \) value is a critical factor. Below is a list of various acid-base pairs with their respective \( pK_a \) values:1. **ICH\(_2\)COO\(^-\)** - Parent Acid: ICH\(_2\)COOH - \( pK_a = 3.2 \)2. **CH\(_2\)NO\(_2^-\)** - Parent Acid: CH\(_3\)NO\(_2\) - \( pK_a = 10.2 \)3. **CCl\(_3^-\)** - Parent Acid: CHCl\(_3\) - \( pK_a = 25 \)4. **Br\(^-\)** - Parent Acid: HBr - \( pK_a = -9 \)5. **NH\(_3\)** - Parent Acid: NH\(_4^+\) - \( pK_a = 9.4 \)### Option:- None of the above### Explanation:- **\( pK_a \) Values:** - Lower \( pK_a \) values indicate stronger acids. - Negative \( pK_a \) values are characteristic of very strong acids.- **Evaluation Notes:** - ICH\(_2\)COOH is a relatively strong acid with a low \( pK_a \). - CH\(_3\)NO\(_2\) and NH\(_4^+\) are weak acids. - CHCl\(_3\) has a very high \( pK_a \), indicating it is a very weak acid. - HBr is an extremely strong acid with a negative \( pK_a \).This assessment aids in understanding the relative strengths of these acids and their conjugate bases within a chemical context.

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.Those base can deprotonate Acetic Acid whose conjugate acid is a weaker acid than acetic acid.That means the conjugate acid should have pka higher than that of Acetic Acid.This is true for nitromethane, chloroform and ammonium ion. So, their conjugate base can abstract proton from acetic acid.Option -B,C,E are correct