Which bases are strong enough to deprotonate the acid, NH, so that the equilibrium favors the products? Check all that apply. Note: Reference the p K values for selected organic molecules table for more information. HSO4 CH₂COO NaNH, None of the above X

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### Question:

**Which bases are strong enough to deprotonate the acid, \( \text{NH}_4^+ \), so that the equilibrium favors the products? Check all that apply.**

*Note*: Reference the \( pK_a \) *values for selected organic molecules* table for more information.

#### Options:

- [ ] \( \text{HSO}_4^- \)
- [ ] \( \text{CH}_3\text{COO}^- \)
- [ ] \( \text{NaNH}_2 \)
- [ ] None of the above

### Explanation:

To solve this question, you need to understand the concept of acid-base equilibrium, particularly the relationship between the strength of a base and its ability to deprotonate an acid, which is often compared using \( pK_a \) values. Stronger bases have higher \( pK_a \) values, enabling them to deprotonate weaker acids.

Please consult the \( pK_a \) table for the specific values of each base to decide which are capable of deprotonating \( \text{NH}_4^+ \).

### Diagram/Visual Aid:

There are three checkboxes corresponding to each base option and one for "None of the above," indicating a multiple-choice selection environment. The clickable interface likely allows users to select one or multiple answers.
Transcribed Image Text:### Question: **Which bases are strong enough to deprotonate the acid, \( \text{NH}_4^+ \), so that the equilibrium favors the products? Check all that apply.** *Note*: Reference the \( pK_a \) *values for selected organic molecules* table for more information. #### Options: - [ ] \( \text{HSO}_4^- \) - [ ] \( \text{CH}_3\text{COO}^- \) - [ ] \( \text{NaNH}_2 \) - [ ] None of the above ### Explanation: To solve this question, you need to understand the concept of acid-base equilibrium, particularly the relationship between the strength of a base and its ability to deprotonate an acid, which is often compared using \( pK_a \) values. Stronger bases have higher \( pK_a \) values, enabling them to deprotonate weaker acids. Please consult the \( pK_a \) table for the specific values of each base to decide which are capable of deprotonating \( \text{NH}_4^+ \). ### Diagram/Visual Aid: There are three checkboxes corresponding to each base option and one for "None of the above," indicating a multiple-choice selection environment. The clickable interface likely allows users to select one or multiple answers.
Expert Solution
Step 1: Define Acidity

Acidity is defined as the ability of a molecule to release protons.  If a compound  easily donats proton it is highly acidic.  it depends on the stability of the conjugate base.

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