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Question
question 40 (1 point)
from the table given below, which base is the strongest?
| row | base | $k_b$ |
|---|---|---|
| b. | nh₃, ammonia | 1.75 × 10⁻⁵ |
| c. | c₂h₅nh₂, ethylamine | 5.6 × 10⁻⁴ |
| d. | c₅h₅n, pyridine | 1.7 × 10⁻⁹ |
| e. | c₆h₅nh₂, aniline | 4 × 10⁻¹⁰ |
options: a, b, c, d, e
Step1: Recall the relationship between \( K_b \) and base strength
A larger \( K_b \) value indicates a stronger base because \( K_b \) (base dissociation constant) measures the extent of base dissociation in water. A higher \( K_b \) means more hydroxide ions (\( OH^- \)) are produced, making the base stronger.
Step2: Compare the \( K_b \) values of all bases
- For A (Methylamine): \( K_b = 4.4 \times 10^{-4} \)
- For B (Ammonia): \( K_b = 1.75 \times 10^{-5} \)
- For C (Ethylamine): \( K_b = 5.6 \times 10^{-4} \)
- For D (Pyridine): \( K_b = 1.7 \times 10^{-9} \)
- For E (Aniline): \( K_b = 4 \times 10^{-10} \)
Now, compare the magnitudes of these \( K_b \) values. We can see that \( 5.6 \times 10^{-4} \) (Ethylamine) is larger than \( 4.4 \times 10^{-4} \) (Methylamine), and both are larger than the \( K_b \) values of Ammonia, Pyridine, and Aniline.
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C. \( \text{C}_2\text{H}_5\text{NH}_2 \), Ethylamine