Q. \(pKa\) of \(\mathrm{NH_3}\).

Answer

The p\(K_a\) of aqueous ammonia, \( \text{NH}_3 \), is based on the equilibrium \( \text{NH}_3 + \text{H}_2\text{O} \rightleftharpoons \text{NH}_4^+ + \text{OH}^- \). For the conjugate acid \( \text{NH}_4^+ \), \( pK_a \approx 9.25 \), so for ammonia as a base its \( pK_a \) (often reported as \(pK_b\) or equivalently from \(pK_w\)) is:

\[
pK_b(\text{NH}_3) = 4.75
\]
\[
pK_a(\text{NH}_4^+) = 14.00 – pK_b = 14.00 – 4.75 = 9.25
\]

Final result: \(pK_a(\text{NH}_3)\) is typically reported via its conjugate acid as \(9.25\) (with \(pK_b = 4.75\)).

Detailed Explanation

Goal: Find the pKa of \( \mathrm{NH_3} \).

Step 1: Identify what “pKa of \( \mathrm{NH_3} \)” refers to

The value of \( \mathrm{p}K_a \) for a species refers to the equilibrium of its acid form donating a proton.

For ammonia, \( \mathrm{NH_3} \) acts as a base in water, but it can be treated as the conjugate acid/base system as follows.

In water, \( \mathrm{NH_3} \) accepts a proton to form the ammonium ion \( \mathrm{NH_4^+} \). The relevant acid for \( \mathrm{p}K_a \) is the conjugate acid \( \mathrm{NH_4^+} \).

Step 2: Write the relevant acid dissociation equilibrium

Consider the dissociation of ammonium:

\[
\mathrm{NH_4^+ \rightleftharpoons NH_3 + H^+}
\]

The acid dissociation constant for this reaction is \( K_a \), and the corresponding pKa is the value we report as “the pKa of \( \mathrm{NH_3} \)” (because \( \mathrm{NH_3} \) and \( \mathrm{NH_4^+} \) are a conjugate acid/base pair).

Step 3: Use the standard tabulated value

The pKa of \( \mathrm{NH_4^+} \) (at \(25^\circ \mathrm{C}\)) is commonly tabulated as:

\[
\mathrm{p}K_a(\mathrm{NH_4^+}) \approx 9.25
\]

Therefore, the pKa associated with \( \mathrm{NH_3} \) is:

\[
\mathrm{p}K_a(\mathrm{NH_3}) \approx 9.25
\]

Final Answer

\[
\boxed{\mathrm{p}K_a(\mathrm{NH_3}) \approx 9.25}
\]

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General Chemistry FAQs

What is the \(pK_a\) of \(NH_3\) in water?

\(NH_3\) is a weak base. Its conjugate acid is \(NH_4^+\). The relevant acidity constant is \(pK_a(NH_4^+ \rightarrow NH_3 + H^+)\approx 9.25\) at \(25^\circ C\).

How do I find \(pK_a\) for \(NH_3\) using \(K_b\) or \(K_w\)?

For \(NH_3\): \(K_b=\dfrac{[NH_4^+][OH^-]}{[NH_3]}\). Then \(K_a=\dfrac{K_w}{K_b}\) and \(pK_a = 14 - pK_b\) (at \(25^\circ C\)).

What are the \(pK_b\) and \(pK_a\) relationships for \(NH_3/NH_4^+\)?

\(pK_b(NH_3)= -\log K_b\). For the conjugate acid: \(pK_a(NH_4^+)=14 - pK_b(NH_3)\) in water at \(25^\circ C\).

Is \(pK_a\) of \(NH_3\) the same as the \(pK_a\) of \(NH_4^+\)?

Not exactly as written. \(NH_3\) is not an acid in water; \(NH_3\) has \(pK_a\) only through its conjugate acid \(NH_4^+\). So the quoted \(pK_a\) for \(NH_3\) refers to \(pK_a\) of \(NH_4^+\).

What reaction corresponds to the \(pK_a\) used for \(NH_4^+\)?

\(NH_4^+ \rightleftharpoons NH_3 + H^+\). The \(pK_a\) is for this dissociation in water.

What typical numeric value should I memorize for \(NH_4^+\) \(pK_a\)?

A common classroom value is \(pK_a(NH_4^+) \approx 9.25\) (about \(9.2\) to \(9.3\) depending on the reference temperature/conditions).
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