QUESTION IMAGE
Question
an aqueous solution contains 0.23 m nitrous acid.
one liter of this solution could be converted into a buffer by the addition of:
(assume that the volume remains constant as each substance is added.)
(select all that apply.)
0.24 mol hcl
0.06 mol ba(oh)₂
0.11 mol hcl
0.23 mol kcl
0.24 mol kno₂
To form a buffer with nitrous acid ($\ce{HNO_2}$), we need a conjugate base (like $\ce{NO_2^-}$) or a strong base that partially neutralizes $\ce{HNO_2}$ to form the conjugate base (without completely consuming the acid). Let's analyze each option:
Step 1: Analyze 0.24 mol HCl
HCl is a strong acid. Adding it to $\ce{HNO_2}$ (a weak acid) will increase $\ce{H^+}$ but not form a conjugate base - it will suppress dissociation, not form a buffer. So this is incorrect.
Step 2: Analyze 0.06 mol $\ce{Ba(OH)_2}$
$\ce{Ba(OH)_2}$ is a strong base. The reaction is: $\ce{2HNO_2 + Ba(OH)_2 -> Ba(NO_2)_2 + 2H_2O}$. Moles of $\ce{OH^-}$ from $\ce{Ba(OH)_2}$: $0.06\ \text{mol} \times 2 = 0.12\ \text{mol}$. Moles of $\ce{HNO_2}$ initially: $0.23\ \text{mol}$ (from $0.23\ \text{M}$ in $1\ \text{L}$). After reaction, moles of $\ce{HNO_2}$ remaining: $0.23 - 0.12 = 0.11\ \text{mol}$, and moles of $\ce{NO_2^-}$ formed: $0.12\ \text{mol}$ (from the reaction, since 2 moles $\ce{HNO_2}$ give 1 mole $\ce{Ba(NO_2)_2}$, so moles of $\ce{NO_2^-}$ is $0.12\ \text{mol}$). Now we have a weak acid ($\ce{HNO_2}$) and its conjugate base ($\ce{NO_2^-}$) - a buffer.
Step 3: Analyze 0.11 mol HCl
HCl is a strong acid. It will react with any conjugate base, but we don't have a conjugate base initially. Adding HCl to $\ce{HNO_2}$ will just make the solution more acidic, no buffer. Incorrect.
Step 4: Analyze 0.23 mol KCl
KCl is a neutral salt (from strong acid and strong base). It doesn't react with $\ce{HNO_2}$ or provide a conjugate base. So it won't form a buffer. Incorrect.
Step 5: Analyze 0.24 mol $\ce{KNO_2}$
$\ce{KNO_2}$ dissociates to give $\ce{NO_2^-}$ (conjugate base of $\ce{HNO_2}$). Now we have $\ce{HNO_2}$ (weak acid) and $\ce{NO_2^-}$ (conjugate base) - this is a buffer (weak acid + conjugate base).
Wait, wait, initial moles of $\ce{HNO_2}$: $0.23\ \text{mol}$ (1 L of 0.23 M). Let's re - check the $\ce{KNO_2}$ option:
Moles of $\ce{NO_2^-}$ from $\ce{KNO_2}$: $0.24\ \text{mol}$. Moles of $\ce{HNO_2}$: $0.23\ \text{mol}$. So we have a weak acid and its conjugate base (even though the conjugate base is in slight excess), this is a buffer.
Wait, earlier analysis of $\ce{Ba(OH)_2}$:
Moles of $\ce{HNO_2}$: $0.23\ \text{mol}$ (1 L * 0.23 M). Moles of $\ce{OH^-}$ from $\ce{Ba(OH)_2}$: $0.06\ \text{mol} \times 2 = 0.12\ \text{mol}$. The reaction is $\ce{HNO_2 + OH^- -> NO_2^- + H_2O}$. So moles of $\ce{HNO_2}$ remaining: $0.23 - 0.12 = 0.11\ \text{mol}$, moles of $\ce{NO_2^-}$ formed: $0.12\ \text{mol}$. So we have $\ce{HNO_2}$ (0.11 mol) and $\ce{NO_2^-}$ (0.12 mol) - buffer.
For $\ce{KNO_2}$:
Moles of $\ce{NO_2^-}$: $0.24\ \text{mol}$, moles of $\ce{HNO_2}$: $0.23\ \text{mol}$. So weak acid and conjugate base - buffer.
Wait, but let's check the initial problem again. The initial solution is 0.23 M $\ce{HNO_2}$ in 1 L, so 0.23 mol $\ce{HNO_2}$.
Wait, maybe I made a mistake with $\ce{Ba(OH)_2}$:
The reaction is $\ce{2HNO_2 + Ba(OH)_2 -> Ba(NO_2)_2 + 2H_2O}$. So 1 mole $\ce{Ba(OH)_2}$ reacts with 2 moles $\ce{HNO_2}$. Moles of $\ce{Ba(OH)_2}$: 0.06 mol, so moles of $\ce{HNO_2}$ reacted: $0.06 \times 2 = 0.12$ mol. Moles of $\ce{HNO_2}$ remaining: $0.23 - 0.12 = 0.11$ mol. Moles of $\ce{NO_2^-}$ formed: $0.12$ mol (since 2 moles $\ce{HNO_2}$ produce 2 moles $\ce{NO_2^-}$? Wait, no: $\ce{Ba(NO_2)_2}$ dissociates into $\ce{Ba^{2+}}$ and $2\ce{NO_2^-}$. So moles of $\ce{NO_2^-}$ from $\ce{Ba(NO_2)_2}$: $0.06\ \text{mol} \times 2 = 0.12\ \text{mol}$. So now we have $\ce{HNO_2}$ (0.11 mol) and $\ce{NO_2^-}$ (0.12 mol) - buffer.
For $\ce{KNO_2}$:…
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0.06 mol $\ce{Ba(OH)_2}$, 0.24 mol $\ce{KNO_2}$