MY ⇌ M + + Y – s s s K sp = s.s = s 2 s =
= 7.87 × 10 –7 mol L –1 NY 3 ⇌ N + + 3Y – s s 3s K sp = s.(3s) 3 = 27s 4 6.2 × 10 –13 = 27s 4 s = 3.89 × 10 –4 mol L –1 Hence, molar solubility of MY in water is less than that of NY 3 .
MY ⇌ M + + Y – s s s K sp = s.s = s 2 s =
= 7.87 × 10 –7 mol L –1 NY 3 ⇌ N + + 3Y – s s 3s K sp = s.(3s) 3 = 27s 4 6.2 × 10 –13 = 27s 4 s = 3.89 × 10 –4 mol L –1 Hence, molar solubility of MY in water is less than that of NY 3 .
HCl + NaOH NaCl + H 2 O Initial 0.01 0.1 0 0 Final 0 0.09 0.01 0.01 As equal volumes of HCl and NaOH are added so the volume of resulting solution becomes double and the concentration of the solution becomes half.
[OH - ] =
= 0.045 M pOH = – log[OH – ] = –log [0.045] = 1.35 pH = 14 – pOH = 14 – 1.35 = 12.65
An acidic buffer is a mixture of a weak acid and its salt with a strong base.
Among CH 3 COOH, H 2 CO 3 , H 3 PO 4 and HClO 4 , the HClO 4 is a strong acid while all other are weak acid thus, HClO 4 and NaClO 4 does not constitute to form an acidic buffer.
From the Ksp values of the given salts calculate the solubility values.
Salt having highest solubility will precipitate at last. <table class=tg> <tbody><tr> <th class=tg-nrix>AgCrO<sub>4</sub></th> <th class=tg-nrix>⇌</th> <th class=tg-baqh>2Ag<sup>+</sup></th> <th class=tg-baqh>+</th> <th class=tg-baqh>CrO<sub>4</sub><sup>2-</sup></th> </tr> <tr> <td class=tg-nrix>s</td> <td class=tg-nrix></td> <td class=tg-baqh>2s</td> <td class=tg-baqh></td> <td class=tg-baqh>s</td> </tr> </tbody></table> <br><br>K<sub>sp</sub> = (2s)<sup>2</sup>(s) = 1.1 × 10<sup>–12</sup> <br><br> s = 0.65 × 10<sup>–4</sup> <br><br> <table class=tg> <tbody><tr> <th class=tg-nrix>AgCl</th> <th class=tg-nrix>⇌</th> <th class=tg-baqh>Ag<sup>+</sup></th> <th class=tg-baqh>+</th> <th class=tg-baqh>Cl<sup>-</sup></th> </tr> <tr> <td class=tg-nrix>s</td> <td class=tg-nrix></td> <td class=tg-baqh>s</td> <td class=tg-baqh></td> <td class=tg-baqh>s</td> </tr> </tbody></table> <br><br>K<sub>sp</sub> = s × s <br><br> 1.8 × 10<sup>–10</sup> = s <sup>2</sup> <br><br> s = 1.34 × 10<sup>–5</sup> <br><br> <table class=tg> <tbody><tr> <th class=tg-nrix>AgBr</th> <th class=tg-nrix>⇌</th> <th class=tg-baqh>Ag<sup>+</sup></th> <th class=tg-baqh>+</th> <th class=tg-baqh>Br<sup>-</sup></th> </tr> <tr> <td class=tg-nrix>s</td> <td class=tg-nrix></td> <td class=tg-baqh>s</td> <td class=tg-baqh></td> <td class=tg-baqh>s</td> </tr> </tbody></table> <br><br>K<sub>sp</sub> = s × s <br><br> 5 × 10<sup>–13</sup> = s<sup>2</sup> <br><br> s = 0.71 × 10<sup>–6</sup> <br><br> <table class=tg> <tbody><tr> <th class=tg-nrix>AgI</th> <th class=tg-nrix>⇌</th> <th class=tg-baqh>Ag<sup>+</sup></th> <th class=tg-baqh>+</th> <th class=tg-baqh>I<sup>-</sup></th> </tr> <tr> <td class=tg-nrix>s</td> <td class=tg-nrix></td> <td class=tg-baqh>s</td> <td class=tg-baqh></td> <td class=tg-baqh>s</td> </tr> </tbody></table> <br><br>K<sub>sp</sub> = s × s <br><br> 8.3 × 10<sup>–17</sup> = s<sup>2</sup> <br><br> s = 0.9 × 10<sup>–8</sup> <br><br> Solubility of Ag<sub>2</sub>CrO<sub>4</sub> is maximum so, it will precipitate at last.
Na 2 CO 3 is salt of strong base, NaOH and weak acid, H 2 CO 3 hence the pH value of the solution will be high.
Given, K a = 1 × 10 –4 pK a = – log (1× 10 –4 ) = 4 pH = pK a + log
5 = 4 + log
log
= 1
= 10 = 10 : 1
K w at 25 o C = 1 × 10 –14 At 25ºC K w = [H + ] [OH – ] = 10 –14 At 100°C (given) K w = [H + ] [OH – ] = 55 × 10 –14 for a neutral solution [H + ] = [OH – ] [H + ] 2 = 55 × 10 –14 or [H + ] = (55 × 10–14) 1/2 pH = – log [H + ] On taking log on both side – log [H + ] = –log (55 × 10 –14 ) 1/2 pH =
- log55 - 14log10 pH = 6.13
<table class=tg> <tbody><tr> <th class=tg-9wq8>CaCO<sub>3</sub></th> <th class=tg-9wq8></th> <th class=tg-c3ow>Ca<sup>2+</sup></th> <th class=tg-c3ow>+</th> <th class=tg-c3ow>CO<sub>3</sub><sup>2-</sup></th> </tr> <tr> <td class=tg-9wq8></td> <td class=tg-9wq8></td> <td class=tg-c3ow>x</td> <td class=tg-c3ow></td> <td class=tg-c3ow>x</td> </tr> </tbody></table> <br> <table class=tg> <tbody><tr> <th class=tg-9wq8>CaC<sub>2</sub>O<sub>4</sub></th> <th class=tg-9wq8></th> <th class=tg-c3ow>Ca<sup>2+</sup></th> <th class=tg-c3ow>+</th> <th class=tg-c3ow>C<sub>2</sub>O<sub>4</sub><sup>2-</sup></th> </tr> <tr> <td class=tg-9wq8></td> <td class=tg-9wq8></td> <td class=tg-c3ow>y</td> <td class=tg-c3ow></td> <td class=tg-c3ow>y</td> </tr> </tbody></table> <br><br>[Ca<sup>2+</sup>] = x + y <br><br>Now, K<sub>sp</sub> (CaCO<sub>3</sub>) = [Ca<sup>2+</sup>] [CO<sub>3</sub> <sup>2-</sup>] <br><br>or 4.7 × 10<sup>–9</sup> = (x + y)x .......(1) <br><br>similarly, K<sub>sp</sub> (CaC<sub>2</sub>O<sub>4</sub>) = [Ca<sup>2+</sup>] [C<sub>2</sub>O<sub>4</sub><sup>2–</sup>] <br><br>or 1.3 × 10<sup>–9</sup> = (x + y)y .......(2) <br><br>Dividing equation (1) and (2), we get <br><br>
<br><br> x = 3.6y <br><br>Putting in equation (2) we get <br><br>y(3.6y + y) = 1.3 × 10<sup>–9</sup> <br><br> y = 1.68 10<sup>-5</sup> <br><br>and x = 3.6 1.68 10<sup>-5</sup> = 6.048 10<sup>-5</sup> <br><br> [Ca<sup>2+</sup>] = (x + y) = (6.048 10<sup>-5</sup>) + (1.68 10<sup>-5</sup>) <br><br> [Ca<sup>2+</sup>] = 7.746 × 10<sup>–5</sup> M
0.037 =
K a = (0.037) 2 0.10 = 1.37 ×10 –4
1.4 10 4
KOH is the base thus, it gives OH – ions thus it cannot remove OH – ions from reaction mixture but it adds on the concentration of OH – ions.
So, an acid must be added but if a strong acid is added to the reaction mixture then in acidic condition the MnO 4 – formed reduces to give Mn 2+ thus, HCl which is a strong acid and SO 2 which on treating with water forms a strong H 2 SO 4 cannot be used for this purpose.
Thus, CO 2 which forms H 2 CO 3 a weak acid reacts to remove OH – but not that much acidic that MnO 4 – undergo reduction.
Thus, CO 2 is used for this reaction for completion.