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3 years ago

Part A

Chemistry

1 answer:

den301095 [7]3 years ago

3 0

Answer:

$n_{Cl_2}=0.3molCl_2$

Explanation:

Hello there!

In this case, according to the given chemical reaction whereas the sodium chloride is in a 2:1 mole ratio with chlorine, the required moles of the later are computed as shown below:

$n_{Cl_2}=0.6molNaCl*\frac{1molCl_2}{2molNaCl}$

So we cancel out the moles of NaCl to obtain:

$n_{Cl_2}=0.3molCl_2$

Best regards!

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Compare and contrast the functions of each of the following types of flasks: filter, Erlenmeyer, volumetric.

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4 years ago

What are the missing coefficents for the following equation? __N2+__H2->__NH3

vivado [14]

Answer:

1, 3, 2

Explanation:

N2 + H2 → NH3

I usually find that the best way to systematically balance an equation by inspection is to start with the most complicated-looking formula and then balance atoms in the order:

All atoms other than O and H
O
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(a) The most complicated formula is NH3.

(b) Balance N.

We have 1 H in NH3, but 2 N on the left. We need 2 N on the right. Put a 1 in front of N2 and a 2 in front of NH3.

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3 years ago

50.0 mL solution of 0.160 M potassium alaninate ( H 2 NC 2 H 5 CO 2 K ) is titrated with 0.160 M HCl . The p K a values for the

scZoUnD [109]

Answer:

a) 6.12

b) 1.87

Explanation:

At the onset of the equivalence point (i.e the first equivalence point); alaninate is being converted to alanine.

$H_2NC_2H_5CO^-_2$ $+$ $H^+$ ------> $H_3}^+NC_2H_5CO^-_2$

1 mole of alaninate react with 1 mole of acid to give 1 mole of alanine;

therefore 50.0 mL of 0.160 M alaninate required 50.0 mL of 0.160M HCl to reach the first equivalence point.

The concentration of alanine can be gotten via the following process as shown below;

$[H_3}^+NC_2H_5CO^-_2]$ = $\frac{initial moles of alaninate}{total volume}$

$[H_3}^+NC_2H_5CO^-_2]$ = $\frac{(50.0mL)*(0.160M)}{(50.0mL+50.0mL)}$

$[H_3}^+NC_2H_5CO^-_2]$ = $\frac{8}{100mL}$

$[H_3}^+NC_2H_5CO^-_2]$ = 0.08 M

Alanine serves as an intermediary form, however the concentration of $H^+$ and the pH can be determined as follows;

$[H^+]$ = $\sqrt{\frac{K_{a1}K_{a2}{[H_3}^+NC_2H_5CO^-_2]+K_{a1}K_w}{ K_{a1}{[H_3}^+NC_2H_5CO^-_2] } }$

$[H^+]$ = $\sqrt{\frac{ (10^{-pK_{a1})}(10^{-pK_{a2})}(0.08)+(10^{-pK_{a1})}(1.0*10^{-14})} {(10^{-pK_{a1}})+(0.08)} }$

$[H^+]$ = $\sqrt{\frac{ (10^{-2.344})(10^{-9.868})(0.08)+(10^{-2.344})(1.0*10^{-14})} {(10^{-2.344})+(0.08)} }$

$[H^+]$ = $7.63*10^{-7}M$

pH = - log $[H^+]$

pH = $-log[7.63*10^{-7}]$

pH= 6.12

Therefore, the pH of the first equivalent point = 6.12

b) At the second equivalence point; all alaninate is converted into protonated alanine.

$H_2NC_2H_5CO^-_2$ $+$ $H^+$ -----> $H^+_3NC_2H_5CO^-_2$

$H^+_3NC_2H_5CO^-_2$ $+$ $H^+$ -----> $H^+_3NC_2H_5CO_2H$

Here; we have a situation where 1 mole of alaninate react with 2 moles of acid to give 1 mole of protonated alanine;

Moreover, 50.0 mL of 0.160 M alaninate is needed to produce 100.0mL of 0.160 M HCl in order to achieve the second equivalence point.

Thus, the concentration of protonated alanine can be determined as:

$[H^+_3NC_2H_5CO_2H]$ = $\frac{initial moles of alaninate}{total volume}$

$[H^+_3NC_2H_5CO_2H]$ = $\frac{(50.0mL)*(0.160M)}{(50.0mL+100.0mL)}$

$[H^+_3NC_2H_5CO_2H]$ = $\frac{8}{150}$

$[H^+_3NC_2H_5CO_2H]$ = 0.053 M

The pH at the second equivalence point can be calculated via the dissociation of protonated alanine at equilibrium which is represented as:

$H^+_3NC_2H_5CO_2H$ ⇄ $H^+_3NC_2H_5CO^-_2$ $+$ $H^+$

(0.053 - x) x x

$K_{a1}$ = $\frac{[H^+] [H^+_3NC_2H_5CO^-_2]}{[H^+_3NC_2H_5CO_2H]}$

$10^{-PK_{a1}}$ = $\frac{x*x}{(0.053-x)}$

$10^{-2.344} =\frac{x^2}{(0.053-x)}$

$0.00453 = \frac{x^2}{(0.053-x)}$

$0.00453(0.053-x) =x^2$

$x^2+0.00453x-(2.4009*10^{-4})$

Using quadratic equation formula;

$\frac{-b+/-\sqrt{b^2-4ac} }{2a}$

we have:

$\frac{-0.00453+\sqrt{(0.00453)^2-4(1)(-2.4009*10^{-4})} }{2(1)}$ OR $\frac{-0.00453-\sqrt{(0.00453)^2-4(1)(-2.4009*10^{-4})} }{2(1)}$

= 0.0134 OR -0.0179

So; we go by the positive integer which says

x = 0.0134

So $[H^+]=[H_3^+NC_2H_5CO^-_2]= 0.0134 M$

pH = $-log[H^+]$

pH = $-log[0.0134]$

pH = 1.87

Thus, the pH of the second equivalent point = 1.87

3 0

4 years ago