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Lana71 [14]
3 years ago
6

Calculate the number of moles of HCl(g) that must be added to 1.0 L of 0.80 M NaC2H3O2 to produce a solution buffered at pH = pK

a. Ka(CH3CO2H) = 1.8×10-5 Number of moles = mol Submit b Calculate the number of moles of HCl(g) that must be added to 1.0 L of 0.80 M NaC2H3O2 to produce a solution buffered at pH = 4.20. Ka(CH3CO2H) = 1.8×10-5 Number of moles = mol c Calculate the number of moles of HCl(g) that must be added to 1.0 L of 0.80 M NaC2H3O2 to produce a solution buffered at pH = 5.00. Ka(CH3CO2H) = 1.8×10-5 Number of moles = mol
Chemistry
1 answer:
GREYUIT [131]3 years ago
4 0

Answer:

a.  0.40

b.  0 .62 mol HCl

c.   0.29 mol HCl

Explanation:

Lets call A⁻ the molar concentration of the weak base A⁻, and HA the acid concentration of HA

a. pH = pKa

from Henderson-Hasselbach equation for buffer solutions:

pH = pKa - log(( A⁻/HA))

we can see that pH = Pka when the  log(( A⁻/HA)) is 0 which is the case for the log 1 hence

A⁻ =HA  and

Ka=  H⁺ x  A ⁻/ HA  

Now for the equilibrium of the weak acid  we have

R                     HA==================  H⁺ + A⁻

Initially            0.80                                    0     0

Change            -x                                     + x    +  x

Equilibrium     0.80 - x                               x      x

Since x = A⁻ and HA = 0.80- x

x/ (0.80-x) =1  

x = 0.80 -x      2x = 0.80

x = 0.40

b. From the Henderson-Hasselbach eqn:

pH = pKa - log ((A⁻/HA))

4.20-4.74 = log ((0 .80-x)/x)  (the negative log of A⁻/HA is the same as log HA/A⁻)

-0.54 = log ((0.80-x)/x)

0.29 = (0.80-x)/x

0.29 x = 0.80 - x

1.29 x = 0.80 moles HCL

x = 0.62

c.  pH= 5.00

Using the same relationships as in b.

5.00-4.74 = log ((0.80-x)/x)

1.80 =( 0.80 - x) /x

2.8 x = 0.80

x = 0.29

0.29 mol HCl needed

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The question is incomplete, here is the complete question:

While ethanol is produced naturally by fermentation, e.g. in beer- and wine-making, industrially it is synthesized by reacting ethylene with water vapor at elevated temperatures.

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<u>Explanation:</u>

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Initial partial pressure of water vapor = 4.7 atm

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Equilibrium partial pressure of water vapor = 4.06 atm

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                     CH_2CH_2(g)+H_2O(g)\rightleftharpoons CH_3CH_2OH(g)

<u>Initial:</u>                  1.8                4.7

<u>At eqllm:</u>           1.8-x             4.7-x

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p_{CH_2CH_2}=1.16atm\\p_{H_2O}=4.06atm\\p_{CH_3CH_2OH}=0.64atm

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<u>Initial:</u>                2.36             4.06               0.64

<u>At eqllm:</u>           2.36-x        4.06-x             0.64+x

Putting value in the equilibrium constant expression, we get:

0.136=\frac{(0.64+x)}{(2.36-x)\times (4.06-x)}\\\\x=0.363,13.41

Neglecting the value of x = 13.41 because equilibrium partial pressure of ethylene and water vapor will become negative, which is not possible.

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