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lisabon 2012 [21]
3 years ago
7

Using any data you can find in the ALEKS Data resource, calculate the equilibrium constant K at 30.0 °C for the following reacti

on CH3OH(g) + C0(g) → HCH,CO2(l) Round your answer to 2 significant digits. K= x10
Chemistry
1 answer:
gayaneshka [121]3 years ago
4 0

Answer : The value of K for this reaction is, 2.6\times 10^{15}

Explanation :

The given chemical reaction is:

CH_3OH(g)+CO(g)\rightarrow HCH_3CO_2(g)

Now we have to calculate value of (\Delta G^o).

\Delta G^o=G_f_{product}-G_f_{reactant}

\Delta G^o=[n_{HCH_3CO_2(g)}\times \Delta G^0_{(HCH_3CO_2(g))}]-[n_{CH_3OH(g)}\times \Delta G^0_{(CH_3OH(g))}+n_{CO(g)}\times \Delta G^0_{(CO(g))}]

where,

\Delta G^o = Gibbs free energy of reaction = ?

n = number of moles

\Delta G^0_{(HCH_3CO_2(g))} = -389.8 kJ/mol

\Delta G^0_{(CH_3OH(g))} = -161.96 kJ/mol

\Delta G^0_{(CO(g))} = -137.2 kJ/mol

Now put all the given values in this expression, we get:

\Delta G^o=[1mole\times (-389.8kJ/mol)]-[1mole\times (-163.2kJ/mol)+1mole\times (-137.2kJ/mol)]

\Delta G^o=-89.4kJ/mol

The relation between the equilibrium constant and standard Gibbs, free energy is:

\Delta G^o=-RT\times \ln K

where,

\Delta G^o = standard Gibbs, free energy  = -89.4 kJ/mol = -89400 J/mol

R = gas constant  = 8.314 J/L.atm

T = temperature  = 30.0^oC=273+30.0=303K

K = equilibrium constant = ?

Now put all the given values in this expression, we get:

-89400J/mol=-(8.314J/L.atm)\times (303K)\times \ln K

K=2.6\times 10^{15}

Thus, the value of K for this reaction is, 2.6\times 10^{15}

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Read 2 more answers
A buffer solution is made that is 0.347 M in H2C2O4 and 0.347 M KHC2O4.
irga5000 [103]

Answer:

1. pH = 1.23.

2. H_2C_2O_4(aq) +OH^-(aq)\rightarrow HC_2O_4^-(aq)+H_2O(l)

Explanation:

Hello!

1. In this case, for the ionization of H2C2O4, we can write:

H_2C_2O_4\rightleftharpoons HC_2O_4^-+H^+

It means, that if it is forming a buffer solution with its conjugate base in the form of KHC2O4, we can compute the pH based on the Henderson-Hasselbach equation:

pH=pKa+log(\frac{[base]}{[acid]} )

Whereas the pKa is:

pKa=-log(Ka)=-log(5.90x10^{-2})=1.23

The concentration of the base is 0.347 M and the concentration of the acid is 0.347 M as well, as seen on the statement; thus, the pH is:

pH=1.23+log(\frac{0.347M}{0.347M} )\\\\pH=1.23+0\\\\pH=1.23

2. Now, since the addition of KOH directly consumes 0.070 moles of acid, we can compute the remaining moles as follows:

n_{acid}=0.347mol/L*1.00L=0.347mol\\\\n_{acid}^{remaining}=0.347mol-0.070mol=0.277mol

It means that the acid remains in excess yet more base is yielded due to the effect of the OH ions provided by the KOH; therefore, the undergone chemical reaction is:

H_2C_2O_4(aq) +OH^-(aq)\rightarrow HC_2O_4^-(aq)+H_2O(l)

Which is also shown in net ionic notation.

Best regards!

4 0
3 years ago
You have a solution that is 0.02M formate (HCOO-) and 0.03M formic acid (HCOOH), which has a Ka of 1.8x10-4. What is the pH of t
lisov135 [29]

Answer:

3.6

Explanation:

Step 1: Given data

  • Concentration of formic acid: 0.03 M
  • Concentration of formate ion: 0.02 M
  • Acid dissociation constant (Ka): 1.8 × 10⁻⁴

Step 2: Calculate the pH

We have a buffer system formed by a weak acid (HCOOH) and its conjugate base (HCOO⁻). We can calculate the pH using the <em>Henderson-Hasselbach equation</em>.

pH = pKa +log\frac{[base]}{[acid]} = -log 1.8 \times 10^{-4} + log \frac{0.02}{0.03} = 3.6

6 0
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