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Elina [12.6K]
3 years ago
6

How many kJ of energy will be released when 4.72g of carbon react with excess oxygen to produce carbon dioxide (delta H is -393.

5 kJ)

Chemistry
1 answer:
ivolga24 [154]3 years ago
7 0

Answer:

155 kJ of energy will be released.

Explanation:

The \rm \Delta H\textdegree (\rm \Delta H \textdegree_\text{rxn} in some textbooks) here stands for standard enthalpy change per mole reaction. To find the amount of energy released in this reaction, start by finding the number of moles of this reaction that will take place.

How many <em>moles</em> of atoms in 4.72 grams of carbon?

Relative atomic mass data from a modern periodic table:

  • C: 12.01.

\displaystyle n = \frac{m}{M} = \rm \frac{4.72\;g}{12.01\; g\cdot mol^{-1}} = 0.393006\; mol.

The coefficient of carbon in the equation is one. In other words, each mole of the reaction will consume one mole of carbon. Oxygen is in excess. As a result, \rm 0.393006\; mol of carbon will support \rm 0.393006\; mol of the reaction.

How much energy will be released?

The \rm \Delta H\textdegree{} value here is negative. But don't panic. \rm \Delta H\textdegree{} is the same as the chemical potential energy of the reactants minus the products in one mole of the reaction. \rm \Delta H\textdegree{} = -393.5\;kJ means that the chemical potential energy drops by \rm 393.5\; kJ during each mole of the reaction (with the coefficients as-is.) Those energy difference will be released as heat. In other words, one mole of the reaction will release \rm 393.5\;kJ of energy.

The 4.72 grams of carbon will support \rm 0.393006\; mol of this reaction. How much heat will that \rm 0.393006\; mol of reaction release?

Q = n \cdot (-\Delta \text{H}\textdegree{}) = \rm 0.393006\times 393.5 = 155\;kJ.

As a side note, the mass of carbon 4.72 grams is the least significant data in this question. There are three significant figures in this value. As a result, keep more than three significant figures in calculations but round the final result to three significant figures.

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Calculate the pH for each of the following cases in the titration of 50.0 mL of 0.210 M HClO(aq) with 0.210 M KOH(aq).
Degger [83]
a) before addition of any KOH : 

when we use the Ka equation & Ka = 4 x 10^-8 : 

Ka = [H+]^2 / [ HCIO]

by substitution:

4 x 10^-8 = [H+]^2 / 0.21

[H+]^2 = (4 x 10^-8) * 0.21

           = 8.4 x 10^-9

[H+] = √(8.4 x 10^-9)

       = 9.2 x 10^-5 M

when PH = -㏒[H+]

   PH = -㏒(9.2 x 10^-5)

        = 4  

b)After addition of 25 mL of KOH: this produces a buffer solution 

So, we will use Henderson-Hasselbalch equation to get PH:

PH = Pka +㏒[Salt]/[acid]


first, we have to get moles of HCIO= molarity * volume

                                                           =0.21M * 0.05L

                                                           = 0.0105 moles

then, moles of KOH = molarity * volume 

                                  = 0.21 * 0.025

                                  =0.00525 moles 

∴moles HCIO remaining = 0.0105 - 0.00525 = 0.00525

and when the total volume is = 0.05 L + 0.025 L =  0.075 L

So the molarity of HCIO = moles HCIO remaining / total volume

                                        = 0.00525 / 0.075

                                        =0.07 M

and molarity of KCIO = moles KCIO / total volume

                                    = 0.00525 / 0.075

                                    = 0.07 M

and when Ka = 4 x 10^-8 

∴Pka =-㏒Ka

         = -㏒(4 x 10^-8)

         = 7.4 

by substitution in H-H equation:

PH = 7.4 + ㏒(0.07/0.07)

∴PH = 7.4 

c) after addition of 35 mL of KOH:

we will use the H-H equation again as we have a buffer solution:

PH = Pka + ㏒[salt/acid]

first, we have to get moles HCIO = molarity * volume 

                                                        = 0.21 M * 0.05L

                                                        = 0.0105 moles

then moles KOH = molarity * volume
                            =  0.22 M* 0.035 L 

                            =0.0077 moles 

∴ moles of HCIO remaining = 0.0105 - 0.0077=  8 x 10^-5

when the total volume = 0.05L + 0.035L = 0.085 L

∴ the molarity of HCIO = moles HCIO remaining / total volume 

                                      = 8 x 10^-5 / 0.085

                                      = 9.4 x 10^-4 M

and the molarity of KCIO = moles KCIO / total volume

                                          = 0.0077M / 0.085L

                                          = 0.09 M

by substitution:

PH = 7.4 + ㏒( 0.09 /9.4 x 10^-4)

∴PH = 8.38

D)After addition of 50 mL:

from the above solutions, we can see that 0.0105 mol HCIO reacting with 0.0105 mol KOH to produce 0.0105 mol KCIO which dissolve in 0.1 L (0.5L+0.5L) of the solution.

the molarity of KCIO = moles KCIO / total volume

                                   = 0.0105mol / 0.1 L

                                   = 0.105 M

when Ka = KW / Kb

∴Kb = 1 x 10^-14 / 4 x 10^-8

       = 2.5 x 10^-7

by using Kb expression:

Kb = [CIO-] [OH-] / [KCIO]

when [CIO-] =[OH-] so we can substitute by [OH-] instead of [CIO-]

Kb = [OH-]^2 / [KCIO] 

2.5 x 10^-7 = [OH-]^2 /0.105

∴[OH-] = 0.00016 M

POH = -㏒[OH-]

∴POH = -㏒0.00016

           = 3.8
∴PH = 14- POH

        =14 - 3.8

PH = 10.2

e) after addition 60 mL of KOH:

when KOH neutralized all the HCIO so, to get the molarity of KOH solution

M1*V1= M2*V2

 when M1 is the molarity of KOH solution

V1 is the total volume = 0.05 + 0.06 = 0.11 L

M2 = 0.21 M 

V2 is the excess volume added  of KOH = 0.01L

so by substitution:

M1 * 0.11L = 0.21*0.01L

∴M1 =0.02 M

∴[KOH] = [OH-] = 0.02 M

∴POH = -㏒[OH-]

           = -㏒0.02 

           = 1.7

∴PH = 14- POH

       = 14- 1.7 

      = 12.3 
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