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kakasveta [241]
3 years ago
9

Glycine, C2H5O2N, is important for biological energy. The combustion reaction of glycine is described by the following thermoche

mical equation. 4C2H5O2N(s) + 9O2(g) → 8CO2(g) + 10H2O(l) + 2N2(g) ΔH°rxn = –3896 kJ/molWhat is the standard enthalpy of formation of solid glycine?–51.90 kJ/mol–527.5 kJ/mol–974.0 kJ/mol–1502 kJ/mol–2476 kJ/mol
Chemistry
1 answer:
vredina [299]3 years ago
6 0

Answer:

-537.25 kJ/mol is the standard enthalpy of formation of solid glycine.

Explanation:

4C_2H_5O_2N(s) + 9O_2(g)\rightarrow 8CO_2(g) + 10H_2O(l) + 2N_2(g) ,\Delta H^{rxn} =-3896 kJ/mol

Standard enthalpy of formation of oxygen gas= \Delta H_{f,O_2}=0

Standard enthalpy of formation of carbon dioxide= \Delta H_{f,CO_2}=-393.5 kJ/mol

Standard enthalpy of formation of water = \Delta H_{f,H_2O}=-285.8 kJ/mol

Standard enthalpy of formation of nitrogen gas= \Delta H_{f,N_2}=0

Standard enthalpy of formation of glycine = \Delta H_{f,gly}=?

Enthalpy of the reaction = H_{rxn}=-3896 kJ/mol

H_{rxn} =

=8\times \Delta H_{f,CO_2} +10\times \Delta H_{f,H_2O}+2\times \Delta H_{f,N_2} - (4\times \Delta H_{f,gly}+9\times \Delta H_{f,O_2})

-3896 kJ/mol=8\times (-393.5 kJ/mol)+ 10\times (-285.8 kJ/mol)+0 - (4\times \Delta H_{f,gly} +0)

On rearranging :

4\times \Delta H_{f,gly}=8\times (-393.5 kJ/mol)+ 10\times (-285.8 kJ/mol)+ 3896 kJ/mol

\Delta H_{f,gly}=\frac{-2149 kJ/mol}{4}=-537.25 kJ/mol

-537.25 kJ/mol is the standard enthalpy of formation of solid glycine.

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The balanced redox reaction is

3Fe + 2NO₃⁻+ 8H+ → 3Fe²⁺ + 2NO + 4H2O

<h3>What is Galvanic cell? </h3>

It is a device that is used for the conversion of the chemical energy which is produce in the redox reaction into the electrical energy. It is also termed as the voltaic cell or electrochemical cell.

In the voltaic cell, at anode which is negative electrode of voltaic cell oxidation occurs and at the cathode which is positive electrode, reduction occurs

<h3>What is redox reaction? </h3>

The reaction in which both reduction and oxidation reaction takes place simultaneously is known as redox reaction.

<h3>What is oxidation reaction? </h3>

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<h3>What is reduction reaction? </h3>

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The given two-half reactions are:

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3Fe → 3Fe²⁺ + 6e-

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8H(+) + 2NO₃⁻ → 2NO + 4H2O

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3Fe + 2NO₃⁻+ 8H+ → 3Fe²⁺ + 2NO + 4H2O

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All four forms of energy are quantised and the quanta ‘gap’ differences increases from trans. KE ==> electronic.

Entropy (S) and energy distribution: The energy is distributed amongst the energy levels in the particles to maximise their entropy.

Entropy is a measure of both the way the particles are arranged AND the ways the quanta of energy can be arranged.

We can apply ΔSθsys/surr/tot ideas to chemical changes to test feasibility of a reaction:

ΔSθtot = ΔSθsys +  ΔSθsurr

ΔSθtot must be >=0 for a chemical change to be feasible.

For example: CaCO3(s) ==> CaO(s) + CO2(g) 

ΔSθsys = ΣSθproducts – ΣSθreactants 

ΔSθsys = SθCaO(s) + SθCO2(g) – SθCaCO3(s) 

ΔSθsurr is –ΔHθ/T(K) and ΔH is very endothermic (very +ve),

Now ΔSθsys is approximately constant with temperature and at room temperature the ΔSθsurr term is too negative for ΔSθtot to be plus overall.

But, as the temperature is raised, the ΔSθsurr term becomes less negative and eventually at about 800oCΔSθtot becomes plus overall (and ΔGθ becomes negative), so the decomposition is now chemically, and 'commercially' feasible in a lime kiln.

CaCO3(s) ==> CaO(s) + CO2(g)  ΔHθ = +179 kJ mol–1  (very endothermic)

This important industrial reaction for converting limestone (calcium carbonate) to lime (calcium oxide) has to be performed at high temperatures in a specially designed limekiln – which these days, basically consists of a huge rotating angled ceramic lined steel tube in which a mixture of limestone plus coal/coke/oil/gas? is fed in at one end and lime collected at the lower end. The mixture is ignited and excess air blasted through to burn the coal/coke and maintain a high operating temperature.
ΔSθsys = ΣSθproducts – ΣSθreactants
ΔSθsys = SθCaO(s) + SθCO2(g) – SθCaCO3(s) = (40.0) + (214.0) – (92.9) = +161.0 J mol–1 K–1
ΔSθsurr is –ΔHθ/T = –(179000/T)
ΔSθtot = ΔSθsys +  ΔSθsurr
ΔSθtot = (+161) + (–179000/T) = 161 – 179000/T
If we then substitute various values of T (in Kelvin) you can calculate when the reaction becomes feasible.
For T = 298K (room temperature)

ΔSθtot = 161 – 179000/298 = –439.7 J mol–1 K–1, no good, negative entropy change

For T = 500K (fairly high temperature for an industrial process)

ΔSθtot = 161 – 179000/500 = –197.0, still no good

For T = 1200K (limekiln temperature)

ΔSθtot = 161 – 179000/1200 = +11.8 J mol–1 K–1, definitely feasible, overall positive entropy change

Now assuming ΔSθsys is approximately constant with temperature change and at room temperature the ΔSθsurr term is too negative for ΔSθtot to be plus overall. But, as the temperature is raised, the ΔSθsurr term becomes less negative and eventually at about 800–900oC ΔSθtot becomes plus overall, so the decomposition is now chemically, and 'commercially' feasible in a lime kiln.
You can approach the problem in another more efficient way by solving the total entropy expression for T at the point when the total entropy change is zero. At this point calcium carbonate, calcium oxide and carbon dioxide are at equilibrium.
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This means that 1112 K is the minimum temperature to get an economic yield. Well at first sight anyway. In fact because the carbon dioxide is swept away in the flue gases so an equilibrium is never truly attained so limestone continues to decompose even at lower temperatures.

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