CHEM ENERGETICS

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30 Terms

1
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Define △H atomisation for elements and compounds. Is it exothermic or endothermic?

For elements, it is the energy required to form 1 mole of gaseous atoms from the element in its standard state under standard conditions, at a specified temperature, usually 298K.

For compounds, it is the energy required to form gaseous atoms from 1 mole of the compound in its standard state under standard conditions, at a specified temperature, usually 298K.

→ endo

<p>For elements, it is the energy <u>required</u> to form <u>1 mole of gaseous atoms</u> from the <u>element in its standard state</u> under <u>standard conditions</u>, at a specified temperature, usually 298K.</p><p>For compounds, it is the energy <u>required</u> to form <u>gaseous atoms</u> from <u>1 mole of the compound in its standard state</u> under <u>standard conditions</u>, at a specified temperature, usually 298K.</p><p>→ endo</p>
2
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Define BE (bond energy). Is it exothermic or endothermic?

It is the average energy required to break 1 mole of covalent bond between 2 atoms in gaseous state.

→ endothermic

<p>It is the <u>average</u> energy required to <u>break 1 mole of covalent </u>bond between 2 atoms in <u>gaseous state</u>.</p><p>→ endothermic</p>
3
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Define △H combustion. Is it exothermic or endothermic?

It is the energy released when 1 mole of substance is completely burnt in excess oxygen under standard conditions, at a specified temperature, usually 298K.

→ exothermic

<p>It is the energy <u>released</u> when <u>1 mole of substance is completely burnt in excess oxygen</u> under <u>standard conditions</u>, at a specified temperature, usually 298K.</p><p>→ exothermic</p>
4
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Define △H formation. Is it exothermic or endothermic?

It is the enthalpy change when 1 mole of substance is formed from its constituent elements in their standard states under standard conditions, at a specified temperature, usually 298K.

→ exo or endo (can be both)

<p>It is the enthalpy change when <u>1 mole of substance</u> is formed <u>from its constituent elements in their standard states</u> under <u>standard conditions</u>, at a specified temperature, usually 298K.</p><p>→ exo or endo (can be both)</p>
5
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Define △H hydration. Is it exothermic or endothermic?

It is the energy released when 1 mole of free gaseous ions is hydrated under standard conditions, at a specified temperature, usually 298K.

→ exo

→ note that ion-dipole interactions between gaseous ions and polar water molecules are formed during hydration. the stronger the ion-dipole interactions, the more exothermic the △H hyd.

<p>It is the energy <u>released</u> when <u>1 mole of free gaseous ions is hydrated</u> under <u>standard conditions</u>, at a specified temperature, usually 298K.</p><p>→ exo</p><p>→ note that ion-dipole interactions between gaseous ions and polar water molecules are formed during hydration. the stronger the ion-dipole interactions, the more exothermic the △H hyd.</p>
6
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Define LE (lattice energy) / △H LE. Is it exothermic or endothermic?

It is the energy released when 1 mole of solid ionic compound is formed from its constituent gaseous ions

→ exo

→ note that generally, the larger the magnitude / numerical value of LE, the stronger the ionic bonds are

<p>It is the energy <u>released</u> when <u>1 mole of solid ionic compound </u>is formed from its constituent gaseous ions</p><p>→ exo </p><p>→ note that generally, the larger the magnitude / numerical value of LE, the stronger the ionic bonds are </p>
7
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Define △H neutralisation. Is it exothermic or endothermic?

It is the energy released when 1 mole of water is formed in a neutralisation reaction between an acid and a base under standard conditions, at a specified temperature, usually 298K.

→ exo

→ note that △H neut involving weak acid or weak base may be less exo since energy is absorbed to dissociate/ionise the undissociated/unionised weak acid or weak base.

<p>It is the energy <u>released</u> when <u>1 mole of water is formed</u> in a <u>neutralisation reaction</u> between an acid and a base under <u>standard conditions</u>, at a specified temperature, usually 298K.</p><p>→ exo</p><p>→ note that △H neut involving weak acid or weak base may be less exo since energy is absorbed to dissociate/ionise the undissociated/unionised weak acid or weak base.</p>
8
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Define △H solution. Is it exothermic or endothermic?

It is the energy change when 1 mole of substance is completely dissolved in an infinite volume of solvent under standard conditions, at a specified temperature, usually 298K.

→ exo or endo (can be both)

<p>It is the <u>energy change</u> when <u>1 mole of substance</u> is <u>completely dissolved in an infinite volume of solvent</u> under <u>standard conditions</u>, at a specified temperature, usually 298K.</p><p>→ exo or endo (can be both)</p>
9
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Define 1st electron affinity (EA). Is it exothermic or endothermic?

It is the energy change when 1 mole of electrons is added to 1 mole of gaseous atoms to form 1 mole of singly charged gaseous anions.

→ exo or endo (can be both)

<p>It is the <u>energy change</u> when <u>1 mole of electrons is added to 1 mole of gaseous atoms</u> to form <u>1 mole of singly charged gaseous anions</u>.</p><p>→ exo or endo (can be both)</p>
10
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Define 1st ionisation energy (IE). Is it exothermic or endothermic?

It is the energy absorbed when 1 mole of electrons is removed from 1 mole of gaseous atoms to form 1 mole of singly charged gaseous cations.

→ endo

<p>It is the energy <u>absorbed</u> when <u>1 mole of electrons</u> is <u>removed</u> from <u>1 mole of gaseous atoms</u> to form <u>1 mole of singly charged gaseous cations</u>.</p><p>→ endo </p>
11
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What is the equation / relationship between △H soln, △H hyd and △H LE?

△H soln = △H hyd - △H LE

12
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Distinguish ionisation from dissociation (for understanding)

→ Dissociation is the separation of particles from an ionic compounds.

→ Ionisation is the process that produces new charged particles.

13
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What conditions are standard?

→ pressure = 1 bar / 10^5 Pa

→ conc for solutions = 1 moldm^-3

→ any temp ok, but usually 298K / 25 °C

14
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Define Hess’ Law.

Hess’ Law states that the enthalpy change of a reaction is determined only by the initial and final states and is independent of the reaction pathway taken.

15
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Define q = -mc△T.

→ q is the heat change, in J

→ m is the mass of solution, in g

→ c is the specific heat capacity of water, at 4.18 or 4.2 J g^-1 K^-1

→ △T is the temperature change of solution, final temp - initial temp, in K or °C

16
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Define q = -C△T.

→ q is the heat change, in J

→ C is the heat capacity of the solution, in J K^-1

→ △T is the temp change of the solution, final temp - initial temp, in K or °C

17
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Define △H reaction = q/n

→ q is the heat change of reaction, = -mc△T or -C△T.

→ n is the amount of limiting reagent or specified substance

→ sign of △Hr (+ or -) denotes whether reaction is endothermic or exothermic

18
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Calculate the efficiency of a combustion reaction.

q’ = x/100 q

where

→ q’ is heat absorbed by calorimeter (including its contents)

→ q is the total heat released from combustion

→ x is the efficiency of combustion reaction

19
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What is the relationship between total BE of bonds broken and total BE of bonds formed?

△Hrxn = Σ (B.E. of bonds broken) − Σ (B.E. of bonds formed)

note: remember you need to break bonds of the reactants to form the bonds of the products

20
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What is the relationship between ΣnHf (products) and ΣmHf (reactants)?

△Hrxn = ΣnHf (products) - ΣmHf (reactants)

note: remember acronym FPR, “fdr”

21
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What is the relationship between ΣnHc (products) and ΣmHc (reactants)?

△Hrxn = ΣnHc (reactants) - ΣmHc (products)

note: remember acronym CRP, “crap”

22
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Why may △Hr differ from actual △H?

1) If BE was used to calculate △Hr, BE are average values and may not be accurate

2) Heat loss to / gain from surroundings was not taken into account

23
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<p>If the standard state of an element is a monoatomic solid, atomisation will involve raising the temperature to melting point, the melting of the element (△H fusion)<em>,</em> raising of the temperature to boiling point, and then vaporisation (△H vaporisation).</p><p>For a monoatomic solid that undergoes sublimation, △H atomisation is the same as the standard enthalpy change of sublimation (△H sublimation.</p><p><em>→ E.g.</em> Na(s) → Na(g)</p><p>→ △H at = △H fus + △H vap + Cm (solid)△T + Cm (liquid)△T, where <em>C</em>m is the molar heat capacity</p>

If the standard state of an element is a monoatomic solid, atomisation will involve raising the temperature to melting point, the melting of the element (△H fusion), raising of the temperature to boiling point, and then vaporisation (△H vaporisation).

For a monoatomic solid that undergoes sublimation, △H atomisation is the same as the standard enthalpy change of sublimation (△H sublimation.

→ E.g. Na(s) → Na(g)

→ △H at = △H fus + △H vap + Cm (solid)△T + Cm (liquid)△T, where Cm is the molar heat capacity

△H at vs △H vap

→ △H vap does not break any covalent bonds, only overcomes IMF attraction to bring an element/compound from liquid to gaseous state

→ △H at breaks covalent bonds to form gaseous atoms

<p>△H at vs △H vap</p><p>→ △H vap does not break any covalent bonds, only overcomes IMF attraction to bring an element/compound from liquid to gaseous state</p><p>→ △H at breaks covalent bonds to form gaseous atoms</p>
24
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27
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Define entropy.

Entropy is a measure of the level of disorderliness or randomness in a system.

28
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List the factors that affect entropy.

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29
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What is the Gibbs fire energy equation and what they represent?

→ △G = △H - T△S

where

→ △G < 0 indicates spontaneous change, △G = 0 indicates dynamic equilibrium, △G > 0 indicates non-spontaneous change , in kJ mol^-1

→ △H is the enthalpy change, in kJ mol^-1

→ T is temperature, in K

→ △S is entropy change, in kJ mol^-1 K^-1

<p>→ △G = △H - T△S</p><p>where</p><p>→ △G &lt; 0 indicates spontaneous change, △G = 0 indicates dynamic equilibrium, △G &gt; 0 indicates non-spontaneous change , in kJ mol^-1</p><p>→ △H is the enthalpy change, in kJ mol^-1</p><p>→ T is temperature, in K</p><p>→ △S is entropy change, in kJ mol^-1 K^-1</p>
30
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Explain the effect of temperature on △G

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