Deck 4: energetics 1 and 2 Flashcards

(43 cards)

1
Q

Enthalpy

A

measure of the energy content of the system

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2
Q

Enthalpy change

A

difference between the quantity of heat absorbed to break the bonds in the reactants and that released during the formation of new bonds in the products at constant pressure

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3
Q

units of enthalpy change

A

kj mol-1

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4
Q

activation energy

A

minimum amount of energy that the reactant particles must possess before they can collide successfully to form products

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5
Q

enthalpy change of reaction

A

energy change in a chemical reaction when the molar quantities of reactants stated in the chemical equation react under standard conditions (ie. 1 bar and 298K)

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6
Q

enthalpy change of formation

A

energy change when 1 mole of the pure substance in a specified state is formed from its constituent elements in their standard states under standard conditions (ie. 1 bar and 298K)

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7
Q

enthalpy change of combustion

A

energy released (cause always exo) when 1 mole of the substance is completely burnt in excess oxygen under standard conditions (ie. 1 bar and 298K)

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8
Q

enthalpy change of neutralisation

A

between an acid and a base is the energy change when the acid and the base react to form 1 mole of water under standard conditions (ie. 1 bar and 298K)

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9
Q

value for enthalpy change of neutralisation for strong acid and base

A

-57.3 kj mol-1

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10
Q

explanation for less exo neutralisation for weak acid strong base

A
  1. weak acid exists mainly as molecules hence further dissociation is required to produce more H+ ions
  2. dissociation involves the breaking of the O-H bond (for the case of CH3COOH) which is an endothermic process and the hydration of the CH3COO- and H+ ions which is an exothermic process
  3. overall, the dissociation process is endothermic
  4. thus as energy is consumed for further dissociation, the energy released by the reaction will be reduced and it will be less exothermic
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11
Q

enthalpy change of atomisation

A

energy absorbed when 1 mole of gaseous atoms is formed from the element under standard conditions (ie. 1 bar and 298K)

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12
Q

enthalpy change of atomisation of a compound

A

energy absorbed (always endo cos breaking bonds) when 1 mole of the compound is converted to gaseous atoms under standard conditions (ie. 1 bar and 298K)

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13
Q

enthalpy change of hydration

A

of an ion is the energy released (always exo) when 1 mole of gaseous ions is dissolved in water to form 1 mole of aqueous ions under standard conditions (ie. 1 bar and 298K)

  • PROPORTIONAL TO CHARGE DENSITYTYTYTYT to charge over radius (charge density)
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14
Q

enthalpy change of solution

A

of a substance is the energy change when 1 mole of the substance is completely dissolved in a solvent to form an infinitely dilute solution (does not produce any further enthalpy change when more solvent is added) under standard conditions (ie. 1 bar and 298K)

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15
Q

bond dissociation energy

A

BDE of a X-Y bond is the energy required to break 1 mole of that particular X-Y bond in a particular compound in gaseous state

always positive

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16
Q

bond energy

A

of a X-Y bond is the average energy required to break 1 mole of the X-Y bond in the gaseous state

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17
Q

ionisation energy 1st and 2nd

A

The first ionisation energy (1st IE) of an element is the energy required to remove 1 mole of electrons from 1 mole of gaseous atoms to form 1 mole of singly positively charge gaseous ions

The second ionisation energy (2nd IE) of an element is the energy required to remove 1 mole of electrons from 1 mole of singly positively charged gaseous ions to form 1 mole of doubly positively charge gaseous ions

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18
Q

electron affinity

A

→ The first electron affinity (1st EA) of an element is the energy CHANGE when 1 mole of gaseous atoms acquires 1 mole of electrons to form 1 mole of singly negatively charged gaseous ions

→ The second electron affinity (2nd EA) of an element is the energy ABSORBED when 1 mole of singly negatively charged gaseous ions acquires 1 mole of electrons to form 1 mole of doubly negatively charged gaseous ions

19
Q

lattice energy

A

of an ionic compound is the energy released when 1 mole of the solid ionic compound is formed from its constituent gaseous ions under standard conditions

20
Q

specific heat capacity/heat capacity

A

quantity of heat required to raise the temperature of 1g of the substance by 1˚C

quantity of heat required to raise the temperature of the substance by 1˚C

21
Q

assumptions for the calculations

A
  1. negligible heat loss to the surroundings due to insulation
  2. specific heat capacity of solution is approx that of water (4.18J g-1 K-1)
  3. density of solution is approx that of water (1.00g cm-3)
22
Q

Hess Law

A

enthalpy change of reaction is determined by the initial and final states of the system and is independent of the pathways taken

23
Q

explain theoretical and experimental LE deviation

A

in agreement
- predominantly ionic
- fits in the purely ionic model which consists of spherical ions with evenly distributed charge

differ by quite a bit
- not purely ionic
- has covalent character due to the substantial polarisation of the anion by the cation
- if the value is more negative, suggests that bonding is stronger than that suggested by the purely ionic model

24
Q

dissolving steps

A
  1. Separation of the ionic crystal lattice into its gaseous ions
    - breaking down of the solid ionic crystal lattice
    - endothermic
    - proportional to q+q-/r+ +r-
  2. Hydration of the gaseous ions
    - formation of ion dipole moments between the gaseous ions and water molecules to form hydrated ions in aqueous solution
    - exothermic
    - proportional to charge density

for dissolution of smth in water
= -LE + enthalpy change of hydration for each ion

25
Solubility
- more soluble when enthalpy change of solution is more negative (less when positive) - when it is negative, the hydration energy released is sufficient to compensate for the energy required to break the solid ionic crystal lattice and vice versa
26
Spontaneous and non spontaneous
Spontaneous - once started will continue without external assistance (not part of definition but always trying to achieve a lower energy state and reach a state of greater entropy) Non spontaneous - will not occur unless external assistance is continuously applied
27
Entropy
of a system is a measure of the disorder of matter and energy in the system. The more ways matter in the system can be arranged, the more ways energy in the system can be dispersed, the more disordered the system is and the larger is its entropy
28
entropy change and what do positive and negative values mean
measure of change of disorder of a system positive means disorder has increased and vice versa
29
factors affecting LE
LE is proportionate to |(q+q-)/(r+ + r-)| - greater the charge and smaller the cationic/anionic size, the greater the LE (NOTOTOTOTOOTOTOT CHARGE DENSITY)
30
what is the born haber cycle to determine LE
Formation Atomisation Ionisation (IE and EA) LE
31
how to find enthalpy change from combustion, reaction and formation
combustion: reactants - products reaction: reactants - products formation: products - reactants
32
Factors affecting entropy (brief)
change in temperature change in phase change in number of particles mixing of particles
33
how does change in temperature lead to change in entropy
As the temp increases, there is a broadening of the Boltzmann energy distribution of the particles. Thus there are more possible energy states in which the particles can adopt at a higher temp. Hence an increase in temp leads to an increase in entropy
34
how does change in phase affect entropy + graph
graph is step looking thing solid to liquid - order in the solid is destroyed, particles in a liquid are more randomly arranged and more disordered than in the solid liquid to gas - gas particles can move freely and are the most randomly arranged - large increase in volume
35
how does change in number of particles affect entropy
with more particles, there are more ways to arrange the particles and more ways to distribute the energy in the system
36
how does mixing of particles affect entropy
mix gas - gases always mix completely to create a more disordered state - each gas expands to occupy a large volume - increase in S as there are now more ways for the molecules to arrange themselves in the larger volume mix liquids - solution where the molecules are randomly mixed (greater S than in unmixed state) - greater number of ways to arrange the greater number of molecules in a greater volume dissolution of ionic solid - depends on the ions to determine whether S increases/decreases
37
explain dissolution of ionic solid effect on entropy (increase and decrease + example)
Increase NaCl - disruption of crystal lattice increases disorder (LE?) - hydration decreases disorder as it puts the hydrating water molecules into an orderly arrangement about the Na+ and Cl- ions - net increase Decrease CaSO4 - more highly charged ions, more water molecules ordered about the ions - net decrease
38
standard gibbs free energy change equation
ΔG = ΔH - TΔS rmb to check units because S is usully in J mol-1 K-1 and H is in kJ mol-1
39
what does sign of ΔG mean for spontaneity and limitation
ΔG < 0 spontaneous ΔG > 0 non spontaneous ΔG = 0 at equilibrium does not give info about kinetic feasibility related to activation energy
40
just read
ΔG = products - reactants
41
why is enthalpy change of H2O2 --> H2O + 1/2O2 < 0
H2O and O2 are energetically more stable than H2O2 as the bonds in H2O and O2 are overall stronger compared to in H2O2
42
what is the graph of ΔG
vertical intercept of ΔH and gradient of -ΔS it is NEGATIVEIVIEIVE ΔS not positive
43
jsut read
due to the increased charge and decreased size of Mg2+ ions compared to Na+ ions, more water molecules are ordered around the Mg2+. Hence on average, the entropy change in hydration process decreases more for Mg2+ hence net entropy change of solution of Mg(OH)2 is likely to be more negative than NaOH