Energetics Definitions Flashcards

1
Q

Standard Enthalpy Change of Formation

A

of a substance is the enthalpy change that occurs when one mole of the substance is formed from its elements in their standard states

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2
Q

Bond Enthalpy

A

is the energy needed to break one mole of bonds in gaseous molecules under standard conditions.

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3
Q

First Ionisation Energy

A

is the minimum energy required to remove one mole of electrons from one mole of gaseous atoms
X(g) —> X+(g) + e
(endothermic) +

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4
Q

First Electron Affinity

A

is the enthalpy change when one mole of gaseous electrons is added to one mole of gaseous atoms.
X(g) + e —> X-(g)
(exothermic) -

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5
Q

Lattice Enthalpy

A

is the enthalpy change that occurs when one mole of a solid ionic compound is separated into gaseous ions under standard conditions.
XY(s) —> X+(g) + Y-(g)
(endothermic)

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6
Q

Enthalpy Change of Atomisation

A

is the enthalpy change that occurs when one mole of gaseous atoms is formed from the element in its standard state
X(s) —> X(g)

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7
Q

Enthalpy Change of Solution

A

is the enthalpy change when one mole of a solute is dissolved in a solvent to infinite dilution under standard conditions of temperature
related to the lattice enthalpy and the hydration enthalpies of the constituent ions

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8
Q

Enthalpy of Hydration of an Ion

A

is the enthalpy change that occurs when one mole of gaseous ions is dissolved to form an infinitely dilute solution of one mole of aqueous ions
(exothermic)

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9
Q

Entropy

A

refers to the distribution of available energy among the particles, the more ways energy can be distributed the higher the entropy
or
a measure of the disorder or randomness of the particles

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10
Q

Gibbs Free Energy

A

relates to the energy that can be obtained from a chemical reaction to the change in enthalpy, change in entropy and absolute temperature

measure of the driving force of a reaction, its tendency to proceed spontaneously

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11
Q

Enthalpy

A

is the heat content of a system

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12
Q

Endothermic

A

heat is added to a system
enthalpy change is positive
graph shows products have higher energy than reactants

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13
Q

Exothermic

A

heat is released to the surroundings
enthalpy change is negative
graph shows products of lower energy than reactants

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14
Q

Standard Enthalpy Change of Combustion

A

the enthalpy change for the complete combustion of one mole of a substance in its standard state in excess oxygen under standard conditions

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15
Q

Why do experimental values of standard enthalpy of combustion differ from data booklet ones?

A
  • not all the heat produced by the combustion reaction is transferred to the water, some is needed to heat the calorimeter and some has passed to the surroundings
  • the combustion of the ethanol is unlikely to be complete owing to the limited oxygen available, as assumed by the literature value
  • some experiments may not be carried out under standard conditions
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16
Q

Hess’s Law

A

the enthalpy change for a reaction that is carried out in a series of steps is equal to the sum of the enthalpy

17
Q

Why are bonds in oxygen and ozone broken by UV of different wavelengths?

A

O2 has a higher bond enthalpy because it has a double bond (bond order 2) and therefore needs a shorter wavelength of higher energy.
O3 has a lower bond enthalpy (bond order 1.5) due to delocalisation. Therefore it needs UV light of a longer wavelength (less energy)

18
Q

Steps of the natural formation and depletion of Ozone

A

step 1:
O2 –> 2O.
endothermic
high energy needed
step 2:
O. + O2 (in eq. with) O3
forward is exothermic
lower energy
step 3:
O3 + O. –> 2O2
exothermic

19
Q

Born Haber Cycle

A

is an energy cycle based on Hess’s Law but shows the formation of an ionic compound

20
Q

What do lattice enthalpies depend on?

A

depends on the product of the ionic charges and the sum of the ionic radii
- an increase in the ionic radius of one of the ions decreases the attraction between the ions
- an increase in the ionic charge increases the ionic attraction between the ions

21
Q

G and Spontaneity

A

if G < 0 it is a spontaneous reaction
if G > 0 it is not a spontaneous reaction
if G = 0 the reaction is at equilibrium

22
Q

Determining G and spontaneity based on H and S

A

H = + and S = + : G depends on T and reaction is only spontaneous at high T
H = + and S = - : G always + so reaction is never spontaneous
H = - and S = + : G is always negative so the reaction is always spontaneous
H = - and S = - : G depends on T and the reaction is only spontaneous at low T

23
Q

What do values of S mean?

A

if deltaS is + there has been an increase in the disorder of the system
if deltas is - there has been a decrease in disorder (become more ordered)

24
Q

Formula for enthalpy for calorimetry (experimental data)

A

H = q/n
enthalpy change = heat energy / number of moles

25
Q

Formula to use when directed to enthalpy of formations

A

H = sum of Hf products - sum of Hf reactants
* remember Hf of elements = 0

26
Q

Formula to use when directed to bond enthalpies

A

H = H bonds broken - H bonds formed

27
Q

Formula to use when finding change in entropy

A

S = sum S products - sum of S reactants

28
Q

Formula to use when finding G not using H or T or S

A

G = G products - G reactants