3.1.8 Thermodynamics Flashcards

1
Q

The standard molar enthalpy of formation

A

When one mol of a compound is formed from its elements at standard states at standard conditions.

Elements → compound

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2
Q

The standard enthalpy of atomisation

A

The enthalpy change of one mol of gaseous atoms form the elements at standard states understandard conditions.

Atom → 1 mol of gaseous atom

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3
Q

First ionisation energy

A

The standard enthalpy changes when 1 mol of gaseous atoms is converted to one mol of gaseous ions each with a single positive charge.

Metal atom → 1+ion

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4
Q

Second ionisation energy

A

The loss of a mol of electrons from a mol of 1+ions

1+ion → 2+ion

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5
Q

First electron affinity

A

When a mol of gaseous atoms is converted to a mol of gaseous 1- ions

Non metal atom → 1-ion

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6
Q

Second electron affinity

A

When a mol of electrons is added to a mol of gaseous ions with a 1- charge

1-ion → 2-ion

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7
Q

Lattice enthalpy of formation

A

When one mol of solid ionic compound is formed from its gaseous ions

Gaseous ions → ionic compound

When a lattice is formed energy is released. Separating requires energy.

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8
Q

Trends in lattice enthalpy

A

Larger ion = smaller lattice enthalpy (as the opposite charges are further apart)
For ions of a similar radius it increases with the charge of the ion.

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9
Q

Theoretical compound

A

Can predict lattice enthalpy of formation theoretically using born haber cycles.
Can you predict from the size of the metal ion and the structure of the crystals ???

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10
Q

find the enthalpy change of hydration when an ionic solid is dissolved in water

A

Enthalpy change of Lattice of dissociation
Pos ions hydrated lattice enthalpy of hydration given out
Neg ions hydrated lattice enthalpy of hydration given out

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11
Q

Lattice enthalpy of dissociation

A

The ionic lattice breaks to give separate gaseous ions.

ionic lattice → separate gaseous ions

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12
Q

Difference between theoretical lattice enthalpy predictions

A

Polarisation when small highly charged negative ions disrupt large highly charged negative ions. Leading to a degree of covalent bonding. Causing a difference between theoretical values.

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13
Q

Forces that make chemical reactions happen

A

Increase in entropy - increase in randomness delta S
Decrease in enthalpy - decrease in energy delta H

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14
Q

What are feasible reactions favoured by

A

Positive entropy changes +delta s (products more random than reactants)
Negative enthalpy changes (energy given out)

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15
Q

Gibbs free energy equation

A

delta G = delta H - T delta S
T = temperature

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16
Q

Value of delatG where it is feasible

A

0
So can calculate the temperature at which the reaction becomes feasible

17
Q

born habour cycle calculation

A

arrow going oposite to direction = arrows going the correct direction

18
Q

delta H of solution

A

= delat H lattice dissociation - (delta H hydra cation + delat H of hydr of anion)

multiply the delta hydra by the nub of ion present for the anion or cation

19
Q

entropy at diffrent states

A

gas is more disordered than a solid

20
Q

when us teh standard entropy os a substance 0

A

at OK
as particals are stationary meaning no vibration
meaning no dissorder

21
Q

difference between boiling and melting

A

boiling has a bigger change in dissorder thena melting

22
Q

delta G =

A

AH -TAS

linear realtionship

23
Q

why delta G decreases as T increases

A

as Tdelta S gets bigger as the particals are moving more meaning ore dissorder

24
Q

frsible when …

A

delta G is negative

25
Q

how to calculate delat S from a table

A

products - reactants

26
Q

what happens at a standard state

A

entropy data is wrong

27
Q

reason the first elctron affinity of oxygen in an exothermic process

A

attractive force between the nucleas of atom and external electron

28
Q

dela solution of a compound =

A

A H lattce enthalpy of the compound

29
Q
A