5.2 Energy Flashcards

1
Q

bond enthalpy definition

A

(average) energy required to break 1 mole of bonds in gaseous particles

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2
Q

enthalpy change of combustion definition

A

enthalpy change when 1 mole of substance is burnt completely, in excess oxygen

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3
Q

enthalpy change of reaction definition

A

energy change when the amount in moles of the substances as written react

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4
Q

enthalpy change of formation definition

A

enthalpy change when 1 mole of substance is formed from its elements in their standard states

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5
Q

enthalpy change of neutralisation definition

A

enthalpy change when 1 mole of water is formed in a reaction between an acid and a base

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6
Q

lattice enthalpy definition

A

enthalpy change when 1 mole of ionic solid is formed from its gaseous ions

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7
Q

factor affecting lattice bond enthalpy

A

size of ions (larger ions = lower charge density = less energy released during formation / absorbed during break down due to weaker bond formed = less negative lattice enthalpy)

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8
Q

enthalpy change of atomisation definition

A

enthalpy change when 1 mole of gaseous atom is formed from an element in its standard state

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9
Q

enthalpy change of electron affinity

A

enthalpy change when each atom in 1 mole of gaseous atoms takes up 1 electron to form 1 mole of gaseous 1- ions

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10
Q

enthalpy of solution definition

A

enthalpy change when 1 mole of a solid compound is dissolved in water to form an infinitely dilute solution

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11
Q

enthalpy change of hydration definition

A

enthalpy change when 1 mole of gaseous ions is dissolved in water to form an infinitely dilute solution
e.g. K+(g) + aq -> K+(aq)

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12
Q

relationship between lattice enthalpy and breaking of lattice

A

energy involved in breaking the lattice is directly involved in forming the lattice
opposites

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13
Q

enthalpy of solution exo or endothermic

A

depends on balance between magnitudes of lattice enthalpy and enthalpy of hydration

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14
Q

entropy definition

A

measure of dispersal of energy in a system

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15
Q

entropy organised or disorganised

A

the greater the entropy, the more disordered the system

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16
Q

standard entropy definition

A

entropy content of one mole of substance under standard conditions
measured in J K^-1 mol^-1

17
Q

how reaction is feasible

A

overall energy of products is lower than overall energy of reactants
negative ∆G

18
Q

Gibbs free energy change formula

A

∆G = ∆H - T∆S

19
Q

entropy change of surroundings formula

A

∆S (surroundings) = ∆H(reactions)/T

20
Q

why feasible reactions may not happen

A

activation energy may be too high

rate of reaction may be very slow

21
Q

free energy and feasability when -ve enthalpy, -ve entropy

A

-ve ∆G at low temperatures

only feasible at low temperatures

22
Q

free energy and feasability when -ve enthalpy, +ve entropy

A

always -ve ∆G

always feasible

23
Q

free energy and feasability when +ve enthalpy, -ve entropy

A

always +ve ∆G

never feasible

24
Q

free energy and feasability when +ve enthalpy, +ve entropy

A

-ve ∆G at high temperatures

feasible at high temperatures

25
Q

calculating enthalpy/entropy change of reaction from given enthalpy change of formation/entropy values

A

products - reactants

26
Q

why is it difficult to predict whether enthalpy change of solution becomes more exothermic or less endothermic down group 7

A

ionic radius increases going down the group
lattice enthalpy becomes less exothermic when going down the group (enthalpy change of solution would be more exothermic)
enthalpy of hydration becomes less exothermic going down the group (enthalpy change of solution would be less exothermic)
difficult to predict whether enthalpy change of solution is exothermic or endothermic

27
Q

why second electron affinity is endothermic

A

X- ion repels the electron being added

requires heat energy to overcome repulsion