chem energetics Flashcards

1
Q

standard enthalpy change of combustion

A

energy evolved when one mole of the substance is completely burnt in oxygen under standard conditions

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2
Q

define standard enthalpy change of hydration

A

energy evolved when one mole of gaseous ions is hydrated under standard conditions

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3
Q

define standard enthalpy change of solution

A

energy change when one mole of the substance is completely dissolved in a solvent to form an infinitely dilute solution under standard conditions

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4
Q

standard enthalpy change of neutralisation

A

energy evolved when one mole of water is formed from the neutralisation between acid and base under standard conditions

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5
Q

define standard enthalpy change of atomisation

A

energy absorbed when one mole of gaseous atoms is formed from the element under standard conditoins

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6
Q

define bond energy

A

average energy adsorbed to break one mole of covalent bonds between 2 atoms in the gaseous state to form gaseous atoms under standard conditions

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6
Q

define lattice energy

A

energy evolved when one mole of the solid ionic compound is formed from its constituent gaseous ions under standard conditions

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6
Q

effect of ionic charge and of ionic radius on the numerical magnitude of a
lattice energy

A

|△Hlatt|∝ (q+)(q-) /(r+)+(r-)

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7
Q

define entropy

A

measures the degree of disorder/randomness in a system

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8
Q

effects on the entropy of a chemical system

A

(i) change in temperature
- more energy to distribute the particles

(ii) change in phase (solid < liquid < gas)
-move more freely and with greater speeds, more ways..

(iii) change in the number of particles (especially for gaseous systems)
- arrangement of molecules more disordered, more gasesous particles moving randomly, more ways..)

(iv) mixing of particles(expansion of volume for gaseous system)
- more ways @ larger volume!!!

more ways to distribute the particles and energy

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9
Q

limitations in the use of ΔG⦵
to predict the spontaneity of a reaction

A

a) only valid for STANDARD CONDITIONS
b) kinetic feasibility not considered

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10
Q

define standard enthalpy change of formation

A

energy change when one mole of the substance is formed from its constituent elements under standard conditions

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10
Q

define 1st ionisation energy

A

energy absorbed when one mole of gaseous atoms loses one mole of electrons to form one mole of singly positively charged gaseous ions

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11
Q

define 2nd ionisation energy

A

energy absorbed when one mole of singly positively charged gaseous ions loses one mole of electrons to form one mole of doubly positively charged gaseous ions

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12
Q

define first electron affinity

A

energy evolved when on mole of gaseous atoms acquires one mole of electrons to give one mole of singly negatively change gaseous ions

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13
Q

ΔHr =

A

ΔHf products - ΔHf reactants

ΔHc reactants - ΔHc products

BE reactants - BE products

14
Q

why ΔHn (weak acid/base) < 57.0?

A
  • weak acids/bases are only sightly dissociated in aq solution. ionisation, which involves bond breaking, is an endo process.
  • some energy evolved from neutralisation process is used to further dissociate the weak acid/base completely
    -thus lest exo
15
Q

why 2d E.A is endo while 1st E.A is exo?

A

2nd EA also endo since e is added to -vely charged ion.
energy has to be supplied to overcome repulsive forces between 2 -vely charged species

16
Q

ΔHf of an element at 25C/298K is always

A

zero

17
Q

manyy enthalpy changes cannot be determined directly by experiments due to :

A
  1. reaction does not take place at standard conditions upon mixing reactants
  2. ΔHrxn is just a theoretical value as reaction does not take place in practice
18
Q

assumptions of conducting experiment in calorimeter: (2)

A
  1. negligible heat lose to or gained from the surroundings due to insulation -> 100% efficiency
  2. specific heat capacity of solution = specific heat capacity of water = 4.18

density of solution = desity of water = 1.00gcm3

19
Q

theoretical vs experimental lattice energies differs due to

A

partial covalent character in the ionic bond has not been accounted for by the theoretical ionic compound model.

this results in discrepancy between ..

more exo experimental lattice energies = stronger ionic bonding

20
Q

salt is likely to be soluble when

A

ΔHsoln < 0. |ΔHhyd|(enough to compensate for latt energy) > |L.E.|

and vice versa

21
Q

At ΔG =0,

A

reaction is at equilibrium (PHASE CHANGES (melting, freezing, vapourisation, condensation, sublimation) OCCURS AT EQUILIBRIUM!!!)

22
Q

why there is a diff in value for theoretical and experimental values for bond energy?

A

bond energy values taken from data booklet for C-H and O-H bonds are only average values obtained from polyatomic molecules

23
Q

ΔHsoln =

A

+|ΔHlatt| - |ΔHhyd|

24
Q

Energetic stability of a substance arises when

A

its enthalpy content is relatively lower than that of the product of a chemical reaction

25
Q

Kinetic stability of a substance arises when

A

the rate of chemical reaction is extremely slow, or negligible. this occurs when Ea is extremely high

26
Q

spontaneous reaction

A

can occur without any external assistance. it is irreversible as it cannot be brought back to its original state again under the same conditions

27
Q
A