Thermodynamics Flashcards

1
Q

The standard molar enthalpy of formation, ▲fH

A

The standard molar enthalpy of formation is the enthalpy change when ONE MOLE OF A COMPOUND IS FORMED FROM ITS CONSTITUENT ELEMENTS under standard conditions, all reactants and products in their standard states.

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2
Q

The standard molar enthalpy change of combustion, ▲cH

A

The standard molar enthalpy change of combustion is the enthalpy change when ONE MOLE OF A SUBSTANCE IS COMPLETELY BURNT IN OXYGEN.

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3
Q

The standard enthalpy of atomisation, ▲atH

A

The standard enthalpy of atomisation is the enthalpy change WHICH ACCOMPANIES THE FORMATION OF ONE MOLE GASEOUS ATOMS FROM THE ELEMENT in its standard state under standard conditions.

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4
Q

First ionisation energy, ▲iH

A

First IE is the standard enthalpy change when ONE MOLE OF GASEOUS ATOMS IS CONVERTED TO A MOLE OF GASEOUS IONS, EACH WITH A SINGLE POSTITIVE CHARGE.

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5
Q

Second ionisation energy

A

Second IE refers to the LOSS OF A MOLE OF ELECTRONS FROM A MOLE OF SINGLY POSITIVELY CHARGED IONS.

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6
Q

First electron affinity, ▲eaH

A

The first electron affinity is the standard enthalpy change when A MOLE OF GASEOUS ATOMS IS CONVERTED TO A MOLE OF GASEOUS IONS, EACH WITH A SINGLE NEGATIVE CHARGE.

E.g.

O(g) + e- —> O- (g)

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7
Q

Second electron affinity

A

Second ▲ eaH is the enthalpy change when A MOLE OF ELECTRONS IS ADDED TO A MOLE OF GASEOUS IONS EACH WITH A SINGLE NEGATIVE CHARGE TO FORM IONS WITH TWO NEGATIVE CHARGES.

E.g.

O- (g) + e- —> O^2- (g)

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8
Q

Lattice enthalpy of formation, ▲L H

A

Lattice enthalpy of formation is the standard enthalpy change when ONE MOLE OF A SOLID IONIC COMPOUND IS FORMED FROM ITS GASEOUS IONS

E.g.

Na+ (g) + Cl- (g) —> NaCl (s)

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9
Q

Lattice enthalpy of dissociation

A

Lattice enthalpy of dissociation, is the standard enthalpy change when ONE MOLE OF SOLID IONIC COMPOUND DISSOCIATED INTO ITS GASEOUS IONS.

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10
Q

Enthalpy of hydration, ▲hyd H

A

Enthalpy of hydration is the standard enthalpy change when 1 MOLE OF GASOUS IONS ARE CONVERTED INTO AQUEOUS IONS / AN AQUEOUS SOLUTION.

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11
Q

Enthalpy of solution, ▲sol H

A

enthalpy of solution is the standard enthalpy change when ONE MOLE OF SOLUTE DISSOLVES COMPLETELY IN SUFFICIENT SOLVENT TO FORM A SOLUTION IN WHICH THE MOLECULES OR IONS ARE FAR ENOUGH APART NOT TO INTERACT WITH EACH OTHER.

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12
Q

Mean bond enthalpy

A

mean bond enthalpy is the enthalpy change when ONE MOLE OF GASEOUS MOLECULES EACH BREAKS A COVALENT BOND TO FORM TWO FREE RADICALS, AVERAGED OVER A RANGE OF COMPOUNDS.

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13
Q

Overall entropy change equation

A

▲S total = ▲S products - ▲S reactants

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14
Q

Gibbs’s free energy equation

With units

A

▲G = ▲H - T ▲S

▲G = kJmol-1
T = Kelvin, K

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15
Q

What does ▲G value have to be for spontaneous reactions

A

▲G is negative for all spontaneous reactions.

This becomes true at a certain, specific temperature which can be found by putting ▲G equal to zero.

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16
Q

What will change the feasibility of the reaction happening?

A

Changing the temperature or the type of reaction occurring will change the feasibility of the reaction happening.

17
Q

If ▲H = positive and ▲S = positive

  • what happens as temp. Increases?
  • is the reaction feasible?
A

As temp increases… makes T ▲S > ▲H

Yes, the reaction is feasible above a certain temperature

18
Q

If ▲H = negative and ▲S = positive

  • what happens as temp. Increases?
  • is the reaction feasible?
A

As temp increases… makes ▲G more negative

Yes, the reaction is always feasible

19
Q

If ▲H = positive and ▲S = negative

  • what happens as temp. Increases?
  • is the reaction feasible?
A

As temp increases… no effect: ▲G always positive

20
Q

If ▲H = negative and ▲S = negative

  • what happens as temp. Increases?
  • is the reaction feasible?
A

As temp increases… unlikely to make T▲S > ▲H

Usually feasible

21
Q

Theoretical VS Experimental values of lattice dissociation enthalpy

A
  • theoretical values calculated using pure ionic model which assumes ions are perfect spheres and have their charge evenly distributed around them. Positive and negative ions cannot be exactly spherical.
  • experimental values calculated from Born-Haber cycles. -Additional covalent bonding as well as ionic bonding causes the greater experimental value.