A2 2 Definitions Flashcards

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1
Q

Standard Enthalpy of formation

A

The Enthalpy change when 1 mole of a substance is formed from its elements, in their natural state, under standard conditions

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2
Q

Standard Enthalpy of atomisation

A

The Enthalpy change when 1 mole of gaseous atoms is formed from its elements in its standard state

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3
Q

1st ionisation energy

A

The energy required to remove 1 electron from each atom in one mole of gaseous atoms, to form one mole of gaseous 1+ ions

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4
Q

2nd ionisation energy

A

The energy required to remove one electron from each ion in one mole of gaseous 1+ ions to form one mole of gaseous 2+ ions

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5
Q

1st electron affinity

A

The energy required to form one mole of negatively charged ions from one mole of atoms, in the gaseous state

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6
Q

2nd electron affinity

A

The energy required to form 1 mole of 2- ions from one mole of 1- ions, in the gaseous state

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7
Q

Hess’ Law

A

The Enthalpy change for a reaction is the same,irrespective of the route taken, provided the initial and final conditions are the same

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8
Q

Standard Enthalpy of solution

A

Enthalpy change when one mole of a compound is completely dissolved in water, under standard conditions

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9
Q

Standard Enthalpy of hydration

A

The Enthalpy change that takes place when one mole of isolated gaseous ions is dissolved in water, forming one mole of aqueous ions, under standard conditions

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10
Q

Entropy

A

A measure of disorder in a system (S)

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11
Q

Standard electrode potential

A

The voltage of a half cell, compared to a standard hydrogen half cell, measured at 298K, with solution concentrations of 1moldm-3 and a gas pressure of 1atm

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12
Q

Standard Lattice Enthalpy

A

The Enthalpy change when one mole of a solid ionic lattice is formed, from its gaseous ions under standard conditions. Always exothermic

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13
Q

Transition element

A

A d block element, that forms an ion with an incomplete d sub shell

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14
Q

Catalyst

A

Increases the rate of reaction, without being used up. Provides an alternative route, with lower activation energy

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15
Q

Ligand

A

A molecule or ion which possesses at least one lone pair of electrons, which can be donated into vacant d orbitals of a metal ion, by forming a co-ordinate bond

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16
Q

Co-ordination number

A

The total number of co-ordinate bonds formed between a central metal ion and it’s ligands

17
Q

Bidentate ligand

A

Can donate two lone pairs of electrons into the vacant d orbitals of a metal ion, forming two co-ordinate bonds

18
Q

Dynamic equilibrium

A

Reached in a closed system where:

  • rate of forward reaction equals the rate of the reverse reaction
  • the concentrations of the reactants and products remain the same but are constantly interchanging
19
Q

Le Chatelier’s principle

A

When a system in equilibrium is subjected to a change, the position of equilibrium will shift to minimise that change

20
Q

Bronstead Lowry theory

A

Acid: proton donor
Base: proton acceptor

21
Q

Buffer

A

Minimises changes in pH, on addition of small amounts of acid or base

22
Q

Titration end point

A

The stage where the indicator used has a colour halfway between it’s extreme colours

23
Q

Equivalence point

A

The point of neutralisation - when an acid and a base have completely reacted

24
Q

Standard Enthalpy change of Neutralisation

A

The energy change when an aqueous acid is neutralised by an aqueous base, to form one mole of water, under standard conditions

25
Q

Oxidation state

A

State which a metal achieves as a result of losing electrons

26
Q

Precipitation reaction

A

A reaction in which soluble ions, in separate solutions, are mixed together to produce an insoluble compound or precipitate

27
Q

Order

A

The power to which the concentration of a reactant is raised in the rate equation

28
Q

Rate determining step

A

The slowest step in the reaction mechanism of a multi step reaction

29
Q

Rate

A

Change in concentration of a reactant or product with time

30
Q

Initial Rate

A

The rate at the start of a reaction, when t=0