definitions Flashcards

1
Q

Rate of reaction

A

Change in concentration of a reactant or product over time

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2
Q

Order

A

Power a concentration of a reactant is raised to in a rate equation, matching its stoichiometry in the RDS

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3
Q

Overall order

A

The sum of all orders in the rate equation

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4
Q

Rate constant

A

k in Rate = k[A]m[B]n…

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5
Q

Half-life

A

Time taken for the concentration of a reactant to reduce by half

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6
Q

Rate determining step

A

The slowest step in a reaction mechanism

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7
Q

Mole fraction

A

Moles of gas divided by the total moles of all gases

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8
Q

Partial pressure

A

Pressure from gas divided by the total pressure from all gasses

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9
Q

Brønsted-Lowry acid

A

donates a proton

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10
Q

Brønsted-Lowry base

A

accepts a proton

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11
Q

Monobasic acid

A

one mole of acid dissociates to form one mole of H+ ions

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12
Q

Dibasic acid

A

one mole of acid dissociates to form two moles of H+ ions

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13
Q

Tribasic acid

A

one mole of acid dissociates to form 3 moles of H+ ions

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14
Q

Buffer solution

A

A system that minimises pH changes on addition of small amounts of an acid or base

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15
Q

Oxidising agent

A

Oxidises another element, it is itself reduced

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16
Q

Reducing agent

A

Reduces another element, it is itself oxidised

17
Q

Standard electrode (redox) potential, Eθ

A

The EMF of a half-cell compared to a standard hydrogen electrode under standard conditions, 298 K, 100 kPa and 1 mol dm-3

18
Q

Transition elements

A

d-block elements that have a stable ion with an incomplete d-sub-shell

19
Q

Ligand

A

A molecule or ion that can donate a lone pair to form a coordinate (dative covalent) bond to a metal ion or metal

20
Q

Bidentate ligand

A

A molecule or ion that can donate two lone pairs to form two coordinate (dative covalent) bond to a metal ion or metal

21
Q

Complex ion

A

Metal cation surrounded by coordinately bonded ligands

22
Q

Coordination number

A

Total number of coordinate bonds formed with the central metal ion

23
Q

Entropy

A

A measure of the dispersal of energy in a system which is greater the more disordered a system

24
Q

which enthalpy term can be either endo or exothermic

A

enthalpy of formation and solution

25
Q

which enthalpy terms are always exothermic

A
  • first electron affinity
  • lattice enthalpy
  • enthalpy change of hydration
26
Q

Enthalpy change of hydration

A
  • Dissolving of 1 mol of gaseous ions in water, ∆hydH
  • K+ (g) —-> K+ (aq)
  • exothermic as water molecules surround ions to form new forces of attraction. Energy is released.
27
Q

Enthalpy change of solution
KCl

A
  • Dissolving of 1 mol of solute in water, ∆solH
  • KCl (s) —> K+ (aq) + Cl- (aq)
  • endo/exothermic as ‘amount of heat’ released or absorbed in the dissolving process depends on whether the lattice enthalpy or hydration enthalpy is greater.
28
Q

enthalpy of atomisation, ΔatH
F

A
  • ΔH when 1 mol of gaseous atoms is formed from its element
  • 1/2 F2 (g) —-> F (g)
  • endothermic only as energy required to break bonds between the atoms of an element.
29
Q

bond enthalpy
CF4

A
  • enthalpy required to break 1 mol of a specific gaseous covalent bond
  • 1/4 CF4 (g) —> 1/4 C (g) + F (g)
  • endothermic only as energy required to break bonds between the atoms.
30
Q

first electron affinity ΔEA1H
Cl

A
  • enthalpy released when 1 mol of gaseous atoms gains 1 mol of e- to form one mole of gaseous 1- ions
  • Cl (g) + e- —> Cl- (g)
  • mostly exothermic because electrostatic attraction between +ve nuclei and -ve e- formed. Can be +ve if it doesn’t form a stable ion
31
Q

second electron affinity ΔEA2H
S

A
  • enthalpy released when 1 mol of 1- gaseous ions gains 1 mol of e- to form one mole of gaseous 2- ions
  • S- (g) + e- —> S^2- (g)
  • always endothermic as repulsion is being forced between to -ve charges
  • Increased electron-electron repulsions in a dianion > the attraction of electrons to the nucleus. Electrostatic repulsion from negative ion and the electron being gained.
32
Q

lattice enthalpy, ΔLEH
NaCl

A
  • ΔH when 1 mol of an ionic compound is formed from its gaseous ions
  • Na+ (g) + Cl- (g) —> NaCl (s)
  • always exothermic because bonds formed by ions combining, large release of energy. Ionic compound more stable than its gaseous ions.
  • Strong electrostatic forces of attraction between oppositely charged ions
33
Q

Enthalpy of formation, ΔfH

A
  • one mole of a compound from its constituent elements
  • Na (s) + ½ Cl2 (g) —> NaCl (s) ΔHfꝋ
  • endo/exothermic because:
    Bonds broken – bonds formed = overall enthalpy change