Definitions Year 2 Flashcards

1
Q

acid dissociation content (Kₐ)

A

Equilibrium constant that shows extent of dissociation of a weak acid.

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2
Q

acid

A

Species that releases H+ ions in aq solution

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3
Q

acid-base pair

A

A pair of two species that transform into each other by gain or loss of a proton

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4
Q

Bronsted-Lowry acid

A

species that is a proton (H+) donor

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5
Q

Bronsted-Lowry base

A

species that is a proton (H+) acceptor

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6
Q

buffer solution

A

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

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7
Q

chemical shift

A

A scale, in ppm, that compares frequency of an NMR absorption with the frequency of reference TMS (0 ppm)

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8
Q

chiral carbon

A

carbon atom attached to four different atoms or groups of atoms

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9
Q

chromatogram

A

A visible record showing the result of separation of the components of a mixture by chromatography

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10
Q

complex ion

A

A transition metal ion bonded to ligands by coordinate bonds (dative covalent bonds)

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11
Q

concentration

A

amount of solute (in moles) dissolved in 1dm3 of solution

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12
Q

condensation reaction

A

A reaction in which two small molecules react together to form a larger molecule with elimination of aa small molecule such as water

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13
Q

conjugate acid

A

a species that releases a proton to form a conjugate base

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14
Q

conjugate base

A

a species that accepts a proton to form a conjugate acid

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15
Q

coordination number

A

Total number of coordinate bonds formed between a central metal ion and ligands (not number of ligands)

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16
Q

electrophilic substitution

A

A type of substitution reaction in which an electrophile is attracted to an electron rich centre or atom, where it accepts a pair of electrons to form a new covalent bond

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17
Q

enantiomers

A

Stereoisomers that are non-superimposable mirror images of each other, (aka Optical Isomers)

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18
Q

end point

A

The point in a titration where the indicator changes colour, the end point indicates when the reaction is just complete

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19
Q

entropy (S)

A

The dispersal of energy, disorder and randomness within a chemical system

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20
Q

equivalence point

A

The point in a titration at which the volume of one solution has reacted exactly with the volume of the second solution

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21
Q

esterification

A

A reaction in which a carboxylic acid reacts with an alcohol to form an ester and water

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22
Q

first electron affinity

A

The enthalpy change that takes place when one electron is added to each atom in one mole of gaseous atoms to form one mole of gaseous 1- ions

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23
Q

first ionisation energy

A

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

24
Q

free energy change (ΔG) & equation

A

The balance between enthalpy, entropy and temperature for a process given by
ΔG = ΔH - TΔS

25
feasibility
ΔG < 0
26
half-life
The time taken for the concentration of a reactant to decrease by half
27
heterogeneous equilibrium
an equilibrium in which the species making up the reactants and products have different physical states
28
homogeneous equilibrium
An equilibrium in which all the species making up the reactants and products have the same physical state
29
hydrolysis
A reaction with water that breaks a chemical compound into two compounds, the H and OH in a water molecule becomes incorporated into the two compounds
30
initial rate of reaction
the change in concentration of a reactant or product per unit time at the start of the reaction: t = 0
31
ionic product of water Kᵥᵥ
The product of the ions formed in the partial dissociation of water, given by Kᵥᵥ = [H⁺(aq)][OH⁻(aq)]
32
lattice enthalpy
The enthalpy change that accompanies the formation of one mole of an ionic compound from its gaseous ions under standard conditions.
33
ligand
A molecule or ion that can donate a pair of electrons to the transition metal ion
34
ligand substitution
A reaction in which one or more ligands in a complex ion are replaced by different ligands.
35
mobile phase
The phase that moves in chromatography
36
optical isomers
Stereosiomers that are non-superimosaable mirror images of each other (aka enantiomers)
37
order
The power to which the concentration of a reactant is raised in the rate equation
38
overall order
The sum of the individual orders of reactants in the rate equation: m + n
39
pH
The expression pH = -log[H⁺(aq)]
40
precipitation reaction
The formation of a solid from a solution during a chemical reaction. Precipitates are often formed when two aq solutions are mixed together
41
rate constant (k)
The constant that links the rate of reaction with the concentrations of the reactants raised to the powers of their orders in the rate equation
42
rate equation
For reaction: A + B -> C, - order m for A, n for B Rate equation= k[A]ᵐ[B]ⁿ
43
rate determining step
The slowest step in the reaction mechanism of a multi-step reaction.
44
retention time
In gas chromatography, the time for a component to pass from the column inlet to the detector
45
Rf value
Rf = distance moved by component / distance moved by solvent
46
second electron affinity
The enthalpy change that takes place when one electron is added to each ion in one mole of gaseous 1- ions to form one mole of gaseous 2- ions
47
second ionisation energy
The energy required to remove one electron from each ion in one mole of gaseous 1+ ions of an element to form one mole of gaseous 2+ ions
48
spin-spin coupling
In an NMR spectrum the interaction between spin states of non-equivalent nuclei that results in the splitting of a signal
49
standard conditions
Pressure: 100 kPa Temperature: 298 K (25ºC) Concentration: 1 mol dm-3
50
standard electrode potential
The e.m.f. of a half-cell compared with a standard hydrogen half-cell measured at 298 K with a solution concentrations of 1 mol dm-3 and a gas pressure of 100 kPa
51
standard enthalpy change of atomisation
The enthalpy change that takes place when one mole of gaseous atoms forms from the element in its standard state.
52
standard enthalpy change of formation ΔfH°
The enthalpy change that takes place when one mole of a compound is formed from its constituent elements in their standard states under standard conditions
53
standard enthalpy change of hydration
The enthalpy change that takes place when one mole of isolated gaseous ions is dissolved in water forming one mole of aq ions under standard conditions
54
standard enthalpy change of solution
The enthalpy change that takes place when one mole of a compound is completely dissolved in water under standard conditions
55
stationary phase
The phrase that doesn't move in chromatography
56
transition element
A d-block element which forms an ion with an incomplete d sub-shell