Chemistry Key Definitions And Things To Remember Flashcards

(70 cards)

1
Q

Define The Standard Enthalpy Of Formation.

A

The enthalpy change when one mole of a compound is formed from its elements under standard conditions, all reactants and products in their standard states.

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2
Q

Define The Standard Enthalpy Of Combustion.

A

The enthalpy change when one mole of a compound is completely burned in oxygen under standard conditions, all reactants and products in their standard states.

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3
Q

Define The Standard Enthalpy Of Atomisation.

A

The standard enthalpy change when one mole of gaseous atoms is formed from an element in its standard state.

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4
Q

Define Mean Bond Enthalpy (Aka bond dissociation enthalpy).

A

The enthalpy change when one mole of gaseous molecules each break a covalent bond to form to free radicals (atoms), averaged over a range of compounds.

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5
Q

Define 1st Ionisation Enthalpy.

A

The standard enthalpy change when one mole of electrons is removed from one mole of gaseous atoms to give one mole of gaseous ions with a single positive charge.

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6
Q

Define 2nd Ionisation Enthalpy.

A

The standard enthalpy change when one mole of electrons is removed from one mole of gaseous 1+ ions to give one mole of gaseous ions each with a 2+ charge.

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7
Q

Define 1st Electron Affinity.

A

The standard enthalpy change when one mole of gaseous atoms is converted into a mole of gaseous ions each with a single negative charge under standard conditions.

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8
Q

Define 2nd Electron Affinity.

A

The standard enthalpy change when one mole of electrons is added to a mole of gaseous ions each with a single negative charge, to form a mole of ions each with a two negative charge.

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9
Q

Define Lattice Formation Enthalpy.

A

The standard enthalpy change when one mole of a solid ionic compound is formed from its gaseous ions.

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10
Q

Define Lattice Dissociation Enthalpy.

A

The standard enthalpy change when one mole of a solid ionic compound dissociates into its gaseous ions.

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11
Q

Define Standard Enthalpy Of Solution.

A

The standard enthalpy change when one mole of a solute dissolves in enough solvent to form a solution in which the ions are far enough apart to not interact with each other.

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12
Q

Define The Standard Enthalpy Of Hydration.

A

The standard enthalpy change when one mole of gaseous ions is converted to one mole of aqueous ions.

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13
Q

Define Hess’s Law.

A

The enthalpy change for a chemical reaction is the same, regardless of the route taken from reactants to products.

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14
Q

State the meaning of the term periodicity.

A

Repeating patterns/trends of physical or chemical properties across a period.

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15
Q

If something can act as either an acid or base, it is:

A

Amphoteric

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16
Q

Give the percentage uncertainty equation.

A

% Uncertainty = (uncertainty/value measured) x100

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17
Q

What is the half neutralisation point of a pH curve?

A

The point when enough base has been added to neutralise exactly half of the acid (or vice versa). On a pH curve: half way between 0 and equivalence point on x-axis. [HA]=[A-] so equal moles of salt and acid so Ka=[H+] therefore pKa=pH.

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18
Q

What are the bond angles and shape for a molecule with 2 bonding pairs?

A

Linear, 180°

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19
Q

What are the bond angles and shape of a molecule with 3 bonding pairs?

A

Trigonal Planar, 120°

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20
Q

What are the bond angles and shape of a molecule with 4 bonding pairs?

A

Tetrahedral, 109.5°

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21
Q

What are the bond angles and shape of a molecule with 5 bonding pairs?

A

Trigonal Bipyramidal, 120° and 90°

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22
Q

What are the bond angles and shape of a molecule with 6 bonding pairs?

A

Octahedral, 90°

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23
Q

What are the bond angles and shape of a molecule with 2 bonding pairs and 1 lone pair?

A

V-Shaped, 117.5° (120-2.5 as one lone pair)

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24
Q

What are the bond angles and shape of a molecule with 3 bonding pairs and 1 lone pair?

A

Trigonal Pyramidal, 107° (109.5-2.5 as one lone pair)

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25
What are the bond angles and shape of a molecule with 2 bonding pairs and 2 lone pairs?
V-Shaped, 104.5° (109.5-2(2.5) as 2.5 for each lone pair)
26
What are the bond angles and shape of a molecule with 4 bonding pairs and 1 lone pair.
Seesaw Molecule, 119°, 89° (More than 5 e- pairs so different rules, angles from original structure have 1° subtracted from them)
27
What are the bond angles and shape of a molecule with 3 bonding pairs and 2 lone pairs? (Two answers)
T-Shaped, 89° (90-1, despite having two lone pairs. You just need to know this one, don't try and figure it out with logic) Or Trigonal Planar, 120°, lone pairs are in an axial position (on opposite sides) so their stronger repulsion cancels each other out leaving, a trigonal planar shape as if they didn't exist in the first place (still draw them though)
28
What are the bond angles and shape of a molecule with 5 bonding pairs and 1 lone pair?
Square Pyramidal, 89° (more than 5 pairs so different rules. 90-1 as original structure is octahedral but one lone pair instead of a bonding pair)
29
What are the bond angles and shape of a molecule with 4 bonding pairs and 2 lone pairs?
Square Planar, 90°, Lone e- pairs in axial position (Opposite each other) so their stronger repulsions cancel out leaving essentially an octahedral, 90°, but without the top and bottom bonding pairs.
30
Give an equation to represent the ionisation of a molecule 'X' in Electrospray Ionisation.
X(g) + H+ ---> XH+(g) (Remember, when looking at the mass spectrum, the Mr will be the Mr of 'X' +1 as it had gained a proton, so its actual relative molecular mass one subtracted from the value in the spectrum)
31
Give an equation to represent the ionisation of a molecule 'X' in Electron Impact Ionisation.
X(g) ---> X+(g) + e- | Electrons collide with electrons in molecule, ionising them
32
Heterogeneous Catalyst Example, Haber Process. Name catalyst and show reversible equation (making ammonia)
Catalysed by Solid Fe | 3H2+N2 (reversible arrow) 2NH3
33
Heterogeneous Catalyst Example Contact Process Name catalyst and show reaction equation (making sulfuric acid) and catalyst reformation. Give a suggestion for the use of the product
Vanadium (V) Oxide SO2(g) + V2O5(s) ---> SO3(g) + V2O4(s) V2O4(s) + 1/2O2(g) ---> V2O5(s) Used to make sulfuric acid (group 3) SO3 + H2O ---> H2SO4
34
Heterogeneous Catalyst Example | Manufacturing of methanol
Solid Cr2O3 Catalyst CH4(g) + H2O(g) --> CO(g) + 3H2(g) CO(g) + 2H2(g) --> CH3OH(g)
35
How does a solid Heterogeneous Catalyst work for gas/liquid reactants
- Reaction occurs on the active sight of the surface of the catalyst - Reactants adsorb into surface - Bonds weaken - Reaction occurs - Products desorb from the surface
36
How to make a solid Heterogeneous Catalyst more efficient
Increase its surface area and spread it over an inert support medium
37
How do solid Heterogeneous Catalysts get poisoned? And how is it prevented?
-Impurities block the active sights (Stronger adsorb and don't desorb) -Purifying the reactants prevents poisoning
38
For Homogeneous Catalyst Reaction, Peroxudisulfate ions to oxidise iodide ions to iodine, give the half equations uncatalysed and explain why this his high activation energy
``` S2O8^2- + 2e- --> 2SO4^2- 2I- ---> I2 + 2e- So overall S2O8^2- + 2I- ---> 2SO4^2- + I2 Which has two -ve ions reacting and therefore they repel, so high Ea ```
39
For Homogeneous Catalyst Reaction, Peroxudisulfate ions to oxidise iodide ions to iodine, give the half equations catalysed and name the catalyst. Explain why this has a much lower Ea
``` Catalysed by Fe2+ ions in 2 step process (Or Fe3+ and swap steps 1 and 2) Step 1: 2Fe2+ ---> 2Fe3+ + 2e- S2O8^2- + 2e- ---> 2SO4^2- Step 2 (Catalyst Re-Formed) 2I- ---> I2 + 2e- 2e- + 2Fe3+ ---> 2Fe2+ Has +ve and -ve ions reacting so they attract so low Ea ```
40
Give the half equations for the reaction you need to know for Autocatalysis when uncatalysed and explain the low Ea (Oxidation of ethanedioc acid by manganate (VII) ions)
5e- + 8H+ MnO4- ---> Mn2+ + 4H2O C2O4^2- ---> 2CO2 + 2e- High Ea as two -ve ions repel
41
Give the half equations for the reaction you need to know for Autocatalysis when catalysed by its own product, and mention what the product is and why it decreases Ea
``` Catalyst: Mn2+ Step 1: 5e- + 8H+ + MnO4- ---> Mn2+ + H2O Mn2+ ---> Mn3+ + e- Step 2: C2O4^2- ---> 2CO2 + 2e- 2e- + 2Mn3+ ---> 2Mn2+ ``` -ve ions and +ve ions attract so low Ea
42
Explain concentration against time graph for Autocatalysis reaction
- Slow rate at start - As no catalyst initially - So high Ea as two -ve ions react - More Mn2+ formed so faster rate - Due to increasingly catalyst reaction - Rate decreases again and levels off - As reactants get used up
43
Give the colour change for MnO4- ---> Mn2+
Purple to colourless
44
To form Vanadium (II), (III) and (IV) ions from Vanadium (V), what is required, and what is the colour of Vanadium (V)
Zinc (Zn) to be oxidised to Zn2+ | Colour: Yellow
45
Colour of Vanadium ions, from (V) to (II)
``` Ya. Yellow. (V) Bastard. Blue. (IV) Got Green. (III) Punched. Purple. (II) Going down (like the bastard) form V ```
46
What happens to Cobalt (II) hexa-aqua ions in Alkaline conditions? E.g H2O2, NH3, or O2
Oxidised to Cobalt (III)
47
Half equations for Cobalt (II) Hexa-aqua ions (acts as acid) reacting with H2O2 (base so dissociation)
H2O2 + 2e- ---> 2OH- | [Co(OH)6]4- ---> [Co(OH)6]3- + e-
48
Equations for the reaction of Cobalt (II) hexa- aqua ions with NaOH (like the same reaction with Cu instead) and give the colour change
[Co(H2O)6]2+(aq) + 2OH- ---> [Co(H2O)4(OH)2](s) + 2H2O | Pink solution to blue ppt
49
Reaction of [Co(H2O)4(OH)2](s) with NH3 and state colour change
Reaction of [Co(H2O)4(OH)2](s) + 6NH3 ---> [Co(NH3)6]2+ (aq) + 4H2O + 2OH- Blue precipitate to pale brown solution
50
Give the half equations for the reaction of [Co(NH3)6]2+ (aq) with O2 and H2O
O2 + 2H2O + 4e- ---> 4OH- | [Co(NH3)6]2+ (aq) ---> [Co(NH3)6]3+ (aq) + e-
51
Give the colour change for Fe2+ to Fe3+
Green to brown
52
Give the colour change for Cr2O7 2- to Cr3+
Orange to green
53
How are Transition Metal Ions Coloured?
- Transition metals are coloured due to partially filled d-sub shell - In pure transition metal, d-orbitals are of equal energy AKA 'ground state' - In transition metal compounds, due to other atoms present, d-orbitals have slightly different energies - So e- can be excited from one d-orbital to another - When one e- moves from lower energy d-orbital to a higher one, energy is needed to make the transition. - This energy is taken from white light and a specific wavelength of light is absorbed which is missing from the light that gets reflected/transmitted to give the compound it's colour.
54
What are the steps of using Colorimetry for finding the concentration of a solution
1. Multiple samples if known different concs of solution, with appropriate ligand added to intensify the colour 2. Test each known sample for transmittance/absorbance 3. Plot Conc Vs transmittance graphs 4. Test solution of unknown concentration for transmittance 5. Use graph to find corresponding concentration (Transmittance -> 1.0 = All light passed through, 0.5=50% absorbed, 0=All light absorbed)
55
What happens when chlorine is added to water, what type of reaction is it and why is the product useful?
Cl2 + H2O HClO + HCl Disproportionation (Oxidised and Reduced) HClO kills bacteria
56
How is bleach made? (NaClO)
Cl2 + 2NaOH ---> NaClO + NaCl + H2O
57
What happens when Chlorine reacts with water in sunlight?
2Cl2 + 2H2O ---> 4HCl + O2
58
What does CRAM stand for and how do we use it to distinguish which has the more exothermic lattice formation enthalpy, MgO or Na2O
Charge, Radius, Attraction, More exothermic or endothermic Mg2+ has greater charge than Na+, and a smaller atomic radius so a greater attraction to O2- so MgO has a more exothermic lattice formation enthalpy
59
When conditions change for an electrode, what may happen? (e.g altered temp, Conc, pressure)
Equilibrium position will shift More or less e- produced Larger or smaller E° Affects calc
60
What is a salt bridge and what is its purpose?
Salt bridge is a solution and connects both beakers. It's ions are free to move and balance the charges in either electrode. It must be UNREACTIVE with half cells. (KNO3 usually used)
61
If two metal ions have SAME state, how are they indicated in cell representation?
With a comma
62
When given a table of electrode potentials what is the main rule?
For most positive E°, SOWR strongest oxidising agent on left Weakest reducing agent on right
63
When are platinum electrodes used?
When no solid metal in reaction, so metal ions with two diff charges in same solution E.g FeSO4 and Fe2(SO4)3 is a solution of Fe2+ and Fe3+ It is unreactive but still conductive
64
What is the half equation for a standard hydrogen electrode? And what are the conditions? Does the other electrode need the conditions?
2H+ + 2e- (reversible arrow) H2 Temp: 298k Conc: 1moldm-3 of H+ sol (e.g 1moldm-3 of HCl or 0.5moldm-3 of H2SO4) Pressure: 100KPa Connected electrode must also have these same conditions
65
How can you test for Ammonium Ions
Add NaOH NH4+ + -OH ---> NH3(g) + H2O Red litmus paper turns blue
66
What is an example of a reachable battery?
Lithium Ion battery
67
What occurs at the negative electrode of a lithium Ion battery?
Graphite (carbon) with a layer of Li(s) on it dissociates | Li(s) --> Li+ + e-
68
What happens on the positive electrode of a lithium ion battery
Li+ ions and CoO2 from electrolyte (both have same state) form lithium cobalt oxide Li(CoO2)(s) on a platinum electrode CoO2 + Li+ + e- ---> Li(CoO2)
69
For an alkaline membrane hydrogen oxygen fuel cell, give the half equation for the anode (negative electrode) and the cathode (positive electrode).
H2(g) + 2OH-(aq) reversible arrow 2H2O(l) + 2e- | 0.5O2(g) + H2(g) + 2e- reversible arrow 2OH- (aq)
70
For an acidic membrane hydrogen oxygen fuel cell, give the half equation for the anode (negative electrode) and the cathode (positive electrode).
H2(g) Reversible Arrow 2H+(aq) + 2e- | 0.5O2(g) + H2(g) + 2e- reversible arrow H2O(l)