R3 Flashcards

(84 cards)

1
Q

Brønsted-Lowry acid

A

A proton donor

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2
Q

Brønsted-Lowry base

A

A proton acceptor

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3
Q

Types of Acids

A

Binary Acids (Hydrogen halide, HCl, HF, etc) ; Oxyacids (Derived from polyatomic ions, HNO3, H2CO3, H2SO4) ; Organic Acids (Containing a carboxyl groups, CH3COOH) ; Monoprotic (donate one proton) ; Diprotic (donate two protons) ; Triprotic (donate three protons)

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4
Q

Conjugate acid-base pairs

A

A pair of species in a reaction that differ by a proton (H+) ; The stronger the acid the weaker the conjugate base ; The stronger the base the weaker the conjugate acid

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5
Q

Amphiprotic Species

A

Species that can act as both a Brønsted-Lowry acid/base by both donating and accepting at least one proton

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6
Q

Amphoteric Species

A

Species that can act as both an acid and a base

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7
Q

The ionic product of water, Kw

A

The ionic product of water is the product of the [H+] and [OH−] in water at a particular temperature.

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8
Q

Strong acids/bases

A

Species that completely dissociate/ionise into ions in aqueous solution

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9
Q

Weak acids/bases

A

Species that only partially dissociate/ionise into ions in aqueous solution

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10
Q

Titration

A

A method of combining a reactant solution of known concentration, standard solution, with a reactant solution of unknown concentration in order to find the unknown concentration.

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11
Q

Acid/Base dissociation constant Ka/b

A

A measure of the strength of an acid/base by measuring the extent of it’s dissociation into ions ; A high Ka/Kb will mean a strong acid/base and vice versa

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12
Q

pKa/pKb

A

Exactly like pH and pOH but just for Ka and Kb, a low pKa/pKb means a strong acid/base

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13
Q

Acid Equations

A

Kw = Ka x Kb
pKa + pKb = 14
pH + pOH = 14
Ka = [H⁺]² / [HA]
pOH = pKb + log10 (HB+/B)
pH = pKa + log10 (A-/HA)

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14
Q

Salt Hydrolysis

A

The interaction between a salt’s ions and water

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15
Q

Salt Hydrolysis Weak Acid Strong Base

A

CH3COOH + NaOH -> CH3COONa + H2O

The CH3COO- in the CH3COONa can undergo salt hydrolysis

CH3COO- + H2O -> CH3COOH + OH- (increasing the pH)

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16
Q

Salt Hydrolysis Strong Acid Weak Base

A

HCl + NH3 -> NH4Cl

The NH4+ in the NH4Cl can undergo salt hydrolysis

NH4+ + H2O -> NH3 + H3O+ (decreasing the pH)

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17
Q

Salt Hydrolysis Weak Acid Weak Base

A

CH3COOH + NH3 -> CH3COOHNH4

Both the CH3COO- and the NH4+ can undergo salt hydrolysis and so the pH will only change depending on the relative size of their respective Ka and Kb values

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18
Q

Salt Hydrolysis Strong Acid Strong Base

A

NaOH + HCl -> NaCl + H2O

Cl- + H2O -> HCl + OH-
Na+ + H2O -> NaOH + H+

However in reality this won’t occur since both NaOH and HCl are strong bases/acids so will fully dissociate/ionise so the reverse reaction can’t occur so no salt hydrolysis can occur

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19
Q

pH curves

A

It will start at the pH of the Analyte then hit the equivalence point and finish at the pH of the Titrant ; Strong acid and Strong base will be the simplest graph ; Weak base and Strong acid will have a buffer solution at the start (top) and have the half equivalent point pH < 7 ; Weak acid and Strong base will have a buffer solution at the start (bottom) and have the half equivalence point pH > 7 ; Weak acid and Weak base will be like the strong acid and base but be much tighter

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20
Q

Analyte

A

The solution of unknown concentration

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21
Q

Titrant

A

The solution of known concentration

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22
Q

Indicators Equation

A

HIn (aq) <-> H+ (aq) + In- (aq)
Colour A Colour B

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23
Q

Buffer solution definition

A

A solution that resists changes in pH when small amounts of acid or base are added

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24
Q

Buffer solution explanations

A

As you put a little bit of acid or base, the equilibrium position shifts to return back to equilibrium and so produces more of H+ or uses H+ ions returning the pH back to the original buffer solution pH ; Weak acid/base and a salt containing it’s conjugate base/acid (ensuring that the salt doesn’t offer acid/base activity or any salt hydrolysis) like CH3COOH and CH3COONa ; You could also add to a weak acid/base, strong base/acid to half neutralise it

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25
Oxidation
A reaction in which a species gains oxygen, increases their oxidation state or loses electrons
26
Reduction
A reaction in which a species gains hydrogen, decreases their oxidation state and gains electrons
27
Spectator Ions
Aqueous ions that remain unchanged in a reaction
28
Oxidising agent
A species that has the ability to accept electrons from another species, causing that species to be oxidised and itself to be reduced
29
Reducing agent
A species that has the ability to donate electrons to another species, causing that species to be reduced and itself to be oxidised
30
Redox reactions with halogens/metals
The more reactive halogen/metal (greater (non-)metal tendency) will aim to be in its ion form, to create a complete octet on its outer shell
31
Halogens' colours at room temperature
Chlorine - Yellow/Green Gas Bromine - Orange/Brown Liquid Iodine - Dark Grey Solid
32
Electrochemical Cell (definition)
A system in which a redox reaction occurs
33
Voltaic Cell (definition)
An electrochemical cell that converts chemical energy into electrical energy through redox reactions ; Galvanic cell ; spontaneous
34
Electrolytic Cell (definition)
An electrochemical cell that converts electrical energy into chemical energy through redox reactions ; non-spontaneous
35
Anode and Cathode roles
Anode is always where oxidation occurs whilst the cathode is always where reduction occurs ; The anode is always on the left whilst the cathode is always on the right ; In electrolytic cells the anode is positive (norm) whilst in voltaic cells the anode is negative
36
Voltaic primary cells
Half-cells to allow the electrons in the wire to be transferred and produce electrical energy ; To finish the circuit a salt bridge (normally KNO3) is needed which allows the positive ions in the salt bridge to move to the cathode (replacing the positive ions lost as they are turned into atoms) and vice versa ; Lastly in each half-cell an electrolyte containing the ions of the atom on the electrode is needed
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Salt Bridge
A liquid juncture that allows for the movement of cations and anions in a voltaic cell, which completes the circuit needed for the cell to produce energy through the redox reaction.
38
Cell Diagram example Zn at the anode and Cu at the cathode
Zn (s) | Zn2+ (aq) || Cu2+ (aq) | Cu (s)
39
Rechargeable secondary cells
They use reversible redox reactions ; For example a lithium battery ; At the anode Li (graphite) -> Li+ (electrolyte) + e- as the lithium atoms get oxidised ; The Li+ ions pass through the electrolyte towards the cathode where they then get reduced ; Li+ (electrolyte) + e- + CoO2(s) -> LiCoO2(s) ; These are the formulae for the discharge of the battery, when getting recharge the arrow simply swaps
40
Hydrogen Cell
H2 (g) -> 2H+ (aq) + 2e- 1/2O2 (g) + 2H+ (aq) + 2e- -> H2O (l)
41
Distinctive features of Primary v Secondary v Fuel cells
Single-use battery, non-reversible reaction Rechargeable battery, reversible reaction Continuous reaction as long as fuel and oxidant are available
42
Advantages Primary v Secondary v Fuel Cells
Long shelf life, low cost and high reliability High energy density and rechargeable Continuous reaction as long as fuel and oxidant are available
43
Disadvantages Primary v Secondary v Fuel Cells
Lower energy density and environmental costs Can cause environmental impact, high cost or high maintenance depending on type Safety concerns and lack of fuel availability
44
Use of Primary v Secondary v Fuel Cells
Back-up power generation EVs Fire alarms
45
Molten Electrolytic cells (explanation)
One container and is normally used to purify ores as you can collect the pure metal from its impure form ; The electrolyte needs to contain the molten form of the anode/cathode species ; Due to it being molten the products will mostly be molten
46
Electrolysis of water
In aqueous solutions, the water can also be electrolysed ; At the anode 2H2O (l) → 4H+ (aq) + O2 (g) + 4e– pH decreases due to H+ ions At the cathode 2H2O (l) + 2e– → H2 (g) + 2OH– (aq) pH increases due to OH- ions Both equations are in the formula booklet Overall equation 2H2O (l) → 2H2 (g) + O2 (g)
47
Standard Hydrogen Electrode (SHE)
Used as a reference to measure the standard electrode potentials of all other cells ; Conditions are 100kPa, 298K, 1.00moldm-3 of H+ ; Inert platinum electrode ; The hydrogen half cell given an E of 0V ; Depending on whether it's an anode hydrogen ions form hydrogen gas or vice versa
48
Standard Cell potential
E(cell) = E(reduction) - E(oxidation) ; Not multiplied by the stoichiometry of the equation ; A positive E(cell) means its a spontaneous reaction ; This means that a more positive E value at reduction is favoured whilst a more negative E value at oxidation is favoured
49
Electrolysis of Aqueous ionic solutions
The E value of water at reduction is greater than for most metal ions and so this reaction is favoured as it is a stronger oxidising agent, therefore producing hydrogen gas. This happens unless Copper, silver, gold or platinum ions are used as they are less reactive so more easily reduce into atoms ; The E value of water at oxidation and of halides are very similar and so what occurs depends on the concentration of the halide ions, a high concentration of halides means that the halogen gas will be produced and vice versa
50
Electrolysis of non-inert electrodes (copper sulphate)
When non-inert electrodes are used then the atoms from the anode will be stripped and passed to the cathode ; If the anode doesn't contain the same respective atom as the ions then the colour of the electrolyte will be lost (as the concentration doesn't remain the same)
51
Electroplating (definition)
The electrolytic coating of an object with a thin layer of metal
52
Electroplating (explanation)
Gold-plated for aesthetics ; Iron is galvanised with zinc to prevent the rusting of iron ; The electrolyte needs to contain the same respective ions as the anode's atoms
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Factors affecting the amount of metal electroplated onto the cathode
Time the electrolysis is left on for ; the current supplied ; the charge on the ion
54
Equation using charge
Q = It moles of substance = Q / (number of electrons x F)
55
Oxidation of primary alcohols
Primary alcohols can undergo partial oxidation to aldehyde and complete oxidation to carboxylic acids with a catalyst of acidified potassium dichromate (VI), K₂Cr₂O₇, turning from orange to green, or acidified potassium manganate, K₂MnO₄, turning from purple to colourless ; For the aldehyde heat distillation can be used where the aldehyde is instantly evaporated and removed to avoid complete combustion as it has a lower boiling point than the alcohol and the carboxylic acid, due to no hydrogen bonding ; For the carboxylic acid heat reflux would be used where the condenser is vertical to allow any evaporated aldehyde to be condensed and fully oxidise to a carboxylic acid
56
Oxidation of secondary alcohols
Secondary alcohols fully oxidise to form a ketone under heat reflux ; Tertiary alcohols don't oxidise due to a lack of available hydrogens on the carbon atom that allows oxidation to occur
57
Reduction of alcohols
The opposite of the oxidation of alcohols can occur with catalysts this time of acidified sodiumborohydride (NaBH4) or acidified Lithiumaluminiumhydride (LiAlH4) where the carboxylic acid to the primary alcohol needs the LiAlH4 since it's a stronger reducing agent. Both catalysts need to be acidified to allow the nucleophillic attack (from the H- ion in the catalyset) to occur then a H+ ion to add on to the proton donating oxygen allowing to form an alcohol
58
Reduction of unsaturated compounds
The reduction of unsaturated compounds involves using H2 to react with them (hydrogenation) removing their unsaturated bond (2H2 needed for a triple bond) with a nickel catalyst at 180C
59
Gibbs Energy
The formula uses n where n is the number of electrons (moles of electrons) not the moles of anything else
60
Radicals (definition)
Reactive species or intermediate with an unpaired electron ; Made through the homolytic fission of a species
61
Homolytic fission
The breaking of a covalent bond breaks in such a way that each atom ends up with one of the electrons, forming two radicals
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Homolytic fission conditions
For certain bonds with weak bond enthalpies, UV light can be used to break the bond such as for Cl-Cl, Br-Br or O-O
63
Depletion of ozone with CFCs (chlorofluorocarbons)
CFCs normally form Cl radicals in the presence of UV light (sun) due to the C-Cl bond being longer and hence weaker then the C-F bond. This causes Cl. + O3 -> ClO. + O2 ClO. + O3 -> Cl. + 2O2 This not only breaks the ozone but also replenishes the Cl radical and so the cycle continues The radicals are able to break the bonds in O3 since they are delocalised so slightly less than O2's double bonds, which they cannot break
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Initiation Step
The first step that initiates the formation of a radical. The input of energy is required usually in the form of UV radiation or heat.
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Radical substitution reactions with alkanes
Alkanes are normally very unreactive due to their non-polar bonds and relatively strong bonds (relatively high bond enthalpy) and is the only reaction that alkanes undergo. It needs the initiation step (where the radical is formed), the propagation step (where the radical and the covalent species react to form a new radical and a new covalent species causing a chain reaction) and the termination step (where two radicals come together to form one new covalent species) ; Beware that many species can occur through the halogenoalkanes or longer chain alkanes through two radical alkyl groups being formed and joining together
66
Nucleophile
An electron-rich species that aims to donate a pair of electrons (Lewis base) whilst gaining a nucleus
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Nucleophilic substitution reactions
The nucleophile attacks a carbon that is attached to a halogen (leaving group) that causes both electrons from the C-X bond to go onto the X forming an X- ion whilst the nucleophile provides a pair of electrons and forms a bond with the same carbon C-Nu
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Electrophile
An electron-deficient species that aims to accept a pair of electrons (Lewis acid) whilst losing a nucleus
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Substrate
The molecule that is attacked by the nucleophile in a reaction
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Heterolytic fission
The breaking of a covalent bond in such a way that one atom takes both of the shared electrons, creating a negative ion (anion) and a positive ion (cation) ; It happens due to a difference in electronegativity of above 0.4
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Electrophilic addition
The process of an electrophile being added to an electron rich area
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Electrophilic addition (Halogenation)
The pi electrons in the electron-rich area repel the shared electrons in the X-X bond causing an induced dipole in the X-X causing one to be more electronegative than another so heterolytic fission occurs causing the addition of both (Bromine water test in alkenes)
73
Electrophilic addition (Hydrohalogenation)
The difference in electronegativity between the H and X causes the heterolytic fission and the rest occurs after
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Electrophilic addition (Hydration)
The difference in electronegativity between the O and the H in the water molecule causes the heterolytic fission into a H and an OH, the rest following on from that
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Electrophilic addition (Asymmetrical alkenes)
In the asymmetrical alkenes to carbocations can be formed forming a major and minor product. The favoured and more stable carbocation can be seen by viewing which has the most electron releasing alkyl groups, decreasing the charge on the carbon and making it more stable (positive inductive effect). The more stable one will lead to the major product.
76
Nucleophilic bimolecular substitution (Sn2)
In primary halogenoalkanes, there is little steric hindrance since the nucleophile can attack from the rear, rear-side attack, which causes an inversion of configuration (therefore it's also a stereospecific reaction) but also means that the reaction occurs in one step and the rate is dependent on the ability of the X group to leave and the nucleophile to join so depends on two molecules so is. bimolecular. It also has a transition state that has both on it simultaneously and has a molecular/electron-domain geometry of trigonal bipyramidal
77
Steric hindrance
The prevention or delay of a chemical reaction occurring due to the presence of a bulky group which has a large atomic radius.
78
Nucleophilic unimolecular substitution (Sn1)
In tertiary halogenoalkanes there is very large steric hindrance so then X first has to leave (which is the slowest and rate-determine step and only relies on the X leaving group hence why it's unimolecular) before the nucleophile can join in that same position. The nucleophile however can join from any position so enantiomers can form but due to the probability of attacking from any direction is the same a racemic mixture is formed. The tertiary carbocation is also more stable due to the positive inductive effect which allows it to be an intermediate and no a transition state
79
Trend in leaving groups
A leaving group is a better leaving group and hence the rate will be lower if the bond is weaker. In halogens this occurs when you go down a group as the ability to attract a pair of electrons decreases. This decrease in the covalent bond strength means its easier to break heterolytically so it will be a faster rate of reaction
80
Electrophilic addition benzene (nitration)
As previously discussed due to benzene's delocalised structure it doesn't undergo electrophilic addition but instead electrophilic substitution with nitrate ions (which are formed via nitric and sulphuric acid reacting together H2SO4 + HNO3 <-> HSO4- + H2NO3+ H2NO3+ <-> NO2+ + H2O) Then the benzene donates from it's electron rich region (inside the ring) to the NO2+. This first step causes a horseshoe positive benzene ring with both a H and a NO2 group attached. However, the C-H then breaks heterolytically causing the shape to return to neutral and the aromatic ring with the NO2 group instead of the H atom
81
Lewis acid
An electron-pair acceptor
82
Lewis base
An electron-pair donor
83
Lewis acid/base reactions
Due to the electron pairs being accepted/donated, coordinate bonds are formed. This is especially notable in forming complex ions where the ligands are the lewis bases whilst the central metal ion are lewis acids
84
Coordination Number
The total amount of coordinate bonds formed (can be two from the same species)