π A strong acid dissociates completely, whereas a weak acid establishes an equilibrium represented by β.
π Formula β The acid dissociation constant is and the acidity is .
π Formula β The relationships for amount, concentration, dilution, and conjugate pairs are , , , and .
At the equivalence point of a 1:
A strong acidβstrong base titration has equivalence pH 7, a weak acidβstrong base titration has equivalence pH above 7, and a strong acidβweak base titration has equivalence pH below 7.
Identify β calculate β titrate
Oxidation occurs at the anode and reduction occurs at the cathode; oxidation loses electrons and reduction gains electrons.
In a galvanic cell, the anode is negative and produces electrons, while the cathode is positive and uses electrons.
Electrons flow from the anode to the cathode in a galvanic cell, while salt-bridge anions migrate to the anode and cations migrate to the cathode.
During electrolysis of molten NaCl, NaβΊ is reduced to sodium at the cathode and chloride ions are oxidised to chlorine at the anode.
AN OX, RED CAT
Adding a reactant shifts equilibrium toward products, whereas adding a product shifts equilibrium toward reactants.
Increasing pressure shifts a gaseous equilibrium toward fewer gas particles, while decreasing pressure shifts it toward more gas particles.
Increasing temperature favours the endothermic direction, whereas decreasing temperature favours the exothermic direction.
π Formula β The equilibrium constant is expressed as ; indicates products are favoured and indicates reactants are favoured.
Change conditions β equilibrium shift
The functional groups C=C, Cβ‘C, βOH, βCHO, >C=O, βCOOH, βCOOβ, βNHβ, and βCβ‘N are respectively alkene, alkyne, alcohol, aldehyde, ketone, carboxylic acid, ester, amine, and nitrile.
An alkene reacts with bromine by addition across the C=C bond.
A primary alcohol can oxidise to an aldehyde and then to a carboxylic acid, whereas a secondary alcohol oxidises to a ketone.
Reduction of a nitrile produces an amine.
π Structural isomers have the same molecular formula but different connectivity, whereas E/Z isomers have a C=C bond with different groups on both carbons and differ in spatial arrangement.
Alcohol β aldehyde β carboxylic acid
IR absorptions at 3200β3600 cmβ»ΒΉ broad, 2500β3000 cmβ»ΒΉ very broad, approximately 1700 cmβ»ΒΉ strong, 1600β1680 cmβ»ΒΉ, and 2850β3100 cmβ»ΒΉ identify alcohol OβH, carboxylic-acid OβH, C=O, C=C, and CβH respectively.
A strong approximately 1700 cmβ»ΒΉ peak with a very broad 2500β3000 cmβ»ΒΉ peak indicates a carboxylic acid, while a 1700 cmβ»ΒΉ peak without OβH indicates an aldehyde or ketone.
The highest molecular peak in a mass spectrum is the molecular ion MβΊ.
π An amino acid is positive when pH<pI, neutral when pH=pI, and negative when pH>pI.
During electrophoresis, positive ions move toward the negative electrode and negative ions move toward the positive electrode.
The relative strength of intermolecular forces is hydrogen bonding greater than dipoleβdipole forces greater than dispersion forces.
OH, COOH, and NHβ groups increase solubility through hydrogen bonding with water, while longer hydrocarbon chains lower solubility.
π In an acidic hydrogen fuel cell, HβΊ moves to the cathode, whereas in an alkaline hydrogen fuel cell, OHβ» moves to the anode.
π Formula β Atom economy is calculated as , and a higher atom economy is better.
π Formula β The E-factor is calculated as , and a lower E-factor is better.
Higher atom economy, lower E-factor
π Formula β Use for moles, for concentration, for dilution, for pH, and for pKa.
For Calculate questions, write the formula, substitute values, and give the answer with units.
Justify responses should contain a claim, relevant data, and chemical reasoning.
A two-mark short response requires an answer and a reason, while a three-mark response requires a prediction, chemical reason, and evidence or data.
Formula β substitution β answer with units
Titration Equivalence pH
| Titration | Equivalence pH | Indicator condition |
|---|---|---|
| Strong acid + strong base | 7 | Indicator range overlaps pH 7 |
| Weak acid + strong base | >7 | Indicator range overlaps pH above 7 |
| Strong acid + weak base | <7 | Indicator range overlaps pH below 7 |
Test your knowledge on Chemistry Revision Map with 33 multiple-choice questions with detailed corrections.
1. How does a weak acid differ from a strong acid in aqueous solution?
2. How many protons can a diprotic acid donate per molecule?
Memorize the key concepts of Chemistry Revision Map with 60 interactive flashcards.
How does a strong acid differ from a weak acid in dissociation?
A strong acid dissociates completely, a weak acid establishes an equilibrium.
How many HβΊ ions can a diprotic acid donate?
Two HβΊ ions.
What is the formula for the acid dissociation constant Kβ?
Kβ = [HβΊ][Aβ»] / [HA].
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