Revision sheet: Chemistry Revision Map

Course Outline

  1. Acids Bases and Titrations
  2. Redox and Electrochemistry
  3. Equilibrium and Le Chatelier
  4. Organic Functional Groups
  5. Organic Reactions and Isomers
  6. Spectroscopy and Mass Spectrometry
  7. Amino Acids and Intermolecular Forces
  8. Fuel Cells and Green Chemistry
  9. Calculations and Written Responses

1. Acids Bases and Titrations

Essential Points

πŸ“Œ A strong acid dissociates completely, whereas a weak acid establishes an equilibrium represented by β‡Œ.

  • A monoprotic acid can donate one H⁺, whereas a diprotic acid can donate two H⁺ ions.

πŸ“ Formula β€” The acid dissociation constant is Ka=[H+][Aβˆ’][HA]K_a=\frac{[H^+][A^-]}{[HA]} and the acidity is pKa=βˆ’log⁑KapK_a=-\log K_a.

πŸ“ Formula β€” The relationships for amount, concentration, dilution, and conjugate pairs are n=cVn=cV, c=nVc=\frac{n}{V}, c1V1=c2V2c_1V_1=c_2V_2, and pKa+pKb=14pK_a+pK_b=14.

  • At the equivalence point of a 1:

    • 1 titration
    • the amount of acid equals the amount of base
    • volumes must be expressed in litres
  • A strong acid–strong base titration has equivalence pH 7, a weak acid–strong base titration has equivalence pH above 7, and a strong acid–weak base titration has equivalence pH below 7.

Memory Hook

Identify β†’ calculate β†’ titrate

2. Redox and Electrochemistry

Essential Points

  • 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, Na⁺ is reduced to sodium at the cathode and chloride ions are oxidised to chlorine at the anode.

Memory Hook

AN OX, RED CAT

3. Equilibrium and Le Chatelier

Essential Points

  • 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.

πŸ“ Formula β€” The equilibrium constant is expressed as Kc=[products]coefficients[reactants]coefficientsK_c=\frac{[products]^{coefficients}}{[reactants]^{coefficients}}; Kc>1K_c>1 indicates products are favoured and Kc<1K_c<1 indicates reactants are favoured.

Memory Hook

Change conditions β†’ equilibrium shift

4. Organic Functional Groups

Essential Points

  • The functional groups C=C, C≑C, –OH, –CHO, >C=O, –COOH, –COO–, –NHβ‚‚, and –C≑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.

5. Organic Reactions and Isomers

Key Concepts & Definitions

  • Ester : Contains the functional group R–COO–R.

Essential Points

  • 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.

πŸ“Œ 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.

Memory Hook

Alcohol β†’ aldehyde β†’ carboxylic acid

6. Spectroscopy and Mass Spectrometry

Essential Points

  • IR absorptions at 3200–3600 cm⁻¹ broad, 2500–3000 cm⁻¹ very broad, approximately 1700 cm⁻¹ strong, 1600–1680 cm⁻¹, and 2850–3100 cm⁻¹ identify alcohol O–H, carboxylic-acid O–H, C=O, C=C, and C–H respectively.

  • A strong approximately 1700 cm⁻¹ peak with a very broad 2500–3000 cm⁻¹ peak indicates a carboxylic acid, while a 1700 cm⁻¹ peak without O–H indicates an aldehyde or ketone.

  • The highest molecular peak in a mass spectrum is the molecular ion M⁺.

7. Amino Acids and Intermolecular Forces

Essential Points

πŸ“Œ 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 dipole–dipole forces greater than dispersion forces.

  • OH, COOH, and NHβ‚‚ groups increase solubility through hydrogen bonding with water, while longer hydrocarbon chains lower solubility.

8. Fuel Cells and Green Chemistry

Essential Points

πŸ“Œ In an acidic hydrogen fuel cell, H⁺ moves to the cathode, whereas in an alkaline hydrogen fuel cell, OH⁻ moves to the anode.

  • Electrons travel through the external circuit and ions travel through the electrolyte in a hydrogen fuel cell.

πŸ“ Formula β€” Atom economy is calculated as AE=Mr(desiredΒ product)Mr(allΒ reactants)Γ—100AE=\frac{M_r(\text{desired product})}{M_r(\text{all reactants})}\times100, and a higher atom economy is better.

πŸ“ Formula β€” The E-factor is calculated as E=wasteproductE=\frac{\text{waste}}{\text{product}}, and a lower E-factor is better.

Memory Hook

Higher atom economy, lower E-factor

9. Calculations and Written Responses

Essential Points

πŸ“ Formula β€” Use n=cVn=cV for moles, c=nVc=\frac{n}{V} for concentration, c1V1=c2V2c_1V_1=c_2V_2 for dilution, pH=βˆ’log⁑[H+]pH=-\log[H^+] for pH, and pKa=βˆ’log⁑KapK_a=-\log K_a 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.

Memory Hook

Formula β†’ substitution β†’ answer with units

Synthesis Tables

Titration Equivalence pH

TitrationEquivalence pHIndicator condition
Strong acid + strong base7Indicator range overlaps pH 7
Weak acid + strong base>7Indicator range overlaps pH above 7
Strong acid + weak base<7Indicator range overlaps pH below 7

Test your knowledge

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?

Take the quiz β†’

Review with flashcards

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 H⁺ ions can a diprotic acid donate?

Two H⁺ ions.

What is the formula for the acid dissociation constant Kₐ?

Kₐ = [H⁺][A⁻] / [HA].

See flashcards β†’

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