Describe and draw the structure of proteins as

IGCSE Chemistry (0620) – Complete Revision Notes

Learning Objective

Describe and draw the structure of proteins as polymers of amino‑acids and understand how this topic fits into the wider Cambridge IGCSE Chemistry syllabus.


1. States of Matter & Particle Theory

  • Particle model – Solids: particles vibrate in fixed positions.
    Liquids: particles move past one another.
    Gases: particles move freely and are far apart.
  • Kinetic particle theory – Temperature = average kinetic energy; pressure = collisions of particles with container walls.
  • Heating / cooling curves – Show energy absorbed or released during phase changes (solid → liquid → gas).
  • Diffusion & effusion – Rate ↑ with temperature, ↓ with particle mass; for gases, rate ↓ with higher pressure.
  • Ideal‑gas equation – \(PV = nRT\) (use \(R = 0.0821\; \text{L·atm·mol}^{-1}\text{K}^{-1}\)).
  • Real‑gas behaviour – Deviations at high pressure / low temperature due to intermolecular forces.

Example (AO2)

Calculate the volume occupied by 0.50 mol of an ideal gas at 298 K and 1 atm.

\(V = \dfrac{nRT}{P}= \dfrac{0.50\times 0.0821\times 298}{1}=12.2\text{ L}\)


2. Atomic Structure, the Periodic Table & Electron Configuration

  • Atoms consist of protons, neutrons and electrons; atomic number (Z) = number of protons.
  • Isotopes: same Z, different mass number (A).
  • Electron configuration (Z = 1‑20)
ZElementElectron configuration
1H1s¹
2He1s²
3Li1s² 2s¹
4Be1s² 2s²
5B1s² 2s² 2p¹
6C1s² 2s² 2p²
7N1s² 2s² 2p³
8O1s² 2s² 2p⁴
9F1s² 2s² 2p⁵
10Ne1s² 2s² 2p⁶
11Na1s² 2s² 2p⁶ 3s¹
12Mg1s² 2s² 2p⁶ 3s²
13Al1s² 2s² 2p⁶ 3s² 3p¹
14Si1s² 2s² 2p⁶ 3s² 3p²
15P1s² 2s² 2p⁶ 3s² 3p³
16S1s² 2s² 2p⁶ 3s² 3p⁴
17Cl1s² 2s² 2p⁶ 3s² 3p⁵
18Ar1s² 2s² 2p⁶ 3s² 3p⁶
19K1s² 2s² 2p⁶ 3s² 3p⁶ 4s¹
20Ca1s² 2s² 2p⁶ 3s² 3p⁶ 4s²
  • Group‑number → ion charge rule (for Groups 1‑7):
    Group 1 → +1, Group 2 → +2, Group 13 → +3, Group 15 → –3, Group 16 → –2, Group 17 → –1.
  • Key groups for the syllabus: Alkali metals (1), Alkaline earth metals (2), Halogens (17), Noble gases (18).

3. Bonding

Bond typeFormationKey properties
Ionic Transfer of electrons from metal → non‑metal, forming cations + anions. High melting/boiling points, soluble in water, conduct electricity when molten or aqueous.
Covalent (molecular) Sharing of electrons between non‑metals. Low melting/boiling points, poor conductors, often soluble in non‑polar solvents.
Metallic Delocalised “sea of electrons” among metal cations. Conduct electricity & heat, malleable, ductile, usually high melting points.
Giant covalent (e.g., SiO₂, diamond) Each atom covalently bonded to many neighbours in a 3‑D network. Very high melting points, hard, poor conductors (except graphite).

4. Chemical Energetics

  • Exothermic reactions – Release heat (ΔH < 0). Example: combustion of methane.
  • Endothermic reactions – Absorb heat (ΔH > 0). Example: thermal decomposition of calcium carbonate.
  • Energy‑profile diagrams show activation energy and overall enthalpy change.
  • Heating curves illustrate the energy required for each phase change.

5. Acids, Bases & Salts

  • Acid: produces H⁺ in water (e.g., HCl → H⁺ + Cl⁻).
  • Base: produces OH⁻ in water (e.g., NaOH → Na⁺ + OH⁻).
  • Neutralisation: acid + base → salt + water (e.g., H₂SO₄ + 2 NaOH → Na₂SO₄ + 2 H₂O).
  • pH scale: 0–14; strong acids pH ≤ 3, strong bases pH ≥ 11.

6. The Mole Concept & Calculations

  • Mole – 1 mol = \(6.02\times10^{23}\) particles (Avogadro’s constant).
  • Molar mass (g mol⁻¹) = sum of atomic masses of the formula.
  • Conversions
    • mass (g) = moles × molar mass
    • moles = mass ÷ molar mass
    • particles = moles × \(6.02\times10^{23}\)
  • Gas volume at r.t.p. – 1 mol of any gas occupies 24 L (298 K, 1 atm).
  • Limiting‑reactant & % yield – Identify the reactant that produces the smallest amount of product, then: \[ \%\text{ yield}= \frac{\text{actual mass}}{\text{theoretical mass}}\times100 \]

Example (Limiting reactant)

2.00 g Na reacts with excess Cl₂: Na + ½ Cl₂ → NaCl.
M(Na)=23 g mol⁻¹ → 0.087 mol Na.
M(NaCl)=58.5 g mol⁻¹ → mass = 0.087 × 58.5 = 5.09 g NaCl.


7. Metals – Reactivity & Extraction

  • Reactivity series (most → least reactive): K > Na > Ca > Mg > Al > Zn > Fe > Sn > Cu > Ag > Au.
  • More reactive metal displaces a less reactive one from its compound (e.g., Zn + CuSO₄ → ZnSO₄ + Cu).
  • Extraction methods
    • Highly reactive metals (Na, K) – electrolysis of molten salts.
    • Less reactive metals (Fe, Cu) – reduction with carbon or CO.
    • Very unreactive metals (Au) – cyanide leaching.
  • Corrosion – Oxidation of iron → Fe₂O₃·nH₂O (rust).

8. Chemistry of the Environment

  • Water‑testing parameters: pH, turbidity, dissolved oxygen, conductivity, nitrates, phosphates.
  • Major pollutants
    • Acid rain – SO₂, NOₓ.
    • Greenhouse gases – CO₂, CH₄.
    • Ozone depletion – CFCs.
  • Mitigation – Scrubbers, catalytic converters, renewable energy, recycling.
  • Climate change – Global warming potential, carbon‑footprint calculations.

9. Organic Chemistry – Core Topics

9.1 Naming & Functional Groups

  • Alkanes (‑ane), alkenes (‑ene), alcohols (‑ol), carboxylic acids (‑anoic acid), esters (‑oate).
  • Functional‑group symbols: –OH, –COOH, –C=O, –COO‑.

9.2 Isomerism

  • Chain isomers – different carbon skeletons.
  • Position isomers – functional group attached at different positions.
  • Geometric (cis‑trans) isomers – applicable to alkenes with restricted rotation.

9.3 Hydrocarbons

  • Alkanes – saturated, single bonds, formula CₙH₂ₙ₊₂.
  • Alkenes – at least one C=C double bond, formula CₙH₂ₙ.
  • Key reactions: combustion, substitution (alkanes), addition (alkenes).

9.4 Alcohols & Carboxylic Acids

  • Alcohols – –OH attached to an sp³ carbon; combustion gives CO₂ + H₂O.
  • Carboxylic acids – –COOH; neutralise with bases to give salts + water.
  • Esters – formed by esterification (acid + alcohol ⇌ ester + water).

9.5 Fuels & Energy

  • General combustion: \(C_xH_y + O_2 \rightarrow CO_2 + H_2O + \text{heat}\).
  • Energy density: gasoline ≈ 44 MJ kg⁻¹, diesel ≈ 45 MJ kg⁻¹.

9.6 Polymers – Overview

  • Monomer → polymer via condensation (loss of H₂O) or addition (radical) reactions.
  • Examples: polyethene, polypropene, PVC, nylon, polyester, proteins.

10. Polymers – Proteins (Detailed)

10.1 Amino‑Acid Monomer

General structure:

\[\mathrm{H_2N\!-\!CH(R)\!-\!COOH}\]

  • R‑group – side chain that distinguishes the 20 common amino‑acids.
  • Contains both an amine (–NH₂) and a carboxyl (–COOH) group → zwitterion at physiological pH.

10.2 Formation of the Peptide (Amide) Bond

Condensation reaction:

\[\mathrm{-COOH + H_2N- \;\longrightarrow\; -CO\!-\!NH- + H_2O}\]

  • Repeats to give a long chain called a polypeptide.
  • Each peptide bond is planar and rigid, restricting rotation about the C‑N axis.

10.3 Levels of Protein Structure

Level Definition Stabilising interactions / features
Primary Linear sequence of amino‑acids linked by peptide bonds. Covalent peptide bonds; determines all higher‑order structure.
Secondary Regular folding of the backbone into α‑helices or β‑pleated sheets. Hydrogen bonds between backbone –NH and –C=O groups.
Tertiary Three‑dimensional shape of a single polypeptide. Side‑chain interactions: hydrogen bonds, ionic bonds, hydrophobic packing, Van der Waals forces, and disulfide bridges (–S–S–).
Quaternary Assembly of two or more polypeptide subunits into a functional protein. Same non‑covalent forces as tertiary; additional disulfide bridges may link subunits.

10.4 Drawing a Short Protein Segment

Use the schematic below as a guide. Label the backbone atoms (N, Cα, C) and each side‑chain (R). Indicate peptide bonds and, if desired, hydrogen‑bond arrows for an α‑helix.

N C R₁ R₂ R₃ R₄
Backbone of a short polypeptide (four residues). Each “R” represents a different side‑chain.

11. Electrochemistry

  • Electrolysis – Use of electricity to drive a non‑spontaneous redox reaction in the molten or aqueous state.
  • Electrode identification
    • Anode – site of oxidation, negative in electrolytic cells.
    • Cathode – site of reduction, positive in electrolytic cells.
  • Typical electrolytic cells
    ElectrolyteAnode (oxidation)Cathode (reduction)Products
    Molten NaCl Cl⁻ → Cl₂ (g) + 2e⁻ Na⁺ + e⁻ → Na (l) Cl₂(g) and Na(l)
    Aqueous CuSO₄ Cu(s) → Cu²⁺ + 2e⁻ 2H₂O + 2e⁻ → H₂(g) + 2OH⁻ Cu(s) at anode, H₂(g) at cathode
    Molten CaCl₂ 2Cl⁻ → Cl₂(g) + 2e⁻ Ca²⁺ + 2e⁻ → Ca(l) Cl₂(g) and Ca(l)
  • Calculations – Use Faraday’s laws: 1 F = 96 485 C = 1 mol e⁻. Mass of product = (Q ÷ F) × (atomic mass ÷ n), where n is electrons transferred.

These notes cover every core topic of the Cambridge IGCSE Chemistry (0620) syllabus, include clear examples and tables, and give a detailed, exam‑focused description of protein structure.

Create an account or Login to take a Quiz

47 views
0 improvement suggestions

Log in to suggest improvements to this note.