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Edexcel AS Chemistry

Revision Notes

Home / AS / Chemistry / Edexcel / Revision Notes / 3. Organic Chemistry / 3.3 Alkenes / 3.3.2 Bonding in Alkenes


3.3.2 Bonding in Alkenes


Bonding in Alkenes

  • Each carbon atom has four electrons in its outer shell (electronic configuration: 1s22s22p2)
  • Carbon atoms share these four electrons in four covalent bonds with other atoms to achieve a full outer shell configuration
  • These electrons are found in orbitals within the respective atoms
  • When forming a covalent bond, the orbitals overlap in such a way to form two types of bonds
    • Sigma bonds (σ)
    • Pi bonds (π)
  • When carbon atoms use only three of their electron pairs to form a σ bond, each carbon atom will have a p orbital which contains one spare electron
  • When the p orbitals of two carbon atoms overlap with each other, a π bond is formed (the π bond contains two electrons)
  • The two orbitals that form the π bond lie above and below the plane of the two carbon atoms to maximise bond overlap

σ bonds

  • Sigma (σ) bonds are formed from the end to end overlap of atomic orbitals
  • s orbitals overlap this way as well as p orbitals

Chemical Bonding Bond Overlap in Sigma Orbitals, downloadable AS & A Level Chemistry revision notes

Sigma orbitals can be formed from the end to end overlap of s orbitals 

  • The electron density in a σ bond is symmetrical about a line joining the nuclei of the atoms forming the bond
  • The pair of electrons is found between the nuclei of the two atoms
  • The electrostatic attraction between the electrons and nuclei bonds the atoms to each other

Hydrogen

  • The hydrogen atom has only one s orbital
  • The s orbitals of the two hydrogen atoms will overlap to form a σ bond

Chemical Bonding Orbital Overlap in Hydrogen, downloadable AS & A Level Chemistry revision notes

π bonds

  • Pi (π) bonds are formed from the sideways overlap of adjacent p orbitals
  • The two lobes that make up the π bond lie above and below the plane of the σ bond
  • This maximises overlap of the p orbitals
  • A single π bond is drawn as two electron clouds, one arising from each lobe of the p orbitals
  • The two clouds of electrons in a π bond represent one bond containing two electrons

Chemical Bonding Bond Overlap in Pi Orbitals, downloadable AS & A Level Chemistry revision notes

π orbitals can be formed from the sideways overlap of p orbitals

Ethene

  • Each carbon atom uses three of its four electrons to form σ bonds
  • Two σ bonds are formed with the hydrogen atoms
  • One σ bond is formed with the other carbon atom
  • The fourth electron from each carbon atom occupies a p orbital which overlaps sideways with another p orbital on the other carbon atom to form a π bond
  • This means that the C-C is a double bond: one σ and one π bond

Chemical Bonding Electron Density in Ethene, downloadable AS & A Level Chemistry revision notes

Each carbon atom in ethene forms two sigma bonds with hydrogen atoms and one σ bond with another carbon atom. The fourth electron is used to form a π bond between the two carbon atoms



  • 1. Physical Chemistry
    • 1.1 Atomic Structure
      • 1.1.1 Structure of the Atom
        • 1.1.2 Isotopes
          • 1.1.3 Relative Mass
            • 1.1.4 Mass Spectrometry
            • 1.2 Ions & Electrons
              • 1.2.1 Ionisation Energy
                • 1.2.2 Quantum Shells
                  • 1.2.4 Electronic Configurations
                  • 1.3 The Periodic Table
                    • 1.3.1 Periodicity
                    • 1.4 Bonding
                      • 1.4.1 Ionic Bonding Overview
                        • 1.4.2 Representing Ionic Bonding
                          • 1.4.3 Ionic Trends
                            • 1.4.4 Physical Properties of Ionic Compounds
                              • 1.4.5 Covalent Bonding Overview
                                • 1.4.6 Covalent Dot-and-Cross Diagrams
                                  • 1.4.7 Bond Length & Bond Strength
                                    • 1.4.8 Shapes of Covalent Compounds
                                    • 1.5 Structure
                                      • 1.5.1 Electronegativity
                                        • 1.5.2 Intermolecular Forces
                                          • 1.5.3 Hydrogen Bonding
                                            • 1.5.4 Intermolecular Forces & Physical Properties
                                              • 1.5.5 Metallic Bonding
                                                • 1.5.6 Giant Lattices
                                                  • 1.5.7 Covalent Structures
                                                    • 1.5.8 Predicting Structures
                                                    • 1.6 Formulae, Equations & Avogadro
                                                      • 1.6.1 Empirical & Molecular Formulae
                                                        • 1.6.4 The Mole & the Avogadro Constant
                                                        • 1.7 Reaction Calculations
                                                          • 1.7.1 Reacting Volume Calculations
                                                            • 1.7.2 Titrations
                                                              • 1.7.3 Error & Uncertainty
                                                                • 1.7.4 Yield & Atom Economy
                                                                • 1.8 Energetics I
                                                                  • 1.8.1 Enthalpy Changes
                                                                    • 1.8.3 Calorimetry
                                                                      • 1.8.4 Hess Cycles
                                                                        • 1.8.5 Bond Enthalpy
                                                                          • Enthalpy Level Diagrams
                                                                          • 1.9 Kinetics
                                                                            • 1.9.1 Collision Theory & Rates
                                                                              • 1.9.2 Calculating Rates of Reaction
                                                                                • 1.9.3 Maxwell-Boltzmann Distributions
                                                                                  • 1.9.4 Catalysts in Industry
                                                                                  • 1.10 Equilibrium I
                                                                                    • 1.10.2 Le Chatelier's Principle
                                                                                      • 1.10.3 The Rate & Yield Compromise
                                                                                        • 1.10.4 Deducing Kc Expressions
                                                                                      • 2. Inorganic Chemistry
                                                                                        • 2.1 Redox I
                                                                                          • 2.1.1 Oxidation Number
                                                                                            • 2.1.2 Types of Reduction & Oxidation
                                                                                              • 2.1.3 Redox & Disproportionation
                                                                                                • 2.1.4 Ionic Equations
                                                                                                • 2.2 Groups 1 & 2
                                                                                                  • 2.2.1 Explaining Group 2 Trends
                                                                                                    • 2.2.2 Reactions of Group 2
                                                                                                      • 2.2.3 Group 2 Hydroxides & Sulfates
                                                                                                        • 2.2.4 Group 2 Carbonates & Nitrates
                                                                                                          • 2.2.5 Flame Tests
                                                                                                          • 2.3 Group 7
                                                                                                            • 2.3.1 Group 7 Trends
                                                                                                              • 2.3.2 Halogen Displacement Reactions
                                                                                                                • 2.3.3 Halogen Redox Reactions
                                                                                                                  • 2.3.4 Halide Ion Reactions
                                                                                                                • 3. Organic Chemistry
                                                                                                                  • 3.1 Introduction to Organic Chemistry
                                                                                                                    • 3.1.1 formulae of organic compounds
                                                                                                                      • 3.1.2 Homologous Series and Functional Groups
                                                                                                                        • 3.1.3 Nomenclature and Classification
                                                                                                                          • 3.1.4 Structural Isomerism
                                                                                                                            • 3.1.5 Stereoisomerism
                                                                                                                            • 3.2 Alkanes
                                                                                                                              • 3.2.1 Describing Alkanes
                                                                                                                                • 3.2.2 Alkane Fuels
                                                                                                                                  • 3.2.3 Pollution from Combustion
                                                                                                                                    • 3.2.4 Reducing Pollution
                                                                                                                                      • 3.2.5 Free Radicals
                                                                                                                                      • 3.3 Alkenes
                                                                                                                                        • 3.3.1 Describing Alkenes
                                                                                                                                          • 3.3.2 Bonding in Alkenes
                                                                                                                                            • 3.3.3 Electrophilic addition
                                                                                                                                              • 3.3.4 Electrophilic Addition Mechanism
                                                                                                                                                • 3.3.5 Saturation Test
                                                                                                                                                  • 3.3.6 Addition Polymerisation
                                                                                                                                                    • 3.3.7 Waste Polymers
                                                                                                                                                    • 3.4 Halogenoalkanes
                                                                                                                                                      • 3.4.1 Classifying Halogenoalkanes
                                                                                                                                                        • 3.4.2 Nucleophilic Substitution
                                                                                                                                                          • 3.4.3 Nucleophilic Substitution Mechanism
                                                                                                                                                            • 3.4.4 Hydrolysis of Halogenoalkanes
                                                                                                                                                              • 3.4.5 Reactivity of Halogenoalkanes
                                                                                                                                                              • 3.5 Alcohols
                                                                                                                                                                • 3.5.1 Classifying Alcohols
                                                                                                                                                                  • 3.5.2 Reactions of Alcohols
                                                                                                                                                                    • 3.5.3 Organic Liquid Preparation & Purification
                                                                                                                                                                    • 3.6 Modern Analytical Techniques I
                                                                                                                                                                      • 3.6.1 Mass Spectrometry
                                                                                                                                                                        • 3.6.2 Infrared (IR) Spectroscopy
                                                                                                                                                                      • 4. Core Chemistry Practicals
                                                                                                                                                                        • 4.1 Physical Chemistry Core Practicals
                                                                                                                                                                          • 4.1.1 Molar Volume of a Gas
                                                                                                                                                                            • 4.1.2 Standard Solutions
                                                                                                                                                                              • 4.1.3 Determining Concentrations
                                                                                                                                                                                • 4.1.4 Determining Enthalpy Change of Reaction
                                                                                                                                                                                • 4.2 Inorganic & Organic Chemistry Core Practicals
                                                                                                                                                                                  • 4.2.1 Hydrolysis of Halogenoalkanes
                                                                                                                                                                                    • 4.2.2 Ethanol Oxidation
                                                                                                                                                                                      • 4.2.3 Chlorination of 2-Methylpropan-2-ol
                                                                                                                                                                                        • 4.2.4 Qualitative Analysis


                                                                                                                                                                                        DOWNLOAD PDF

                                                                                                                                                                                      Author: Sonny



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