2.3.4
Resonance Structures
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Resonance Structures
In structures with multiple bonds and when more than one Lewis structure can be drawn for the same molecule, the true structure is best represented by a resonance hybrid.

Resonance
- Resonance shows the delocalisation of electrons in a molecule and this needs to be considered when more than one Lewis structure can be drawn for the same molecule.
- None of the Lewis structures drawn represents the true structure and the electron density is averaged over all positions.
- The delocalisation of electrons gives more space for the electrons to move and molecules with resonance structures are more stable as a consequence.
- This higher stability is known as resonance stability.
- Resonance occurs in structures with multiple bonds.

Example: Ozone
- The Lewis structure of ozone can be represented by the two diagrams above.
- The two structures can be interconverted by moving the non-bonding electron domain across from one oxygen to the other.
- Neither of these structures is the true structure and ozone is best represented by a resonance hybrid structure.
- This is supported by the bond lengths and strengths, which are consistent with a bond order of 1.5.

Example: Carbonate ion
- Three resonance structures can be drawn for the carbonate ion and the bond order is best described as 1.3.

Example: Nitrate ion
- Three resonance structures can be drawn for the nitrate ion and the bond order is best described as 1.3.

Example: Carboxylate ion
- On removing a proton from a carboxylic acid, a carboxylate ion is formed in which the two carbon-oxygen bonds become equivalent and can be considered to have a bond order of 1.5.

Example: Benzene
- An important example with delocalised electrons is benzene.
- In benzene, the π-bonds are shared equally between the six positions.
Graphene
Graphene is an important example where its structure, containing delocalised electrons, confers very useful properties.

Graphene
- Graphene is a recently discovered allotrope of carbon, which is related to the structure of graphite with just one layer of atoms.
 2.3.3.1 - The structure of graphene-min,h_400,q_80,w_640.png)
Graphene structure
- Each carbon atom bonds with three others to give a hexagon.
- Each carbon is sp2 hybridized.
- Each carbon atom has a spare electron, which is delocalised around the whole structure.
- This structure is often described as a honeycomb structure.

Properties
- Excellent conductor
- Very strong, but also very light
- Transparent

Applications
- Drug delivery in carbon nanotubes
- Electronics
- Touch screens
- Photovoltaics
1Structure - Models of the Particulate of Matter
1.1Introduction to the Particulate Model of Matter
1.2The Nuclear Atom
1.3Electron Configuration
1.4Counting Particles by Mass: The Mole
1.6Elements, Compounds & Mixtures
1.7States of Matter & Changes of State
1.8Reacting Masses &. Volumes
1.9Solutions
2Structure - Models of Bonding & Structure
2.1The Ionic Model
2.2The Covalent Model
2.3Covalent Structures
2.4The Metallic Model
2.5From Models to Materials
2.6Valence Electrons & Ionic Compounds
2.7Molecular Shape
3Structure - Classification of Matter
3.1The Periodic Table: Classification of Elements
3.2Periodic Trends
3.3Group 1 Alkali Metals
3.4Halogens
3.5Noble gases, group 18
3.6Functional Groups: Classification of Organic
3.7Functional Group Chemistry
3.8Alkanes
3.9Alcohols
4Reactivity - What Drives Chemical Reaction?
4.1Endothermic & Exothermic Reactions
4.2Enthalpy of Reaction, Formation, & Hess' Law
5Reactivity - How Much, How Fast & How Far?
5.1Kinetics
5.2Rates of Reaction
5.3Stoichometry
5.4Le Châtelier’s Principle
5.5Introduction to Equilibrium
5.6Equilibrium Constant
5.7Reaction Quotient & Equilibrium Constant
6Reactivity - The Mechanisms of Chemical Change
6.1Proton Transfer Reactions
6.2The pH Scale
6.3Strong & Weak Acids and Bases
6.4Acid Deposition
6.5Types of Organic Reactions
6.6Oxidation & Reduction
6.7Electrochemical Cells
6.9Acid-Base Titrations
6.9.1Titration Calculation Weak Acid & Strong Base6.9.2Titration Experimental Detail6.9.3Extended Response - Titration6.9.4Titration Calculations6.9.5Titration Curves6.9.6Titration Calculation Strong Acid & Weak Base6.9.7IB Multiple Choice - Titrations6.9.8Polyprotic Acids6.9.9Titration Calculations Strong Acid & Strong Base6.9.10Titrations Curves 2
7Measurement, Data Processing & Analysis
7.1Uncertainties & Errors in Measurements & Results
7.2Graphical Techniques
7.3Spectroscopic Identification of Organic Compounds
7.4Infrared Spectroscpy
Jump to other topics
1Structure - Models of the Particulate of Matter
1.1Introduction to the Particulate Model of Matter
1.2The Nuclear Atom
1.3Electron Configuration
1.4Counting Particles by Mass: The Mole
1.6Elements, Compounds & Mixtures
1.7States of Matter & Changes of State
1.8Reacting Masses &. Volumes
1.9Solutions
2Structure - Models of Bonding & Structure
2.1The Ionic Model
2.2The Covalent Model
2.3Covalent Structures
2.4The Metallic Model
2.5From Models to Materials
2.6Valence Electrons & Ionic Compounds
2.7Molecular Shape
3Structure - Classification of Matter
3.1The Periodic Table: Classification of Elements
3.2Periodic Trends
3.3Group 1 Alkali Metals
3.4Halogens
3.5Noble gases, group 18
3.6Functional Groups: Classification of Organic
3.7Functional Group Chemistry
3.8Alkanes
3.9Alcohols
4Reactivity - What Drives Chemical Reaction?
4.1Endothermic & Exothermic Reactions
4.2Enthalpy of Reaction, Formation, & Hess' Law
5Reactivity - How Much, How Fast & How Far?
5.1Kinetics
5.2Rates of Reaction
5.3Stoichometry
5.4Le Châtelier’s Principle
5.5Introduction to Equilibrium
5.6Equilibrium Constant
5.7Reaction Quotient & Equilibrium Constant
6Reactivity - The Mechanisms of Chemical Change
6.1Proton Transfer Reactions
6.2The pH Scale
6.3Strong & Weak Acids and Bases
6.4Acid Deposition
6.5Types of Organic Reactions
6.6Oxidation & Reduction
6.7Electrochemical Cells
6.9Acid-Base Titrations
6.9.1Titration Calculation Weak Acid & Strong Base6.9.2Titration Experimental Detail6.9.3Extended Response - Titration6.9.4Titration Calculations6.9.5Titration Curves6.9.6Titration Calculation Strong Acid & Weak Base6.9.7IB Multiple Choice - Titrations6.9.8Polyprotic Acids6.9.9Titration Calculations Strong Acid & Strong Base6.9.10Titrations Curves 2
7Measurement, Data Processing & Analysis
7.1Uncertainties & Errors in Measurements & Results
7.2Graphical Techniques
7.3Spectroscopic Identification of Organic Compounds
7.4Infrared Spectroscpy
Practice questions on Resonance Structures
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- 1Which of these statements is NOT true?Multiple choice
- 2
- 3Which of these is NOT a potential application of graphene?Multiple choice
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