Alkanes do not react with most reagents for two reasons. First, carbon-carbon and carbon-hydrogen single bonds are very strong due to good orbital overlap. Second, the carbon-hydrogen bonds make alkane molecules neither acidic nor basic because the electronegativity of both elements is very similar. This similarity gives the carbonhydrogen bond little polarity, and without polarity, proton loss is difficult. Thus, alkanes make poor acids. Likewise, a lack of nonbonded electron pairs on either the carbon or hydrogen atoms makes alkanes poor bases. However, under proper conditions, alkanes can react with halogens and oxygen.
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- Atomic Structure
- Lewis Structures
- Ionic Bonding
- Covalent Bonding and Electronegativity
- Brønsted‐Lowry Theory of Acids and Bases
- Lewis Theory of Acids and Bases
- Mechanisms
- Bond Rupture and Formation
- Properties of Electrons
- Molecular Orbitals
- Hybridization of Atomic Orbitals
- Three‐Dimensional Shapes of Molecules
- Free Rotation Around Single Bonds
- Nonrotation Around Multiple Bonds
- Structural Isomers and Stereoisomers
- Hydrocarbons
- Alkanes: Molecular and Structural Formulas
- Alkanes: Nomenclature
- Alkanes: Physical Properties
- Alkanes: Natural Sources
- Alkanes: Preparations
- Introduction to Alkanes
- Alkanes: Halogenation
- Alkanes: Kinetics and Rate
- Alkanes: Oxidation
- Alkenes: Molecular and Structural Formulas
- Alkenes: Unsaturation
- Alkenes: Nomenclature
- Alkenes: Physical Properties
- Alkenes: Preparations
- Alkenes: Electrophilic Addition Reactions
- Alkenes: Halogenation
- Alkenes: Hydrohalogenation
- Alkenes: Hydration (Direct Addition of Water)
- Alkenes: Hydroboration‐Oxidation
- Alkenes: Catalytic Addition of Hydrogen
- Alkenes: Addition of Carbenes
- Alkenes: Epoxide Reactions
- Alkenes: Oxidation and Cleavage Reactions
- Alkenes: Polymerization
- Alkynes: Molecular and Structural Formulas
- Alkynes: Unsaturation
- Alkynes: Nomenclature
- Alkynes: Physical Properties
- Alkynes: Acidity
- Alkynes: Preparations
- Alkynes: Addition Reactions
- Cyclohydrocarbons: Structural Formulas
- Cyclohydrocarbons: Nomenclature
- Cyclohydrocarbons: Stereochemistry
- Cyclohydrocarbons: Reactivity, Stresses of Small Rings
- Cyclohydrocarbons: Preparations
- Cyclohydrocarbons: Reactions
- Stereochemistry Defined
- Optical Activity
- Chirality
- Projections
- Enantiomers and Diastereomers
- Racemic Mixtures: Resolving Enantiomers
- Cahn‐Ingold‐Prelog RS Notational System
- Stereochemistry of Reactions
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Introduction to Alkanes
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Review of General Chemistry
Reactions of Alkanes
