🥼organic chemistry review

key term - Alkanes

Definition

Alkanes are a class of saturated hydrocarbons composed entirely of single-bonded carbon and hydrogen atoms. They are the simplest organic compounds and serve as the foundation for many other organic molecules and reactions.

5 Must Know Facts For Your Next Test

  1. Alkanes are the simplest and most saturated hydrocarbons, with the general formula $\ce{C_nH_{2n+2}}$.
  2. The carbon atoms in alkanes are connected by single bonds, and all the hydrogen atoms are bonded to the carbon atoms, resulting in a tetrahedral geometry around each carbon.
  3. Alkanes exhibit low reactivity due to the stability of the carbon-carbon and carbon-hydrogen bonds, making them relatively unreactive under normal conditions.
  4. Alkanes can undergo substitution reactions, such as radical halogenation, to form alkyl halides, which are important precursors for many organic reactions.
  5. The infrared (IR) spectra of alkanes are characterized by the absence of any absorption bands in the carbonyl (C=O) region, as well as the presence of characteristic C-H stretching and bending vibrations.

Review Questions

  • Explain the relationship between alkanes and alkyl groups, and how they are used in the naming of organic compounds.
    • Alkanes are the parent hydrocarbons, while alkyl groups are derived from alkanes by the removal of a single hydrogen atom. Alkyl groups are represented by the general formula $R$ and are used as substituents in the systematic naming of organic compounds. For example, the methyl group ($\ce{CH3-}$) is an alkyl group derived from the simplest alkane, methane ($\ce{CH4}$). Alkyl groups play a crucial role in the IUPAC nomenclature system, as they are used to identify the branching and substituents in more complex organic molecules.
  • Describe the process of radical halogenation and its significance in the preparation of alkyl halides from alkanes.
    • Radical halogenation is a substitution reaction in which a hydrogen atom in an alkane is replaced by a halogen atom, such as chlorine or bromine, through a free-radical mechanism. This reaction is initiated by the homolytic cleavage of the halogen molecule (e.g., $\ce{Cl2}$) to form reactive halogen radicals. These radicals then abstract a hydrogen atom from the alkane, creating an alkyl radical intermediate, which then combines with another halogen atom to form the alkyl halide product. Radical halogenation is an important method for the preparation of alkyl halides, which are versatile intermediates in many organic reactions.
  • Explain how the infrared (IR) spectra of alkanes can be used to identify and characterize these compounds, and discuss the specific features that distinguish the IR spectra of alkanes from other functional groups.
    • The infrared (IR) spectra of alkanes exhibit distinctive features that can be used to identify and characterize these compounds. Alkanes are characterized by the absence of any absorption bands in the carbonyl (C=O) region of the IR spectrum, as they do not contain any carbon-oxygen double bonds. Instead, the IR spectra of alkanes are dominated by the characteristic C-H stretching and bending vibrations. The C-H stretching vibrations typically occur in the range of 2850-3000 cm$^{-1}$, while the C-H bending vibrations are observed in the 1350-1480 cm$^{-1}$ region. These unique IR spectral features, along with the lack of other functional group absorptions, allow for the unambiguous identification of alkanes and their differentiation from other organic compounds with different functional groups.

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