Skip to main content
Library homepage
 
Chemistry LibreTexts

15.S: Benzene and Aromaticity (Summary)

  • Page ID
    214191
  • \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \) \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)\(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\) \(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\)\(\newcommand{\AA}{\unicode[.8,0]{x212B}}\)

    Concepts & Vocabulary

    15.0 Introduction

    • Aromatic compounds contain ring structures with a special type of resonance delocalization.
    • Aromatic compounds can be drawn with alternating single and double bonds, each atom in the ring must have a p-orbital available.

    15.1 Naming Aromatic Compounds

    • Disubstituted benzene derivatives are often named using ortho (1,2), meta (1,3) and para (1,4).
    • There are common benzene derivative names that are used by IUPAC such as toluene, phenol, benzoic acid and benzaldehyde.
    • A benzene group that is named as a substituent is called phenyl.
    • A benzene with a CH2 as a substituent group is called benzyl.

    15.2 Structure and Stability of Benzene

    • Benzene does not undergo the same reactions that alkenes do, due to its aromatic stability.
    • Aromatic molecules must have all ring atoms in the same plane to allow delocalization of the pi electrons.
    • Heats of hydrogenation can be used to show the special stability of benzene compared to what would be expected for a theoretical cyclohexatriene molecule.

    15.3 Aromaticity and the Hückel 4n + 2 Rule

    • The four criteria for aromaticity are that the molecule must:
      • be cyclic
      • be planar
      • be fully conjugated
      • have 4n+2 π Electrons
    • Ionic molecules and heterocyclic molecules can also be aromatic if they meet the four criteria.

    15.4 Aromatic Ions

    • Carbanions and carbocations that meet the rules for aromaticity are also aromatic.

    15.5 Aromatic Heterocycles: Pyridine and Pyrrole

    • Heterocycles that meet the rules for aromaticty are also aromatic.
    • If a lone pair of electrons on a ring atom can result in 4n+2 π Electrons, they will be in a p-orbital. If not, they will remain in hybrid orbitals.

    15.6 Polycyclic Aromatic Compounds

    • Benzene rings can be fused together to give larger aromatic compounds with mutliple rings called polycyclic aromatic compounds (or polycyclic aromatic hydrocarbons).

    15.7 Spectroscopy of Aromatic Compounds

    • Aromatic compounds can be identified by common infrared absorptions in the 3000-3100 cm-1 and 1500-1600 cm-1.
    • In 1H NMR, aromatic hydrogens appear in the 6.5-8 ppm region.

    Skills to Master

    • Skill 15.1 Using IUPAC rules to name substituted benzene molecules.
    • Skill 15.2 Use heats of hydrogenation to explain aromatic stabilization.
    • Skill 15.3 Draw molecular orbital diagram for benzene (all 6 MO's).
    • Skill 15.4 Use the criteria for aromaticity to determine if a molecule is aromatic or not.
    • Skill 15.5 Determine whether lone pairs of electrons for ions and heterocycles will be in p orbitals or hybrid orbitals.
    • Skill 15.6 Identify aromatic absorbances in infrared spectroscopy.
    • Skill 15.7 Identify aromatic resonances in 1H NMR spectroscopy.

    15.S: Benzene and Aromaticity (Summary) is shared under a not declared license and was authored, remixed, and/or curated by Layne Morsch.

    • Was this article helpful?