Solutions for Chapter 11.6: Polycyclic Aromatic Hydrocarbons

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 11.6: Polycyclic Aromatic Hydrocarbons

Solutions for Chapter 11.6
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Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 11.6: Polycyclic Aromatic Hydrocarbons includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 11.6: Polycyclic Aromatic Hydrocarbons have been answered, more than 10867 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • [4+2]-cycloaddition

    A pericyclic reaction, also called a Diels-Alder reaction, that takes place between two different p systems, one of which is associated with four atoms while the other is associated with two atoms.

  • Allylic carbon

    A carbon adjacent to a carbon-carbon double bond.

  • angle strain

    The increase in energy associated with a bond angle that has deviated from the preferred angle of 109.5°.

  • chemical equation

    A representation of a chemical reaction using the chemical formulas of the reactants and products; a balanced chemical equation contains equal numbers of atoms of each element on both sides of the equation. (Section 3.1)

  • conduction band

    A band of molecular orbitals lying higher in energy than the occupied valence band and distinctly separated from it. (Section 12.7)

  • conjugated

    A compound in which two p bonds are separated from each other by exactly one s bond.

  • cyanides.

    Compounds containing the CN2 ion. (22.3)

  • Endergonic reaction

    A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials

  • J value

    When signal splitting occurs in 1H NMR spectroscopy, the distance (in hertz) between the individual peaks of a signal.

  • lipid

    A nonpolar molecule derived from glycerol and fatty acids that is used by organisms for long-term energy storage. (Section 24.9)

  • mass spectrometer

    A device inwhich a compound is first vaporized and convertedinto ions, which are then separated anddetected.

  • nuclear model

    Model of the atom with a nucleus containing protons and neutrons and with electrons in the space outside the nucleus. (Section 2.2)

  • nucleophilic acyl substitution

    A reaction in which a nucleophile attacks a carboxylic acid derivative.

  • protium

    The most common isotope of hydrogen. (Section 22.2)

  • rad

    A measure of the energy absorbed from radiation by tissue or other biological material; 1 rad = transfer of 1 * 10-2 J of energy per kilogram of material. (Section 21.9)

  • rate equation

    An equation thatdescribes the relationship between the rate of a reactionand the concentration of reactants.

  • Sulfi de

    The sulfur analog of an ether; a molecule containing a sulfur atom bonded to two carbon atoms. Sulfi des are also called thioethers

  • Synstereoselective

    The addition of atoms or groups of atoms to the same face of a carbon-carbon double bond.

  • Unimolecular reaction

    A reaction in which only one species is involved in the rate-determining step

  • Wolff-Kishner reduction

    A method for converting a carbonyl group into a methylene group (CH2) under basic conditions.

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