Solutions for Chapter 16.6: Hydrogenation of benzene derivatives

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 16.6: Hydrogenation of benzene derivatives

Solutions for Chapter 16.6
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Chapter 16.6: Hydrogenation of benzene derivatives includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Since 1 problems in chapter 16.6: Hydrogenation of benzene derivatives have been answered, more than 15916 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

Key Chemistry Terms and definitions covered in this textbook
  • Allylic

    Next to a carbon-carbon double bond.

  • Aryl group (Ar -)

    A group derived from an arene by removal of an H.

  • bent

    A type of geometry resulting from an sp3-hybridized atom that has two lone pairs. For example, the oxygen atom in H2O.

  • Betaine

    A neutral molecule with nonadjacent positive and negative charges. An example of a betaine is the intermediate formed by addition of a Wittig reagent to an aldehyde or ketone

  • condensation polymerization

    Polymerization in which molecules are joined together through condensation reactions. (Section 12.8)

  • Crystalline domain

    An ordered crystalline region in the solid state of a polymer. Also called a crystallite.

  • Dispersion forces

    Very weak intermolecular forces of attraction resulting from the interaction between temporary induced dipoles

  • Formal charge

    The charge on an atom in a polyatomic ion or molecule

  • Levorotatory

    Refers to a substance that rotates the plane of polarized light to the left.

  • miscible

    Two liquids that can be mixed with each other in any proportion.

  • molecular solids

    Solids that are composed of molecules. (Sections 12.1 and 12.6)

  • N-bromosuccinimide

    A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.

  • Nitrile

    A compound containing a !C#N (cyano) group bonded to a carbon atom.

  • ortho

    On an aromatic ring, the C2 position.

  • partially condensed structures

    A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.

  • plane of symmetry

    A plane that bisects a compound into two halves that are mirror images of each other.

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

  • Sanger dideoxy method

    A method developed by Frederick Sanger for sequencing DNA molecules

  • Schiemann reaction

    The conversion of an aryl diazonium salt into fluorobenzene upon treatment with fluoroboric acid (HBF4).

  • solubility

    The amount of a substance that dissolves in a given quantity of solvent at a given temperature to form a saturated solution. (Sections 4.2 and 13.2)

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