Solutions for Chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers

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 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers

Solutions for Chapter 2.15
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Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers have been answered, more than 12524 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkylation

    A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.

  • atomic orbital

    A three-dimensional plot of y2 of a wavefunction. It is a region of space that can accommodate electron density.

  • band structure

    The electronic structure of a solid, defining the allowed ranges of energy for electrons in a solid. (Section 12.7)

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • chemical equation.

    An equation that uses chemical symbols to show what happens during a chemical reaction. (3.7)

  • constitutional isomers

    Compounds that have the same molecular formula but differ in the way the atoms are connected.

  • Dextrorotatory

    Refers to a substance that rotates the plane of polarized light to the right

  • effusion

    The escape of a gas through an orifice or hole. (Section 10.8)

  • elastomer

    A material that can undergo a substantial change in shape via stretching, bending, or compression and return to its original shape upon release of the distorting force. (Section 12.6)

  • elimination-addition

    A reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • Exergonic reaction

    A reaction in which the Gibbs free energy of the products is lower than that of the reactants. The position of equilibrium for an exergonic reaction favors products.

  • l-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.

  • metallic character

    The extent to which an element exhibits the physical and chemical properties characteristic of metals, for example, luster, malleability, ductility, and good thermal and electrical conductivity. (Section 7.6)

  • molecular orbital (MO)

    An allowed state for an electron in a molecule. According to molecular-orbital theory, a molecular orbital is entirely analogous to an atomic orbital, which is an allowed state for an electron in an atom. Most bonding molecular orbitals can be classified as s or p, depending on the disposition of electron density with respect to the internuclear axis. (Section 9.7)

  • nitronium ion

    The NO2+ ion, which is present in a mixture of nitric acid and sulfuric acid.

  • Nonbonding electrons

    Valence electrons not involved in forming covalent bonds. Also called unshared pairs or lone pairs.

  • norbornane

    The common name for bicyclo[2.2.1]heptane.

  • observed rotation

    The extent to which plane-polarized light is rotated by a solution of a chiral compound.

  • Observed rotation

    the number of degrees through which a compound rotates the plane of polarized light

  • quartet

    In NMR spectroscopy, a signal that is comprised of four peaks.

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