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Solutions for Chapter 13.16: 13C NMR and Peak Intensities

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 13.16: 13C NMR and Peak Intensities

Solutions for Chapter 13.16
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This expansive textbook survival guide covers the following chapters and their solutions. Since 1 problems in chapter 13.16: 13C NMR and Peak Intensities have been answered, more than 27802 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 13.16: 13C NMR and Peak Intensities includes 1 full step-by-step solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • actual yield.

    The amount of product actually obtained in a reaction. (3.10)

  • bridgeheads

    In a bicyclic system, the carbon atoms where the rings are fused together.

  • bromonium ion

    A positively charged, bridged intermediate formed during the addition reaction that occurs when an alkene is treated with molecular bromine (Br2).

  • cephalins

    Phosphoglycerides that contain ethanolamine.

  • common ion effect.

    The shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved substances. (16.2)

  • degenerate

    A situation in which two or more orbitals have the same energy. (Section 6.7)

  • Enantiomers

    Stereoisomers that are nonsuperposable mirror images of each other; refers to a relationship between pairs of objects

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • hexagonal close packing

    A crystal structure where the atoms are packed together as closely as possible. The close-packed layers adopt a two-layer repeating pattern, which leads to a primitive hexagonal unit cell. (Section 12.3)

  • lanthanide contraction

    The gradual decrease in atomic and ionic radii with increasing atomic number among the lanthanide elements, atomic numbers 57 through 70. The decrease arises because of a gradual increase in effective nuclear charge through the lanthanide series. (Section 23.1)

  • lattice points

    Points in a crystal all of which have identical environments. (Section 12.2)

  • Lewis structure

    A representation of covalent bonding in a molecule that is drawn using Lewis symbols. Shared electron pairs are shown as lines, and unshared electron pairs are shown as pairs of dots. Only the valence-shell electrons are shown. (Section 8.3)

  • low-spin complex

    A metal complex in which the electrons are paired in lower-energy orbitals. (Section 23.6)

  • methine group

    A CH group.

  • oxyanion

    A polyatomic anion that contains one or more oxygen atoms. (Section 2.8)

  • quantum mechanics

    A mathematical description of an electron that incorporates its wavelike properties.

  • quartet

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

  • Staggered conformation

    A conformation about a carbon-carbon single bond in which the atoms or groups on one carbon are as far apart as possible from atoms or groups on an adjacent carbon.

  • Triol

    A compound containing three hydroxyl groups.

  • weak activators

    Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.

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