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Solutions for Chapter 14.1: Organometallic Nomenclature

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 14.1: Organometallic Nomenclature

Solutions for Chapter 14.1
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Chapter 14.1: Organometallic Nomenclature includes 1 full step-by-step solutions. Since 1 problems in chapter 14.1: Organometallic Nomenclature have been answered, more than 36167 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Activation energy

    The difference in Gibbs free energy between reactants and a transition state

  • Alditol

    The product formed when the C"O group of a monosaccharide is reduced to a CHOH group.

  • azo coupling

    An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.

  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • crystalline solid.

    A solid that possesses rigid and long-range order; its atoms, molecules, or ions occupy specific positions. (11.4)

  • cyanides.

    Compounds containing the CN2 ion. (22.3)

  • deposition.

    The process in which the molecules go directly from the vapor into the solid phase. (11.8)

  • eicosanoids

    A class of lipids which includes leukotrienes, prostaglandins, thromboxanes, and prostacyclins.

  • Fischer projection

    A twodimensional representation of a molecule; in these projections, groups on the right and left are by convention in front, while those at the top and bottom are to the rear.

  • formal charge

    The number of valence electrons in an isolated atom minus the number of electrons assigned to the atom in the Lewis structure. (Section 8.5)

  • free energy (Gibbs free energy, G)

    A thermodynamic state function that gives a criterion for spontaneous change in terms of enthalpy and entropy: G = H - TS. (Section 19.5)

  • hydrogen bonding

    A special type of dipole-dipole interaction that occurs between an electronegative atom and a hydrogen atom that is connected to another electronegative atom.

  • J value

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

  • molecular compound

    A compound that consists of molecules. (Section 2.6)

  • photodissociation

    The breaking of a molecule into two or more neutral fragments as a result of absorption of light. (Section 18.2)

  • Photosensitizer

    A compound that absorbs light and transfers the energy to another molecule.

  • polycarbonates

    Polymers that are similar in structure to polyesters but with repeating carbonate groups (!O!CO2!) instead of repeating ester groups (!CO2!). polycyclic aromatic hydrocarbons

  • Quaternary structure

    The arrangement of polypeptide monomers into a noncovalently bonded aggregate.

  • Reaction mechanism

    A step-by-step description of how a chemical reaction occurs.

  • Retrosynthesis

    A process of reasoning backwards from a target molecule to a suitable set of starting materials.

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