Solutions for Chapter 24: Catalytic Carbon-Carbon Bond Formation

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781133952848

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Solutions for Chapter 24: Catalytic Carbon-Carbon Bond Formation

Solutions for Chapter 24
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781133952848. Chapter 24: Catalytic Carbon-Carbon Bond Formation includes 36 full step-by-step solutions. Since 36 problems in chapter 24: Catalytic Carbon-Carbon Bond Formation have been answered, more than 5366 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • (n 1 1) rule

    If a hydrogen has n hydrogens nonequivalent to it but equivalent among themselves on the same or adjacent atom(s), its 1 H!NMR signal is split into (n 1 1) peaks

  • 1,2-Shift

    A type of rearrangement in which an atom or group of atoms with its bonding electrons moves from one atom to an adjacent electron-defi cient atom.

  • alkenes.

    Hydrocarbons that contain one or more carbon-carbon double bonds. They have the general formula CnH2n, where n 5 2,3, . . . . (24.2)

  • antiferromagnetism

    A form of magnetism in which unpaired electron spins on adjacent sites point in opposite directions and cancel each other’s effects. (Section 23.1)

  • Bond dipole moment

    A measure of the polarity of a covalent bond. The product of the charge on either atom of a polar bond times the distance between the atoms

  • chemical kinetics

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (Chapter 14: Introduction)

  • complex lipid

    A lipid that readily undergoes hydrolysis in aqueous acid or base to produce smaller fragments.

  • condensation polymerization

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

  • crossed-linked polymer

    A polymer in which neighboring chains are linked together, for example, by disulfide bonds.

  • Delocalization

    The spreading of electron density over a larger volume of space.

  • diatomic molecule.

    A molecule that consists of two atoms. (2.5)

  • elimination

    A reaction involving the loss of a leaving group and formation of a p bond.

  • enantiomerically pure

    A substance that consists of a single enantiomer, and not its mirror image.

  • hydration

    Solvation when the solvent is water. (Section 13.1)

  • ionic bond

    A bond that results from the force of attraction between two oppositely charged ions.

  • lithium dialkyl cuprate

    A nucleophilic compound with the general structureR2CuLi.

  • nonaromatic

    A compound that lacks a ring with a continuous system of overlapping p orbitals.

  • nucleophile

    A compound containing an electron-rich atom that is capable of donating a pair of electrons.

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • torsional strain

    The difference in energy between staggered and eclipsed conformations (for example, in ethane).

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