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Solutions for Chapter 20: Dienes, Conjugated Systems, and Pericyclic Reactions

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 20: Dienes, Conjugated Systems, and Pericyclic Reactions

Solutions for Chapter 20
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

Organic Chemistry was written by and is associated to the ISBN: 9781133952848. Chapter 20: Dienes, Conjugated Systems, and Pericyclic Reactions includes 50 full step-by-step solutions. Since 50 problems in chapter 20: Dienes, Conjugated Systems, and Pericyclic Reactions have been answered, more than 9940 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • addition to p bond

    One of the six kinds of arrow-pushing patterns used in drawing mechanisms for radical reactions. A radical adds to a p bond, destroying the p bond and generating a new radical.

  • beta (b) rays.

    Electrons. (2.2)

  • blocking group

    A group that can be readily installed and uninstalled. Used for regiochemical control during synthesis.

  • body-centered lattice

    A crystal lattice in which the lattice points are located at the center and corners of each unit cell. (Section 12.2)

  • chemical equilibrium.

    A state in which the rates of the forward and reverse reactions are equal. (14.1)

  • deoxyribonucleic acids (DNA).

    A type of nucleic acid. (25.4)

  • displacement reaction

    A reaction in which an element reacts with a compound, displacing an element from it. (Section 4.4)

  • E,Z system

    A system to specify the confi guration of groups about a carbon-carbon double bond

  • electrostatic potential maps

    A three-dimensional, rainbowlike image used to visualize partial charges in a compound.

  • Endergonic reaction

    A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials

  • high-spin complex

    A complex whose electrons populate the d orbitals to give the maximum number of unpaired electrons. (Section 23.6)

  • hydroxyl group

    An OH group.

  • induction

    The withdrawal of electron density that occurs when a bond is shared by two atoms of differing electronegativity.

  • Monomer

    From the Greek, mono 1 meros, meaning single part. The simplest nonredundant unit from which a polymer is synthesized.

  • retrosynthetic analysis

    A systematic set of principles that enable the design of a synthetic route by working backward from the desired product.

  • sp3 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and three 2p atomic orbitals.

  • Stereochemistry

    The study of three-dimensional arrangements of atoms in molecules

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • Substitution

    A reaction in which an atom or group of atoms in a compound is replaced by another atom or group of atoms.

  • ylide

    A compound with two oppositely charged atoms adjacent to each other.

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