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Solutions for Chapter 9: Nucleophilic Substitution and b-Elimination

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 9: Nucleophilic Substitution and b-Elimination

Solutions for Chapter 9
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

Since 58 problems in chapter 9: Nucleophilic Substitution and b-Elimination have been answered, more than 56827 students have viewed full step-by-step solutions from this chapter. Chapter 9: Nucleophilic Substitution and b-Elimination includes 58 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781133952848.

Key Chemistry Terms and definitions covered in this textbook
  • alpha particles

    Particles that are identical to helium-4 nuclei, consisting of two protons and two neutrons, symbol 4 2He or 4 2a. (Section 21.1)

  • Androgen

    A steroid hormone, such as testosterone, that mediates the development of sexual characteristics of males.

  • Bonding electrons

    Valence electrons involved in forming a covalent bond (i.e., shared electrons).

  • conjugate addition

    An addition reaction in which a nucleophile and a proton are added across the two ends of a conjugated p system.

  • constitutional isomers

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

  • coordination number.

    In a crystal lattice it is defined as the number of atoms (or ions) surrounding an atom (or ion) (11.4). In coordination compounds it is defined as the number of donor atoms surrounding the central metal atom in a complex. (23.3)

  • cycloaddition reactions

    Reactions in which two p systems are joined together in a way that forms a ring. In the process, two p bonds are converted into two s bonds.

  • equatorial position

    For chair conformations of substituted cyclohexanes, a position that is approximately along the equator of the ring.

  • exchange (metathesis) reaction

    A reaction between compounds that when written as a molecular equation appears to involve the exchange of ions between the two reactants. (Section 4.2)

  • homogeneous catalysts

    A catalyst that dissolves in the reaction medium.

  • homogeneous equilibrium

    The equilibrium established between reactant and product substances that are all in the same phase. (Section 15.4)

  • lattice points

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

  • Prostaglandin

    A member of the family of compounds having the 20-carbon skeleton of prostanoic acid

  • pyrimidine

    A compound that is similar in structure to pyridine but contains one extra nitrogen atom at the 3 position.

  • Quantum mechanics

    The branch of science that studies the interaction of matter and radiation.

  • Retrosynthesis

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

  • saturated hydrocarbon

    A hydrocarbon that contains no p bonds.

  • termination

    In radical reactions, a step in which two radicals are joined to give a compound with no unshared electrons.

  • terpenes

    A diverse class of naturally occurring compounds that can be thought of as being assembled from isoprene units, each of which contains five carbon atoms.

  • Wittig reaction

    A reaction that converts an aldehyde or ketone into an alkene, with the introduction of one or more carbon atoms.