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 4551 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 Patricia and is associated to the ISBN: 9781133952848.

Key Chemistry Terms and definitions covered in this textbook
  • acid

    A substance that is able to donate a H+ ion (a proton) and, hence, increases the concentration of H+1aq2 when it dissolves in water. (Section 4.3)

  • alkenes

    Hydrocarbons containing one or more carbon–carbon double bonds. (Section 24.2)

  • antibonding molecular orbital

    A molecular orbital in which electron density is concentrated outside the region between the two nuclei of bonded atoms. Such orbitals, designated as s* or p*, are less stable (of higher energy) than bonding molecular orbitals. (Section 9.7)

  • atactic

    A polymer in which the repeating units contain chirality centers which are not arranged in a pattern (they have random configurations).

  • Brønsted–Lowry acid

    A substance (molecule or ion) that acts as a proton donor. (Section 16.2)

  • chemical equilibrium.

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

  • chemical nomenclature

    The rules used in naming substances. (Section 2.8)

  • donor atom

    The atom of a ligand that bonds to the metal. (Section 23.2)

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • green chemistry

    Chemistry that promotes the design and application of chemical products and processes that are compatible with human health and that preserve the environment. (Section 18.5)

  • isotactic

    A polymer in which the repeating units contain chirality centers which all have the same configuration.

  • liquid

    Matter that has a distinct volume but no specific shape. (Section 1.2)

  • mass spectrum

    In mass spectrometry,a plot that shows the relative abundance ofeach cation that was detected.

  • metallic elements (metals)

    Elements that are usually solids at room temperature, exhibit high electrical and heat conductivity, and appear lustrous. Most of the elements in the periodic table are metals. (Sections 2.5 and 12.1)

  • Plane-polarized light

    Light oscillating in only parallel planes.

  • Polarizability

    A measure of the ease of distortion of the distribution of electron density about an atom or group in response to interaction with other molecules or ions. Fluorine which has a high electronegativity and holds its electrons tightly, has a very low polarizability. Iodine, which has a lower electronegativity and holds its electrons less tightly, has a very high polarizability.

  • Polyunsaturated triglyceride

    A triglyceride having several carbon-carbon double bonds in the hydrocarbon chains of its three fatty acids.

  • Rate determining step

    The step in a multistep reaction sequence that crosses the highest energy barrier.

  • sodium cyanoborohydride

    A selective reducing agent (NaBH3CN) that can be used for reductive amination.

  • Watson-Crick model

    A double-helix model for the secondary structure of a DNA molecule

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