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Solutions for Chapter 14: Ethers, Epoxides, and Thioethers

Organic Chemistry | 9th Edition | ISBN: 9780321971371 | Authors: Leroy G. Wade, Jan W. Simek

Full solutions for Organic Chemistry | 9th Edition

ISBN: 9780321971371

Organic Chemistry | 9th Edition | ISBN: 9780321971371 | Authors: Leroy G. Wade, Jan W. Simek

Solutions for Chapter 14: Ethers, Epoxides, and Thioethers

Solutions for Chapter 14
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Textbook: Organic Chemistry
Edition: 9
Author: Leroy G. Wade, Jan W. Simek
ISBN: 9780321971371

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 9. Chapter 14: Ethers, Epoxides, and Thioethers includes 60 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321971371. Since 60 problems in chapter 14: Ethers, Epoxides, and Thioethers have been answered, more than 46937 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Absorbance (A)

    A quantitative measure of the extent to which a compound absorbs radiation of a particular wavelength. A 5 log (I0/I ) where I0 is the incident radiation and I is the transmitted radiation

  • Alkyne

    An unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds.

  • Bimolecular reaction

    A reaction in which two species are involved in the rate-determining step.

  • bond angles

    The angles made by the lines joining the nuclei of the atoms in a molecule. (Section 9.1)

  • Chain-growth polymerization

    A polymerization that involves sequential addition reactions, either to unsaturated monomers or to monomers possessing other reactive functional groups.

  • chemical equilibrium.

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

  • Conjugated

    A conjugated diene or carbonyl is one in which the double bonds are separated by one single bond

  • decarboxylation

    A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • fission

    The splitting of a large nucleus into two smaller ones. (Section 21.6)

  • ideal solution

    A solution that obeys Raoult’s law. (Section 13.5)

  • mass spectrum

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

  • Nernst equation

    An equation that relates the cell emf, E, to the standard emf, E°, and the reaction quotient, Q: E = E° - 1RT>nF2 ln Q. (Section 20.6)

  • Octet rule

    Group 1A–7A elements react to achieve an outer shell of eight valence electrons.

  • oxymercuration-demercuration

    A two-step process for the Markovnikov addition of water across an alkene. With this process, carbocation rearrangements do not occur.

  • saponification

    The base-catalyzed hydrolysis of an ester. This method is used to make soap.

  • Signal

    A recording in an NMR spectrum of a nuclear magnetic resonance

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • tetravalent

    An element, such as carbon, that forms four bonds.

  • unsaturated

    A compound containingone or more p bonds.

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