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Solutions for Chapter Chapter 14: Ethers, Epoxides, and Thioethers

Organic Chemistry | 8th Edition | ISBN: 9780321811394 | Authors: L.g. Wade, Jr.

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780321811394

Organic Chemistry | 8th Edition | ISBN: 9780321811394 | Authors: L.g. Wade, Jr.

Solutions for Chapter Chapter 14: Ethers, Epoxides, and Thioethers

Solutions for Chapter Chapter 14
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Textbook: Organic Chemistry
Edition: 8
Author: L.g. Wade, Jr.
ISBN: 9780321811394

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Organic Chemistry was written by and is associated to the ISBN: 9780321811394. Chapter Chapter 14: Ethers, Epoxides, and Thioethers includes 51 full step-by-step solutions. Since 51 problems in chapter Chapter 14: Ethers, Epoxides, and Thioethers have been answered, more than 20813 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • aldol addition reaction

    A reaction that occurs when an aldehyde or ketone is attacked by an enolate ion. The product of an aldol addition reaction is always a b-hydroxy aldehyde or ketone.

  • Amino group

    A compound containing an sp3 -hybridized nitrogen atom bonded to one, two, or three carbon atoms

  • bond enthalpy

    The enthalpy change, ?H, required to break a particular bond when the substance is in the gas phase. (Section 8.8)

  • bridgeheads

    In a bicyclic system, the carbon atoms where the rings are fused together.

  • Br√łnsted-Lowry base

    A compound that can serve as a proton acceptor.

  • carboxylic acid

    A compound that contains the ¬COOH functional group. (Sections 16.10 and 24.4)

  • chemical property.

    Any property of a substance that cannot be studied without converting the substance into some other substance. (1.6)

  • conjugate acid

    In an acid-base reaction, the product that results when a base is protonated.

  • Diamagnetic current in NMR

    The circulation of electron density in a molecule in an applied magnetic fi eld.

  • diene

    A compound containing two carbon-carbon p bonds.

  • Eclipsed conformation

    A conformation about a carboncarbon single bond in which the atoms or groups on one carbon are as close as possible to the atoms or groups on an adjacent carbon.

  • formal charge

    A charge associated with any atom that does not exhibit the appropriate number of valence electrons.

  • functional group

    An atom or group of atoms that imparts characteristic chemical properties to an organic compound. (Section 24.1)

  • hyperconjugation

    An effect that explains why alkyl groups stabilize a carbocation.

  • irreversible process

    A process that cannot be reversed to restore both the system and its surroundings to their original states. Any spontaneous process is irreversible. (Section 19.1)

  • isomers

    Compounds whose molecules have the same overall composition but different structures. (Sections 2.9 and 23.4)

  • molecularity

    The number of molecules that participate as reactants in an elementary reaction. (Section 14.6)

  • Radical cation

    A species formed when a neutral molecule loses one electron; it contains both an odd number of electrons and a positive charge.

  • Solvolysis

    A nucleophilic substitution in which the solvent is also the nucleophile

  • ylide

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

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