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Solutions for Chapter 7.11: SYNTHESIS USING ACETYLIDE IONS

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 7.11: SYNTHESIS USING ACETYLIDE IONS

Solutions for Chapter 7.11
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter 7.11: SYNTHESIS USING ACETYLIDE IONS includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Organic Chemistry was written by and is associated to the ISBN: 9780134042282. Since 1 problems in chapter 7.11: SYNTHESIS USING ACETYLIDE IONS have been answered, more than 75335 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkene

    A compound that possesses a carbon-carbon double bond.

  • alkynes.

    Hydrocarbons that contain one or more carbon-carbon triple bonds. They have the general formula CnH2n22, where n 5 2,3, . . . . (24.2)

  • beta (b) rays.

    Electrons. (2.2)

  • chain reaction

    A reaction (generally involving radicals) in which one chemical entity can ultimately cause a chemical transformation for thousands of molecules.

  • crown ether

    Cyclic polyethers whose molecular models resemble crowns.

  • double bond

    A covalent bond involving two electron pairs. (Section 8.3)

  • elastomers

    Polymers that return to their original shape after being stretched.

  • Equatorial bond

    A bond to a chair conformation of cyclohexane that extends from the ring roughly perpendicular to the imaginary axis through the center of the ring; a bond that lies roughly along the equator of a cyclohexane ring

  • melt transition temperature (Tm)

    The temperature at which the crystallineregions of a polymer become amorphous.

  • mercurinium ion

    The intermediateformed during oxymercuration.

  • Polarimeter

    An instrument for measuring the ability of a compound to rotate the plane of plane-polarized light.

  • regioselective

    A reaction that can produce two or more constitutional isomers but nevertheless produces one as the major product.

  • Resonance

    A theory that many molecules and ions are best described as a hybrid of several Lewis structures

  • spectator ions

    Ions that go through a reaction unchanged and that appear on both sides of the complete ionic equation. (Section 4.2)

  • sulfide

    A compound that is similar in structure to an ether, but the oxygen atom has been replaced with a sulfur atom. Also called a thioether.

  • thiolate

    The conjugate base of a thiol.

  • van der Waals forces

    A group of intermolecular attractive forces including dipole-dipole, dipole-induced dipole, and induced dipole-induced dipole (dispersion) forces

  • Watson-Crick model

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

  • weak deactivators

    Groups that weakly deactivate an aromatic ring toward electrophilic aromatic substitution, thereby decreasing the rate of the reaction.

  • Williamson ether synthesis

    A method for preparing an ether from an alkoxide ion and an alkyl halide (via an SN2 process).