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Solutions for Chapter 11.17: Cyclobutadiene and Cyclooctatetraene

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 11.17: Cyclobutadiene and Cyclooctatetraene

Solutions for Chapter 11.17
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 11.17: Cyclobutadiene and Cyclooctatetraene have been answered, more than 18424 students have viewed full step-by-step solutions from this chapter. Chapter 11.17: Cyclobutadiene and Cyclooctatetraene includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • Acetal

    A molecule containing two !OR or !OAr groups bonded to the same carbon

  • acidic oxide (acidic anhydride)

    An oxide that either reacts with a base to form a salt or with water to form an acid. (Section 22.5)

  • activity series

    A list of metals in order of decreasing ease of oxidation. (Section 4.4)

  • alkynes

    Compounds containing a carbon-carbon triple bond.

  • boat conformation

    A conformation of cyclohexane in which all bond angles are fairly close to 109.5° and many hydrogen atoms are eclipsing each other.

  • chromatogram

    In gas chromatography, a plot that identifies the retention time of each compound in the mixture.

  • directed aldol addition

    A techniquefor performing a crossed aldol addition thatproduces one major product.

  • Enantiomeric excess (ee)

    The difference between the percentage of two enantiomers in a mixture

  • ferrimagnetism

    A form of magnetism in which unpaired electron spins on different-type ions point in opposite directions but do not fully cancel out. (Section 23.1)

  • force

    A push or a pull. (Section 5.1)

  • initiation

    In radical reaction mechanisms, a step in which radicals are created.

  • Lewis base

    An electron-pair donor. (Section 16.11)

  • nonpolar covalent bond

    A covalent bond in which the electrons are shared equally. (Section 8.4) normal boiling point The boiling point at 1 atm pressure. (Section 11.5)

  • Oligosaccharide

    A carbohydrate containing four to ten monosaccharide units, each joined to the next by a glycosidic bond.

  • periplanar

    A conformation in which a hydrogen atom and a leaving group are approximately coplanar.

  • photoionization

    The removal of an electron from an atom or molecule by absorption of light. (Section 18.2)

  • Photons

    An alternative way to describe electromagnetic radiation as a stream of particles

  • reducing agent, or reductant

    The substance that is oxidized and thereby causes the reduction of some other substance in an oxidation–reduction reaction. (Section 20.1)

  • spectator ions

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

  • standard atomic weight

    The weighted averages for each element, which takes into account isotopic abundance.

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