Solutions for Chapter 5.14: Dehydrohalogenation of Alkyl Halides

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 5.14: Dehydrohalogenation of Alkyl Halides

Solutions for Chapter 5.14
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Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Since 2 problems in chapter 5.14: Dehydrohalogenation of Alkyl Halides have been answered, more than 10708 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 5.14: Dehydrohalogenation of Alkyl Halides includes 2 full step-by-step solutions.

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

    A reaction in which a reagent adds to the two carbon atoms of a carbon–carbon multiple bond. (Section 24.3)

  • alkynide ion

    The conjugate base of a terminal alkyne.

  • autooxidation

    The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.

  • Chain initiation

    A step in a chain reaction characterized by the formation of reactive intermediates (radicals, anions, or cations) from nonradical or noncharged molecules

  • chirality center

    A tetrahedral carbon atom bearing four different groups.

  • chlorohydrin

    A compound containing a Cl group and a hydroxyl group (OH) on adjacent carbon atoms.

  • combination reaction.

    A reaction in which two or more substances combine to form a single product. (4.4)

  • Conformation

    Any three-dimensional arrangement of atoms in a molecule that results from rotation about a single bond.

  • conjugated diene

    A compound inwhich two carbon-carbon p bonds are separated from each other by exactly one s bond.

  • glass

    An amorphous solid formed by fusion of SiO2, CaO, and Na2O. Other oxides may also be used to form glasses with differing characteristics. (Section 22.10)

  • Hofmann product

    The less substituted product (alkene) of an elimination reaction.

  • Merrifield synthesis

    A method for building a peptide from protected building blocks.

  • nematic liquid crystalline phase

    A liquid crystal in which the molecules are aligned in the same general direction, along their long axes, but in which the ends of the molecules are not aligned. (Section 11.7)

  • Newman projection

    A drawing style that is designed to show the conformation of a molecule.

  • Pericyclic reaction

    A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons

  • primary structure

    The sequence of amino acids along a protein chain. (Section 24.7)

  • radical

    A chemical entity with an unpaired electron.

  • resonance stabilization

    The stabilization associated with the delocalization of electrons via resonance.

  • waxes

    High-molecular-weight esters that are constructed from carboxylic acids and alcohols.

  • Williamson ether synthesis

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

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