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Solutions for Chapter 5.10: Regioselectivity in Alcohol Dehydration: The Zaitsev Rule

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 5.10: Regioselectivity in Alcohol Dehydration: The Zaitsev Rule

Solutions for Chapter 5.10
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Since 1 problems in chapter 5.10: Regioselectivity in Alcohol Dehydration: The Zaitsev Rule have been answered, more than 32454 students have viewed full step-by-step solutions from this chapter. Chapter 5.10: Regioselectivity in Alcohol Dehydration: The Zaitsev Rule includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Axial bond

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

  • cathode.

    The electrode at which reduction occurs. (18.2)

  • chemical formula.

    An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)

  • Conjugate acid

    The species formed when a base accepts a proton from an acid

  • electronic charge

    The negative charge carried by an electron; it has a magnitude of 1.602 * 10-19 C. (Section 2.3)

  • Enantiomers

    Stereoisomers that are nonsuperposable mirror images of each other; refers to a relationship between pairs of objects

  • exothermic

    Any process with a negative DH (the system gives energy to the surroundings).

  • Hofmann rule

    Any b-elimination that occurs preferentially to give the less substituted alkene as the major product.

  • hydrofluorocarbons (HFCs)

    Compounds that contain only carbon, fluorine, and hydrogen (no chlorine).

  • hydrophobic

    A nonpolar group that does not have favorable interactions with water.

  • line spectrum

    A spectrum that contains radiation at only certain specific wavelengths. (Section 6.3)

  • LUMO

    The lowest unoccupied molecular orbital.

  • migratory aptitude

    In a BaeyerVilliger oxidation, the migration rates of different groups, which determine the regiochemical outcome of the reaction.

  • natural gas

    A naturally occurring mixture of gaseous hydrocarbon compounds composed of hydrogen and carbon. (Section 5.8)

  • partially condensed structures

    A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.

  • photoionization

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

  • polarizability

    The ease with which the electron cloud of an atom or a molecule is distorted by an outside influence, thereby inducing a dipole moment. (Section 11.2)

  • Regioselective reaction

    An addition or substitution reaction in which one of two or more possible products is formed in preference to all others that might be formed.

  • S (Section 3.3

    From the Latin, sinister, left; used in the R,S convention to show that the order of priority of groups on a chiral center is counterclockwise

  • solvent

    The dissolving medium of a solution; it is normally the component of a solution present in the greater amount. (Section 4.1)

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