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Solutions for Chapter 18.2: eLimination Reactions of vinyLic HaLides

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 18.2: eLimination Reactions of vinyLic HaLides

Solutions for Chapter 18.2
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Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Since 1 problems in chapter 18.2: eLimination Reactions of vinyLic HaLides have been answered, more than 36718 students have viewed full step-by-step solutions from this chapter. Chapter 18.2: eLimination Reactions of vinyLic HaLides includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6.

Key Chemistry Terms and definitions covered in this textbook
  • alpha particles

    Particles that are identical to helium-4 nuclei, consisting of two protons and two neutrons, symbol 4 2He or 4 2a. (Section 21.1)

  • amphoteric oxides and hydroxides

    Oxides and hydroxides that are only slightly soluble in water but that dissolve in either acidic or basic solutions. (Section 17.5)

  • atomic number (Z).

    The number of protons in the nucleus of an atom. (2.3)

  • Atropisomers

    Enantiomers that lack a chiral center and differ because of hindered rotation.

  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • Charles’s law

    A law stating that at constant pressure, the volume of a given quantity of gas is proportional to absolute temperature. (Section 10.3)

  • conjugate base

    A substance formed by the loss of a proton from a Brønsted–Lowry acid. (Section 16.2)

  • continuous-wave (CW) spectrometer

    An NMR spectrometer that holds the magnetic field constant and slowly sweeps through a range of rf frequencies, monitoring which frequencies are absorbed.

  • degree of unsaturation

    The absence of two hydrogen atoms associated with a ring or a p bond.

  • donor atom

    The atom of a ligand that bonds to the metal. (Section 23.2)

  • d–d transition

    The transition of an electron in a transition-metal compound from a lower-energy d orbital to a higher-energy d orbital. (Section 23.6)

  • eicosanoids

    A class of lipids which includes leukotrienes, prostaglandins, thromboxanes, and prostacyclins.

  • electron-sea model

    A model for the behavior of electrons in metals. (Section 12.4)

  • Halohydrin

    A compound containing a halogen atom and a hydroxyl group on adjacent carbons; those containing Br and OH are bromohydrins, and those containing Cl and OH are chlorohydrins.

  • heterogeneous catalyst

    A catalyst that does not dissolve in the reaction medium.

  • instantaneous rate

    The reaction rate at a particular time as opposed to the average rate over an interval of time. (Section 14.2)

  • Micelle

    A spherical arrangement of organic molecules in water solution clustered so that their hydrophobic parts are buried inside the sphere and their hydrophilic parts are on the surface of the sphere and in contact with water

  • Molar absorptivity (e)

    The absorbance of a 1 M solution of a compound.

  • Observed rotation

    the number of degrees through which a compound rotates the plane of polarized light

  • Solvolysis

    A nucleophilic substitution in which the solvent is also the nucleophile

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