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Solutions for Chapter 5.16: Anti Elimination in E2 Reactions: Stereoelectronic Effects

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 5.16: Anti Elimination in E2 Reactions: Stereoelectronic Effects

Solutions for Chapter 5.16
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Since 1 problems in chapter 5.16: Anti Elimination in E2 Reactions: Stereoelectronic Effects have been answered, more than 27766 students have viewed full step-by-step solutions from this chapter. Chapter 5.16: Anti Elimination in E2 Reactions: Stereoelectronic Effects 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. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • alpha (a) anomer

    The cyclic hemiacetal of an aldose in which the hydroxyl group at the anomeric position is trans to the CH2OH

  • Androgen

    A steroid hormone, such as testosterone, that mediates the development of sexual characteristics of males.

  • axial position

    For chair conformations of substituted cyclohexanes, a position that is parallel to a vertical axis passing through the center of the ring.

  • Carboxylic ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • Chiral center

    A tetrahedral atom, most commonly carbon, that is bonded to four different groups; also called a chirality center

  • conjugated

    A compound in which two p bonds are separated from each other by exactly one s bond.

  • diffusion

    The spreading of one substance through a space occupied by one or more other substances. (Section 10.8)

  • doublet

    In NMR spectroscopy, a signal that is comprised of two peaks.

  • equivalence point

    The point in a titration at which the added solute reacts completely with the solute present in the solution. (Section 4.6)

  • exchange (metathesis) reaction

    A reaction between compounds that when written as a molecular equation appears to involve the exchange of ions between the two reactants. (Section 4.2)

  • frontier orbital theory

    The analysis of a reaction using MO theory, where only the frontier orbitals (HOMO and LUMO) are considered.

  • hydrogen deficiency index (HDI)

    A measure of the number of degrees of unsaturation in a compound.

  • hydrophobic

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

  • isoelectric point (pI)

    For an amino acid, the specific pH at which the concentration of the zwitterionic form reaches its maximum value.

  • molecular orbital (MO)

    An allowed state for an electron in a molecule. According to molecular-orbital theory, a molecular orbital is entirely analogous to an atomic orbital, which is an allowed state for an electron in an atom. Most bonding molecular orbitals can be classified as s or p, depending on the disposition of electron density with respect to the internuclear axis. (Section 9.7)

  • Oil

    When used in the context of fats and oils, a mixture of triglycerides that is liquid at room temperature

  • polarizability

    The ability of an atom or molecule to distribute its electron density unevenly in response to external influences.

  • radioactive decay chain

    A series of nuclear reactions that begins with an unstable nucleus and terminates with a stable one. Also called nuclear disintegration series. (Section 21.2)

  • 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.

  • second-order reaction

    A reaction in which the overall reaction order (the sum of the concentration- term exponents) in the rate law is 2. (Section 14.4)

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