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Solutions for Chapter 25.2: Stereochemistry of Amino Acids

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 25.2: Stereochemistry of Amino Acids

Solutions for Chapter 25.2
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Chapter 25.2: Stereochemistry of Amino Acids includes 2 full step-by-step solutions. Since 2 problems in chapter 25.2: Stereochemistry of Amino Acids have been answered, more than 18649 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. 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.

Key Chemistry Terms and definitions covered in this textbook
  • activation energy (Ea).

    The minimum amount of energy required to initiate a chemical reaction. (13.4)

  • alkenes

    Hydrocarbons containing one or more carbon–carbon double bonds. (Section 24.2)

  • broadband decoupling

    In 13C NMR spectroscopy, a technique in which all 13C!1H splitting is suppressed with the use of two rf transmitters.

  • conduction band

    A band of molecular orbitals lying higher in energy than the occupied valence band and distinctly separated from it. (Section 12.7)

  • coordinate covalent bond.

    A bond in which the pair of electrons is supplied by one of the two bonded atoms; also called a dative bond. (9.9)

  • corrosion.

    The deterioration of metals by an electrochemical process. (18.7)

  • Delocalization

    The spreading of electron density over a larger volume of space.

  • Fishhook arrow

    A barbed curved arrow used to show the change in position of a single electron.

  • hybrid orbital

    An orbital that results from the mixing of different kinds of atomic orbitals on the same atom. For example, an sp3 hybrid results from the mixing, or hybridizing, of one s orbital and three p orbitals. (Section 9.5)

  • hydrofluorocarbons (HFCs)

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

  • hydronium ion 1H3O+2

    The predominant form of the proton in aqueous solution. (Section 16.2)

  • Hydrophobic effect

    The tendency of nonpolar groups to cluster so as to shield them from contact with an aqueous environment.

  • Hückel criteria for aromaticity

    To be aromatic, a monocyclic compound must have one 2p orbital on each atom of the ring, be planar or nearly so, and have (4n 1 2) p electrons in the cyclic arrangement of 2p orbitals

  • intermolecular forces

    The attractive forces between molecules.

  • isomers

    Compounds whose molecules have the same overall composition but different structures. (Sections 2.9 and 23.4)

  • lanthanide contraction

    The gradual decrease in atomic and ionic radii with increasing atomic number among the lanthanide elements, atomic numbers 57 through 70. The decrease arises because of a gradual increase in effective nuclear charge through the lanthanide series. (Section 23.1)

  • leveling effect

    An effect thatprevents the use of bases stronger than hydroxidewhen the solvent is water.

  • lithium dialkyl cuprate

    A nucleophilic compound with the general structureR2CuLi.

  • Orthogonal

    Having no net overlap.

  • Watson-Crick model

    A double-helix model for the secondary structure of a DNA molecule

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