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Solutions for Chapter 6.17: Enantiomers Can Be Distinguished by Biological Molecules

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 6.17: Enantiomers Can Be Distinguished by Biological Molecules

Solutions for Chapter 6.17
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Since 1 problems in chapter 6.17: Enantiomers Can Be Distinguished by Biological Molecules have been answered, more than 35732 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. Chapter 6.17: Enantiomers Can Be Distinguished by Biological Molecules includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • calcination

    The heating of an ore to bring about its decomposition and the elimination of a volatile product. For example, a carbonate ore might be calcined to drive off CO2. (Section 23.2)

  • Correlation tables

    Tables of data on absorption patterns of functional groups.

  • Diazonium ion

    An ArN2 1 or RN2 1 ion

  • doublet

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

  • hydrochlorofluorocarbons, (HCFCs)

    Compounds that are similar in structure to CFCs but also possess at least one C!Hbond.

  • hydronium ion 1H3O+2

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

  • Infrared (IR) spectroscopy

    A spectroscopic technique in which a compound is irradiated with infrared radiation, absorption of which causes covalent bonds to change from a lower vibration state to a higher one. Infrared spectroscopy is particularly valuable for determining the kinds of functional groups present in a molecule.

  • lattice vectors

    The vectors a, b, and c that define a crystal lattice. The position of any lattice point in a crystal can be represented by summing integer multiples of the lattice vectors. (Section 12.2)

  • Le Châtelier’s principle

    A principle stating that when we disturb a system at chemical equilibrium, the relative concentrations of reactants and

  • Meso compound

    An achiral compound possessing two or more chiral centers that also has chiral isomers

  • Nernst equation

    An equation that relates the cell emf, E, to the standard emf, E°, and the reaction quotient, Q: E = E° - 1RT>nF2 ln Q. (Section 20.6)

  • nuclear transmutation

    A conversion of one kind of nucleus to another. (Section 21.3)

  • Octet rule

    Group 1A–7A elements react to achieve an outer shell of eight valence electrons.

  • Primary structure of proteins

    The sequence of amino acids in the polypeptide chain, read from the N-terminal amino acid to the C-terminal amino acid.

  • resonance stabilization

    The stabilization associated with the delocalization of electrons via resonance.

  • s-cis

    A conformation of a conjugated diene in which the disposition of the two p bonds with regard to the connecting single bond is cis-like (a dihedral angle of 0°).

  • salt

    An ionic compound formed by replacing one or more hydrogens of an acid by other cations. (Section 4.3)

  • solid

    Matter that has both a definite shape and a definite volume. (Section 1.2)

  • Twist-boat conformation

    A nonplanar conformation of a cyclohexane ring that is twisted from and slightly more stable than a boat conformation.

  • 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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