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Solutions for Chapter 6.2: nomEnClaturE of EnantiomErs

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 6.2: nomEnClaturE of EnantiomErs

Solutions for Chapter 6.2
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Since 2 problems in chapter 6.2: nomEnClaturE of EnantiomErs have been answered, more than 17870 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 6.2: nomEnClaturE of EnantiomErs includes 2 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6.

Key Chemistry Terms and definitions covered in this textbook
  • absolute zero.

    Theoretically the lowest attainable temperature. (5.3)

  • Atropisomers

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

  • autocatalytic

    A reaction for which the reagent necessary to catalyze the reaction is produced by the reaction itself.

  • Avogadro’s law

    A statement that the volume of a gas maintained at constant temperature and pressure is directly proportional to the number of moles of the gas. (Section 10.3)

  • Bonding electrons

    Valence electrons involved in forming a covalent bond (i.e., shared electrons).

  • Conjugate acid

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

  • coordination-sphere isomers

    Structural isomers of coordination compounds in which the ligands within the coordination sphere differ. (Section 23.4)

  • crystallite

    A region of a polymer inwhich the chains are linearly extended and closein proximity to one another, resulting in van der Waals forces that hold the chains close together.

  • diamagnetic anisotropy

    An effect that causes different regions of space to be characterized by different magnetic field strengths.

  • dilution.

    A procedure for preparing a less concentrated solution from a more concentrated solution. (4.5)

  • Dispersion forces

    Very weak intermolecular forces of attraction resulting from the interaction between temporary induced dipoles

  • element

    A substance consisting of atoms of the same atomic number. Historically defined as a substance that cannot be separated into simpler substances by chemical means. (Sections 1.1 and 1.2)

  • Hydroboration-oxidation

    A method for converting an alkene to an alcohol. The alkene is treated with borane (BH3) to give a trialkylborane, which is then oxidized with alkaline hydrogen peroxide to give an alcohol

  • isoelectronic series

    A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)

  • law of definite proportions

    A law that states that the elemental composition of a pure substance is always the same, regardless of its source; also called the law of constant composition. (Section 1.2)

  • mole fraction

    The ratio of the number of moles of one component of a mixture to the total moles of all components; abbreviated X, with a subscript to identify the component. (Section 10.6)

  • oxonium ion

    An intermediate with a positively charged oxygen atom.

  • specific heat 1Cs2

    The heat capacity of 1 g of a substance; the heat required to raise the temperature of 1 g of a substance by 1 °C. (Section 5.5)

  • Transition state

    The highest energy point on a reaction coordinate diagram. The chemical structure at this point is commonly called an activated complex.

  • weak activators

    Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.

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