Solutions for Chapter 7.6: The CahnIngoldPrelog RS Notational System

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 7.6: The CahnIngoldPrelog RS Notational System

Solutions for Chapter 7.6
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Since 2 problems in chapter 7.6: The CahnIngoldPrelog RS Notational System have been answered, more than 10972 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 7.6: The CahnIngoldPrelog RS Notational System includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • 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)

  • Boat conformation

    A nonplanar conformation of a cyclohexane ring in which carbons 1 and 4 of the ring are bent toward each other

  • Brønsted base.

    A substance capable of accepting a proton. (4.3)

  • Codon

    A triplet of nucleotides on mRNA that directs incorporation of a specifi c amino acid into a polypeptide sequence.

  • column chromatography

    A technique by which compounds are separated from each other based on a difference in the way they interact with the medium (the adsorbent) through which they are passed.

  • crystalline solid.

    A solid that possesses rigid and long-range order; its atoms, molecules, or ions occupy specific positions. (11.4)

  • cumulated diene

    A compound containing two adjacent p bonds.

  • dextrorotatory

    A compound that rotates plane-polarized light in a clockwise direction (+).

  • E1cb mechanism

    An eliminationreaction in which the leaving group only leavesafter deprotonation occurs. This process occurs atthe end of an aldol condensation.

  • Edman degradatio

    A method for selectively cleaving and identifying the N-terminal amino acid of a polypeptide chain.

  • flagpole interactions

    For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.

  • Freons

    CFCs that were heavily used for a wide variety of commercial applications, including as refrigerants, as propellants, in the production of foam insulation, as fire-fighting materials, and many other useful applications.

  • Heterocyclic aromatic amine

    An amine in which nitrogen is one of the atoms of an aromatic ring.

  • Homotopic groups

    Atoms or groups on an atom that give an achiral molecule when one of the groups is replaced by another group. The hydrogens of the CH2 group of propane, for example, are homotopic. Replacing either one of them with deuterium gives 2-deuteropropane, which is achiral. Homotopic groups have identical chemical shifts under all conditions

  • phase change

    The conversion of a substance from one state of matter to another. The phase changes we consider are melting and freezing 1solid ? liquid2, sublimation and deposition, and vaporization and condensation 1liquid ? gas2. (Section 11.4)

  • phase diagram

    A graphic representation of the equilibria among the solid, liquid, and gaseous phases of a substance as a function of temperature and pressure. (Section 11.6)

  • reaction order

    The power to which the concentration of a reactant is raised in a rate law. (Section 14.3)

  • rotational motion

    Movement of a molecule as though it is spinning like a top. (Section 19.3)

  • tertiary alkyl halide

    An organohalide in which the alpha (a) position is connected to three alkyl groups.

  • Wolff-Kishner reduction

    A method for converting a carbonyl group into a methylene group (CH2) under basic conditions.

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