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Solutions for Chapter 5.1: Alkene Nomenclature

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 5.1: Alkene Nomenclature

Solutions for Chapter 5.1
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Since 2 problems in chapter 5.1: Alkene Nomenclature have been answered, more than 33809 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 5.1: Alkene Nomenclature includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkynes.

    Hydrocarbons that contain one or more carbon-carbon triple bonds. They have the general formula CnH2n22, where n 5 2,3, . . . . (24.2)

  • alpha (a) helix

    For proteins, a feature of secondary structure that forms when a portion of the protein twists into a spiral.

  • atomic number

    The number of protons in the nucleus of an atom of an element. (Section 2.3)

  • biochemistry

    The study of the chemistry of living systems. (Chapter 24: Introduction)

  • bonding atomic radius

    The radius of an atom as defined by the distances separating it from other atoms to which it is chemically bonded. (Section 7.3)

  • carbide

    A binary compound of carbon with a metal or metalloid. (Section 22.9)

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • crystalline solid.

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

  • dipole-dipole interactions

    Theresulting net attraction between two dipoles.

  • enthalpy

    A quantity defined by the relationship H = E + PV; the enthalpy change, ?H, for a reaction that occurs at constant pressure is the heat evolved or absorbed in the reaction: ?H = qp. (Section 5.3)

  • Enthalpy change, DH

    The difference in total bond strengths and solvation between various points under comparison on a reaction coordinate diagram

  • hydroboration-oxidation

    A twostep process that achieves an anti-Markovnikov addition of a proton and a hydroxyl group (OH) across an alkene.

  • Hydrogen bonding

    The attractive interaction between a hydrogen atom bonded to an atom of high electronegativity (most commonly O or N) and a lone pair of electrons on another atom of high electronegativity (again, most commonly O or N).

  • immiscible liquids

    Liquids that do not dissolve in one another to a significant extent. (Section 13.3)

  • l amino acid

    Amino acids with Fischer projections that resemble the Fischer projections of l sugars.

  • percent ionization

    The percent of a substance that undergoes ionization on dissolution in water. The term applies to solutions of weak acids and bases. (Section 16.6)

  • phenyl group

    A C6H5 group.

  • R (Section 3.3)

    From the Latin, rectus, straight, correct; used in the R,S convention to show that the order of priority of groups on a chiral center is clockwise.

  • Steric hindrance

    The ability of groups, because of their size, to hinder access to a reaction site within a molecule.

  • Thermoset plastic

    A polymer that can be molded when it is fi rst prepared, but once cooled, hardens irreversibly and cannot be remelted.

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