Solutions for Chapter 6.14: Free-Radical Polymerization of Alkenes

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 6.14: Free-Radical Polymerization of Alkenes

Solutions for Chapter 6.14
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Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 6.14: Free-Radical Polymerization of Alkenes includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 1 problems in chapter 6.14: Free-Radical Polymerization of Alkenes have been answered, more than 10702 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • 1,4-adduct

    The product obtained from 1,4-addition across a conjugated p system.

  • acidic anhydride (acidic oxide)

    An oxide that forms an acid when added to water; soluble nonmetal oxides are acidic anhydrides. (Section 22.5)

  • amorphous solid.

    A solid that lacks a regular three-dimensional arrangement of atoms or molecules. (11.7)

  • aromatic

    A compound containing a planar ring of continuously overlapping p orbitals with 4n+2p electrons.

  • carbide

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

  • carboxylic acids.

    Acids that contain the carboxyl group —COOH. (24.4)

  • cumulated diene

    A compound containing two adjacent p bonds.

  • Decarboxylation

    Loss of CO2 from a carboxyl group.

  • dipole–dipole force

    A force that becomes significant when polar molecules come in close contact with one another. The force is attractive when the positive end of one polar molecule approaches the negative end of another. (Section 11.2)

  • electronic structure

    The arrangement of electrons in an atom or molecule. (Chapter 6:Introduction)

  • heterogeneous equilibrium

    The equilibrium established between substances in two or more different phases, for example, between a gas and a solid or between a solid and a liquid. (Section 15.4)

  • irreversible process

    A process that cannot be reversed to restore both the system and its surroundings to their original states. Any spontaneous process is irreversible. (Section 19.1)

  • kinetics

    A term that refers to the rate of a reaction.

  • lock-and-key model

    A model of enzyme action in which the substrate molecule is pictured as fitting rather specifically into the active site on the enzyme. It is assumed that in being bound to the active site, the substrate is somehow activated for reaction. (Section 14.7)

  • Optical purity

    The specifi c rotation of a mixture of enantiomers divided by the specifi c rotation of the enantiomerically pure substance (expressed as a percent). Optical purity is numerically equal to enantiomeric excess, but experimentally determined.

  • Part per million (ppm)

    Units used on NMR spectra to record chemical shift relative to the TMS standard.

  • period

    The row of elements that lie in a horizontal row in the periodic table. (Section 2.5)

  • S (Section 3.3

    From the Latin, sinister, left; used in the R,S convention to show that the order of priority of groups on a chiral center is counterclockwise

  • sulfoxide

    A compound containing an SRO bond that is flanked on both sides by R groups.

  • Wolff-Kishner reduction

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

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