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Solutions for Chapter 10: States of Matter

Modern Chemistry | 1st Edition | ISBN: 9780030735462 | Authors: Rinehart & Winston Holt

Full solutions for Modern Chemistry | 1st Edition

ISBN: 9780030735462

Modern Chemistry | 1st Edition | ISBN: 9780030735462 | Authors: Rinehart & Winston Holt

Solutions for Chapter 10: States of Matter

Solutions for Chapter 10
4 5 0 320 Reviews
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Textbook: Modern Chemistry
Edition: 1
Author: Rinehart & Winston Holt
ISBN: 9780030735462

This textbook survival guide was created for the textbook: Modern Chemistry, edition: 1. Since 44 problems in chapter 10: States of Matter have been answered, more than 16449 students have viewed full step-by-step solutions from this chapter. Modern Chemistry was written by and is associated to the ISBN: 9780030735462. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 10: States of Matter includes 44 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Axial bond

    A bond to a chair conformation of cyclohexane that extends from the ring parallel to the imaginary axis through the center of the ring; a bond that lies roughly perpendicular to the equator of the ring.

  • bond cleavage

    The breaking of a bond, either homolytically or heterolytically. bond dissociation energy (Sect. 6.1): The energy required to achieve homolytic bond cleavage (generating radicals).

  • Bond dipole moment

    A measure of the polarity of a covalent bond. The product of the charge on either atom of a polar bond times the distance between the atoms

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • Chain-transfer reaction

    The transfer of reactivity of an endgroup from one chain to another during a polymerization

  • chemical properties

    Properties that describe a substance’s composition and its reactivity; how the substance reacts or changes into other substances. (Section 1.3)

  • chemical property.

    Any property of a substance that cannot be studied without converting the substance into some other substance. (1.6)

  • Dextrorotatory

    Refers to a substance that rotates the plane of polarized light to the right

  • Downfield

    A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.

  • Enantioselective reaction

    A reaction that produces one enantiomer in preference to the other.

  • imine

    A compound containing a CRN bond.

  • Ka

    A measure of the strength of an acid: Ka = Keq 3H2O4 = 3H3O+ 4 3A- 4 3HA4

  • Living polymer

    A polymer chain that continues to grow without chain-termination steps until either all of the monomer is consumed or some external agent is added to terminate the chain. The polymer chains will continue to grow if more monomer is added.

  • miscible liquids

    Liquids that mix in all proportions. (Section 13.3)

  • 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)

  • nuclear binding energy

    The energy required to decompose an atomic nucleus into its component protons and neutrons. (Section 21.6)

  • protic solvent

    A solvent that contains at least one hydrogen atom connected directly to an electronegative atom.

  • singlet

    In NMR spectroscopy, a signal that is comprised of only one peak.

  • spectrochemical series

    A list of ligands arranged in order of their abilities to split the d-orbital energies (using the terminology of the crystal-field model). (Section 23.6)

  • Syndiotactic polymer

    A polymer with alternating R and S confi gurations at the chiral centers along its chain, as, for example, syndiotactic polypropylene

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