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Solutions for Chapter 11.3SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 11.3SE

Solutions for Chapter 11.3SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 11.3SE includes 2 full step-by-step solutions. Since 2 problems in chapter 11.3SE have been answered, more than 66110 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • addition polymerization

    Polymerization that occurs through coupling of monomers with one another, with no other products formed in the reaction. (Section 12.8)

  • amorphous solid.

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

  • amplitude.

    The vertical distance from the middle of a wave to the peak or trough. (7.1)

  • aromatic hydrocarbon.

    A hydrocarbon that contains one or more benzene rings. (24.1)

  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • cation

    A structure that bears a positive charge.

  • colligative properties.

    Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)

  • configuration

    The 3D spatial orientation of the groups connected to a chirality center (R or S ) or of the groups in a stereoisiomeric alkene (E or Z).

  • Conjugation

    A situation in which two multiple bonds are separated by a single bond. Alternatively, a series of overlapping 2p orbitals. 1,3-butadiene, for example, is a conjugated diene, and 3-butene-2-one is a conjugated enone

  • E1

    A unimolecular b-elimination reaction

  • enantiomers

    Two mirror-image molecules of a chiral substance. The enantiomers are nonsuperimposable. (Section 23.4)

  • Ground state

    The lowest energy state of a system.

  • Hammond postulate

    In an exothermic process the transition state is closer in energy to the reactants than to the products, and therefore the structure of the transition state more closely resembles the reactants. In contrast, the transition state in an endothermic process is closer in energy to the products, and therefore the transition state more closely resembles the products.

  • kinetic energy

    The energy that an object possesses by virtue of its motion. (Section 5.1)

  • mass spectrometer

    An instrument used to measure the precise masses and relative amounts of atomic and molecular ions. (Section 2.4)

  • periodic table

    The arrangement of elements in order of increasing atomic number, with elements having similar properties placed in vertical columns. (Section 2.5)

  • pH titration curve

    A graph of pH as a function of added titrant. (Section 17.3)

  • quartet

    In NMR spectroscopy, a signal that is comprised of four peaks.

  • spin-pairing energy

    The energy required to pair an electron with another electron occupying an orbital. (Section 23.6)

  • Valence electrons

    Electrons in the valence (outermost) shell of an atom.

Textbook Survival Guides

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