Solutions for Chapter 17.12SE: 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 17.12SE

Solutions for Chapter 17.12SE
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Chapter 17.12SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 17.12SE have been answered, more than 146716 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxide

    The conjugate base of an alcohol.

  • chemical nomenclature

    The rules used in naming substances. (Section 2.8)

  • critical temperature (Tc).

    The temperature above which a gas will not liquefy. (11.8)

  • crystallization.

    The process in which dissolved solute comes out of solution and forms crystals. (12.1)

  • dispersion forces

    Intermolecular forces resulting from attractions between induced dipoles. Also called London dispersion forces. (Section 11.2)

  • disrotatory

    In electrocyclicreactions, a type of rotation in which the orbitalsbeing used to form the new s bond must rotate in opposite directions (one rotates clockwise while the other rotates counterclockwise).

  • Energy diagram

    A graph showing the changes in energy that occur during a chemical reaction; energy is plotted on the vertical axis, and reaction progress is plotted on the horizontal axis. Also called a reaction coordinate diagram

  • Equatorial bond

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

  • frequency

    For electromagnetic radiation, the number of wavelengths that pass a particular point in space per unit time.

  • frontier orbitals

    The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) that participate in a reaction.

  • hydrate

    A compound containing two hydroxyl groups (OH) connected to the same carbon atom.

  • Methylene

    A !CH2! group.

  • Nitrogen rule

    A rule stating that the molecular ion of a compound with an odd number of nitrogen atoms has an odd m/z ratio; if zero or an even number of nitrogen atoms, the molecular ion has an even m/z ratio

  • phenolate

    The conjugate base of phenol or a substituted phenol.

  • Polyester

    A polymer in which each monomer unit is joined to the next by an ester bond, as, for example, poly(ethylene terephthalate).

  • Polyurethane

    A polymer containing the !NHCO2! group as a repeating unit

  • primary structure

    For proteins, the sequence of amino acid residues.

  • Reactive intermediate

    A high-energy species formed between two successive reaction steps, that lies in an energy minimum between the two transition states

  • Schiemann reaction

    The conversion of an aryl diazonium salt into fluorobenzene upon treatment with fluoroboric acid (HBF4).

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

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