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Solutions for Chapter 14.2SE: 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 14.2SE

Solutions for Chapter 14.2SE
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter 14.2SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 14.2SE have been answered, more than 66507 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417.

Key Chemistry Terms and definitions covered in this textbook
  • aldaric acid

    A dicarboxylic acid that is produced when an aldose or ketose is treated with a strong oxidizing agent, such as HNO3.

  • amidomalonate synthesis

    A synthetic method that employs diethyl acetamidomalonate as the starting material and enables the preparation of racemic a-amino acids.

  • Anion

    An atom or group of atoms bearing a negative charge.

  • antibonding molecular orbital

    A molecular orbital in which electron density is concentrated outside the region between the two nuclei of bonded atoms. Such orbitals, designated as s* or p*, are less stable (of higher energy) than bonding molecular orbitals. (Section 9.7)

  • antioxidants

    Radical scavengers that prevent autooxidation by preventing radical chain reactions from beginning.

  • bimolecular

    For mechanisms, a step that involves two chemical entities.

  • cathode

    An electrode at which reduction occurs. (Section 20.3)

  • deactivate

    For a substitutedaromatic ring, the effect of an electronwithdrawingsubstituent that decreases therate of electrophilic aromatic substitution.

  • formal charge

    The number of valence electrons in an isolated atom minus the number of electrons assigned to the atom in the Lewis structure. (Section 8.5)

  • Functional group

    An atom or group of atoms within a molecule that shows a characteristic set of physical and chemical properties

  • Hertz (Hz)

    The unit in which frequency is measured: s 21 (read “per second”).

  • integration

    In 1H NMR spectroscopy, the area under a signal indicates the number of protons giving rise to the signal.

  • Node

    A point in space where the value of a wave function is zero

  • nuclear disintegration series

    A series of nuclear reactions that begins with an unstable nucleus and terminates with a stable one; also called a radioactive series. (Section 21.2)

  • optically active

    Possessing the ability to rotate the plane of polarized light. (Section 23.4)

  • Oxymercuration-reduction

    A method for converting an alkene to an alcohol. The alkene is treated with mercury(II) acetate followed by reduction with sodium borohydride.

  • quantitative analysis

    The determination of the amount of a given substance that is present in a sample. (Section 17.7)

  • rare earth element

    See lanthanide element. (Sections 6.8 and 6.9)

  • superimposable

    Two objects that are identical.

  • Transfer RNA (tRNA

    A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes

Textbook Survival Guides

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