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Solutions for Chapter 23: The Transition Elements and Their Coordination Compounds

Chemistry: The Molecular Nature of Matter and Change | 5th Edition | ISBN: 9780077216504 | Authors: Martin S. Silberberg

Full solutions for Chemistry: The Molecular Nature of Matter and Change | 5th Edition

ISBN: 9780077216504

Chemistry: The Molecular Nature of Matter and Change | 5th Edition | ISBN: 9780077216504 | Authors: Martin S. Silberberg

Solutions for Chapter 23: The Transition Elements and Their Coordination Compounds

Solutions for Chapter 23
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Textbook: Chemistry: The Molecular Nature of Matter and Change
Edition: 5
Author: Martin S. Silberberg
ISBN: 9780077216504

Since 144 problems in chapter 23: The Transition Elements and Their Coordination Compounds have been answered, more than 99151 students have viewed full step-by-step solutions from this chapter. Chapter 23: The Transition Elements and Their Coordination Compounds includes 144 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Molecular Nature of Matter and Change was written by and is associated to the ISBN: 9780077216504. This textbook survival guide was created for the textbook: Chemistry: The Molecular Nature of Matter and Change, edition: 5.

Key Chemistry Terms and definitions covered in this textbook
  • Baeyer-Villiger oxidation

    A reaction in which a ketone is treated with a peroxy acid and is converted into an ester via the insertion of an oxygen atom.

  • boranes

    Covalent hydrides of boron. (Section 22.11)

  • carbides.

    Ionic compounds containing the C2 22 or C42 ion. (22.3)

  • cation.

    An ion with a net positive charge. (2.5)

  • Chain-growth polymerization

    A polymerization that involves sequential addition reactions, either to unsaturated monomers or to monomers possessing other reactive functional groups.

  • Claisen condensation

    A nucleophilic acyl substitution reaction in which the nucleophile is an ester enolate and the electrophile is an ester.

  • condensation polymerization

    Polymerization in which molecules are joined together through condensation reactions. (Section 12.8)

  • Deshielding

    The term used to express the concept of less shielding in NMR

  • E1

    A unimolecular b-elimination reaction

  • electron affinity

    The energy change that occurs when an electron is added to a gaseous atom or ion. (Section 7.5)

  • electrospray ionization (ESI):

    In mass spectrometry, an ionization technique in which the compound is first dissolved in a solvent and then sprayed via a high-voltage needle into a vacuum chamber. The tiny droplets of solution become charged by the needle, and subsequent evaporation forms gas-phase molecular ions that typically carry one or more charges.

  • Hertz (Hz)

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

  • Infrared active

    Any molecular vibration that leads to a substantial change in dipole moment and is observed in an IR spectrum.

  • mass percentage

    The number of grams of solute in each 100 g of solution. (Section 13.4)

  • mass spectrum

    In mass spectrometry,a plot that shows the relative abundance ofeach cation that was detected.

  • Phasing

    The sign of the wave function at particular coordinates in space, either plus or minus. Phasing is often represented by colors, such as red or blue

  • SN1 reaction

    A unimolecular nucleophilic substitution reaction.

  • Stereoselective reaction

    A reaction in which one stereoisomer is formed in preference to all others. A stereoselective reaction may be enantioselective or diastereoselective, as the case may be.

  • sulfonation

    An electrophilic aromatic substitution reaction in which an SO3H group is installed on an aromatic ring.

  • thiolate

    The conjugate base of a thiol.

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