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Solutions for Chapter 23: Transition Metals Chemistry and Coordination Compounds

Chemistry | 12th Edition | ISBN: 9780078021510 | Authors: Raymond Chang; Kenneth Goldsby

Full solutions for Chemistry | 12th Edition

ISBN: 9780078021510

Chemistry | 12th Edition | ISBN: 9780078021510 | Authors: Raymond Chang; Kenneth Goldsby

Solutions for Chapter 23: Transition Metals Chemistry and Coordination Compounds

Solutions for Chapter 23
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Textbook: Chemistry
Edition: 12
Author: Raymond Chang; Kenneth Goldsby
ISBN: 9780078021510

Chapter 23: Transition Metals Chemistry and Coordination Compounds includes 76 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry, edition: 12. Since 76 problems in chapter 23: Transition Metals Chemistry and Coordination Compounds have been answered, more than 47683 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry was written by and is associated to the ISBN: 9780078021510.

Key Chemistry Terms and definitions covered in this textbook
  • Alkene metathesis

    A reaction in which two alkenes interchange the carbons attached to their double bonds.

  • alkylation

    A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.

  • Center of symmetry

    A point so situated that identical components of an object are located on opposite sides and equidistant from that point along any axis passing through it.

  • chain-growth polymer

    A polymer that is formed under conditions in which the monomers do not react directly with each other, but rather, each monomer is added to the growing chain, one at a time.

  • chromatogram

    In gas chromatography, a plot that identifies the retention time of each compound in the mixture.

  • desalination

    The removal of salts from seawater, brine, or brackish water to make it fit for human consumption. (Section 18.4)

  • downfield

    The left side of an NMR spectrum.

  • 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.

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • liquid

    Matter that has a distinct volume but no specific shape. (Section 1.2)

  • monosaccharide

    A simple sugar, most commonly containing six carbon atoms. The joining together of monosaccharide units by condensation reactions results in formation of polysaccharides. (Section 24.8)

  • Nucleophilicity

    A kinetic property measured by the rate at which a nucleophile causes nucleophilic substitution on a reference compound under a standardized set of experimental conditions.

  • polyether

    A compound containing several ether groups.

  • proton transfer

    One of the four arrow-pushing patterns for ionic reactions.

  • Raoult’s law

    A law stating that the partial pressure of a solvent over a solution, Psolution, is given by the vapor pressure of the pure solvent, P° solvent, times the mole fraction of a solvent in the solution, Xsolvent: Psolution = XsolventP° solvent. (Section 13.5)

  • replacement test

    A test for determining the relationship between two protons. The compound is drawn two times, each time replacing one of the protons with deuterium. If the two compounds are identical, the protons are homotopic. If the two compounds are enantiomers, the protons are enantiotopic. If the two compounds are diastereomers, the protons are diastereotopic.

  • representative (main-group) element

    An element from within the s and p blocks of the periodic table (Figure 6.29). (Section 6.9)

  • s-cis

    A conformation of a conjugated diene in which the disposition of the two p bonds with regard to the connecting single bond is cis-like (a dihedral angle of 0°).

  • Steric hindrance

    The ability of groups, because of their size, to hinder access to a reaction site within a molecule.

  • Valence-shell electron-pair repulsion (VSEPR)

    A method for predicting bond angles based on the idea that electron pairs repel each other and keep as far apart as possible.

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