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Solutions for Chapter 23: Transition Metals and Coordination Chemistry

Chemistry: The Central Science | 14th Edition | ISBN: 9780134414232 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 14th Edition

ISBN: 9780134414232

Chemistry: The Central Science | 14th Edition | ISBN: 9780134414232 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 23: Transition Metals and Coordination Chemistry

Solutions for Chapter 23
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Textbook: Chemistry: The Central Science
Edition: 14
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus
ISBN: 9780134414232

Summary of Chapter 23: Transition Metals and Coordination Chemistry

We focus on the rich and important chemistry associated with such complex assemblies of metal ions surrounded by molecules and ions. Metal compounds of this kind are called coordination compounds, and the branch of chemistry that focuses on them is called coordination chemistry

Chemistry: The Central Science was written by and is associated to the ISBN: 9780134414232. This expansive textbook survival guide covers the following chapters and their solutions. Since 88 problems in chapter 23: Transition Metals and Coordination Chemistry have been answered, more than 29036 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 14. Chapter 23: Transition Metals and Coordination Chemistry includes 88 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkenes.

    Hydrocarbons that contain one or more carbon-carbon double bonds. They have the general formula CnH2n, where n 5 2,3, . . . . (24.2)

  • amino acid residue

    The individual repeating units in a polypeptide chain or protein.

  • band

    An array of closely spaced molecular orbitals occupying a discrete range of energy. (Section 12.4)

  • chemical bond

    A strong attractive force that exists between atoms in a molecule. (Section 8.1)

  • chlor-alkali process.

    The production of chlorine gas by the electrolysis of aqueous NaCl solution. (22.6)

  • dehydration

    An elimination reaction involving the loss of H and OH.

  • Electron affinity

    Energy added or released when an electron is added to an atom or molecule.

  • electronic structure

    The arrangement of electrons in an atom or molecule. (Chapter 6:Introduction)

  • Endothermic reaction

    A reaction in which the enthalpy of the products is higher than the enthalpy of the reactants; a reaction in which heat is absorbed

  • heterocycle

    A cyclic compound containing at least one heteroatom (such as S, N, or O) in the ring.

  • hydrate

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

  • hyperconjugation

    An effect that explains why alkyl groups stabilize a carbocation.

  • lipid bilayer

    The main fabricof cell membranes, assembled primarily fromphosphoglycerides.

  • Nucleoside

    A building block of nucleic acids, consisting of d-ribose or 2-deoxy-d-ribose bonded to a heterocyclic aromatic amine base by a b-N-glycosidic bond

  • organohalide

    An organic compound containing at least one halogen.

  • reduction

    A reaction in which a compound undergoes a decrease in oxidation state.

  • Reduction

    The gain of electrons. Alternatively, either the gain of hydrogen, loss of oxygen, or both

  • retrosynthetic analysis

    A systematic set of principles that enable the design of a synthetic route by working backward from the desired product.

  • second order

    A reaction that has a rate equation in which the sum of all exponents is two.

  • sulfone

    A compound that contains a sulfur atom that has double bonds with two oxygen atoms and is flanked on both sides by R groups.