Solutions for Chapter 16.6SE: 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 16.6SE

Solutions for Chapter 16.6SE
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Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 16.6SE 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 16.6SE have been answered, more than 144504 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
  • alcohol

    A compound that possesses a hydroxyl group (OH).

  • buffer capacity

    The amount of acid or base a buffer can neutralize before the pH begins to change appreciably. (Section 17.2)

  • colligative properties.

    Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)

  • complete ionic equation

    A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)

  • condensation reaction.

    A reaction in which two smaller molecules combine to form a larger molecule. Water is invariably one of the products of such a reaction. (24.4)

  • coordination compound.

    A neutral species containing one or more complex ions. (23.3)

  • Cycloalkane

    A saturated hydrocarbon that contains carbons joined to form a ring

  • Gilman reagent

    A lithium dialkyl cuprate (R2CuLi).

  • Keq

    A term that describes the position of equilibrium for a reaction: Keq = 3H3O+ 4 3A- 4 3HA4 3H2O4

  • methyl shift

    A type of carbocation rearrangement in which a methyl group migrates.

  • Nucleophilic aromatic substitution

    A reaction in which a nucleophile, most commonly a halogen, on an aromatic ring is replaced by another nucleophile.

  • partially condensed structures

    A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.

  • Polyunsaturated fatty acid

    A fatty acid with two or more carbon-carbon double bonds in its hydrocarbon chain

  • protecting group

    A group that is used during synthesis to protect a functional group from the reaction conditions.

  • radioactive decay chain

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

  • singlet

    In NMR spectroscopy, a signal that is comprised of only one peak.

  • solvent extraction

    A process by which one or more compounds are removed from a mixture of organic compounds, based on a difference in solubility and/or acid-base properties.

  • sulfonation

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

  • tertiary

    A term used to indicate that exactly three alkyl groups are attached directly to a particular position. For example, a tertiary carbocation has three alkyl groups attached directly to the electrophilic carbon atom (C+).

  • Thermoset plastic

    A polymer that can be molded when it is fi rst prepared, but once cooled, hardens irreversibly and cannot be remelted.

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