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Solutions for Chapter 7: Reactions In Aqueous Solution

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Full solutions for Chemistry: The Central Science | 12th Edition

ISBN: 9780321696724

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Solutions for Chapter 7: Reactions In Aqueous Solution

Solutions for Chapter 7
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Textbook: Chemistry: The Central Science
Edition: 12
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward
ISBN: 9780321696724

Summary of Chapter 7: Reactions In Aqueous Solution

Examine chemical reactions that take place in aqueous solutions. In addition, extend the concepts of stoichiometry by considering how solution concentrations are expressed and used.

Since 115 problems in chapter 7: Reactions In Aqueous Solution have been answered, more than 605316 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321696724. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 12. Chapter 7: Reactions In Aqueous Solution includes 115 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • addition reaction

    A reaction in which a reagent adds to the two carbon atoms of a carbon–carbon multiple bond. (Section 24.3)

  • alpha (a) helix

    For proteins, a feature of secondary structure that forms when a portion of the protein twists into a spiral.

  • Boyle’s law

    A law stating that at constant temperature, the product of the volume and pressure of a given amount of gas is a constant. (Section 10.3)

  • carboxylic acids.

    Acids that contain the carboxyl group —COOH. (24.4)

  • conduction band

    A band of molecular orbitals lying higher in energy than the occupied valence band and distinctly separated from it. (Section 12.7)

  • Dienophile

    A compound containing a double bond (consisting of one or two C, N, or O atoms) that can react with a conjugated diene to give a Diels-Alder adduct.

  • Hydration

    The addition of water.

  • hydronium ion 1H3O+2

    The predominant form of the proton in aqueous solution. (Section 16.2)

  • hydrophilic

    Water attracting. The term is often used to describe a type of colloid. (Section 13.6)

  • imine

    A compound containing a CRN bond.

  • Markovnikov addition

    In additionreactions, the observation that the hydrogen atomis generally placed at the vinylic position alreadybearing the larger number of hydrogen atoms.

  • metallic bond

    Bonding, usually in solid metals, in which the bonding electrons are relatively free to move throughout the three-dimensional structure. (Section 8.1)

  • phospholipids

    Esterlike derivatives of phosphoric acid.

  • photochemical reaction

    A reaction that is performed with photochemical excitation (usually UV light).

  • polar aprotic solvent

    A solvent that lacks hydrogen atoms connected directly to an electronegative atom.

  • radical

    A chemical entity with an unpaired electron.

  • salinity

    A measure of the salt content of seawater, brine, or brackish water. It is equal to the mass in grams of dissolved salts present in 1 kg of seawater. (Section 18.3)

  • Steric hindrance

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

  • vinylic

    The carbon atoms of a carbon-carbon double bond.

  • Wolff-Kishner reduction

    A method for converting a carbonyl group into a methylene group (CH2) under basic conditions.