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Solutions for Chapter 13.1: Compounds in Aqueous Solutions

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition

ISBN: 9780547586632

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Solutions for Chapter 13.1: Compounds in Aqueous Solutions

Modern Chemistry: Student Edition 2012 was written by Patricia and is associated to the ISBN: 9780547586632. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 13.1: Compounds in Aqueous Solutions includes 5 full step-by-step solutions. Since 5 problems in chapter 13.1: Compounds in Aqueous Solutions have been answered, more than 14181 students have viewed full step-by-step solutions from this chapter.

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)

  • aldonic acid

    The product obtained when the aldehyde group of an aldose is oxidized.

  • boat conformation

    A conformation of cyclohexane in which all bond angles are fairly close to 109.5° and many hydrogen atoms are eclipsing each other.

  • broadband decoupling

    In 13C NMR spectroscopy, a technique in which all 13C!1H splitting is suppressed with the use of two rf transmitters.

  • chain reaction

    A reaction (generally involving radicals) in which one chemical entity can ultimately cause a chemical transformation for thousands of molecules.

  • Chromatography

    A separation method involving passing a vapor or solution mixture through a column packed with a material with different affi nities for different components of the mixture.

  • core electrons.

    All nonvalence electrons in an atom. (8.2)

  • desalination

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

  • Friedel-Crafts acylation

    An electrophilic aromatic substitution reaction that installs an acyl group on an aromatic ring.

  • Haloalkane (alkyl halide)

    A compound containing a halogen atom covalently bonded to an sp3 -hybridized carbon atom. Given the symbol R!X.

  • heat of vaporization

    The enthalpy change, ?H, for vaporization of a liquid. (Section 11.4)

  • hydroboration-oxidation

    A twostep process that achieves an anti-Markovnikov addition of a proton and a hydroxyl group (OH) across an alkene.

  • hydrogen deficiency index (HDI)

    A measure of the number of degrees of unsaturation in a compound.

  • net ionic equation

    A chemical equation for a solution reaction in which soluble strong electrolytes are written as ions and spectator ions are omitted. (Section 4.2)

  • Nonbonding electrons

    Valence electrons not involved in forming covalent bonds. Also called unshared pairs or lone pairs.

  • nucleotide

    Compounds formed from a molecule of phosphoric acid, a sugar molecule, and an organic nitrogen base. Nucleotides form linear polymers called DNA and RNA, which are involved in protein synthesis and cell reproduction. (Section 24.10)

  • Prochiral hydrogens

    Refers to two hydrogens bonded to a carbon atom. When a different atom replaces one or the other, the carbon becomes a chiral center. The hydrogens of the CH2 group of ethanol, for example, are prochiral. Replacing one of them by deuterium gives (R)-1-deuteroethanol; replacing the other gives (S)-1-deuteroethanol

  • Synstereoselective

    The addition of atoms or groups of atoms to the same face of a carbon-carbon double bond.

  • Tripeptide

    A molecule containing three amino acid units, each joined to the next by a peptide bond

  • zwitterion

    A net neutral compound that exhibits charge separation. Amino acids exist as zwitterions at physiological pH.

Textbook Survival Guides

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