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Solutions for Chapter 5.3: Names and Formulas of Ionic Compounds

Modern Chemistry: Student Edition 2006 | 1st Edition | ISBN: 9780030391071 | Authors: R. Thomas Myers, Keith B. Oldham, Salvatore Tocci

Full solutions for Modern Chemistry: Student Edition 2006 | 1st Edition

ISBN: 9780030391071

Modern Chemistry: Student Edition 2006 | 1st Edition | ISBN: 9780030391071 | Authors: R. Thomas Myers, Keith B. Oldham, Salvatore Tocci

Solutions for Chapter 5.3: Names and Formulas of Ionic Compounds

This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2006, edition: 1. Chapter 5.3: Names and Formulas of Ionic Compounds includes 8 full step-by-step solutions. Since 8 problems in chapter 5.3: Names and Formulas of Ionic Compounds have been answered, more than 23164 students have viewed full step-by-step solutions from this chapter. Modern Chemistry: Student Edition 2006 was written by and is associated to the ISBN: 9780030391071.

Key Chemistry Terms and definitions covered in this textbook
  • Absorbance (A)

    A quantitative measure of the extent to which a compound absorbs radiation of a particular wavelength. A 5 log (I0/I ) where I0 is the incident radiation and I is the transmitted radiation

  • alkenes

    Hydrocarbons containing one or more carbon–carbon double bonds. (Section 24.2)

  • asymmetric stretching

    In IR spectroscopy, when two bonds are stretching out of phase with each other.

  • azo coupling

    An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.

  • Beer’s law

    The light absorbed by a substance (A) equals the product of its extinction coefficient 1e2, the path length through which the light passes (b), and the molar concentration of the substance (c): A = ebc. (Section 14.2)

  • beta (b) pleated sheet

    For proteins, a feature of secondary structure that forms when two or more protein chains line up side-by-side.

  • Birch reduction

    A reaction in which benzene is reduced to give 1,4-cyclohexadiene.

  • chemical formula

    A notation that uses chemical symbols with numerical subscripts to convey the relative proportions of atoms of the different elements in a substance. (Section 2.6)

  • chlorohydrin

    A compound containing a Cl group and a hydroxyl group (OH) on adjacent carbon atoms.

  • doublet

    In NMR spectroscopy, a signal that is comprised of two peaks.

  • flagpole interactions

    For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.

  • Fourier transform NMR (FT-NMR)

    The modern NMR method that is based on a constant magnetic fi eld, a short pulse of electromagnetic radiation, and a mathematical Fourier transform to produce the spectrum

  • Lewis base

    Any molecule or ion that can form a new covalent bond by donating a pair of electrons.

  • main-group elements

    Elements in the s and p blocks of the periodic table. (Section 6.9)

  • molality

    The concentration of a solution expressed as moles of solute per kilogram of solvent; abbreviated m. (Section 13.4)

  • optically active

    A compound that rotates plane-polarized light.

  • oxirane

    A cyclic ether containing a three-membered ring system. Also called an epoxide.

  • radical inhibitor

    A compound that prevents a radical chain process from either getting started or continuing.

  • 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)

  • Thermodynamic control

    Experimental conditions that permit the establishment of equilibrium between two or more products of a reaction. The composition of the product mixture is determined by the relative stabilities of the products.

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