Solutions for Chapter 7.3: Using Chemical Formulas

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 7.3: Using Chemical Formulas

Chapter 7.3: Using Chemical Formulas includes 6 full step-by-step solutions. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1. Since 6 problems in chapter 7.3: Using Chemical Formulas have been answered, more than 24502 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Modern Chemistry: Student Edition 2012 was written by and is associated to the ISBN: 9780547586632.

Key Chemistry Terms and definitions covered in this textbook
  • accuracy

    A measure of how closely individual measurements agree with the correct value. (Section 1.5)

  • alkene

    A compound that possesses a carbon-carbon double bond.

  • benzyne

    A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.

  • Charles’ law.

    The volume of a fixed amount of gas maintained at constant pressure is directly proportional to the absolute temperature of the gas. (5.3)

  • chemical equation

    A representation of a chemical reaction using the chemical formulas of the reactants and products; a balanced chemical equation contains equal numbers of atoms of each element on both sides of the equation. (Section 3.1)

  • chromatogram

    In gas chromatography, a plot that identifies the retention time of each compound in the mixture.

  • Energy

    The ability to do work.

  • homogeneous equilibrium

    The equilibrium established between reactant and product substances that are all in the same phase. (Section 15.4)

  • hydrocarbons

    Compounds composed of only carbon and hydrogen. (Section 2.9)

  • lock-and-key model

    A model of enzyme action in which the substrate molecule is pictured as fitting rather specifically into the active site on the enzyme. It is assumed that in being bound to the active site, the substrate is somehow activated for reaction. (Section 14.7)

  • mass spectrometer

    An instrument used to measure the precise masses and relative amounts of atomic and molecular ions. (Section 2.4)

  • mass-to-charge ratio(m/z)

    Thedetermining factor by which ions are separatedfrom each other in mass spectrometry.

  • Meta (m)

    Refers to groups occupying 1,3-positions on a benzene ring.

  • molar mass

    The mass of one mole of a substance in grams; it is numerically equal to the formula weight in atomic mass units. (Section 3.4)

  • optically pure

    A solution containing just one enantiomer, but not its mirror image.

  • Organic synthesis

    A series of reactions by which a set of organic starting materials is converted to a more complicated structure.

  • Polypeptide

    A macromolecule containing many amino acid units, each joined to the next by a peptide bond

  • sigma complex

    The positively charged intermediate of an electrophilic aromatic substitution reaction.

  • smectic liquid crystalline phase

    A liquid crystal in which the molecules are aligned along their long axes and arranged in sheets, with the ends of the molecules aligned. There are several different kinds of smectic phases. (Section 12.8)

  • VSEPR theory

    Valence Shell Electron Pair Repulsion theory, which can be used to predict the geometry around an atom.

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