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Solutions for Chapter 4: Reactions in Aqueous Solutions

Chemistry | 12th Edition | ISBN: 9780078021510 | Authors: Raymond Chang; Kenneth Goldsby

Full solutions for Chemistry | 12th Edition

ISBN: 9780078021510

Chemistry | 12th Edition | ISBN: 9780078021510 | Authors: Raymond Chang; Kenneth Goldsby

Solutions for Chapter 4: Reactions in Aqueous Solutions

Solutions for Chapter 4
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Textbook: Chemistry
Edition: 12
Author: Raymond Chang; Kenneth Goldsby
ISBN: 9780078021510

Chemistry was written by and is associated to the ISBN: 9780078021510. This textbook survival guide was created for the textbook: Chemistry, edition: 12. This expansive textbook survival guide covers the following chapters and their solutions. Since 174 problems in chapter 4: Reactions in Aqueous Solutions have been answered, more than 98479 students have viewed full step-by-step solutions from this chapter. Chapter 4: Reactions in Aqueous Solutions includes 174 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Aldonic acid

    The product formed when the !CHO group of an aldose is oxidized to a !COOH group

  • alkanes

    Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)

  • Arene

    A term used to classify benzene and its derivatives.

  • Boyle’s law.

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

  • cephalins

    Phosphoglycerides that contain ethanolamine.

  • chiral

    A term describing a molecule or an ion that cannot be superimposed on its mirror image. (Sections 23.4 and 24.5)

  • density

    The ratio of an object’s mass to its volume. (Section 1.4)

  • DEPT 13C NMR

    In 13C NMR spectroscopy, a technique that utilizes two rf radiation emitters and provides information regarding the number of protons attached to each carbon atom in a compound.

  • Disaccharide

    A carbohydrate containing two monosaccharide units joined by a glycosidic bond.

  • Frost circles

    A simple method for drawing the relative energy levels of the MOs for a ring assembled from continuously overlapping p orbitals.

  • homopolymer

    A polymer constructed from a single type of monomer.

  • isothermal process

    One that occurs at constant temperature. (Section 19.1)

  • leveling effect

    An effect thatprevents the use of bases stronger than hydroxidewhen the solvent is water.

  • pi 1P2 molecular orbital

    A molecular orbital that concentrates the electron density on opposite sides of an imaginary line that passes through the nuclei. (Section 9.8)

  • Polypeptide

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

  • reaction order

    The power to which the concentration of a reactant is raised in a rate law. (Section 14.3)

  • staggered conformation

    A conformation in which nearby groups in a Newman projection have a dihedral angle of 60°.

  • Tertiary structure of nucleic acids

    The threedimensional arrangement of all atoms of a nucleic acid, commonly referred to as supercoiling

  • torsional angle

    The angle between two groups in a Newman projection, also called the dihedral angle.

  • torsional strain

    The difference in energy between staggered and eclipsed conformations (for example, in ethane).