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Solutions for Chapter 23.4SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 23.4SE

Solutions for Chapter 23.4SE
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter 23.4SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 23.4SE have been answered, more than 66232 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • alcohol

    A compound that possesses a hydroxyl group (OH).

  • axial position

    For chair conformations of substituted cyclohexanes, a position that is parallel to a vertical axis passing through the center of the ring.

  • Base peak

    The peak caused by the most abundant ion in a mass spectrum; the most intense peak. It is assigned an arbitrary intensity of 100

  • calorie

    A unit of energy; it is the amount of energy needed to raise the temperature of 1 g of water by 1 °C from 14.5 °C to 15.5 °C. A related unit is the joule: 1 cal = 4.184 J. (Section 5.1)

  • Carboxyl group (Section 1.3D)

    A !COOH group.

  • combination reaction.

    A reaction in which two or more substances combine to form a single product. (4.4)

  • coupling (of protons)

    A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms in which the multiplicity of each signal is affected by the other.

  • directed aldol addition

    A techniquefor performing a crossed aldol addition thatproduces one major product.

  • Downfield

    A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.

  • first law of thermodynamics

    A statement that energy is conserved in any process. One way to express the law is that the change in internal energy, ?E, of a system in any process is equal to the heat, q, added to the system, plus the work, w, done on the system by its surroundings: ?E = q + w. (Section 5.2)

  • formal charge

    A charge associated with any atom that does not exhibit the appropriate number of valence electrons.

  • free induction decay

    In NMR spectroscopy, a complex signal which is a combination of all of the electrical impulses generated by each type of proton.

  • Heterolytic bond cleavage

    Cleavage of a bond so that one fragment retains both electrons and the other retains none.

  • Organic synthesis

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

  • polar covalent bond

    A bond in which the difference in electronegative values of the two atoms is between 0.5 and 1.7.

  • reaction quotient (Q)

    The value that is obtained when concentrations of reactants and products are inserted into the equilibrium expression. If the concentrations are equilibrium concentrations, Q = K; otherwise, Q ? K. (Section 15.6)

  • Sandmeyer reactions

    Reactions that utilize copper salts (CuX) and enable the installation of a halogen or a cyano group on an aromatic ring.

  • Schiff base

    An alternative name for an imine

  • secondary cell

    A voltaic cell that can be recharged. (Section 20.7)

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

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