Solutions for Chapter 11.2SE: 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 11.2SE

Solutions for Chapter 11.2SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 11.2SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 11.2SE have been answered, more than 147986 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxymercuration-demercuration

    A two-step process that achieves Markovnikov addition of an alcohol (H and OR) across an alkene. The product of this process is an ether.

  • Avogadro‚Äôs number (NA).

    6.022 3 1023; the number of particles in a mole. (3.2)

  • biochemistry

    The study of the chemistry of living systems. (Chapter 24: Introduction)

  • deposition.

    The process in which the molecules go directly from the vapor into the solid phase. (11.8)

  • diastereotopic

    Nonequivalent protons for which the replacement test produces diastereomers.

  • diene

    A compound containing two carbon-carbon p bonds.

  • Dipeptide

    A molecule containing two amino acid units joined by a peptide bond

  • HOMO

    The highest occupied molecular orbital.

  • metalloids

    Elements that lie along the diagonal line separating the metals from the nonmetals in the periodic table; the properties of metalloids are intermediate between those of metals and nonmetals. (Section 2.5)

  • ortho-para director

    A group that directs the regiochemistry of an electrophilic aromatic substitution reaction such that the incoming electrophile is installed at the ortho or para positions.

  • oxyacid

    A compound in which one or more OH groups, and possibly additional oxygen atoms, are bonded to a central atom. (Section 16.10)

  • Polynuclear aromatic hydrocarbon (PAH)

    A hydrocarbon containing two or more fused benzene rings

  • R

    A term used to designate the configuration of a chirality center, determined in the following way: Each of the four groups is assigned a priority, and the molecule is then rotated (if necessary) so that the #4 group is directed behind the page (on a dash). A clockwise sequence for 1-2-3 is designated as R.

  • Reductive elimination

    Elimination of two substituents at a metal center, causing the oxidation state of the metal to decrease by two.

  • SI units

    The preferred metric units for use in science. (Section 1.4)

  • sigma (s) bond

    A bond that is characterized by circular symmetry with respect to the bond axis.

  • spectroscopy

    The study of the interaction between matter and electromagnetic radiation.

  • Staggered conformation

    A conformation about a carbon-carbon single bond in which the atoms or groups on one carbon are as far apart as possible from atoms or groups on an adjacent carbon.

  • thermodynamics

    The study of how energy is distributed under the influence of entropy. For chemists, the thermodynamics of a reaction specifically refers to the study of the relative energy levels of reactants and products.

  • tosylate

    An excellent leaving group (OTs). transition state (Sect. 6.6): A state through which a reaction passes. On an energy diagram, a transition state corresponds with a local maximum.

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