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Solutions for Chapter 5.10SE: 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 5.10SE

Solutions for Chapter 5.10SE
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Chapter 5.10SE includes 2 full step-by-step solutions. Since 2 problems in chapter 5.10SE have been answered, more than 65296 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • annulenes

    Compounds consisting of a single ring containing a fully conjugated p system. Benzene is [6]annulene.

  • antioxidants

    Radical scavengers that prevent autooxidation by preventing radical chain reactions from beginning.

  • Avogadro’s number (NA)

    The number of 12C atoms in exactly 12 g of 12C; it equals 6.022 * 1023 mol-1. (Section 3.4)

  • binary compounds.

    Compounds formed from just two elements. (2.7)

  • cathode

    An electrode at which reduction occurs. (Section 20.3)

  • covalent bond

    A bond that results when two atoms share a pair of electrons.

  • Disproportionation

    A termination process that involves the abstraction of a hydrogen atom from the beta position of the propagating radical of one chain by the radical endgroup of another chain.

  • doping

    Incorporation of a hetero atom into a solid to change its electrical properties. For example, incorporation of P into Si. (Section 12.7)

  • effusion

    The escape of a gas through an orifice or hole. (Section 10.8)

  • elastomers

    Polymers that return to their original shape after being stretched.

  • energy-level diagram

    A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived. Also called a molecular-orbital diagram. (Section 9.7)

  • Fischer projection

    A twodimensional representation of a molecule; in these projections, groups on the right and left are by convention in front, while those at the top and bottom are to the rear.

  • Inductive effect

    The polarization of the electron density of a covalent bond caused by the electronegativity of a nearby atom.

  • percent yield

    The ratio of the actual (experimental) yield of a product to its theoretical (calculated) yield, multiplied by 100. (Section 3.7)

  • photoelectric effect

    The emission of electrons from a metal surface induced by light. (Section 6.2)

  • Polyester

    A polymer in which each monomer unit is joined to the next by an ester bond, as, for example, poly(ethylene terephthalate).

  • Pro-S-hydrogen

    Replacing this hydrogen by deuterium gives a chiral center with an S confi guration

  • racemic mixture

    A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)

  • Radical cation

    A species formed when a neutral molecule loses one electron; it contains both an odd number of electrons and a positive charge.

  • sulfone

    A compound that contains a sulfur atom that has double bonds with two oxygen atoms and is flanked on both sides by R groups.

Textbook Survival Guides

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