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Solutions for Chapter 17.12SE: 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 17.12SE

Solutions for Chapter 17.12SE
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Chapter 17.12SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 17.12SE have been answered, more than 67761 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkanes

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

  • allylic carbocation

    A carbocation in which the positive charge is adjacent to a carbon-carbon double bond.

  • Birch reduction

    A reaction in which benzene is reduced to give 1,4-cyclohexadiene.

  • diatomic molecule.

    A molecule that consists of two atoms. (2.5)

  • Elastomer

    A material that, when stretched or otherwise distorted, returns to its original shape when the distorting force is released.

  • Functional group

    An atom or group of atoms within a molecule that shows a characteristic set of physical and chemical properties

  • homogeneous catalyst

    A catalyst that is in the same phase as the reactant substances. (Section 14.7)

  • Hydrophobic effect

    The tendency of nonpolar groups to cluster so as to shield them from contact with an aqueous environment.

  • hyperconjugation

    An effect that explains why alkyl groups stabilize a carbocation.

  • hypothesis

    A tentative explanation of a series of observations or of a natural law. (Section 1.3)

  • J value

    When signal splitting occurs in 1H NMR spectroscopy, the distance (in hertz) between the individual peaks of a signal.

  • Messenger RNA (mRNA)

    A ribonucleic acid that carries coded genetic information from DNA to the ribosomes for the synthesis of proteins

  • Newman projection

    A drawing style that is designed to show the conformation of a molecule.

  • nuclear transmutation

    A conversion of one kind of nucleus to another. (Section 21.3)

  • optically pure

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

  • Part per million (ppm)

    Units used on NMR spectra to record chemical shift relative to the TMS standard.

  • Quaternary structure

    The arrangement of polypeptide monomers into a noncovalently bonded aggregate.

  • radioactive

    Possessing radioactivity, the spontaneous disintegration of an unstable atomic nucleus with accompanying emission of radiation. (Section 2.2; Chapter 21: Introduction)

  • Reaction mechanism

    A step-by-step description of how a chemical reaction occurs.

  • staggered conformation

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

Textbook Survival Guides

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