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Solutions for Chapter 13.8SE: 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 13.8SE

Solutions for Chapter 13.8SE
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter 13.8SE includes 2 full step-by-step solutions. Since 2 problems in chapter 13.8SE have been answered, more than 65383 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.

Key Chemistry Terms and definitions covered in this textbook
  • addition reaction.

    A reaction in which one molecule adds to another. (24.2)

  • addition to p bond

    One of the six kinds of arrow-pushing patterns used in drawing mechanisms for radical reactions. A radical adds to a p bond, destroying the p bond and generating a new radical.

  • alkanamine

    A format for naming primary amines containing a complex alkyl group.

  • amplitude.

    The vertical distance from the middle of a wave to the peak or trough. (7.1)

  • axis of symmetry

    An axis about which a compound possesses rotational symmetry.

  • 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

  • conversion factor

    A ratio relating the same quantity in two systems of units that is used to convert the units of measurement. (Section 1.6)

  • Crown ether

    A cyclic polyether derived from ethylene glycol and substituted ethylene glycols.

  • directed aldol addition

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

  • disulfide

    A compound with the structure R!S!S!R.

  • fingerprint region

    The region of an IR spectrum that contains signals resulting from the vibrational excitation of most single bonds (stretching and bending).

  • Haloarene (aryl halide)

    A compound containing a halogen atom bonded to a benzene ring. Given the symbol Ar!X

  • HOMO

    The highest occupied molecular orbital.

  • Meso compound

    An achiral compound possessing two or more chiral centers that also has chiral isomers

  • nucleotides

    The product formed when a nucleoside is coupled to a phosphate group

  • peptidases

    A variety of enzymes that selectively hydrolyze specific peptide bonds.

  • Pericyclic reaction

    A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons

  • spectrochemical series

    A list of ligands arranged in order of their abilities to split the d-orbital energies (using the terminology of the crystal-field model). (Section 23.6)

  • Tollens’ reagent

    A solution prepared by dissolving Ag2O in aqueous ammonia; used for selective oxidation of an aldehyde to a carboxylic acid.

  • Woodward-Fieser rules

    Rules for predicting the wavelength of maximum absorption for a compound with extended conjugation.

Textbook Survival Guides

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