Solutions for Chapter 21.5SE: 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 21.5SE

Solutions for Chapter 21.5SE
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter 21.5SE includes 2 full step-by-step solutions. Since 2 problems in chapter 21.5SE have been answered, more than 122414 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
  • 1,2-Shift

    A type of rearrangement in which an atom or group of atoms with its bonding electrons moves from one atom to an adjacent electron-defi cient atom.

  • a-Helix

    A type of secondary structure in which a section of polypeptide chain coils into a spiral, most commonly a right-handed spiral.

  • absorption spectrum

    A pattern of variation in the amount of light absorbed by a sample as a function of wavelength. (Section 23.5)

  • Acyl group

    An RCO! or ArCO! group.

  • amidomalonate synthesis

    A synthetic method that employs diethyl acetamidomalonate as the starting material and enables the preparation of racemic a-amino acids.

  • amine

    Compounds containing a nitrogen atom that is connected to one, two, or three alkyl or aryl groups.

  • b-Elimination

    A reaction in which a molecule, such as HCl, HBr, HI, or HOH, is split out or eliminated from adjacent carbons

  • carbocation

    An intermediate containing a positively charged carbon atom.

  • Contributing structures

    Representations of a molecule or ion that differ only in the distribution of valence electrons.

  • E,Z system

    A system to specify the confi guration of groups about a carbon-carbon double bond

  • fuel cell

    A voltaic cell that utilizes the oxidation of a conventional fuel, such as H2 or CH4, in the cell reaction. (Section 20.7)

  • hydrophilic

    A polar group that has favorable interactions with water.

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • mass-to-charge ratio(m/z)

    Thedetermining factor by which ions are separatedfrom each other in mass spectrometry.

  • Nucleophilicity

    A kinetic property measured by the rate at which a nucleophile causes nucleophilic substitution on a reference compound under a standardized set of experimental conditions.

  • retrosynthetic analysis

    A systematic set of principles that enable the design of a synthetic route by working backward from the desired product.

  • sp3 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and three 2p atomic orbitals.

  • spontaneous process

    A process that is capable of proceeding in a given direction, as written or described, without needing to be driven by an outside source of energy. A process may be spontaneous even though it is very slow. (Section 19.1)

  • torsional strain

    The difference in energy between staggered and eclipsed conformations (for example, in ethane).

  • Zaitsev’s rule

    A rule stating that the major product of a b-elimination reaction is the most stable alkene; that is, it is the alkene with the greatest number of substituents on the carboncarbon double bond

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