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Solutions for Chapter A: Chemistry: The Central Science 12th Edition

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Full solutions for Chemistry: The Central Science | 12th Edition

ISBN: 9780321696724

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Solutions for Chapter A

Solutions for Chapter A
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This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 12. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321696724. Since 2 problems in chapter A have been answered, more than 201629 students have viewed full step-by-step solutions from this chapter. Chapter A includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkanamine

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

  • alkenes

    Hydrocarbons containing one or more carbon–carbon double bonds. (Section 24.2)

  • amphoteric oxides and hydroxides

    Oxides and hydroxides that are only slightly soluble in water but that dissolve in either acidic or basic solutions. (Section 17.5)

  • asymmetric hydrogenation

    The addition of H2 across only one face of a p bond.

  • Beer’s law

    In UV-Vis spectroscopy, an equation describing the relationship between molar absorptivity (e), absorbance (A), concentration (C), and path length (l): e = A (C Ž l)

  • Carboxyl group (Section 1.3D)

    A !COOH group.

  • 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.

  • Fluid-mosaic model

    A biological membrane that consists of a phospholipid bilayer with proteins, carbohydrates, and other lipids on the surface and embedded in the bilayer

  • hydration

    Solvation when the solvent is water. (Section 13.1)

  • Hydrogenolysis

    Cleavage of a single bond by H2, most commonly accomplished by treating a compound with H2 in the presence of a transition metal catalyst.

  • optically active

    A compound that rotates plane-polarized light.

  • polyvinyl chloride, (PVC)

    A polymer formed from the polymerization of vinyl chloride (H2CRCHCl).

  • product

    A substance produced in a chemical reaction; it appears to the right of the arrow in a chemical equation. (Section 3.1)

  • reaction mechanism

    A series of intermediates and curved arrows that show howthe reaction occurs in terms of the motion of electrons.

  • secondary cell

    A voltaic cell that can be recharged. (Section 20.7)

  • silicates

    Compounds containing silicon and oxygen, structurally based on SiO4 tetrahedra. (Section 22.10)

  • Thermoset plastic

    A polymer that can be molded when it is fi rst prepared, but once cooled, hardens irreversibly and cannot be remelted.

  • third order

    A reaction that has a rate equation in which the sum of all exponents is three

  • VSEPR theory

    Valence Shell Electron Pair Repulsion theory, which can be used to predict the geometry around an atom.

  • Woodward-Fieser rules

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

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