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> > General, Organic, and Biological Chemistry: Structures of Life 4

General, Organic, and Biological Chemistry: Structures of Life 4th Edition - Solutions by Chapter

General, Organic, and Biological Chemistry: Structures of Life | 4th Edition | ISBN: 9780321750891 | Authors: Karen Timberlake

Full solutions for General, Organic, and Biological Chemistry: Structures of Life | 4th Edition

ISBN: 9780321750891

General, Organic, and Biological Chemistry: Structures of Life | 4th Edition | ISBN: 9780321750891 | Authors: Karen Timberlake

General, Organic, and Biological Chemistry: Structures of Life | 4th Edition - Solutions by Chapter

This expansive textbook survival guide covers the following chapters: 24. Since problems from 24 chapters in General, Organic, and Biological Chemistry: Structures of Life have been answered, more than 25867 students have viewed full step-by-step answer. This textbook survival guide was created for the textbook: General, Organic, and Biological Chemistry: Structures of Life, edition: 4. The full step-by-step solution to problem in General, Organic, and Biological Chemistry: Structures of Life were answered by Patricia, our top Chemistry solution expert on 05/06/17, 06:54PM. General, Organic, and Biological Chemistry: Structures of Life was written by Patricia and is associated to the ISBN: 9780321750891.

Key Chemistry Terms and definitions covered in this textbook
  • Alcohol

    A compound containing an !OH (hydroxyl) group bonded to a carbon atom

  • Alkylation reaction

    Any reaction in which a new carbon-carbon bond to an alkyl group is formed.

  • anti addition

    An addition reaction in which two groups are installed on opposite sides of a p bond.

  • asymmetric hydrogenation

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

  • atomic mass.

    The mass of an atom in atomic mass units. (3.1)

  • base

    A substance that is an H+ acceptor; a base produces an excess of OH-1aq2 ions when it dissolves in water. (Section 4.3)

  • chemical properties

    Properties that describe a substance’s composition and its reactivity; how the substance reacts or changes into other substances. (Section 1.3)

  • complex ion.

    An ion containing a central metal cation bonded to one or more molecules or ions. (16.10)

  • conformation

    A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.

  • enantiomer

    A nonsuperimposable mirror image.

  • exothermic process

    A process in which a system releases heat to its surroundings. (Section 5.2)

  • Friedel-Crafts acylation

    An electrophilic aromatic substitution reaction that installs an acyl group on an aromatic ring.

  • Le Châtelier’s principle

    A principle stating that when we disturb a system at chemical equilibrium, the relative concentrations of reactants and

  • Photolysis

    Cleavage by light.

  • polyprotic acid

    A substance capable of dissociating more than one proton in water; H2SO4 is an example. (Section 16.6)

  • Reductive elimination

    Elimination of two substituents at a metal center, causing the oxidation state of the metal to decrease by two.

  • secondary

    A term used to indicate that exactly two alkyl groups are attached directly to a particular position. For example, a secondary carbocation has two alkyl groups attached directly to the electrophilic carbon atom (C+).

  • solvent extraction

    A process by which one or more compounds are removed from a mixture of organic compounds, based on a difference in solubility and/or acid-base properties.

  • tetrahedral

    The geometry of an atom with four bonds separated from each other by 109.5°.

  • Upfield

    A signal of an NMR spectrum that is shifted toward the right (smaller chemical shift) on the chart paper.

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