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Textbooks / Chemistry / General Chemistry: Principles and Modern Applications 10

General Chemistry: Principles and Modern Applications 10th Edition - Solutions by Chapter

General Chemistry: Principles and Modern Applications | 10th Edition | ISBN: 9780132064521 | Authors: Ralph Petrucci

Full solutions for General Chemistry: Principles and Modern Applications | 10th Edition

ISBN: 9780132064521

General Chemistry: Principles and Modern Applications | 10th Edition | ISBN: 9780132064521 | Authors: Ralph Petrucci

General Chemistry: Principles and Modern Applications | 10th Edition - Solutions by Chapter

The full step-by-step solution to problem in General Chemistry: Principles and Modern Applications were answered by , our top Chemistry solution expert on 12/23/17, 04:52PM. General Chemistry: Principles and Modern Applications was written by and is associated to the ISBN: 9780132064521. This expansive textbook survival guide covers the following chapters: 28. This textbook survival guide was created for the textbook: General Chemistry: Principles and Modern Applications, edition: 10. Since problems from 28 chapters in General Chemistry: Principles and Modern Applications have been answered, more than 27506 students have viewed full step-by-step answer.

Key Chemistry Terms and definitions covered in this textbook
  • acyl peroxide

    A peroxide for which each oxygen atom is connected to an acyl group. Acyl peroxides are often used as radical initiators, because the O!O bond is especially weak.

  • Allylic substitution

    Any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon.

  • base-dissociation constant (Kb)

    An equilibrium constant that expresses the extent to which a base reacts with solvent water, accepting a proton and forming OH-1aq2. (Section 16.7)

  • Carbenoid

    A compound that delivers the elements of a carbene without actually producing a free carbene.

  • carboxylic acids.

    Acids that contain the carboxyl group —COOH. (24.4)

  • Cyanohydrin

    A molecule containing an !OH group and a !CN group bonded to the same carbon.

  • diborane

    B2H6. A dimeric structure formed when one borane molecule reacts with another.

  • endo

    In Diels-Alder reactions that produce bicyclic structures, the positions that are syn to the larger bridge.

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • hydration

    A reaction in which a proton and a hydroxyl group (OH) are added across a p bond.

  • keto-enol tautomerization

    The equilibrium that is established between an enol and a ketone in either acid-catalyzed or basecatalyzed conditions.

  • Orbital

    A region of space that can hold two electrons

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • rare earth element

    See lanthanide element. (Sections 6.8 and 6.9)

  • resonance

    A method that chemists use to deal with the inadequacy of bond-line drawings.

  • standard atomic weight

    The weighted averages for each element, which takes into account isotopic abundance.

  • Stereochemistry

    The study of three-dimensional arrangements of atoms in molecules

  • Steric strain

    The strain that arises when nonbonded atoms separated by four or more bonds are forced closer to each other than their atomic (contact) radii would allow. Steric strain is also called non-bonded interaction strain, or van der Waals strain.

  • symmetry allowed

    A reaction that obeys conservation of orbital symmetry.

  • Valence electrons

    Electrons in the valence (outermost) shell of an atom.

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