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Solutions for Chapter 8.6SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 8.6SE

Solutions for Chapter 8.6SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 8.6SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 8.6SE have been answered, more than 263903 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkylthio group

    An SR group.

  • Aprotic acid

    An acid that is not a proton donor; an acid that is an electron pair acceptor in a Lewis acid-base reaction.

  • azide synthesis

    A method for preparing primary amines that avoids the formation of secondary and tertiary amines.

  • carbonyl group

    The C “O double bond, a characteristic feature of several organic functional groups, such as ketones and aldehydes. (Section 24.4)

  • Carboxylic acid

    A compound containing a carboxyl, !COOH, group.

  • catalyst.

    A substance that increases the rate of a chemical reaction without itself being consumed. (13.6)

  • cyanides.

    Compounds containing the CN2 ion. (22.3)

  • Delocalization

    The spreading of electron density over a larger volume of space.

  • E1cb mechanism

    An eliminationreaction in which the leaving group only leavesafter deprotonation occurs. This process occurs atthe end of an aldol condensation.

  • 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)

  • Heat of combustion (DH0 )

    Standard heat of combustion is the heat released when one mole of a substance in its standard state (gas, liquid, solid) is oxidized completely to carbon dioxide and water.

  • homogeneous catalyst

    A catalyst that is in the same phase as the reactant substances. (Section 14.7)

  • Ligand

    A Lewis base bonded to a metal atom in a coordination compound. It may bond strongly or weakly.

  • mass-to-charge ratio(m/z)

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

  • pericylic reactions

    Reactions that occur via a concerted process and do not involve either ionic or radical intermediates.

  • period

    The row of elements that lie in a horizontal row in the periodic table. (Section 2.5)

  • radical initiator

    A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.

  • saturated hydrocarbon

    A hydrocarbon that contains no p bonds.

  • silica

    Common name for silicon dioxide. (Section 22.4)

  • sulfonation

    An electrophilic aromatic substitution reaction in which an SO3H group is installed on an aromatic ring.

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