Solutions for Chapter 17.1SE: 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 17.1SE

Solutions for Chapter 17.1SE
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This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 17.1SE have been answered, more than 106432 students have viewed full step-by-step solutions from this chapter. Chapter 17.1SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417.

Key Chemistry Terms and definitions covered in this textbook
  • addition polymerization

    Polymerization that occurs through coupling of monomers with one another, with no other products formed in the reaction. (Section 12.8)

  • alkylthio group

    An SR group.

  • benzylic position

    A carbon atom that is immediately adjacent to a benzene ring.

  • Curved arrow

    A symbol used to show the redistribution of valence electrons in resonance contributing structures or reactions, symbolizing movement of two electrons

  • density

    The ratio of an object’s mass to its volume. (Section 1.4)

  • dispersion forces

    Intermolecular forces resulting from attractions between induced dipoles. Also called London dispersion forces. (Section 11.2)

  • Electrophoresis

    The process of separating compounds on the basis of their electric charge

  • Ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • excited state

    A higher energy state than the ground state. (Section 6.3)

  • Halohydrin

    A compound containing a halogen atom and a hydroxyl group on adjacent carbons; those containing Br and OH are bromohydrins, and those containing Cl and OH are chlorohydrins.

  • hydride shift

    A type of carbocation rearrangement that involves the migration of a hydride ion (H-).

  • ion-product constant

    For water, Kw is the product of the aquated hydrogen ion and hydroxide ion concentrations: 3H+43OH-4 = Kw = 1.0 * 10-14 at 25 °C. (Section 16.3)

  • linkage isomers

    Structural isomers of coordination compounds in which a ligand differs in its mode of attachment to a metal ion. (Section 23.4)

  • Part per million (ppm)

    Units used on NMR spectra to record chemical shift relative to the TMS standard.

  • primary

    A term used to indicate that exactly one alkyl group is attached directly to a particular position. For example, a primary carbocation has one alkyl group (not more) attached directly to the electrophilic carbon atom (C+).

  • prosthetic group

    A nonprotein unit attached to a protein, such as heme in hemoglobin.

  • protecting group

    A group that is used during synthesis to protect a functional group from the reaction conditions.

  • reducing agent

    A compound that reduces another compound and in the process is itself oxidized. Sodium borohydride and lithium aluminum hydride are reducing agents.

  • regiochemistry

    A term describing a consideration that must be taken into account for a reaction in which two or more constitutional isomers can be formed.

  • silica

    Common name for silicon dioxide. (Section 22.4)

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