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Solutions for Chapter 17: 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 17

Solutions for Chapter 17
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Textbook: Chemistry: The Central Science
Edition: 12
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward
ISBN: 9780321696724

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 128 problems in chapter 17 have been answered, more than 198922 students have viewed full step-by-step solutions from this chapter. Chapter 17 includes 128 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • activated complex (transition state)

    The particular arrangement of atoms found at the top of the potential-energy barrier as a reaction proceeds from reactants to products. (Section 14.5)

  • activity series

    A list of metals in order of decreasing ease of oxidation. (Section 4.4)

  • alternating copolymers

    A copolymer that contains an alternating distribution of repeating units.

  • Anti conformation

    A conformation about a single bond in which two groups on adjacent carbons lie at a dihedral angle of 180°.

  • Axial bond

    A bond to a chair conformation of cyclohexane that extends from the ring parallel to the imaginary axis through the center of the ring; a bond that lies roughly perpendicular to the equator of the ring.

  • Bond dissociation enthalpy

    The amount of energy required to break a bond into two radicals in the gas phase at 25°C, A!B !> A• 1 •B

  • calorimeter

    An apparatus that measures the heat released or absorbed in a chemical or physical process. (Section 5.5)

  • Chair conformation

    The most stable nonplanar conformation of a cyclohexane ring; all bond angles are approximately 109.5°, and all bonds on adjacent carbons are staggered.

  • conjugate base

    A substance formed by the loss of a proton from a Brønsted–Lowry acid. (Section 16.2)

  • diastereomers

    Stereoisomers that are not mirror images of one another.

  • disulfide

    A compound with the structure R!S!S!R.

  • geometric isomerism

    A form of isomerism in which compounds with the same type and number of atoms and the same chemical bonds have different spatial arrangements of these atoms and bonds. (Sections 23.4 and 24.4)

  • globular proteins

    Proteins that consist of chains that are coiled into compact shapes.

  • hydrophobic

    A nonpolar group that does not have favorable interactions with water.

  • ortho-para director

    A group that directs the regiochemistry of an electrophilic aromatic substitution reaction such that the incoming electrophile is installed at the ortho or para positions.

  • oxymercuration-demercuration

    A two-step process for the Markovnikov addition of water across an alkene. With this process, carbocation rearrangements do not occur.

  • SN1 reaction

    A unimolecular nucleophilic substitution reaction.

  • sp-hybridized

    Atomic orbitals that are achieved by mathematically averaging one s orbital with only one p orbital to form two hybridized atomic orbitals.

  • sp2-hybridized orbitals

    Atomic orbitals that are achieved by mathematically averaging one s orbital with two p orbitals to form three hybridized atomic orbitals.

  • sulfoxide

    A compound containing an SRO bond that is flanked on both sides by R groups.

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