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Solutions for Chapter 20: Electrochemistry

Chemistry: The Central Science | 14th Edition | ISBN: 9780134414232 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 14th Edition

ISBN: 9780134414232

Chemistry: The Central Science | 14th Edition | ISBN: 9780134414232 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 20: Electrochemistry

Solutions for Chapter 20
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Textbook: Chemistry: The Central Science
Edition: 14
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus
ISBN: 9780134414232

Summary of Chapter 20: Electrochemistry

Electrochemistry is the study of the relationships between electricity and chemical reactions. It includes the study of both spontaneous and nonspontaneous processes.

This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 14. Chemistry: The Central Science was written by and is associated to the ISBN: 9780134414232. Chapter 20: Electrochemistry includes 118 full step-by-step solutions. Since 118 problems in chapter 20: Electrochemistry have been answered, more than 17805 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • activated complex.

    The species temporarily formed by the reactant molecules as a result of the collision before they form the product. (13.4)

  • aldehydes.

    Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)

  • Antiaromatic compound

    A monocyclic compound that is planar or nearly so, has one 2p orbital on each atom of the ring, and has 4n p electrons in the cyclic arrangement of overlapping 2p orbitals, where n is an integer. Antiaromatic compounds are especially unstable

  • bromonium ion

    A positively charged, bridged intermediate formed during the addition reaction that occurs when an alkene is treated with molecular bromine (Br2).

  • calorimeter

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

  • cephalins

    Phosphoglycerides that contain ethanolamine.

  • Cycloalkane

    A saturated hydrocarbon that contains carbons joined to form a ring

  • deactivate

    For a substitutedaromatic ring, the effect of an electronwithdrawingsubstituent that decreases therate of electrophilic aromatic substitution.

  • ester

    An organic compound that has an OR group attached to a carbonyl; it is the product of a reaction between a carboxylic acid and an alcohol. (Section 24.4)

  • hybrid orbital

    An orbital that results from the mixing of different kinds of atomic orbitals on the same atom. For example, an sp3 hybrid results from the mixing, or hybridizing, of one s orbital and three p orbitals. (Section 9.5)

  • Lactam

    A cyclic amide.

  • metal complex

    An assembly of a metal ion and the Lewis bases bonded to it. (Section 23.2)

  • noble gases

    Members of group 8A in the periodic table. (Section 7.8)

  • 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.

  • phase change

    The conversion of a substance from one state of matter to another. The phase changes we consider are melting and freezing 1solid ? liquid2, sublimation and deposition, and vaporization and condensation 1liquid ? gas2. (Section 11.4)

  • phosphoglycerides

    Compounds that are very similar in structure to triglycerides, with the main difference being that one of the three fatty acid residues is replaced by a phosphoester group.

  • Radical cation

    A species formed when a neutral molecule loses one electron; it contains both an odd number of electrons and a positive charge.

  • resonance

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

  • solvolysis

    A substitution reaction in which the solvent functions as the nucleophile.

  • upfield

    The right side of an NMRspectrum.