Solutions for Chapter 20.1: Introduction to Electrochemistry

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition

ISBN: 9780547586632

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Solutions for Chapter 20.1: Introduction to Electrochemistry

Modern Chemistry: Student Edition 2012 was written by Patricia and is associated to the ISBN: 9780547586632. Since 4 problems in chapter 20.1: Introduction to Electrochemistry have been answered, more than 17865 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 20.1: Introduction to Electrochemistry includes 4 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • bond order

    The number of bonding electron pairs shared between two atoms, minus the number of antibonding electron pairs: bond order = (number of bonding electrons - number of antibonding electrons)/2. (Section 9.7)

  • carbides.

    Ionic compounds containing the C2 22 or C42 ion. (22.3)

  • coordinate covalent bond.

    A bond in which the pair of electrons is supplied by one of the two bonded atoms; also called a dative bond. (9.9)

  • critical mass.

    The minimum mass of fissionable material required to generate a self-sustaining nuclear chain reaction. (19.5)

  • diazotization

    The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.

  • divalent

    An element that forms two bonds, such as oxygen.

  • Electromagnetic radiation

    Light and other forms of radiant energy.

  • electronic structure

    The arrangement of electrons in an atom or molecule. (Chapter 6:Introduction)

  • energy-level diagram

    A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived. Also called a molecular-orbital diagram. (Section 9.7)

  • frontier orbitals

    The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) that participate in a reaction.

  • heterocycle

    A cyclic compound containing at least one heteroatom (such as S, N, or O) in the ring.

  • Hückel’s rule

    The requirement for an odd number of p electron pairs in order for a compound to be aromatic.

  • node

    In atomic and molecular orbitals, a location where the value of y is zero.

  • Nucleophilicity

    A kinetic property measured by the rate at which a nucleophile causes nucleophilic substitution on a reference compound under a standardized set of experimental conditions.

  • Phenyl group

    A group derived by removing an H from benzene; abbreviated C6H5! or Ph!.

  • phospholipids

    Esterlike derivatives of phosphoric acid.

  • photoionization

    The removal of an electron from an atom or molecule by absorption of light. (Section 18.2)

  • Steric hindrance

    The ability of groups, because of their size, to hinder access to a reaction site within a molecule.

  • Tripeptide

    A molecule containing three amino acid units, each joined to the next by a peptide bond

  • Twist-boat conformation

    A nonplanar conformation of a cyclohexane ring that is twisted from and slightly more stable than a boat conformation.

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