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Solutions for Chapter 8: Basic Concepts of Chemical Bonding

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 8: Basic Concepts of Chemical Bonding

Solutions for Chapter 8
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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 8: Basic Concepts of Chemical Bonding

We examine the relationship between the electronic structure of atoms and the ionic and covalent chemical bonds they form

This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 14. Since 110 problems in chapter 8: Basic Concepts of Chemical Bonding have been answered, more than 28875 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by and is associated to the ISBN: 9780134414232. Chapter 8: Basic Concepts of Chemical Bonding includes 110 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • allylic carbocation

    A carbocation in which the positive charge is adjacent to a carbon-carbon double bond.

  • anion

    A negatively charged ion. (Section 2.7)

  • Benzyl group (C6H5CH2!)

    The group derived from toluene by removing a hydrogen from its methyl group.

  • condensation.

    The phenomenon of going from the gaseous state to the liquid state. (11.8)

  • degenerate orbitals

    Orbitals that have the same energy.

  • enantiomeric excess

    For a mixture containing two enantiomers, the difference between the percent concentration of the major enantiomer and the percent concentration of its mirror image.

  • exothermic

    Any process with a negative DH (the system gives energy to the surroundings).

  • functional group

    An atom or group of atoms that imparts characteristic chemical properties to an organic compound. (Section 24.1)

  • Haloalkene (vinylic halide)

    A compound containing a halogen atom bonded to one of the carbons of a carbon-carbon double bond.

  • Henderson–Hasselbalch equation

    The relationship among the pH, pKa, and the concentrations of acid and conjugate base in an aqueous solution: pH = pKa + log 3base4 3acid4. (Section 17.2)

  • high-spin complex

    A complex whose electrons populate the d orbitals to give the maximum number of unpaired electrons. (Section 23.6)

  • lactone

    A cyclic ester.

  • levorotatory

    A compound thatrotates plane-polarized light in a counterclockwisedirection (-).

  • mercurinium ion

    The intermediateformed during oxymercuration.

  • proton

    A positively charged subatomic particle found in the nucleus of an atom. (Section 2.3)

  • second order

    A reaction that has a rate equation in which the sum of all exponents is two.

  • solvent

    The dissolving medium of a solution; it is normally the component of a solution present in the greater amount. (Section 4.1)

  • stereoisomers

    Compounds that have the same constitution but differ in the 3D arrangement of atoms.

  • tetravalent

    An element, such as carbon, that forms four bonds.

  • Williamson ether synthesis

    A method for preparing an ether from an alkoxide ion and an alkyl halide (via an SN2 process).