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Solutions for Chapter 11: Theories of Covalent Bonding

Chemistry: The Molecular Nature of Matter and Change | 5th Edition | ISBN: 9780073048598 | Authors: Martin S. Silberberg

Full solutions for Chemistry: The Molecular Nature of Matter and Change | 5th Edition

ISBN: 9780073048598

Chemistry: The Molecular Nature of Matter and Change | 5th Edition | ISBN: 9780073048598 | Authors: Martin S. Silberberg

Solutions for Chapter 11: Theories of Covalent Bonding

Solutions for Chapter 11
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Textbook: Chemistry: The Molecular Nature of Matter and Change
Edition: 5
Author: Martin S. Silberberg
ISBN: 9780073048598

This expansive textbook survival guide covers the following chapters and their solutions. Since 59 problems in chapter 11: Theories of Covalent Bonding have been answered, more than 34924 students have viewed full step-by-step solutions from this chapter. Chemistry: The Molecular Nature of Matter and Change was written by and is associated to the ISBN: 9780073048598. This textbook survival guide was created for the textbook: Chemistry: The Molecular Nature of Matter and Change , edition: 5. Chapter 11: Theories of Covalent Bonding includes 59 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Aceto group

    A CH3CO! group; also called an acetyl group

  • Activating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be greater than that for benzene.

  • alkene

    A compound that possesses a carbon-carbon double bond.

  • amalgam.

    An alloy of mercury with another metal or metals. (21.2)

  • band theory.

    Delocalized electrons move freely through “bands” formed by overlapping molecular orbitals. (21.3)

  • Bile acid

    A cholesterol-derived detergent molecule, such as cholic acid, which is secreted by the gallbladder into the intestine to assist in the absorption of dietary lipids.

  • 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.

  • common-ion effect

    A shift of an equilibrium induced by an ion common to the equilibrium. For example, added Na2SO4 decreases the solubility of the slightly soluble salt BaSO4, or added NaF decreases the percent ionization of HF. (Section 17.1)

  • condensation polymer

    A polymer,that is formed via a condensation reaction.

  • denaturation

    A process during which a protein unfolds under conditions of mild heating.

  • dipole moment

    A measure of the separation and magnitude of the positive and negative charges in polar molecules. (Section 8.4)

  • Double-headed arrow

    A symbol used to show that structures on either side of it are resonance-contributing structures

  • enantiomer

    A nonsuperimposable mirror image.

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • halogenation

    A reaction that involves the addition of X2 (either Br2 or Cl2) across an alkene.

  • ionic reaction

    A reaction that involves the participation of ions as reactants, intermediates, or products.

  • Nucleophilic acyl substitution

    A reaction in which a nucleophile bonded to the carbon of an acyl group is replaced by another nucleophile.

  • Para (p)

    Refers to groups occupying l,4-positions on a benzene ring

  • saponification

    Hydrolysis of an ester in the presence of a base. (Section 24.4)

  • torsional angle

    The angle between two groups in a Newman projection, also called the dihedral angle.

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