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Solutions for Chapter 3: Acids and Bases

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition

ISBN: 9781118452288

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Solutions for Chapter 3: Acids and Bases

Solutions for Chapter 3
4 5 0 296 Reviews
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Textbook: Organic Chemistry, - Standalone Book
Edition: 2
Author: David R. Klein
ISBN: 9781118452288

This expansive textbook survival guide covers the following chapters and their solutions. Chapter 3: Acids and Bases includes 73 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Since 73 problems in chapter 3: Acids and Bases have been answered, more than 66014 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, - Standalone Book was written by and is associated to the ISBN: 9781118452288.

Key Chemistry Terms and definitions covered in this textbook
  • acceptor impurities.

    Impurities that can accept electrons from semiconductors. (21.3)

  • bimolecular

    For mechanisms, a step that involves two chemical entities.

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • buffer solution.

    A solution of (a) a weak acid or base and (b) its salt; both components must be present. The solution has the ability to resist changes in pH upon the addition of small amounts of either acid or base. (16.3)

  • chromatogram

    In gas chromatography, a plot that identifies the retention time of each compound in the mixture.

  • crystallization.

    The process in which dissolved solute comes out of solution and forms crystals. (12.1)

  • Dalton’s law of partial pressures.

    The total pressure of a mixture of gases is just the sum of the pressures that each gas would exert if it were present alone. (5.6)

  • decomposition reaction.

    The breakdown of a compound into two or more components. (4.4)

  • dilution

    The process of preparing a less concentrated solution from a more concentrated one by adding solvent. (Section 4.5)

  • Edman degradatio

    A method for selectively cleaving and identifying the N-terminal amino acid of a polypeptide chain.

  • endergonic

    Any process with a positive DG.

  • Equatorial bond

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

  • Hydroboration-oxidation

    A method for converting an alkene to an alcohol. The alkene is treated with borane (BH3) to give a trialkylborane, which is then oxidized with alkaline hydrogen peroxide to give an alcohol

  • monodentate ligand

    A ligand that binds to the metal ion via a single donor atom. It occupies one position in the coordination sphere. (Section 23.3)

  • partially condensed structures

    A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.

  • Polycarbonate

    A polyester in which the carboxyl groups are derived from carbonic acid

  • polypeptide

    A polymer of amino acids that has a molecular weight of less than 10,000. (Section 24.7)

  • Principle of microscopic reversibility

    This principle states that the sequence of transition states and reactive intermediates in the mechanism of any reversible reaction must be the same, but in reverse order, for the reverse reaction as for the forward reaction

  • sulfoxide

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

  • Thermochemistry

    The study of the energy of chemical structures.

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