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Solutions for Chapter 3: Stereoisomerism and Chirality

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781133952848

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Solutions for Chapter 3: Stereoisomerism and Chirality

Solutions for Chapter 3
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

Chapter 3: Stereoisomerism and Chirality includes 36 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781133952848. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 36 problems in chapter 3: Stereoisomerism and Chirality have been answered, more than 10903 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • anion

    A negatively charged ion. (Section 2.7)

  • carboxylic acid

    A compound that contains the ¬COOH functional group. (Sections 16.10 and 24.4)

  • carboxylic acids.

    Acids that contain the carboxyl group —COOH. (24.4)

  • closest packing.

    The most efficient arrangements for packing atoms, molecules, or ions in a crystal. (11.4)

  • decarboxylation

    A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.

  • delocalized

    A lone pair or charge that is participating in resonance.

  • electron impact ionization (EI)

    In mass spectrometry, an ionization technique that involves bombarding a compoundwith high-energy electrons.

  • Glycosidic bond

    The bond from the anomeric carbon of a glycoside to an !OR group

  • indicator

    A substance added to a solution that changes color when the added solute has reacted with all the solute present in solution. The most common type of indicator is an acid–base indicator whose color changes as a function of pH. (Section 4.6)

  • isolated diene

    A compound containing two carbon-carbon p bonds that are separated by two or more s bonds.

  • limiting reactant (limiting reagent)

    The reactant present in the smallest stoichiometric quantity in a mixture of reactants; the amount of product that can form is limited by the complete consumption of the limiting reactant. (Section 3.7)

  • mass defect

    The difference between the mass of a nucleus and the total masses of the individual nucleons that it contains. (Section 21.6)

  • metallic character

    The extent to which an element exhibits the physical and chemical properties characteristic of metals, for example, luster, malleability, ductility, and good thermal and electrical conductivity. (Section 7.6)

  • miscible

    Two liquids that can be mixed with each other in any proportion.

  • polarimeter

    A device that measures the rotation of plane-polarized light caused by optically active compounds.

  • Racemic mixture

    A mixture of equal amounts of two enantiomers.

  • racemic mixture

    A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)

  • radial probability function

    The probability that the electron will be found at a certain distance from the nucleus. (Section 6.6)

  • rate-determining step

    The sloweststep in a multistep reaction which determines the rate of the reaction.

  • Schiff base

    An alternative name for an imine

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