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Solutions for Chapter 6: Chemical Reactivity and Mechanisms

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 6: Chemical Reactivity and Mechanisms

Solutions for Chapter 6
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Textbook: Organic Chemistry, - Standalone Book
Edition: 2
Author: David R. Klein
ISBN: 9781118452288

Chapter 6: Chemical Reactivity and Mechanisms includes 64 full step-by-step solutions. Since 64 problems in chapter 6: Chemical Reactivity and Mechanisms have been answered, more than 41960 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Organic Chemistry, - Standalone Book was written by and is associated to the ISBN: 9781118452288. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • aldose

    A carbohydrate that contains an aldehyde group.

  • amino sugars

    Carbohydrate derivatives in which an OH group has been replaced with an amino group.

  • anti addition

    An addition reaction in which two groups are installed on opposite sides of a p bond.

  • Crown ether

    A cyclic polyether derived from ethylene glycol and substituted ethylene glycols.

  • disulfide

    A compound with the structure R!S!S!R.

  • Endergonic reaction

    A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials

  • Enol

    A compound containing a hydroxyl group bonded to a doubly bonded carbon atom.

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • irreversible process

    A process that cannot be reversed to restore both the system and its surroundings to their original states. Any spontaneous process is irreversible. (Section 19.1)

  • Lipid

    A biomolecule isolated from plant or animal sources by extraction with nonpolar organic solvents, such as diethyl ether and hexane.

  • methyl shift

    A type of carbocation rearrangement in which a methyl group migrates.

  • Michael reaction

    A reaction in which a nucleophile attacks a conjugated p system, resulting in a 1,4-addition.

  • Nucleophilic substitution

    Any reaction in which one nucleophile is substituted for another at a tetravalent carbon atom.

  • periplanar

    A conformation in which a hydrogen atom and a leaving group are approximately coplanar.

  • quantum

    The smallest increment of radiant energy that may be absorbed or emitted; the magnitude of radiant energy is hn. (Section 6.2)

  • quantum mechanics

    A mathematical description of an electron that incorporates its wavelike properties.

  • rearrangement

    One of the four arrow-pushing patterns for ionic reactions.

  • Sharpless asymmetric epoxidation

    A reaction that converts an alkene into an epoxide via a stereospecific pathway.

  • spectrochemical series

    A list of ligands arranged in order of their abilities to split the d-orbital energies (using the terminology of the crystal-field model). (Section 23.6)

  • Terpene

    A compound whose carbon skeleton can be divided into two or more units identical with the carbon skeleton of isoprene

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