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Solutions for Chapter 13: Alcohols and Phenols

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 13: Alcohols and Phenols

Solutions for Chapter 13
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Textbook: Organic Chemistry, - Standalone Book
Edition: 2
Author: David R. Klein
ISBN: 9781118452288

Since 72 problems in chapter 13: Alcohols and Phenols have been answered, more than 61583 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, - Standalone Book was written by and is associated to the ISBN: 9781118452288. This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Chapter 13: Alcohols and Phenols includes 72 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,4-adduct

    The product obtained from 1,4-addition across a conjugated p system.

  • a-Helix

    A type of secondary structure in which a section of polypeptide chain coils into a spiral, most commonly a right-handed spiral.

  • Aglycon

    Lacking a sugar

  • aqueous solution.

    A solution in which the solvent is water. (4.1)

  • Boat conformation

    A nonplanar conformation of a cyclohexane ring in which carbons 1 and 4 of the ring are bent toward each other

  • Carboxylic acid

    A compound containing a carboxyl, !COOH, group.

  • chemical formula.

    An expression showing the chemical composition of a compound in terms of the symbols for the atoms of the elements involved. (2.6)

  • combination reaction.

    A reaction in which two or more substances combine to form a single product. (4.4)

  • divalent

    An element that forms two bonds, such as oxygen.

  • HOMO

    The highest occupied molecular orbital.

  • Molecular orbital (MO) theory

    A theory of chemical bonding in which electrons in molecules occupy molecular orbitals that extend over the entire molecule and are formed by the combination of the atomic orbitals that make up the molecule

  • neutralization reaction

    A reaction in which an acid and a base react in stoichiometrically equivalent amounts; the neutralization reaction between an acid and a metal hydroxide produces water and a salt. (Section 4.3)

  • nuclear transmutation

    A conversion of one kind of nucleus to another. (Section 21.3)

  • polysaccharides

    Polymers made up of repeating monosaccharide units linked together by glycoside bonds.

  • property

    A characteristic that gives a sample of matter its unique identity. (Section 1.1)

  • reaction quotient (Q)

    The value that is obtained when concentrations of reactants and products are inserted into the equilibrium expression. If the concentrations are equilibrium concentrations, Q = K; otherwise, Q ? K. (Section 15.6)

  • secondary alkyl halide

    An organohalide in which the alpha (a) position is connected to exactly two alkyl groups.

  • strong deactivators

    Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

  • Wave function

    A solution to a set of equations that defi nes the energy of an electron in an atom and the region of space it may occupy.

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