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Solutions for Chapter Chapter 10: Structure and Synthesis of Alcohols

Organic Chemistry | 8th Edition | ISBN: 9780321811394 | Authors: L.g. Wade, Jr.

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780321811394

Organic Chemistry | 8th Edition | ISBN: 9780321811394 | Authors: L.g. Wade, Jr.

Solutions for Chapter Chapter 10: Structure and Synthesis of Alcohols

Solutions for Chapter Chapter 10
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Textbook: Organic Chemistry
Edition: 8
Author: L.g. Wade, Jr.
ISBN: 9780321811394

Organic Chemistry was written by and is associated to the ISBN: 9780321811394. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. Chapter Chapter 10: Structure and Synthesis of Alcohols includes 53 full step-by-step solutions. Since 53 problems in chapter Chapter 10: Structure and Synthesis of Alcohols have been answered, more than 21147 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Avogadro‚Äôs law

    A statement that the volume of a gas maintained at constant temperature and pressure is directly proportional to the number of moles of the gas. (Section 10.3)

  • biochemistry

    The study of the chemistry of living systems. (Chapter 24: Introduction)

  • chain reaction

    A reaction (generally involving radicals) in which one chemical entity can ultimately cause a chemical transformation for thousands of molecules.

  • Chiral

    From the Greek, cheir meaning hand; an object that is not superposable on its mirror image; an object that has handedness.

  • covalent bond.

    A bond in which two electrons are shared by two atoms. (9.4)

  • degree of unsaturation

    The absence of two hydrogen atoms associated with a ring or a p bond.

  • donor atom

    The atom of a ligand that bonds to the metal. (Section 23.2)

  • enantiotopic

    Protons that are not interchangeable by rotational symmetry but are interchangeable by reflectional symmetry.

  • 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

  • First ionization potential

    The energy needed to remove the most loosely held electron from an atom or molecule.

  • methylene group

    A CH2 group.

  • Newman projection

    A drawing style that is designed to show the conformation of a molecule.

  • oxymercuration-demercuration

    A two-step process for the Markovnikov addition of water across an alkene. With this process, carbocation rearrangements do not occur.

  • porphyrin

    A complex derived from the porphine molecule. (Section 23.3)

  • Protic solvent

    A solvent that is a hydrogen-bond donor. Common protic solvents are water, low-molecular-weight alcohols, and low-molecular weight carboxylic acids.

  • quaternary structure

    The structure of a protein resulting from the clustering of several individual protein chains into a final specific shape. (Section 24.7)

  • radical inhibitor

    A compound that prevents a radical chain process from either getting started or continuing.

  • root-mean-square (rms) speed 1M2

    The square root of the average of the squared speeds of the gas molecules in a gas sample. (Section 10.7)

  • Schiemann reaction

    The conversion of an aryl diazonium salt into fluorobenzene upon treatment with fluoroboric acid (HBF4).

  • Syndiotactic polymer

    A polymer with alternating R and S confi gurations at the chiral centers along its chain, as, for example, syndiotactic polypropylene

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