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Solutions for Chapter 11: Alcohols and Ethers

Organic Chemistry | 11th Edition | ISBN: 9781118133576 | Authors: T. W. Graham Solomons Craig B. Fryhle, Scott A. Snyder

Full solutions for Organic Chemistry | 11th Edition

ISBN: 9781118133576

Organic Chemistry | 11th Edition | ISBN: 9781118133576 | Authors: T. W. Graham Solomons Craig B. Fryhle, Scott A. Snyder

Solutions for Chapter 11: Alcohols and Ethers

Solutions for Chapter 11
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Textbook: Organic Chemistry
Edition: 11
Author: T. W. Graham Solomons Craig B. Fryhle, Scott A. Snyder
ISBN: 9781118133576

Organic Chemistry was written by and is associated to the ISBN: 9781118133576. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 11. This expansive textbook survival guide covers the following chapters and their solutions. Since 56 problems in chapter 11: Alcohols and Ethers have been answered, more than 43368 students have viewed full step-by-step solutions from this chapter. Chapter 11: Alcohols and Ethers includes 56 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Activation energy

    The difference in Gibbs free energy between reactants and a transition state

  • Alkene metathesis

    A reaction in which two alkenes interchange the carbons attached to their double bonds.

  • Antiaromatic compound

    A monocyclic compound that is planar or nearly so, has one 2p orbital on each atom of the ring, and has 4n p electrons in the cyclic arrangement of overlapping 2p orbitals, where n is an integer. Antiaromatic compounds are especially unstable

  • Aufbau principle.

    As protons are added one by one to the nucleus to build up the elements, electrons similarly are added to the atomic orbitals. (7.9)

  • band

    An array of closely spaced molecular orbitals occupying a discrete range of energy. (Section 12.4)

  • Claisen rearrangement

    A [3,3] sigmatropic rearrangement that is observed for allylic vinylic ethers.

  • fats

    Triglycerides that are solids atroom temperature.

  • isotopes

    Atoms of the same element containing different numbers of neutrons and therefore having different masses. (Section 2.3)

  • loss of a leaving group

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

  • Michael donor

    The nucleophile in a Michael reaction.

  • node

    In atomic and molecular orbitals, a location where the value of y is zero.

  • Oligosaccharide

    A carbohydrate containing four to ten monosaccharide units, each joined to the next by a glycosidic bond.

  • phosphatidic acid

    A phosphoric monoester, which is the simplest kind of phosphoglyceride.

  • plane of symmetry

    A plane that bisects a compound into two halves that are mirror images of each other.

  • positron emission

    A nuclear decay process where a positron, a particle with the same mass as an electron but with a positive charge, symbol 0+1e, or b+ is emitted from the nucleus. (Section 21.1)

  • Potential energy

    The energy that can be released if given an opportunity

  • rad

    A measure of the energy absorbed from radiation by tissue or other biological material; 1 rad = transfer of 1 * 10-2 J of energy per kilogram of material. (Section 21.9)

  • sp2-hybridized orbitals

    Atomic orbitals that are achieved by mathematically averaging one s orbital with two p orbitals to form three hybridized atomic orbitals.

  • specific rotation

    For a chiral compound that is subjected to plane-polarized light, the observed rotation when a standard concentration (1 g/mL) and a standard path length (1 dm) are used.

  • syndiotactic

    A polymer in which the repeating units contain chirality centers which have alternating configuration.

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