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Solutions for Chapter 17.5: allylic and benzylic oXidation

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 17.5: allylic and benzylic oXidation

Since 7 problems in chapter 17.5: allylic and benzylic oXidation have been answered, more than 39614 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Chapter 17.5: allylic and benzylic oXidation includes 7 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • base ionization constant (Kb).

    The equilibrium constant for the base ionization. (15.6)

  • bond enthalpy

    The enthalpy change, ?H, required to break a particular bond when the substance is in the gas phase. (Section 8.8)

  • branched polymer

    A polymer that contains a large number of branches connected to the main chain of the polymer.

  • Celsius scale

    A temperature scale on which water freezes at 0° and boils at 100° at sea level. (Section 1.4)

  • conjugate acid

    A substance formed by addition of a proton to a Brønsted–Lowry base. (Section 16.2)

  • denaturation

    A process during which a protein unfolds under conditions of mild heating.

  • Enamine

    An unsaturated compound derived by the reaction of an aldehyde or ketone and a secondary amine followed by loss of H2O; R2C"CR!NR2

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • halogens

    Members of group 7A in the periodic table. (Section 7.8)

  • homogeneous catalyst

    A catalyst that is in the same phase as the reactant substances. (Section 14.7)

  • Hückel’s rule

    The requirement for an odd number of p electron pairs in order for a compound to be aromatic.

  • ignal splitting in NMR

    Spin-spin coupling with adjacent nuclei split NMR signals depending on the extent of coupling and the number of adjacent equivalent nuclei.

  • Observed rotation

    the number of degrees through which a compound rotates the plane of polarized light

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • partially condensed structures

    A drawing style in which the CH bonds are not drawn explicitly, but all other bonds are drawn.

  • Polysaccharide

    A carbohydrate containing a large number of monosaccharide units, each joined to the next by one or more glycosidic bonds.

  • protecting group

    A group that is used during synthesis to protect a functional group from the reaction conditions.

  • radical inhibitor

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

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

  • Sulfi de

    The sulfur analog of an ether; a molecule containing a sulfur atom bonded to two carbon atoms. Sulfi des are also called thioethers

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