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Solutions for Chapter 6.2: nomEnClaturE of EnantiomErs

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 6.2: nomEnClaturE of EnantiomErs

Solutions for Chapter 6.2
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Since 2 problems in chapter 6.2: nomEnClaturE of EnantiomErs have been answered, more than 40100 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 6.2: nomEnClaturE of EnantiomErs includes 2 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6.

Key Chemistry Terms and definitions covered in this textbook
  • Acylium ion

    A resonance-stabilized cation with the structure [RC"O]1 or [ArC"O]1. The positive charge is delocalized over both the carbonyl carbon and the carbonyl oxygen.

  • anti addition

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

  • base peak

    In mass spectrometry, the tallest peak in the spectrum, which is assigned a relative value of 100%.

  • Brønsted-Lowry acid

    A compound that can serve as a proton donor.

  • combination reaction.

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

  • decomposition reaction.

    The breakdown of a compound into two or more components. (4.4)

  • degenerate

    Having the same energy.

  • E1cb mechanism

    An eliminationreaction in which the leaving group only leavesafter deprotonation occurs. This process occurs atthe end of an aldol condensation.

  • estrogens

    Female sex hormones.

  • fragmentation

    In mass spectrometry, when the molecular ion breaks apart into fragments.

  • Heterocyclic aromatic amine

    An amine in which nitrogen is one of the atoms of an aromatic ring.

  • hydrogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a hydrogen atom is abstracted by a radical, generating a new radical.

  • Hydrogenolysis

    Cleavage of a single bond by H2, most commonly accomplished by treating a compound with H2 in the presence of a transition metal catalyst.

  • lithium dialkyl cuprate

    A nucleophilic compound with the general structureR2CuLi.

  • para

    On an aromatic ring, the C4position.

  • peroxides

    Compounds with the general structure R!O!O!R.

  • polyvinyl chloride, (PVC)

    A polymer formed from the polymerization of vinyl chloride (H2CRCHCl).

  • 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)

  • radiotracer

    A radioisotope that can be used to trace the path of an element in a chemical system. (Section 21.5)

  • unsaturated

    A compound containingone or more p bonds.

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