Solutions for Chapter 10.12: planning an organic synthesis

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 10.12: planning an organic synthesis

Solutions for Chapter 10.12
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Since 1 problems in chapter 10.12: planning an organic synthesis have been answered, more than 11605 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by Patricia and is associated to the ISBN: 9781936221349. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 10.12: planning an organic synthesis includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6.

Key Chemistry Terms and definitions covered in this textbook
  • activity series.

    A summary of the results of many possible displacement reactions. (4.4)

  • alkylthio group

    An SR group.

  • Bicycloalkane

    An alkane containing two rings that share two carbons

  • Bonding molecular orbital

    A molecular orbital in which electrons have a lower energy than they would in isolated atomic orbitals

  • Brønsted-Lowry acid

    A compound that can serve as a proton donor.

  • Chlorofl uorocarbons (CFCs, Freons)

    Compounds with one or two carbons, chlorine, and fl uorine, formerly used as refrigerants

  • crystal lattice

    An imaginary network of points on which the repeating motif of a solid may be imagined to be laid down so that the structure of the crystal is obtained. The motif may be a single atom or a group of atoms. Each lattice point represents an identical environment in the crystal. (Section 12.2)

  • diamagnetic anisotropy

    An effect that causes different regions of space to be characterized by different magnetic field strengths.

  • dipole moment

    A measure of the separation and magnitude of the positive and negative charges in polar molecules. (Section 8.4)

  • disulfide bridge

    The group that is formed when two cysteine residues of a polypeptide or protein are joined together.

  • double helix

    The structure for DNA that involves the winding of two DNA polynucleotide chains together in a helical arrangement. The two strands of the double helix are complementary in that the organic bases on the two strands are paired for optimal hydrogen bond interaction. (Section 24.10)

  • electronic charge

    The negative charge carried by an electron; it has a magnitude of 1.602 * 10-19 C. (Section 2.3)

  • electrospray ionization (ESI):

    In mass spectrometry, an ionization technique in which the compound is first dissolved in a solvent and then sprayed via a high-voltage needle into a vacuum chamber. The tiny droplets of solution become charged by the needle, and subsequent evaporation forms gas-phase molecular ions that typically carry one or more charges.

  • Fischer projection

    A twodimensional representation of a molecule; in these projections, groups on the right and left are by convention in front, while those at the top and bottom are to the rear.

  • Hydroxyl group

    An !OH group

  • Ketone

    A compound containing a carbonyl group bonded to two carbons.

  • Lactam

    A cyclic amide.

  • Markovnikov addition

    In additionreactions, the observation that the hydrogen atomis generally placed at the vinylic position alreadybearing the larger number of hydrogen atoms.

  • Oxidative addition

    Addition of a reagent to a metal center causing it to add two substituents and to increase its oxidation state by two

  • prosthetic group

    A nonprotein unit attached to a protein, such as heme in hemoglobin.

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