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Solutions for Chapter 14.8: organic synthesis Using alkynes

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 14.8: organic synthesis Using alkynes

Solutions for Chapter 14.8
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Chapter 14.8: organic synthesis Using alkynes includes 1 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. Since 1 problems in chapter 14.8: organic synthesis Using alkynes have been answered, more than 39806 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
  • absolute zero

    The lowest attainable temperature; 0 K on the Kelvin scale and -273.15 °C on the Celsius scale. (Section 1.4)

  • alkynes

    Compounds containing a carbon-carbon triple bond.

  • benzylic position

    A carbon atom that is immediately adjacent to a benzene ring.

  • bonding atomic radius

    The radius of an atom as defined by the distances separating it from other atoms to which it is chemically bonded. (Section 7.3)

  • branched polymer

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

  • C terminus

    For a peptide chain,the end that contains the COOH group. carbinolamine (Sect. 20.6): A compound containing a hydroxyl group (OH) and a nitrogen atom, both of which are connceted to the same carbon atom.

  • Chiral center

    A tetrahedral atom, most commonly carbon, that is bonded to four different groups; also called a chirality center

  • closed system.

    A system that enables the exchange of energy (usually in the form of heat) but not mass with its surroundings. (6.2)

  • DEPT 13C NMR

    In 13C NMR spectroscopy, a technique that utilizes two rf radiation emitters and provides information regarding the number of protons attached to each carbon atom in a compound.

  • diffusion.

    The gradual mixing of molecules of one gas with the molecules of another by virtue of their kinetic properties. (5.7)

  • eicosanoids

    A class of lipids which includes leukotrienes, prostaglandins, thromboxanes, and prostacyclins.

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • octet rule

    The observation that second-row elements (C, N, O, and F) will form the necessary number of bonds so as to achieve a full valence shell (eight electrons).

  • Orbital

    A region of space that can hold two electrons

  • Peptide bond

    The special name given to the amide bond formed between the a-amino group of one amino acid and the a-carboxyl group of another amino acid

  • pi (p) bond

    A bond formed from adjacent, overlapping p orbitals.

  • quintet

    In NMR spectroscopy, a signal that is comprised of five peaks.

  • ring flip

    A conformational change in which one chair conformation is converted into the other.

  • Stereospecific reaction

    A special type of stereoselective reaction in which the stereochemistry of the product is dependent on the stereochemistry of the starting material.

  • Z

    For alkenes, a stereodescriptor that indicates that the two priority groups are on the same side of the p bond.

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