Solutions for Chapter 14.1: Structure and Bonding in 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 14.1: Structure and Bonding in alkyneS

Solutions for Chapter 14.1
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Organic Chemistry was written by Patricia and is associated to the ISBN: 9781936221349. Since 1 problems in chapter 14.1: Structure and Bonding in alkyneS have been answered, more than 13601 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Chapter 14.1: Structure and Bonding in alkyneS includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-adduct

    The product obtainedfrom 1,2-addition across a conjugated p system.

  • auxochrome

    When applying Woodward-Fieser rules, the groups attached to the chromophore.

  • beta sheet

    A structural form of protein in which two strands of amino acids are hydrogen-bonded together in a zipperlike configuration. (Section 24.7)

  • buffer solution.

    A solution of (a) a weak acid or base and (b) its salt; both components must be present. The solution has the ability to resist changes in pH upon the addition of small amounts of either acid or base. (16.3)

  • conservation of orbital symmetry

    During a reaction, the requirement that the phases of the frontier MOs must be aligned.

  • 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

  • Energy diagram

    A graph showing the changes in energy that occur during a chemical reaction; energy is plotted on the vertical axis, and reaction progress is plotted on the horizontal axis. Also called a reaction coordinate diagram

  • halogen abstraction

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

  • Heterocyclic aromatic amine

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

  • law of mass action

    The rules by which the equilibrium constant is expressed in terms of the concentrations of reactants and products, in accordance with the balanced chemical equation for the reaction. (Section 15.2)

  • N terminus

    For a peptide chain,the end that contains the amino group.

  • optical isomerism

    A form of isomerism in which the two forms of a compound (stereoisomers) are nonsuperimposable mirror images. (Section 23.4)

  • oxime

    A compound with the structure R2CRN!OH.

  • Pi (p) bond

    A covalent bond formed by the overlap of parallel 2p orbitals.

  • propagation

    For radical reactions,the steps whose sum gives the net chemical reaction.

  • reducing agent

    A compound that reduces another compound and in the process is itself oxidized. Sodium borohydride and lithium aluminum hydride are reducing agents.

  • salinity

    A measure of the salt content of seawater, brine, or brackish water. It is equal to the mass in grams of dissolved salts present in 1 kg of seawater. (Section 18.3)

  • scientific method

    The general process of advancing scientific knowledge by making experimental observations and by formulating hypotheses, theories, and laws. (Section 1.3)

  • Telechelic polymer

    A polymer in which its growing chains are terminated by formation of new functional groups at both ends of its chains. These new functional groups are introduced by adding reagents, such as CO2 or ethylene oxide, to the growing chains.

  • vicinal

    A term used to describe two identical groups attached to adjacent carbon atoms.

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