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Solutions for Chapter 2.9: sp Hybridization and Bonding in Acetylene

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 2.9: sp Hybridization and Bonding in Acetylene

Solutions for Chapter 2.9
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This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Since 1 problems in chapter 2.9: sp Hybridization and Bonding in Acetylene have been answered, more than 25381 students have viewed full step-by-step solutions from this chapter. Chapter 2.9: sp Hybridization and Bonding in Acetylene includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

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

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

  • axis of symmetry

    An axis about which a compound possesses rotational symmetry.

  • catalyst.

    A substance that increases the rate of a chemical reaction without itself being consumed. (13.6)

  • chain-growth polymer

    A polymer that is formed under conditions in which the monomers do not react directly with each other, but rather, each monomer is added to the growing chain, one at a time.

  • changes of state

    Transformations of matter from one state to a different one, for example, from a gas to a liquid. (Section 1.3)

  • electrolytic cell

    A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)

  • enantiomeric excess

    For a mixture containing two enantiomers, the difference between the percent concentration of the major enantiomer and the percent concentration of its mirror image.

  • Ground-state electron confi guration

    The lowest-energy electron confi guration for an atom or molecule.

  • hydrazone

    A compound with the structure R2CRN!NH2.

  • hydrocarbons

    Compounds composed of only carbon and hydrogen. (Section 2.9)

  • ion-product constant

    For water, Kw is the product of the aquated hydrogen ion and hydroxide ion concentrations: 3H+43OH-4 = Kw = 1.0 * 10-14 at 25 °C. (Section 16.3)

  • oils

    Triglycerides that are liquids at room temperature.

  • pericylic reactions

    Reactions that occur via a concerted process and do not involve either ionic or radical intermediates.

  • polarizability

    The ease with which the electron cloud of an atom or a molecule is distorted by an outside influence, thereby inducing a dipole moment. (Section 11.2)

  • proton

    A positively charged subatomic particle found in the nucleus of an atom. (Section 2.3)

  • Radical

    Any chemical species that contains one or more unpaired electrons.

  • semiconductor

    A material that has electrical conductivity between that of a metal and that of an insulator. (Section 12.7)

  • Steric strain

    The strain that arises when nonbonded atoms separated by four or more bonds are forced closer to each other than their atomic (contact) radii would allow. Steric strain is also called non-bonded interaction strain, or van der Waals strain.

  • strong deactivators

    Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

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