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Solutions for Chapter 2.18: Cycloalkane Nomenclature

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 2.18: Cycloalkane Nomenclature

Solutions for Chapter 2.18
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This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 1 problems in chapter 2.18: Cycloalkane Nomenclature have been answered, more than 22646 students have viewed full step-by-step solutions from this chapter. Chapter 2.18: Cycloalkane Nomenclature includes 1 full step-by-step solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • allylic carbocation

    A carbocation in which the positive charge is adjacent to a carbon-carbon double bond.

  • Amino group

    A compound containing an sp3 -hybridized nitrogen atom bonded to one, two, or three carbon atoms

  • anomers

    Stereoisomeric cyclic hemiacetals of an aldose or ketose that differ from each other in their configuration at the anomeric carbon.

  • Antiaromatic compound

    A monocyclic compound that is planar or nearly so, has one 2p orbital on each atom of the ring, and has 4n p electrons in the cyclic arrangement of overlapping 2p orbitals, where n is an integer. Antiaromatic compounds are especially unstable

  • Aramid

    A polyaromatic amide; a polymer in which the monomer units are an aromatic diamine and an aromatic dicarboxylic acid

  • bond length.

    The distance between the nuclei of two bonded atoms in a molecule. (9.4)

  • bromohydrin

    A compound containing a Br group and a hydroxyl group (OH) on adjacent carbon atoms.

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • Cis, trans isomers

    Stereoisomers that have the same connectivity but a different arrangement of their atoms in space as a result of the presence of either a ring or a carboncarbon double bond.

  • entropy

    A thermodynamic function associated with the number of different equivalent energy states or spatial arrangements in which a system may be found. It is a thermodynamic state function, which means that once we specify the conditions for a system—that is, the temperature, pressure, and so on—the entropy is defined. (Section 19.2)

  • First ionization potential

    The energy needed to remove the most loosely held electron from an atom or molecule.

  • fishhook arrow

    A curved arrow with only one barb, indicating the motion of just one electron (also see Sect. 11.1).

  • Friedel-Crafts alkylation

    An electrophilic aromatic substitution reaction that installs an alkyl group on an aromatic ring.

  • indicator

    A substance added to a solution that changes color when the added solute has reacted with all the solute present in solution. The most common type of indicator is an acid–base indicator whose color changes as a function of pH. (Section 4.6)

  • ionic reaction

    A reaction that involves the participation of ions as reactants, intermediates, or products.

  • nitronium ion

    The NO2+ ion, which is present in a mixture of nitric acid and sulfuric acid.

  • ozone

    The name given to O3, an allotrope of oxygen. (Section 7.8)

  • solvent extraction

    A process by which one or more compounds are removed from a mixture of organic compounds, based on a difference in solubility and/or acid-base properties.

  • Steric hindrance

    The ability of groups, because of their size, to hinder access to a reaction site within a molecule.

  • symmetrical ether

    An ether (R!O!R) where both R groups are identical.

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