Solutions for Chapter 5.7: Cycloalkenes

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 5.7: Cycloalkenes

Solutions for Chapter 5.7
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This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 5.7: Cycloalkenes includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Since 1 problems in chapter 5.7: Cycloalkenes have been answered, more than 10876 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • aldol addition reaction

    A reaction that occurs when an aldehyde or ketone is attacked by an enolate ion. The product of an aldol addition reaction is always a b-hydroxy aldehyde or ketone.

  • atomic mass unit (amu)

    A unit based on the value of exactly 12 amu for the mass of the isotope of carbon that has six protons and six neutrons in the nucleus. (Sections 2.3 and 3.3)

  • bending

    In IR spectroscopy, a type of vibration that generally produces a signal in the fingerprint region of an IR spectrum.

  • bimolecular reaction.

    An elementary step that involves two molecules. (13.5)

  • combination reaction

    A chemical reaction in which two or more substances combine to form a single product. (Section 3.2)

  • Cope rearrangement

    A [3,3] sigmatropic rearrangement in which all six atoms of the cyclic transition state are carbon atoms.

  • core electrons.

    All nonvalence electrons in an atom. (8.2)

  • critical mass

    The amount of fissionable material necessary to maintain a nuclear chain reaction. (Section 21.7)

  • delocalized

    A lone pair or charge that is participating in resonance.

  • diazotization

    The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.

  • electronic charge

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

  • functional group

    An atom or group of atoms that imparts characteristic chemical properties to an organic compound. (Section 24.1)

  • liquid crystal

    A substance that exhibits one or more partially ordered liquid phases above the melting point of the solid form. By contrast, in nonliquid crystalline substances the liquid phase that forms upon melting is completely unordered. (Section 11.7)

  • living polymer

    A polymer that isformed via anionic polymerization.

  • nuclear binding energy

    The energy required to decompose an atomic nucleus into its component protons and neutrons. (Section 21.6)

  • Orbital

    A region of space that can hold two electrons

  • Polypeptide

    A macromolecule containing many amino acid units, each joined to the next by a peptide bond

  • quaternary ammonium salt

    An ionic compound containing a positively charged nitrogen atom connected to four alkyl groups.

  • staggered conformation

    A conformation in which nearby groups in a Newman projection have a dihedral angle of 60°.

  • Watson-Crick model

    A double-helix model for the secondary structure of a DNA molecule

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