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Solutions for Chapter 5.3: Isomerism in Alkenes

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 5.3: Isomerism in Alkenes

Solutions for Chapter 5.3
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This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 2 problems in chapter 5.3: Isomerism in Alkenes have been answered, more than 18448 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 5.3: Isomerism in Alkenes includes 2 full step-by-step 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

    Hydrocarbons containing one or more carbon–carbon triple bonds. (Section 24.2)

  • Chain-transfer reaction

    The transfer of reactivity of an endgroup from one chain to another during a polymerization

  • Charles’s law

    A law stating that at constant pressure, the volume of a given quantity of gas is proportional to absolute temperature. (Section 10.3)

  • cycloalkanes.

    Alkanes whose carbon atoms are joined in rings. (24.2)

  • E1cb mechanism

    An eliminationreaction in which the leaving group only leavesafter deprotonation occurs. This process occurs atthe end of an aldol condensation.

  • heat of reaction

    The heat given off during a reaction.

  • Hofmann rule

    Any b-elimination that occurs preferentially to give the less substituted alkene as the major product.

  • l sugar

    A carbohydrate for which the chirality center farthest from the carbonyl group will have an OH group pointing to the left in the Fischer projection.

  • lecithins

    Phosphoglycerides thatcontain choline.

  • Molecular spectroscopy

    The study of which frequencies of radiation are absorbed or emitted by a particular substance and the correlation of these frequencies with details of molecular structure.

  • Nuclear magnetic resonance (NMR) spectroscopy

    A spectroscopic technique that gives information about the number and types of atoms in a molecule, for example, hydrogens (1 H!NMR) and carbons (13C!NMR)

  • ozonolysis

    A reaction in which the CRC bond of an alkene is cleaved to form two CRO bonds.

  • Pi (p) bond

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

  • plasticizers

    Small molecules that are trapped between polymer chains where they function as lubricants, preventing the polymer from being brittle.

  • Polarizability

    A measure of the ease of distortion of the distribution of electron density about an atom or group in response to interaction with other molecules or ions. Fluorine which has a high electronegativity and holds its electrons tightly, has a very low polarizability. Iodine, which has a lower electronegativity and holds its electrons less tightly, has a very high polarizability.

  • Resonance in NMR spectroscopy

    The absorption of electromagnetic radiation by a precessing nucleus and the resulting “fl ip” of its nuclear spin from the lower energy state to the higher energy state.

  • single bond

    A covalent bond involving one electron pair. (Section 8.3)

  • spontaneous process

    A process that is capable of proceeding in a given direction, as written or described, without needing to be driven by an outside source of energy. A process may be spontaneous even though it is very slow. (Section 19.1)

  • systematic name

    A name that is assigned using the rules of IUPAC nomenclature.

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