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Solutions for Chapter 5.4: Naming Stereoisomeric Alkenes by the EZ Notational System

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 5.4: Naming Stereoisomeric Alkenes by the EZ Notational System

Solutions for Chapter 5.4
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 5.4: Naming Stereoisomeric Alkenes by the EZ Notational System includes 3 full step-by-step solutions. Since 3 problems in chapter 5.4: Naming Stereoisomeric Alkenes by the EZ Notational System have been answered, more than 31670 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acetoacetic ester synthesis

    A threestep process that converts an alkyl halide into a methyl ketone with the introduction of three new carbon atoms.

  • amidomalonate synthesis

    A synthetic method that employs diethyl acetamidomalonate as the starting material and enables the preparation of racemic a-amino acids.

  • Basicity

    An equilibrium property measured by the position of equilibrium in an acid-base reaction, as, for example, the acid-base reaction between ammonia and water.

  • chain reaction

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

  • chemical bond

    A strong attractive force that exists between atoms in a molecule. (Section 8.1)

  • Chemical shift (d)

    The shift in parts per million of an NMR signal relative to the signal of TMS

  • covalent compounds.

    Compounds containing only covalent bonds. (9.4)

  • crystallization

    The process in which molecules, ions, or atoms come together to form a crystalline solid. (Section 13.2)

  • delocalized

    A lone pair or charge that is participating in resonance.

  • E,Z system

    A system to specify the confi guration of groups about a carbon-carbon double bond

  • enol

    A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.

  • equivalence point

    The point in a titration at which the added solute reacts completely with the solute present in the solution. (Section 4.6)

  • fuel cell

    A voltaic cell that utilizes the oxidation of a conventional fuel, such as H2 or CH4, in the cell reaction. (Section 20.7)

  • Graham’s law

    A law stating that the rate of effusion of a gas is inversely proportional to the square root of its molecular weight. (Section 10.8)

  • meta director

    An electronwithdrawing group that directs the regiochemistry of an electrophilic aromatic substitution reaction such that the incoming electrophile is installed at the meta position.

  • nucleotide

    Compounds formed from a molecule of phosphoric acid, a sugar molecule, and an organic nitrogen base. Nucleotides form linear polymers called DNA and RNA, which are involved in protein synthesis and cell reproduction. (Section 24.10)

  • Reaction coordinate diagram

    A graph showing the energy changes that occur during a chemical reaction; energy is plotted on the vertical axis and reaction progress is plotted on the horizontal axis.

  • Secondary (2°) amine

    An amine in which nitrogen is bonded to two carbons and one hydrogen

  • 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)

  • stereospecific

    A reaction in which the configuration of the product is dependent on the configuration of the starting material.

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