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Solutions for Chapter 6.2: Stereochemistry of Alkene Hydrogenation

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 6.2: Stereochemistry of Alkene Hydrogenation

Solutions for Chapter 6.2
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Chapter 6.2: Stereochemistry of Alkene Hydrogenation includes 1 full step-by-step solutions. 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 6.2: Stereochemistry of Alkene Hydrogenation have been answered, more than 27308 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-elimination

    An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.

  • alkenes

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

  • 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

  • auxochrome

    When applying Woodward-Fieser rules, the groups attached to the chromophore.

  • bond polarity

    A measure of the degree to which the electrons are shared unequally between two atoms in a chemical bond. (Section 8.4)

  • broadband decoupling

    In 13C NMR spectroscopy, a technique in which all 13C!1H splitting is suppressed with the use of two rf transmitters.

  • cellulose

    A polysaccharide of glucose; it is the major structural element in plant matter. (Section 24.8)

  • conjugate addition

    An addition reaction in which a nucleophile and a proton are added across the two ends of a conjugated p system.

  • doping

    Incorporation of a hetero atom into a solid to change its electrical properties. For example, incorporation of P into Si. (Section 12.7)

  • epimer

    Diastereomers that differ from each other in the configuration of only one chirality center.

  • exothermic

    Any process with a negative DH (the system gives energy to the surroundings).

  • Fat

    A mixture of triglycerides that is semisolid or solid at room temperature.

  • instantaneous rate

    The reaction rate at a particular time as opposed to the average rate over an interval of time. (Section 14.2)

  • interhalogens

    Compounds formed between two different halogen elements. Examples include IBr and BrF3. (Section 22.4)

  • methylene group

    A CH2 group.

  • monodentate ligand

    A ligand that binds to the metal ion via a single donor atom. It occupies one position in the coordination sphere. (Section 23.3)

  • Plane of symmetry

    An imaginary plane passing through an object dividing it so that one half is the mirror image of the other half

  • precipitation reaction

    A reaction that occurs between substances in solution in which one of the products is insoluble. (Section 4.2)

  • solution

    A mixture of substances that has a uniform composition; a homogeneous mixture. (Section 1.2)

  • vicinal

    A term used to describe two identical groups attached to adjacent carbon atoms.

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