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Solutions for Chapter 7.11: Chiral Molecules with Two Chirality Centers

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 7.11: Chiral Molecules with Two Chirality Centers

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 7.11: Chiral Molecules with Two Chirality Centers includes 4 full step-by-step solutions. Since 4 problems in chapter 7.11: Chiral Molecules with Two Chirality Centers have been answered, more than 36794 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
  • 1,2-addition

    A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C2 position.

  • amino sugars

    Carbohydrate derivatives in which an OH group has been replaced with an amino group.

  • covalent compounds.

    Compounds containing only covalent bonds. (9.4)

  • degenerate

    Having the same energy.

  • Diamagnetic current in NMR

    The circulation of electron density in a molecule in an applied magnetic fi eld.

  • Elastomer

    A material that, when stretched or otherwise distorted, returns to its original shape when the distorting force is released.

  • Leaving group

    The group that is displaced in a substitution reaction or the Lewis base that is lost in an elimination reaction

  • lecithins

    Phosphoglycerides thatcontain choline.

  • 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)

  • meso compound

    A compound that possesses chirality centers and an internal plane of symmetry.

  • metalloids

    Elements that lie along the diagonal line separating the metals from the nonmetals in the periodic table; the properties of metalloids are intermediate between those of metals and nonmetals. (Section 2.5)

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • Part per million (ppm)

    Units used on NMR spectra to record chemical shift relative to the TMS standard.

  • photodissociation

    The breaking of a molecule into two or more neutral fragments as a result of absorption of light. (Section 18.2)

  • primitive lattice

    A crystal lattice in which the lattice points are located only at the corners of each unit cell. (Section 12.2)

  • pyrometallurgy

    A process in which heat converts a mineral in an ore from one chemical form to another and eventually to the free metal. (Section 23.2)

  • reaction quotient (Q)

    The value that is obtained when concentrations of reactants and products are inserted into the equilibrium expression. If the concentrations are equilibrium concentrations, Q = K; otherwise, Q ? K. (Section 15.6)

  • retention time

    The amount of time required for a compound to exit from a gas chromatograph.

  • S (Section 3.3

    From the Latin, sinister, left; used in the R,S convention to show that the order of priority of groups on a chiral center is counterclockwise

  • Zaitsev product

    The more substituted product (alkene) of an elimination reaction.

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