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Textbooks / Chemistry / Organic Chemistry 6

Organic Chemistry 6th Edition - Solutions by Chapter

Organic Chemistry | 6th Edition | ISBN: 9780840054982 | Authors: William H. Brown, Christopher S. Foote , Brent L. Iverson, Eric Anslyn

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9780840054982

Organic Chemistry | 6th Edition | ISBN: 9780840054982 | Authors: William H. Brown, Christopher S. Foote , Brent L. Iverson, Eric Anslyn

Organic Chemistry | 6th Edition - Solutions by Chapter

This expansive textbook survival guide covers the following chapters: 29. The full step-by-step solution to problem in Organic Chemistry were answered by , our top Chemistry solution expert on 09/09/17, 04:06AM. Organic Chemistry was written by and is associated to the ISBN: 9780840054982. Since problems from 29 chapters in Organic Chemistry have been answered, more than 63453 students have viewed full step-by-step answer. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6.

Key Chemistry Terms and definitions covered in this textbook
  • aromatic hydrocarbon.

    A hydrocarbon that contains one or more benzene rings. (24.1)

  • atomic orbital.

    The wave function (?) of an electron in an atom. (7.5)

  • chemical kinetics.

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (13.1)

  • chlorophyll

    A plant pigment that plays a major role in conversion of solar energy to chemical energy in photosynthesis. (Section 23.3)

  • closed system.

    A system that enables the exchange of energy (usually in the form of heat) but not mass with its surroundings. (6.2)

  • complete ionic equation

    A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)

  • crystal-field theory

    A theory that accounts for the colors and the magnetic and other properties of transition-metal complexes in terms of the splitting of the energies of metal ion d orbitals by the electrostatic interaction with the ligands. (Section 23.6)

  • Disaccharide

    A carbohydrate containing two monosaccharide units joined by a glycosidic bond.

  • enantiotopic

    Protons that are not interchangeable by rotational symmetry but are interchangeable by reflectional symmetry.

  • geometric isomerism

    A form of isomerism in which compounds with the same type and number of atoms and the same chemical bonds have different spatial arrangements of these atoms and bonds. (Sections 23.4 and 24.4)

  • group

    Elements that are in the same column of the periodic table; elements within the same group or family exhibit similarities in their chemical behavior. (Section 2.5)

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • kinetic-molecular theory

    A set of assumptions about the nature of gases. These assumptions, when translated into mathematical form, yield the ideal-gas equation. (Section 10.7)

  • Nernst equation

    An equation that relates the cell emf, E, to the standard emf, E°, and the reaction quotient, Q: E = E° - 1RT>nF2 ln Q. (Section 20.6)

  • Optically active

    Refers to a compound that rotates the plane of plane-polarized light

  • plastic

    A material that can be formed into particular shapes by application of heat and pressure. (Section 12.8)

  • polyurethanes

    Polymers made up of repeating urethane groups, also sometimes called carbamate groups (!N!CO2!).

  • R (Section 3.3)

    From the Latin, rectus, straight, correct; used in the R,S convention to show that the order of priority of groups on a chiral center is clockwise.

  • resonance structures

    A series of structures that are melded together (conceptually) to circumvent the inadequacies of bond-line drawings.

  • solvation

    The clustering of solvent molecules around a solute particle. (Section 13.1)