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Textbooks / Chemistry / Organic Chemistry 6

Organic Chemistry 6th Edition - Solutions by Chapter

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Organic Chemistry | 6th Edition - Solutions by Chapter

Solutions by Chapter
4 5 0 408 Reviews
Textbook: Organic Chemistry
Edition: 6
Author: Marc Loudon, Jim Parise
ISBN: 9781936221349

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. The full step-by-step solution to problem in Organic Chemistry were answered by , our top Chemistry solution expert on 03/16/18, 03:35PM. This expansive textbook survival guide covers the following chapters: 239. Since problems from 239 chapters in Organic Chemistry have been answered, more than 64346 students have viewed full step-by-step answer. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

Key Chemistry Terms and definitions covered in this textbook
  • amplitude.

    The vertical distance from the middle of a wave to the peak or trough. (7.1)

  • boat conformation

    A conformation of cyclohexane in which all bond angles are fairly close to 109.5° and many hydrogen atoms are eclipsing each other.

  • Charles’ law.

    The volume of a fixed amount of gas maintained at constant pressure is directly proportional to the absolute temperature of the gas. (5.3)

  • delocalized

    A lone pair or charge that is participating in resonance.

  • Diamagnetic current in NMR

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

  • dimensional analysis

    A method of problem solving in which units are carried through all calculations. Dimensional analysis ensures that the final answer of a calculation has the desired units. (Section 1.6)

  • ester

    An organic compound that has an OR group attached to a carbonyl; it is the product of a reaction between a carboxylic acid and an alcohol. (Section 24.4)

  • folding

    The process by which a protein adopts its biologically active shape. (Section 24.7)

  • Haloarene (aryl halide)

    A compound containing a halogen atom bonded to a benzene ring. Given the symbol Ar!X

  • Hess’s law

    The heat evolved in a given process can be expressed as the sum of the heats of several processes that, when added, yield the process of interest. (Section 5.6)

  • ideal gas

    A hypothetical gas whose pressure, volume, and temperature behavior is completely described by the ideal-gas equation. (Section 10.4)

  • 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.

  • malonic ester synthesis

    Asynthetic technique that enables the transformationof a halide into a carboxylic acid with theintroduction of two new carbon atoms.

  • metallic hydrides

    Compounds formed when hydrogen reacts with transition metals; these compounds contain the hydride ion, H-. (Section 22.2)

  • Octet rule

    Group 1A–7A elements react to achieve an outer shell of eight valence electrons.

  • photochemical reaction

    A reaction that is performed with photochemical excitation (usually UV light).

  • pure substance

    Matter that has a fixed composition and distinct properties. (Section 1.2)

  • solution alloy

    A homogeneous alloy, where two or more elements are distributed randomly and uniformly throughout the solid. (Section 12.3)

  • Tertiary (3°) amine

    An amine in which nitrogen is bonded to three carbons

  • Zwitterion

    An internal salt of an amino acid; the carboxylate is negatively charged, and the ammonium group is positively charged