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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 0 429 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 17630 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
  • Alkaloid

    A basic nitrogen-containing compound of plant origin, many of which are physiologically active when administered to humans.

  • alkynes

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

  • anomeric carbon

    The C1 position of the cyclic hemiacetal of an aldose or the C2 position of the cyclic hemiacetal of a ketose.

  • Arene

    A term used to classify benzene and its derivatives.

  • Atropisomers

    Enantiomers that lack a chiral center and differ because of hindered rotation.

  • Brønsted-Lowry acid

    A compound that can serve as a proton donor.

  • capillary action

    The process by which a liquid rises in a tube because of a combination of adhesion to the walls of the tube and cohesion between liquid particles. (Section 11.3)

  • chemical changes

    Processes in which one or more substances are converted into other substances; also called chemical reactions. (Section 1.3)

  • complex lipid

    A lipid that readily undergoes hydrolysis in aqueous acid or base to produce smaller fragments.

  • conjugate acid-base pair.

    An acid and its conjugate base or a base and its conjugate acid. (15.1)

  • conjugate base

    A substance formed by the loss of a proton from a Brønsted–Lowry acid. (Section 16.2)

  • Diol

    A compound containing two hydroxyl groups

  • eicosanoids

    A class of lipids which includes leukotrienes, prostaglandins, thromboxanes, and prostacyclins.

  • electron configuration

    The arrangement of electrons in the orbitals of an atom or molecule (Section 6.8)

  • electronic structure

    The arrangement of electrons in an atom or molecule. (Chapter 6:Introduction)

  • frequency factor (A)

    A term in the Arrhenius equation that is related to the frequency of collision and the probability that the collisions are favorably oriented for reaction. (Section 14.5)

  • instantaneous rate

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

  • melt transition temperature (Tm)

    The temperature at which the crystallineregions of a polymer become amorphous.

  • Mutarotation

    The change in specifi c rotation that occurs when an a or b hemiacetal form of a carbohydrate in aqueous solution is converted to an equilibrium mixture of the two forms.

  • substitution reactions

    Reactions in which one group is replaced by another group.

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