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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 0 359 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 30233 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
  • activation energy (Ea).

    The minimum amount of energy required to initiate a chemical reaction. (13.4)

  • anion.

    An ion with a net negative charge. (2.5)

  • antibonding molecular orbital

    A molecular orbital in which electron density is concentrated outside the region between the two nuclei of bonded atoms. Such orbitals, designated as s* or p*, are less stable (of higher energy) than bonding molecular orbitals. (Section 9.7)

  • bond dipole

    The dipole moment that is due to unequal electron sharing between two atoms in a covalent bond. (Section 9.3)

  • bonding atomic radius

    The radius of an atom as defined by the distances separating it from other atoms to which it is chemically bonded. (Section 7.3)

  • common-ion effect

    A shift of an equilibrium induced by an ion common to the equilibrium. For example, added Na2SO4 decreases the solubility of the slightly soluble salt BaSO4, or added NaF decreases the percent ionization of HF. (Section 17.1)

  • conservation of orbital symmetry

    During a reaction, the requirement that the phases of the frontier MOs must be aligned.

  • Hofmann elimination

    When treated with a strong base, a quaternary ammonium halide undergoes b-elimination by an E2 mechanism to give the less-substituted alkene as the major product

  • l amino acid

    Amino acids with Fischer projections that resemble the Fischer projections of l sugars.

  • lanthanide (rare earth) element

    Element in which the 4f subshell is only partially occupied. (Sections 6.8 and 6.9)

  • miscible liquids

    Liquids that mix in all proportions. (Section 13.3)

  • Oil

    When used in the context of fats and oils, a mixture of triglycerides that is liquid at room temperature

  • Optically active

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

  • Ostwald process

    An industrial process used to make nitric acid from ammonia. The NH3 is catalytically oxidized by O2 to form NO; NO in air is oxidized to NO2; HNO3 is formed in a disproportionation reaction when NO2 dissolves in water. (Section 22.7)

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • rad

    A measure of the energy absorbed from radiation by tissue or other biological material; 1 rad = transfer of 1 * 10-2 J of energy per kilogram of material. (Section 21.9)

  • renewable energy sources

    Energy such as solar energy, wind energy, and hydroelectric energy derived from essentially inexhaustible sources. (Section 5.8)

  • replacement test

    A test for determining the relationship between two protons. The compound is drawn two times, each time replacing one of the protons with deuterium. If the two compounds are identical, the protons are homotopic. If the two compounds are enantiomers, the protons are enantiotopic. If the two compounds are diastereomers, the protons are diastereotopic.

  • resolution

    The separation of enantiomers from a mixture containing both enantiomers.

  • Vibrational infrared region

    A common type of spin-spin coupling involving the H atoms on two C atoms that are bonded to each other.

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