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Organic Chemistry 7th Edition - Solutions by Chapter

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Organic Chemistry | 7th Edition - Solutions by Chapter

Solutions by Chapter
4 5 0 277 Reviews
Textbook: Organic Chemistry
Edition: 7
Author: Paula Yurkanis Bruice
ISBN: 9780321803221

Organic Chemistry was written by Patricia and is associated to the ISBN: 9780321803221. This expansive textbook survival guide covers the following chapters: 354. Since problems from 354 chapters in Organic Chemistry have been answered, more than 7594 students have viewed full step-by-step answer. The full step-by-step solution to problem in Organic Chemistry were answered by Patricia, our top Chemistry solution expert on 03/16/18, 03:38PM. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • Azeotrope

    A liquid mixture of constant composition with a boiling point that is different from that of any of its components.

  • catalytic hydrogenation

    A reaction that involves the addition of molecular hydrogen (H2) across a double bond in the presence of a metal catalyst.

  • colligative property

    A property of a solvent (vapor-pressure lowering, freezing-point lowering, boiling-point elevation, osmotic pressure) that depends on the total concentration of solute particles present. (Section 13.5)

  • Dehydration

    Elimination of water.

  • electrolytic cell

    A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)

  • Electronegativity

    A measure of the force of an atom’s attraction for electrons

  • hydrophilic

    A polar group that has favorable interactions with water.

  • imine

    A compound containing a CRN bond.

  • internal energy

    The total energy possessed by a system. When a system undergoes a change, the change in internal energy, ?E, is defined as the heat, q, added to the system, plus the work, w, done on the system by its surroundings: ?E = q + w. (Section 5.2)

  • Kinetic control

    Experimental conditions under which the composition of the product mixture is determined by the relative rates of formation of each product.

  • kinetics

    A term that refers to the rate of a reaction.

  • leveling effect

    An effect thatprevents the use of bases stronger than hydroxidewhen the solvent is water.

  • Meisenheimer complex

    Theresonance-stabilized intermediate of a nucleophilicaromatic substitution reaction.

  • Sandmeyer reactions

    Reactions that utilize copper salts (CuX) and enable the installation of a halogen or a cyano group on an aromatic ring.

  • Sanger dideoxy method

    A method developed by Frederick Sanger for sequencing DNA molecules

  • Schiemann reaction

    The conversion of an aryl diazonium salt into fluorobenzene upon treatment with fluoroboric acid (HBF4).

  • shielded

    In NMR spectroscopy,protons or carbon atoms whose surrounding electron density is rich.

  • sulfone

    A compound that contains a sulfur atom that has double bonds with two oxygen atoms and is flanked on both sides by R groups.

  • termination

    In radical reactions, a step in which two radicals are joined to give a compound with no unshared electrons.

  • Transition state

    The highest energy point on a reaction coordinate diagram. The chemical structure at this point is commonly called an activated complex.

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