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> > Organic Chemistry, - Standalone Book 2

Organic Chemistry, - Standalone Book 2nd Edition - Solutions by Chapter

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition

ISBN: 9781118452288

Organic Chemistry,  - Standalone Book | 2nd Edition | ISBN: 9781118452288 | Authors: David R. Klein

Organic Chemistry, - Standalone Book | 2nd Edition - Solutions by Chapter

This textbook survival guide was created for the textbook: Organic Chemistry, - Standalone Book, edition: 2. Organic Chemistry, - Standalone Book was written by Patricia and is associated to the ISBN: 9781118452288. Since problems from 27 chapters in Organic Chemistry, - Standalone Book have been answered, more than 13058 students have viewed full step-by-step answer. The full step-by-step solution to problem in Organic Chemistry, - Standalone Book were answered by Patricia, our top Chemistry solution expert on 01/19/18, 05:12PM. This expansive textbook survival guide covers the following chapters: 27.

Key Chemistry Terms and definitions covered in this textbook
  • activate

    For a substituted aromatic ring, the effect of an electron-donating substituent that increases the rate of electrophilic aromatic substitution.

  • aldose

    A carbohydrate that contains an aldehyde group.

  • alpha (a) rays.

    Helium ions with a positive charge of 12. (2.2)

  • Anion

    An atom or group of atoms bearing a negative charge.

  • Basicity

    An equilibrium property measured by the position of equilibrium in an acid-base reaction, as, for example, the acid-base reaction between ammonia and water.

  • broadband decoupling

    In 13C NMR spectroscopy, a technique in which all 13C!1H splitting is suppressed with the use of two rf transmitters.

  • Correlation tables

    Tables of data on absorption patterns of functional groups.

  • covalent compounds.

    Compounds containing only covalent bonds. (9.4)

  • dilution.

    A procedure for preparing a less concentrated solution from a more concentrated solution. (4.5)

  • equilibrium-constant expression

    The expression that describes the relationship among the concentrations (or partial pressures) of the substances present in a system at equilibrium. The numerator is obtained by multiplying the concentrations of the substances on the product side of the equation, each raised to a power equal to its coefficient in the chemical equation. The denominator similarly contains the concentrations of the substances on the reactant side of the equation. (Section 15.2)

  • Geminal coupling

    Spin-spin coupling that occurs between nonequivalent H atoms bonded to the same C atom. The H atoms are generally nonequivalent owing to restricted bond rotation in the molecule

  • Heterolytic bond cleavage

    Cleavage of a bond so that one fragment retains both electrons and the other retains none.

  • homotopic

    Protons that are interchangeable by rotational symmetry.

  • internal alkyne

    A compound with the structure R!C#C!R, where each R group is not a hydrogen atom.

  • nonelectrolyte

    A substance that does not ionize in water and consequently gives a nonconducting solution. (Section 4.1)

  • phenyl group

    A C6H5 group.

  • sulfonate ions

    Common leaving groups. Examples include tosylate, mesylate, and triflate ions.

  • van der Waals forces

    A group of intermolecular attractive forces including dipole-dipole, dipole-induced dipole, and induced dipole-induced dipole (dispersion) forces

  • Wohl degradation

    A process that involves the removal of a carbon atom from an aldose. The aldehyde group is first converted to a cyanohydrin, followed by loss of HCN in the presence of a base.

  • Ylide

    A neutral molecule with positive and negative charges on adjacent atoms

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