Solutions for Chapter 13: Nuclear Magnetic Resonance Spectroscopy

Organic Chemistry | 9th Edition | ISBN: 9780321971371 | Authors: Leroy G. Wade, Jan W. Simek

Full solutions for Organic Chemistry | 9th Edition

ISBN: 9780321971371

Organic Chemistry | 9th Edition | ISBN: 9780321971371 | Authors: Leroy G. Wade, Jan W. Simek

Solutions for Chapter 13: Nuclear Magnetic Resonance Spectroscopy

Solutions for Chapter 13
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Textbook: Organic Chemistry
Edition: 9
Author: Leroy G. Wade, Jan W. Simek
ISBN: 9780321971371

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 9. Since 63 problems in chapter 13: Nuclear Magnetic Resonance Spectroscopy have been answered, more than 12515 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 13: Nuclear Magnetic Resonance Spectroscopy includes 63 full step-by-step solutions. Organic Chemistry was written by Patricia and is associated to the ISBN: 9780321971371.

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.

  • Androgen

    A steroid hormone, such as testosterone, that mediates the development of sexual characteristics of males.

  • C terminus

    For a peptide chain,the end that contains the COOH group. carbinolamine (Sect. 20.6): A compound containing a hydroxyl group (OH) and a nitrogen atom, both of which are connceted to the same carbon atom.

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • degree of substitution

    For alkenes, a classification method that refers to the number of alkyl groups connected to the double bond.

  • diastereomers

    Stereoisomers that are not mirror images of one another.

  • Diaxial interactions

    Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring

  • diene

    A compound containing two carbon-carbon p bonds.

  • Disaccharide

    A carbohydrate containing two monosaccharide units joined by a glycosidic bond.

  • fission

    The splitting of a large nucleus into two smaller ones. (Section 21.6)

  • Haloform

    A compound of the type CHX3 where X is a halogen.

  • halogenation

    A reaction that involves the addition of X2 (either Br2 or Cl2) across an alkene.

  • 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

  • hydrophobic

    A nonpolar group that does not have favorable interactions with water.

  • ideal-gas equation

    An equation of state for gases that embodies Boyle’s law, Charles’s law, and Avogadro’s hypothesis in the form PV = nRT. (Section 10.4)

  • isoprene

    2-Methyl-1,3-butadiene.

  • Meso compound

    An achiral compound possessing two or more chiral centers that also has chiral isomers

  • Pro-S-hydrogen

    Replacing this hydrogen by deuterium gives a chiral center with an S confi guration

  • Schiff base

    An alternative name for an imine

  • thermosetting resins

    Highly crosslinked polymers that are generally very hard and insoluble.

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