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Solutions for Chapter 20.1: MORE ABOUT AMINE NOMENCLATURE

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

Solutions for Chapter 20.1: MORE ABOUT AMINE NOMENCLATURE

Solutions for Chapter 20.1
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Organic Chemistry was written by and is associated to the ISBN: 9780321803221. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 1 problems in chapter 20.1: MORE ABOUT AMINE NOMENCLATURE have been answered, more than 35758 students have viewed full step-by-step solutions from this chapter. Chapter 20.1: MORE ABOUT AMINE NOMENCLATURE includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • amine

    A compound that has the general formula R3N, where R may be H or a hydrocarbon group. (Section 16.7)

  • anion.

    An ion with a net negative charge. (2.5)

  • Avogadro‚Äôs law

    A statement that the volume of a gas maintained at constant temperature and pressure is directly proportional to the number of moles of the gas. (Section 10.3)

  • cephalins

    Phosphoglycerides that contain ethanolamine.

  • chlor-alkali process.

    The production of chlorine gas by the electrolysis of aqueous NaCl solution. (22.6)

  • Confi guration

    Refers to the arrangement of atoms about a stereocenter

  • constructive interference

    When two waves interact with each other in a way that produces a wave with a larger amplitude.

  • Double helix

    A type of secondary structure of DNA molecules in which two anti parallel polynucleotide strands are coiled in a right-handed manner about the same axis

  • electrocyclic reaction

    A pericyclic process in which a conjugated polyene undergoes cyclization. In the process, one p bond is converted into a s bond, while the remaining p bonds all change their location. The newly formed s bond joins the ends of the original p system,thereby creating a ring.

  • Hammond postulate

    In an exothermic process the transition state is closer in energy to the reactants than to the products, and therefore the structure of the transition state more closely resembles the reactants. In contrast, the transition state in an endothermic process is closer in energy to the products, and therefore the transition state more closely resembles the products.

  • heterogeneous catalyst

    A catalyst that does not dissolve in the reaction medium.

  • hydrophilic

    Water attracting. The term is often used to describe a type of colloid. (Section 13.6)

  • mass spectrum

    In mass spectrometry,a plot that shows the relative abundance ofeach cation that was detected.

  • Molar absorptivity (e)

    The absorbance of a 1 M solution of a compound.

  • overall reaction order

    The sum of the reaction orders of all the reactants appearing in the rate expression when the rate can be expressed as rate = k3A4a 3B4b... . (Section 14.3)

  • Reducing sugar

    A carbohydrate that reacts with an oxidizing agent to form an aldonic acid. In this reaction, the carbohydrate reduces the oxidizing agent.

  • Reductive elimination

    Elimination of two substituents at a metal center, causing the oxidation state of the metal to decrease by two.

  • sigma (s) bond

    A bond that is characterized by circular symmetry with respect to the bond axis.

  • Tripeptide

    A molecule containing three amino acid units, each joined to the next by a peptide bond

  • Wittig reaction

    A reaction that converts an aldehyde or ketone into an alkene, with the introduction of one or more carbon atoms.

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