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Solutions for Chapter 20: More About Amines Reactions of Heterocyclic Compounds

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: More About Amines Reactions of Heterocyclic Compounds

Solutions for Chapter 20
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Textbook: Organic Chemistry
Edition: 7
Author: Paula Yurkanis Bruice
ISBN: 9780321803221

Since 23 problems in chapter 20: More About Amines Reactions of Heterocyclic Compounds have been answered, more than 38691 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Chapter 20: More About Amines Reactions of Heterocyclic Compounds includes 23 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Absorbance (A)

    A quantitative measure of the extent to which a compound absorbs radiation of a particular wavelength. A 5 log (I0/I ) where I0 is the incident radiation and I is the transmitted radiation

  • acid-dissociation constant (Ka)

    An equilibrium constant that expresses the extent to which an acid transfers a proton to solvent water. (Section 16.6)

  • Alditol

    The product formed when the C"O group of a monosaccharide is reduced to a CHOH group.

  • aldol condensation

    An aldol addition followed by dehydration to give an a,bunsaturated ketone or aldehyde.

  • amines.

    Organic bases that have the functional group —NR2, where R may be H, an alkyl group, or an aromatic group. (24.4)

  • b-Pleated sheet

    A type of polypeptide secondary structure in which sections of polypeptide chains are aligned parallel or antiparallel to one another.

  • Base peak

    The peak caused by the most abundant ion in a mass spectrum; the most intense peak. It is assigned an arbitrary intensity of 100

  • Brønsted-Lowry acid

    A proton donor

  • E

    For alkenes, a stereodescriptorthat indicates that the two priority groups are on opposite sides of the p bond.

  • enzymes

    Important biological molecules that catalyze virtually all cellular processes.

  • free radical

    A substance with one or more unpaired electrons. (Section 21.9)

  • natural gas

    A naturally occurring mixture of gaseous hydrocarbon compounds composed of hydrogen and carbon. (Section 5.8)

  • polarizability

    The ease with which the electron cloud of an atom or a molecule is distorted by an outside influence, thereby inducing a dipole moment. (Section 11.2)

  • Polyamide

    A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.

  • polysaccharides

    Polymers made up of repeating monosaccharide units linked together by glycoside bonds.

  • Reaction mechanism

    A step-by-step description of how a chemical reaction occurs.

  • secondary structure

    The threedimensional conformations of localized regions of a protein, including helices and b-pleated sheets.

  • substitution reactions

    Reactions in which one group is replaced by another group.

  • Sulfi de

    The sulfur analog of an ether; a molecule containing a sulfur atom bonded to two carbon atoms. Sulfi des are also called thioethers

  • 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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