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Solutions for Chapter 24.5: base-Catalyzed isomerization of aldoses and Ketoses

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 24.5: base-Catalyzed isomerization of aldoses and Ketoses

Solutions for Chapter 24.5
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Since 1 problems in chapter 24.5: base-Catalyzed isomerization of aldoses and Ketoses have been answered, more than 36477 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 24.5: base-Catalyzed isomerization of aldoses and Ketoses includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-addition

    A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C2 position.

  • [4+2]-cycloaddition

    A pericyclic reaction, also called a Diels-Alder reaction, that takes place between two different p systems, one of which is associated with four atoms while the other is associated with two atoms.

  • addition polymers

    Polymers that are formed via cationic addition, anionic addition, or free-radical addition.

  • alkene

    A compound that possesses a carbon-carbon double bond.

  • asymmetric stretching

    In IR spectroscopy, when two bonds are stretching out of phase with each other.

  • chain-growth polymer

    A polymer that is formed under conditions in which the monomers do not react directly with each other, but rather, each monomer is added to the growing chain, one at a time.

  • complete ionic equation

    A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)

  • cycloaddition reactions

    Reactions in which two p systems are joined together in a way that forms a ring. In the process, two p bonds are converted into two s bonds.

  • Epoxide

    A cyclic ether in which oxygen is one atom of a three-membered ring

  • Hell-Volhard-Zelinsky reaction

    A reaction in which a carboxylic acid undergoes a-halogenation when treated with bromine in the presence of PBr3.

  • homotopic

    Protons that are interchangeable by rotational symmetry.

  • Hybrid orbital

    An orbital formed by the combination of two or more atomic orbitals.

  • intensive property

    A property that is independent of the amount of material considered, for example, density. (Section 1.3)

  • isoprene

    2-Methyl-1,3-butadiene.

  • meso compound

    A compound that possesses chirality centers and an internal plane of symmetry.

  • molecular geometry

    The arrangement in space of the atoms of a molecule. (Section 9.2)

  • periplanar

    A conformation in which a hydrogen atom and a leaving group are approximately coplanar.

  • physiological pH

    The pH of blood (approximately 7.3).

  • Reaction mechanism

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

  • Resolution

    Separation of a racemic mixture into its enantiomers; in mass spectrometry, a measure of how well a mass spectrometer separates ions of different mass.

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