Solutions for Chapter 23.6: Cyclic Forms of Carbohydrates: Furanose Forms

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 23.6: Cyclic Forms of Carbohydrates: Furanose Forms

Solutions for Chapter 23.6
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This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Chapter 23.6: Cyclic Forms of Carbohydrates: Furanose Forms includes 2 full step-by-step solutions. Since 2 problems in chapter 23.6: Cyclic Forms of Carbohydrates: Furanose Forms have been answered, more than 10702 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • 1,4-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 C4 position.

  • 1,4-adduct

    The product obtained from 1,4-addition across a conjugated p system.

  • adsorption

    The binding of molecules to a surface. (Section 14.7)

  • alkyl amines

    A format for naming amines containing simple alkyl groups.

  • aromatic hydrocarbon.

    A hydrocarbon that contains one or more benzene rings. (24.1)

  • Charles’ and Gay-Lussac’s law.

    See Charles’ law.

  • core electrons.

    All nonvalence electrons in an atom. (8.2)

  • covalent compounds.

    Compounds containing only covalent bonds. (9.4)

  • dispersion forces

    Intermolecular forces resulting from attractions between induced dipoles. Also called London dispersion forces. (Section 11.2)

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • gauche interaction

    The steric interaction that results when two groups in a Newman projection are separated by a dihedral angle of 60°.

  • homogeneous catalysts

    A catalyst that dissolves in the reaction medium.

  • ion

    Electrically charged atom or group of atoms (polyatomic ion); ions can be positively or negatively charged, depending on whether electrons are lost (positive) or gained (negative) by the atoms. (Section 2.7)

  • ketone

    A compound in which the carbonyl group 1C “O2 occurs at the interior of a carbon chain and is therefore flanked by carbon atoms. (Section 24.4)

  • Levorotatory

    Refers to a substance that rotates the plane of polarized light to the left.

  • localized lone pair

    A lone pair thatis not participating in resonance.

  • polarizability

    The ability of an atom or molecule to distribute its electron density unevenly in response to external influences.

  • polarization

    For light, the orientation of the electric field.

  • Reductive elimination

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

  • solvent

    The dissolving medium of a solution; it is normally the component of a solution present in the greater amount. (Section 4.1)

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