×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide

Solutions for Chapter 23.14: Glycosides: The Fischer Glycosidation

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 23.14: Glycosides: The Fischer Glycosidation

This expansive textbook survival guide covers the following chapters and their solutions. Since 4 problems in chapter 23.14: Glycosides: The Fischer Glycosidation have been answered, more than 36458 students have viewed full step-by-step solutions from this chapter. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Chapter 23.14: Glycosides: The Fischer Glycosidation includes 4 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9.

Key Chemistry Terms and definitions covered in this textbook
  • acid ionization constant (Ka).

    The equilibrium constant for the acid ionization. (15.5)

  • atmospheric pressure.

    The pressure exerted by Earth’s atmosphere. (5.2)

  • chemical reactions

    Processes in which one or more substances are converted into other substances; also called chemical changes. (Section 1.3)

  • Confi guration

    Refers to the arrangement of atoms about a stereocenter

  • desalination

    The removal of salts from seawater, brine, or brackish water to make it fit for human consumption. (Section 18.4)

  • Dipole-dipole interaction

    The attraction between the positive end of one dipole and the negative end of another.

  • doping

    Incorporation of a hetero atom into a solid to change its electrical properties. For example, incorporation of P into Si. (Section 12.7)

  • Enamine

    An unsaturated compound derived by the reaction of an aldehyde or ketone and a secondary amine followed by loss of H2O; R2C"CR!NR2

  • ether

    A compound in which two hydrocarbon groups are bonded to one oxygen. (Section 24.4)

  • flagpole interactions

    For cyclohexane, the steric interactions that occur between the flagpole hydrogen atoms in a boat conformation.

  • hydroboration-oxidation

    A twostep process that achieves an anti-Markovnikov addition of a proton and a hydroxyl group (OH) across an alkene.

  • ionic reaction

    A reaction that involves the participation of ions as reactants, intermediates, or products.

  • kinetic control

    A reaction for which the product distribution is determined by the relative rates at which the products are formed.

  • percent ionization

    The percent of a substance that undergoes ionization on dissolution in water. The term applies to solutions of weak acids and bases. (Section 16.6)

  • phase change

    The conversion of a substance from one state of matter to another. The phase changes we consider are melting and freezing 1solid ? liquid2, sublimation and deposition, and vaporization and condensation 1liquid ? gas2. (Section 11.4)

  • phenoxide

    The conjugate base of phenol or a substituted phenol.

  • Plane of symmetry

    An imaginary plane passing through an object dividing it so that one half is the mirror image of the other half

  • sulfonate ions

    Common leaving groups. Examples include tosylate, mesylate, and triflate ions.

  • Vicinal coupling

    a !CH"CH2 group

  • weak activators

    Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.

×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide
×
Reset your password