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Solutions for Chapter 25.2: pHOSpHORIC ACID DERIVATIVES

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 25.2: pHOSpHORIC ACID DERIVATIVES

This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 25.2: pHOSpHORIC ACID DERIVATIVES includes 3 full step-by-step solutions. Since 3 problems in chapter 25.2: pHOSpHORIC ACID DERIVATIVES have been answered, more than 40146 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

Key Chemistry Terms and definitions covered in this textbook
  • absorbance

    In UV-Vis spectroscopy, the value log (I0/I) where I0 is the intensity of the reference beam and I is the intensity of the sample beam.

  • Alditol

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

  • antioxidants

    Radical scavengers that prevent autooxidation by preventing radical chain reactions from beginning.

  • Bile acid

    A cholesterol-derived detergent molecule, such as cholic acid, which is secreted by the gallbladder into the intestine to assist in the absorption of dietary lipids.

  • biodegradable polymers

    Polymers that can be broken down by enzymes produced by soil microorganisms.

  • bond polarity

    A measure of the degree to which the electrons are shared unequally between two atoms in a chemical bond. (Section 8.4)

  • chlorofluorocarbons (CFCs)

    Compound containing only carbon, chlorine, and fluorine.

  • 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.

  • dihedral angle

    The angle by which two groups are separated in a Newman projection.

  • directed aldol addition

    A techniquefor performing a crossed aldol addition thatproduces one major product.

  • 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.

  • 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

  • first-order reaction

    A reaction in which the reaction rate is proportional to the concentration of a single reactant, raised to the first power. (Section 14.4)

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • Nonpolar covalent bond

    A covalent bond between atoms whose difference in electronegativity is less than approximately 0.5.

  • plane-polarized light

    Light for which all photons have the same polarization, generally formed by passing light through a polarizing filter.

  • saturated hydrocarbon

    A hydrocarbon that contains no p bonds.

  • Tertiary structure of proteins

    The three-dimensional arrangement in space of all atoms in a single polypeptide chain.

  • Torsional strain

    Strain that arises when nonbonded atoms separated by three bonds are forced from a staggered conformation to an eclipsed conformation. Torsional strain is also called eclipsed-interaction strain.

  • Valence Bond Theory

    A model of bonding that places electron pairs between adjacent atoms to create bonds.