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Solutions for Chapter 20.4: acidbase properties of carboxylic acids

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 20.4: acidbase properties of carboxylic acids

Solutions for Chapter 20.4
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Chapter 20.4: acidbase properties of carboxylic acids includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Since 2 problems in chapter 20.4: acidbase properties of carboxylic acids have been answered, more than 39909 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkane

    A hydrocarbon that lacks p bonds.

  • aromatic hydrocarbons

    Hydrocarbon compounds that contain a planar, cyclic arrangement of carbon atoms linked by both s and delocalized p bonds. (Section 24.2)

  • Carbanion

    An ion in which carbon has an unshared pair of electrons and bears a negative charge.

  • diffusion.

    The gradual mixing of molecules of one gas with the molecules of another by virtue of their kinetic properties. (5.7)

  • Disproportionation

    A termination process that involves the abstraction of a hydrogen atom from the beta position of the propagating radical of one chain by the radical endgroup of another chain.

  • Electrophoresis

    The process of separating compounds on the basis of their electric charge

  • Enantiomeric excess (ee)

    The difference between the percentage of two enantiomers in a mixture

  • Endothermic reaction

    A reaction in which the enthalpy of the products is higher than the enthalpy of the reactants; a reaction in which heat is absorbed

  • Haloalkane (alkyl halide)

    A compound containing a halogen atom covalently bonded to an sp3 -hybridized carbon atom. Given the symbol R!X.

  • hole

    A vacancy in the valence band of a semiconductor, created by doping. (Section 12.7)

  • Nucleoside

    A building block of nucleic acids, consisting of d-ribose or 2-deoxy-d-ribose bonded to a heterocyclic aromatic amine base by a b-N-glycosidic bond

  • optically pure

    A solution containing just one enantiomer, but not its mirror image.

  • peptidases

    A variety of enzymes that selectively hydrolyze specific peptide bonds.

  • positron emission

    A nuclear decay process where a positron, a particle with the same mass as an electron but with a positive charge, symbol 0+1e, or b+ is emitted from the nucleus. (Section 21.1)

  • Pyranose

    A six-membered cyclic form of a monosaccharide.

  • Sanger dideoxy method

    A method developed by Frederick Sanger for sequencing DNA molecules

  • Sharpless asymmetric epoxidation

    A reaction that converts an alkene into an epoxide via a stereospecific pathway.

  • terpenes

    A diverse class of naturally occurring compounds that can be thought of as being assembled from isoprene units, each of which contains five carbon atoms.

  • thermodynamics

    The study of how energy is distributed under the influence of entropy. For chemists, the thermodynamics of a reaction specifically refers to the study of the relative energy levels of reactants and products.

  • valence bond theory

    A theory that treats a bond as the sharing of electrons that are associated with individual atoms, rather than being associated with the entire molecule.

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