Solutions for Chapter 15.8: Esterification

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 15.8: Esterification

Solutions for Chapter 15.8
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Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Chapter 15.8: Esterification includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Since 2 problems in chapter 15.8: Esterification have been answered, more than 12742 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • amphoteric

    Compounds that will react with either acids or bases. Amino acids are amphoteric.

  • band structure

    The electronic structure of a solid, defining the allowed ranges of energy for electrons in a solid. (Section 12.7)

  • carbohydrates

    Polyhydroxy aldehydes or ketones with molecular formula CxH2xOx.

  • crystal field splitting (D).

    The energy difference between two sets of d orbitals in a metal atom when ligands are present. (23.5)

  • electrophile

    A compound containing an electron-deficient atom that is capable of accepting a pair of electrons.

  • electrophoresis

    A technique for separating amino acids from each other based on a difference in pI values.

  • Fourier-transform NMR (FT-NMR)

    In nuclear magnetic resonance (NMR) spectroscopy, a technique in which the sample is irradiated with a short pulse that covers the entire range of relevant rf frequencies.

  • frequency

    The number of times per second that one complete wavelength passes a given point. (Section 6.1)

  • Haworth projection

    For substituted cycloalkanes, a drawing style used to clearly identify which groups are above the ring and which groups are below the ring. (See also Sect. 4.14.)

  • Hund’s rule

    When considering electrons in atomic orbitals, a rule that states that one electron is placed in each degenerate orbital first, before electrons are paired up.

  • labile

    Protons that are exchanged at a rapid rate.

  • lithium dialkyl cuprate

    A nucleophilic compound with the general structureR2CuLi.

  • Molecular ion (M1)

    The radical cation formed by removal of a single electron from a parent molecule in a mass spectrometer.

  • oxonium ion

    An intermediate with a positively charged oxygen atom.

  • polyether

    A compound containing several ether groups.

  • protein

    A biopolymer formed from amino acids. (Section 24.7)

  • quantum

    The smallest increment of radiant energy that may be absorbed or emitted; the magnitude of radiant energy is hn. (Section 6.2)

  • reducing sugar

    A carbohydrate that is oxidized upon treatment with Tollens’ reagent, Fehling’s reagent, or Benedict’s reagent.

  • replacement test

    A test for determining the relationship between two protons. The compound is drawn two times, each time replacing one of the protons with deuterium. If the two compounds are identical, the protons are homotopic. If the two compounds are enantiomers, the protons are enantiotopic. If the two compounds are diastereomers, the protons are diastereotopic.

  • stereoselective

    A reaction in which one substrate produces two stereoisomers in unequal amounts.

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