Solutions for Chapter 13.12: 1 H NMR Spectra of Alcohols

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 13.12: 1 H NMR Spectra of Alcohols

Solutions for Chapter 13.12
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 13.12: 1 H NMR Spectra of Alcohols includes 1 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 1 problems in chapter 13.12: 1 H NMR Spectra of Alcohols have been answered, more than 16274 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-Shift

    A type of rearrangement in which an atom or group of atoms with its bonding electrons moves from one atom to an adjacent electron-defi cient atom.

  • activate

    For a substituted aromatic ring, the effect of an electron-donating substituent that increases the rate of electrophilic aromatic substitution.

  • beta (b) pleated sheet

    For proteins, a feature of secondary structure that forms when two or more protein chains line up side-by-side.

  • cathode.

    The electrode at which reduction occurs. (18.2)

  • cation.

    An ion with a net positive charge. (2.5)

  • Conjugate acid

    The species formed when a base accepts a proton from an acid

  • conjugate acid-base pair.

    An acid and its conjugate base or a base and its conjugate acid. (15.1)

  • Downfield

    A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.

  • energy

    The capacity to do work or to transfer heat. (Section 5.1)

  • fossil fuels

    Coal, oil, and natural gas, which are presently our major sources of energy. (Section 5.8)

  • Hofmann rule

    Any b-elimination that occurs preferentially to give the less substituted alkene as the major product.

  • homopolymer

    A polymer constructed from a single type of monomer.

  • Homotopic groups

    Atoms or groups on an atom that give an achiral molecule when one of the groups is replaced by another group. The hydrogens of the CH2 group of propane, for example, are homotopic. Replacing either one of them with deuterium gives 2-deuteropropane, which is achiral. Homotopic groups have identical chemical shifts under all conditions

  • hydroperoxide

    A compound with the structure R!O!O!H.

  • metallurgy

    The science of extracting metals from their natural sources by a combination of chemical and physical processes. It is also concerned with the properties and structures of metals and alloys. (Section 23.1)

  • 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

  • octet rule

    The observation that second-row elements (C, N, O, and F) will form the necessary number of bonds so as to achieve a full valence shell (eight electrons).

  • regiochemistry

    A term describing a consideration that must be taken into account for a reaction in which two or more constitutional isomers can be formed.

  • Resolution

    Separation of a racemic mixture into its enantiomers; in mass spectrometry, a measure of how well a mass spectrometer separates ions of different mass.

  • ribonucleic acid (RNA)

    A polynucleotide in which ribose is the sugar component. (Section 24.10)

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