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Solutions for Chapter 26: Nucleosides, Nucleotides, and Nucleic Acids

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 26: Nucleosides, Nucleotides, and Nucleic Acids

Solutions for Chapter 26
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Textbook: Organic Chemistry,
Edition: 9
Author: Francis A Carey Dr., Robert M. Giuliano
ISBN: 9780073402741

This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. Chapter 26: Nucleosides, Nucleotides, and Nucleic Acids includes 20 full step-by-step solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. This expansive textbook survival guide covers the following chapters and their solutions. Since 20 problems in chapter 26: Nucleosides, Nucleotides, and Nucleic Acids have been answered, more than 36402 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Aceto group

    A CH3CO! group; also called an acetyl group

  • Amino acid

    A compound that contains both an amino group and a carboxyl group

  • band structure

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

  • Base peak

    The peak caused by the most abundant ion in a mass spectrum; the most intense peak. It is assigned an arbitrary intensity of 100

  • combustion reaction.

    A reaction in which a substance reacts with oxygen, usually with the release of heat and light, to produce a flame. (4.4)

  • crystalline solid.

    A solid that possesses rigid and long-range order; its atoms, molecules, or ions occupy specific positions. (11.4)

  • diatomic molecule

    A molecule composed of only two atoms. (Section 2.6)

  • diffusion

    The spreading of one substance through a space occupied by one or more other substances. (Section 10.8)

  • disulfide bridge

    The group that is formed when two cysteine residues of a polypeptide or protein are joined together.

  • Ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • Fourier transform NMR (FT-NMR)

    The modern NMR method that is based on a constant magnetic fi eld, a short pulse of electromagnetic radiation, and a mathematical Fourier transform to produce the spectrum

  • Hydrophobic

    From the Greek, meaning water-fearing.

  • Inductive effect

    The polarization of the electron density of a covalent bond caused by the electronegativity of a nearby atom.

  • Nuclear magnetic resonance (NMR) spectroscopy

    A spectroscopic technique that gives information about the number and types of atoms in a molecule, for example, hydrogens (1 H!NMR) and carbons (13C!NMR)

  • Pauli exclusion principle

    No more than two electrons may be present in an orbital. If two electrons are present, their spins must be paired

  • pyrometallurgy

    A process in which heat converts a mineral in an ore from one chemical form to another and eventually to the free metal. (Section 23.2)

  • Reduction

    The gain of electrons. Alternatively, either the gain of hydrogen, loss of oxygen, or both

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

  • Valence shell

    The outermost occupied electron shell of an atom.

  • Z (Section 5.2C)

    From the German, zusammen, meaning opposite. Specifi es that groups of higher priority on the carbons of a double bond are on the same side

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