Solutions for Chapter 26.2: Nucleosides

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 26.2: Nucleosides

Solutions for Chapter 26.2
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Since 1 problems in chapter 26.2: Nucleosides have been answered, more than 16274 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 26.2: Nucleosides includes 1 full step-by-step solutions. Organic Chemistry, was written by and is associated to the ISBN: 9780073402741.

Key Chemistry Terms and definitions covered in this textbook
  • antiaromatic

    Instability that arises when a planar ring of continuously overlapping p orbitals contains 4n p electrons.

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • catalyst

    A substance that changes the speed of a chemical reaction without itself undergoing a permanent chemical change in the process. (Section 14.7)

  • chain-growth polymer

    A polymer that is formed under conditions in which the monomers do not react directly with each other, but rather, each monomer is added to the growing chain, one at a time.

  • copolymer

    A complex polymer resulting from the polymerization of two or more chemically different monomers. (Section 12.8)

  • corrosion

    The process by which a metal is oxidized by substances in its environment. (Section 20.8)

  • dispersion forces

    Intermolecular forces resulting from attractions between induced dipoles. Also called London dispersion forces. (Section 11.2)

  • Exergonic reaction

    A reaction in which the Gibbs free energy of the products is lower than that of the reactants. The position of equilibrium for an exergonic reaction favors products.

  • first order

    A reaction that has a rate equation in which the sum of all exponents is one.

  • 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)

  • free energy (Gibbs free energy, G)

    A thermodynamic state function that gives a criterion for spontaneous change in terms of enthalpy and entropy: G = H - TS. (Section 19.5)

  • hydroxyl group

    An OH group.

  • Infrared active

    Any molecular vibration that leads to a substantial change in dipole moment and is observed in an IR spectrum.

  • Newman projection

    A way to view a molecule by looking along a carbon-carbon single bond

  • Nucleophile

    From the Greek meaning nucleus-loving. Any species that can donate a pair of electrons to form a new covalent bond; alternatively, a Lewis base

  • reactant

    A starting substance in a chemical reaction; it appears to the left of the arrow in a chemical equation. (Section 3.1)

  • solvent

    The dissolving medium of a solution; it is normally the component of a solution present in the greater amount. (Section 4.1)

  • tertiary alkyl halide

    An organohalide in which the alpha (a) position is connected to three alkyl groups.

  • thioacetal

    A compound that contains two SR groups, both of which are connected to the same carbon atom.

  • torsional angle

    The angle between two groups in a Newman projection, also called the dihedral angle.

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