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Solutions for Chapter 26.1: Pyrimidines and Purines

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 26.1: Pyrimidines and Purines

Chapter 26.1: Pyrimidines and Purines includes 3 full step-by-step solutions. Since 3 problems in chapter 26.1: Pyrimidines and Purines have been answered, more than 32403 students have viewed full step-by-step solutions from this chapter. 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. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • anode.

    The electrode at which oxidation occurs. (18.2)

  • atomic orbital

    A three-dimensional plot of y2 of a wavefunction. It is a region of space that can accommodate electron density.

  • band theory.

    Delocalized electrons move freely through “bands” formed by overlapping molecular orbitals. (21.3)

  • chemical equilibrium

    A state of dynamic balance in which the rate of formation of the products of a reaction from the reactants equals the rate of formation of the reactants from the products; at equilibrium the concentrations of the reactants and products remain constant. (Section 4.1;Chapter 15: Introduction)

  • Chlorofl uorocarbons (CFCs, Freons)

    Compounds with one or two carbons, chlorine, and fl uorine, formerly used as refrigerants

  • corrosion

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

  • Dalton’s law of partial pressures

    A law stating that the total pressure of a mixture of gases is the sum of the pressures that each gas would exert if it were present alone. (Section 10.6)

  • Diol

    A compound containing two hydroxyl groups

  • Enantiomers

    Stereoisomers that are nonsuperposable mirror images of each other; refers to a relationship between pairs of objects

  • Friedel-Crafts acylation

    An electrophilic aromatic substitution reaction that installs an acyl group on an aromatic ring.

  • Glass transition temperature (TG)

    The temperature at which a polymer undergoes the transition from a hard glass to a rubbery state

  • 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

  • ionic bond

    A bond that results from the force of attraction between two oppositely charged ions.

  • Ketose

    A monosaccharide containing a ketone group.

  • Lewis dot structure

    The symbol of an element surrounded by a number of dots equal to the number of electrons in the valence shell of the atom

  • methine group

    A CH group.

  • salt

    An ionic compound formed by replacing one or more hydrogens of an acid by other cations. (Section 4.3)

  • standard atmospheric pressure

    Defined as 760 torr or, in SI units, 101.325 kPa. (Section 10.2)

  • steric number

    The total of (single bonds + lone pairs) for an atom in a compound.

  • vinylic carbocation

    A carbocation in which the positive charge resides on a vinylic carbon atom. This type of carbocation is very unstable and will not readily form in most cases.

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