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Solutions for Chapter 15.14: Splitting Diagrams Explain the Multiplicity of a Signal

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 15.14: Splitting Diagrams Explain the Multiplicity of a Signal

Solutions for Chapter 15.14
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Organic Chemistry was written by and is associated to the ISBN: 9780321803221. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions. Since 1 problems in chapter 15.14: Splitting Diagrams Explain the Multiplicity of a Signal have been answered, more than 37708 students have viewed full step-by-step solutions from this chapter. Chapter 15.14: Splitting Diagrams Explain the Multiplicity of a Signal includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • a-Carbon

    A carbon atom adjacent to a carbonyl group

  • alkynes.

    Hydrocarbons that contain one or more carbon-carbon triple bonds. They have the general formula CnH2n22, where n 5 2,3, . . . . (24.2)

  • amphoteric oxide.

    An oxide that exhibits both acidic and basic properties. (8.6)

  • androgens

    Male sex hormones.

  • autooxidation

    The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.

  • compound

    A substance composed of two or more elements united chemically in definite proportions. (Section 1.2)

  • coordination number

    The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)

  • diborane

    B2H6. A dimeric structure formed when one borane molecule reacts with another.

  • doping

    Incorporation of a hetero atom into a solid to change its electrical properties. For example, incorporation of P into Si. (Section 12.7)

  • Enantiotopic groups

    Atoms or groups on an atom that give a chiral center when one of the groups is replaced by another group. A pair of enantiomers results. The hydrogens of the CH2 group of ethanol, for example, are enantiotopic. Replacing one of them by deuterium gives (R)-1-deuteroethanol; replacing the other gives (S)-1-deuteroethanol. Enantiotopic groups have identical chemical shifts in achiral environments but different chemical shifts in chiral environments.

  • Estrogen

    A steroid hormone, such as estrone and estradiol, that mediates the development of sexual characteristics in females.

  • Hybridization

    The combination of atomic orbitals of different types

  • isolated diene

    A compound containing two carbon-carbon p bonds that are separated by two or more s bonds.

  • ligand

    An ion or molecule that coordinates to a metal atom or to a metal ion to form a complex. (Section 23.2)

  • methine group

    A CH group.

  • octet rule

    A rule stating that bonded atoms tend to possess or share a total of eight valence-shell electrons. (Section 8.1)

  • R (Section 3.3)

    From the Latin, rectus, straight, correct; used in the R,S convention to show that the order of priority of groups on a chiral center is clockwise.

  • Reducing sugar

    A carbohydrate that reacts with an oxidizing agent to form an aldonic acid. In this reaction, the carbohydrate reduces the oxidizing agent.

  • resonance stabilization

    The stabilization associated with the delocalization of electrons via resonance.

  • secondary structure

    The manner in which a protein is coiled or stretched. (Section 24.7)

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