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Solutions for Chapter 16.3: spectroscopy of BeNzeNe Derivatives

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9781936221349

Organic Chemistry | 6th Edition | ISBN: 9781936221349 | Authors: Marc Loudon, Jim Parise

Solutions for Chapter 16.3: spectroscopy of BeNzeNe Derivatives

Chapter 16.3: spectroscopy of BeNzeNe Derivatives includes 8 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Since 8 problems in chapter 16.3: spectroscopy of BeNzeNe Derivatives have been answered, more than 34331 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by and is associated to the ISBN: 9781936221349.

Key Chemistry Terms and definitions covered in this textbook
  • anomers

    Stereoisomeric cyclic hemiacetals of an aldose or ketose that differ from each other in their configuration at the anomeric carbon.

  • basic anhydride (basic oxide)

    An oxide that forms a base when added to water; soluble metal oxides are basic anhydrides. (Section 22.5)

  • cathode rays

    Streams of electrons that are produced when a high voltage is applied to electrodes in an evacuated tube. (Section 2.2)

  • conjugated diene

    A compound inwhich two carbon-carbon p bonds are separated from each other by exactly one s bond.

  • cubic close packing

    A crystal structure where the atoms are packed together as close as possible, and the close-packed layers of atoms adopt a three-layer repeating pattern that leads to a face-centered cubic unit cell. (Section 12.3)

  • Deactivating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.

  • delocalization

    The spreading of a charge or lone pair as described by resonance theory.

  • delocalized molecular orbitals.

    Molecular orbitals that are not confined between two adjacent bonding atoms but actually extend over three or more atoms. (10.8)

  • DEPT 13C NMR

    In 13C NMR spectroscopy, a technique that utilizes two rf radiation emitters and provides information regarding the number of protons attached to each carbon atom in a compound.

  • effusion

    The escape of a gas through an orifice or hole. (Section 10.8)

  • element

    A substance consisting of atoms of the same atomic number. Historically defined as a substance that cannot be separated into simpler substances by chemical means. (Sections 1.1 and 1.2)

  • force

    A push or a pull. (Section 5.1)

  • formal charge

    A charge associated with any atom that does not exhibit the appropriate number of valence electrons.

  • Frequency

    The number of full cycles of a wave that pass a given point in a second, and reported in hertz (Hz), which has the units s21

  • metallic character

    The extent to which an element exhibits the physical and chemical properties characteristic of metals, for example, luster, malleability, ductility, and good thermal and electrical conductivity. (Section 7.6)

  • momentum

    The product of the mass, m, and velocity, v, of an object. (Section 6.4)

  • nucleophilic acyl substitution

    A reaction in which a nucleophile attacks a carboxylic acid derivative.

  • Phenyl group

    A group derived by removing an H from benzene; abbreviated C6H5! or Ph!.

  • primitive lattice

    A crystal lattice in which the lattice points are located only at the corners of each unit cell. (Section 12.2)

  • proton

    A positively charged subatomic particle found in the nucleus of an atom. (Section 2.3)

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