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Solutions for Chapter 7.2: How to Name a Compound That Has More than One Functional Group

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 7.2: How to Name a Compound That Has More than One Functional Group

Solutions for Chapter 7.2
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Chapter 7.2: How to Name a Compound That Has More than One Functional Group includes 2 full step-by-step solutions. 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 2 problems in chapter 7.2: How to Name a Compound That Has More than One Functional Group have been answered, more than 8365 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by Patricia and is associated to the ISBN: 9780321803221.

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

    Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)

  • Alkyne

    An unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds.

  • anti-coplanar

    A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of exactly 180°.

  • cholesteric liquid crystalline phase

    A liquid crystal formed from flat, disc-shaped molecules that align through a stacking of the molecular discs. (Section 11.7)

  • concentration

    The quantity of solute present in a given quantity of solvent or solution. (Section 4.5)

  • coplanar

    Atoms that lie in the same plane.

  • denaturation

    A process during which a protein unfolds under conditions of mild heating.

  • diastereotopic

    Nonequivalent protons for which the replacement test produces diastereomers.

  • E1

    A unimolecular elimination reaction.

  • E2

    A bimolecular b-elimination reaction.

  • Electrophile

    From the Greek meaning electron loving. Any species that can accept a pair of electrons to form a new covalent bond; alternatively, a Lewis acid.

  • gauche interaction

    The steric interaction that results when two groups in a Newman projection are separated by a dihedral angle of 60°.

  • halogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a halogen atom is abstracted by a radical, generating a new radical.

  • high-spin complex

    A complex whose electrons populate the d orbitals to give the maximum number of unpaired electrons. (Section 23.6)

  • lanthanide contraction

    The gradual decrease in atomic and ionic radii with increasing atomic number among the lanthanide elements, atomic numbers 57 through 70. The decrease arises because of a gradual increase in effective nuclear charge through the lanthanide series. (Section 23.1)

  • ortho-para director

    A group that directs the regiochemistry of an electrophilic aromatic substitution reaction such that the incoming electrophile is installed at the ortho or para positions.

  • sigma 1S2 molecular orbital

    A molecular orbital that centers the electron density about an imaginary line passing through two nuclei. (Section 9.7)

  • tautomers

    Constitutional isomers that rapidly interconvert via the migration of a proton.

  • Thermolysis

    Cleavage by heating

  • wavenumber

    In IR spectroscopy, the location of each signal is reported in terms of this frequency-related unit.

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