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Solutions for Chapter 8.4: How to Draw Resonance Contributors

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 8.4: How to Draw Resonance Contributors

Solutions for Chapter 8.4
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Chapter 8.4: How to Draw Resonance Contributors includes 1 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. This expansive textbook survival guide covers the following chapters and their solutions. Since 1 problems in chapter 8.4: How to Draw Resonance Contributors have been answered, more than 42174 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • acetoacetic ester synthesis

    A threestep process that converts an alkyl halide into a methyl ketone with the introduction of three new carbon atoms.

  • amino acid

    A carboxylic acid that contains an amino 1¬NH22 group attached to the carbon atom adjacent to the carboxylic acid 1¬COOH2 functional group. (Section 24.7)

  • atomic orbital

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

  • Bonding molecular orbital

    A molecular orbital in which electrons have a lower energy than they would in isolated atomic orbitals

  • chemistry

    The scientific discipline that studies the composition, properties, and transformations of matter. (Chapter 1: Introduction)

  • Condensation polymerization

    A polymerization in which chain growth occurs in a stepwise manner between difunctional monomers. Also called step-growth polymerization.

  • crossed-linked polymer

    A polymer in which neighboring chains are linked together, for example, by disulfide bonds.

  • E1

    A unimolecular elimination reaction.

  • equilibrium constant

    The numerical value of the equilibrium-constant expression for a system at equilibrium. The equilibrium constant is most usually denoted by Kp for gas-phase systems or Kc for solution-phase systems. (Section 15.2)

  • Ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • formal charge

    The number of valence electrons in an isolated atom minus the number of electrons assigned to the atom in the Lewis structure. (Section 8.5)

  • 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

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • Geminal coupling

    Spin-spin coupling that occurs between nonequivalent H atoms bonded to the same C atom. The H atoms are generally nonequivalent owing to restricted bond rotation in the molecule

  • heterogeneous equilibrium

    The equilibrium established between substances in two or more different phases, for example, between a gas and a solid or between a solid and a liquid. (Section 15.4)

  • radical inhibitor

    A compound that prevents a radical chain process from either getting started or continuing.

  • Raoult’s law

    A law stating that the partial pressure of a solvent over a solution, Psolution, is given by the vapor pressure of the pure solvent, P° solvent, times the mole fraction of a solvent in the solution, Xsolvent: Psolution = XsolventP° solvent. (Section 13.5)

  • Reaction mechanism

    A step-by-step description of how a chemical reaction occurs.

  • Sandmeyer reactions

    Reactions that utilize copper salts (CuX) and enable the installation of a halogen or a cyano group on an aromatic ring.

  • significant figures

    The digits that indicate the precision with which a measurement is made; all digits of a measured quantity are significant, including the last digit, which is uncertain. (Section 1.5)

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