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Solutions for Chapter 8.12: A Molecular Orbital Description of Aromaticity and Antiaromaticity

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 8.12: A Molecular Orbital Description of Aromaticity and Antiaromaticity

Solutions for Chapter 8.12
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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. Since 3 problems in chapter 8.12: A Molecular Orbital Description of Aromaticity and Antiaromaticity have been answered, more than 36045 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 8.12: A Molecular Orbital Description of Aromaticity and Antiaromaticity includes 3 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Aldonic acid

    The product formed when the !CHO group of an aldose is oxidized to a !COOH group

  • bonding molecular orbital

    A molecular orbital in which the electron density is concentrated in the internuclear region. The energy of a bonding molecular orbital is lower than the energy of the separate atomic orbitals from which it forms. (Section 9.7)

  • catalyst.

    A substance that increases the rate of a chemical reaction without itself being consumed. (13.6)

  • collision model

    A model of reaction rates based on the idea that molecules must collide to react; it explains the factors influencing reaction rates in terms of the frequency of collisions, the number of collisions with energies exceeding the activation energy, and the probability that the collisions occur with suitable orientations. (Section 14.5)

  • crossed-linked polymer

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

  • elastomer

    A material that can undergo a substantial change in shape via stretching, bending, or compression and return to its original shape upon release of the distorting force. (Section 12.6)

  • Equivalent hydrogens

    Hydrogens that have the same chemical environment

  • Ether

    A compound containing an oxygen atom bonded to two carbon atoms.

  • free radical

    A substance with one or more unpaired electrons. (Section 21.9)

  • Glycosidic bond

    The bond from the anomeric carbon of a glycoside to an !OR group

  • isoprene

    2-Methyl-1,3-butadiene.

  • ketone

    A compound in which the carbonyl group 1C “O2 occurs at the interior of a carbon chain and is therefore flanked by carbon atoms. (Section 24.4)

  • liquid

    Matter that has a distinct volume but no specific shape. (Section 1.2)

  • Nucleotide

    A nucleoside in which a molecule of phosphoric acid is esterifi ed with an !OH of the monosaccharide, most commonly either the 39!OH or the 59!OH.

  • partial pressure

    The pressure exerted by a particular gas in a mixture. (Section 10.6)

  • quaternary structure

    The structure that arises when a protein consists of two or more folded polypeptide chains that aggregate to form one protein complex.

  • quintet

    In NMR spectroscopy, a signal that is comprised of five peaks.

  • representative (main-group) element

    An element from within the s and p blocks of the periodic table (Figure 6.29). (Section 6.9)

  • Retrosynthesis

    A process of reasoning backwards from a target molecule to a suitable set of starting materials.

  • triglyceride

    A triester formed from glycerol and three long-chain carboxylic acids.

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