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Solutions for Chapter 1.7: ElEctronic StructurES

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 1.7: ElEctronic StructurES

Solutions for Chapter 1.7
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This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Since 1 problems in chapter 1.7: ElEctronic StructurES have been answered, more than 36849 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Chapter 1.7: ElEctronic StructurES includes 1 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • acid-catalyzed hydration

    A reaction that achieves the addition of water across a double bond in the presence of an acid catalyst.

  • Acylium ion

    A resonance-stabilized cation with the structure [RC"O]1 or [ArC"O]1. The positive charge is delocalized over both the carbonyl carbon and the carbonyl oxygen.

  • alkylation

    A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.

  • 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)

  • Aprotic solvent

    A solvent that cannot serve as a hydrogen-bond donor; nowhere in the molecule is there a hydrogen bonded to an atom of high electronegativity. Common aprotic solvents are dichloromethane, diethyl ether, and dimethyl sulfoxide

  • buffered solution (buffer)

    A solution that undergoes a limited change in pH upon addition of a small amount of acid or base. (Section 17.2)

  • Contributing structures

    Representations of a molecule or ion that differ only in the distribution of valence electrons.

  • Disulfide

    A molecule containing an !S!S! group

  • Glycoside

    A carbohydrate in which the !OH on its anomeric carbon is replaced by !OR

  • gray (Gy)

    The SI unit for radiation dose

  • halohydrin formation

    A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.

  • Haworth projection

    A way to view furanose and pyranose forms of monosaccharides. The ring is drawn fl at and most commonly viewed through its edge with the anomeric carbon on the right and the oxygen atom of the ring to the rear

  • Hybrid orbital

    An orbital formed by the combination of two or more atomic orbitals.

  • hydrogen abstraction

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

  • Isomers

    Different compounds with the same molecular formula.

  • Living polymer

    A polymer chain that continues to grow without chain-termination steps until either all of the monomer is consumed or some external agent is added to terminate the chain. The polymer chains will continue to grow if more monomer is added.

  • LUMO

    The lowest unoccupied molecular orbital.

  • precision

    The closeness of agreement among several measurements of the same quantity; the reproducibility of a measurement. (Section 1.5)

  • Quantum mechanics

    The branch of science that studies the interaction of matter and radiation.

  • Terpene

    A compound whose carbon skeleton can be divided into two or more units identical with the carbon skeleton of isoprene

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