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Solutions for Chapter 1.2: ClassIcal theorIes of chemIcal BondIng

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 1.2: ClassIcal theorIes of chemIcal BondIng

Since 7 problems in chapter 1.2: ClassIcal theorIes of chemIcal BondIng have been answered, more than 18024 students have viewed full step-by-step solutions from this chapter. Chapter 1.2: ClassIcal theorIes of chemIcal BondIng includes 7 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. 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.

Key Chemistry Terms and definitions covered in this textbook
  • a-Helix

    A type of secondary structure in which a section of polypeptide chain coils into a spiral, most commonly a right-handed spiral.

  • back-side attack

    In SN2 reactions, the side opposite the leaving group, which is where the nucleophile attacks.

  • bond dipole

    The dipole moment that is due to unequal electron sharing between two atoms in a covalent bond. (Section 9.3)

  • bond enthalpy.

    The enthalpy change required to break a bond in a mole of gaseous molecules. (9.10)

  • C-Terminal amino acid

    The amino acid at the end of a polypeptide chain having the free !COOH group.

  • chemical shift (d)

    In an NMR spectrum, the location of a signal, defined relative to the frequency of absorption of a reference compound, tetramethylsilane (TMS).

  • condensed structure

    A drawing style in which none of the bonds are drawn. Groups of atoms are clustered together when possible. For example, isopropanol has two CH3 groups, both of which are connected to the central carbon atom, shown like this: (CH3)2CHOH.

  • constitutional isomers

    Compounds that have the same molecular formula but differ in the way the atoms are connected.

  • elimination (of radicals)

    In radical reaction mechanisms, a step in which a bond forms between the alpha (a) and beta (b) positions. As a result, a single bond at the b position is cleaved, causing the compound to fragment into two pieces.

  • enzyme

    A protein molecule that acts to catalyze specific biochemical reactions. (Section 14.7)

  • fuel cell

    A voltaic cell that utilizes the oxidation of a conventional fuel, such as H2 or CH4, in the cell reaction. (Section 20.7)

  • gas constant (R)

    The constant of proportionality in the ideal-gas equation. (Section 10.4)

  • Hund’s rule

    When orbitals of equal energy are available but there are not enough electrons to fi ll all of them completely, one electron is put in each before a second electron is added to any

  • liquid crystal

    A substance that exhibits one or more partially ordered liquid phases above the melting point of the solid form. By contrast, in nonliquid crystalline substances the liquid phase that forms upon melting is completely unordered. (Section 11.7)

  • neutralization reaction

    A reaction in which an acid and a base react in stoichiometrically equivalent amounts; the neutralization reaction between an acid and a metal hydroxide produces water and a salt. (Section 4.3)

  • Photolysis

    Cleavage by light.

  • plane-polarized light

    Light for which all photons have the same polarization, generally formed by passing light through a polarizing filter.

  • specific heat 1Cs2

    The heat capacity of 1 g of a substance; the heat required to raise the temperature of 1 g of a substance by 1 °C. (Section 5.5)

  • stretching

    In IR spectroscopy, atype of vibration that generally produces a signal in the diagnostic region of an IR spectrum.

  • symmetry allowed

    A reaction that obeys conservation of orbital symmetry.

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