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Solutions for Chapter 17.1: The Reaction Process

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition

ISBN: 9780547586632

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Solutions for Chapter 17.1: The Reaction Process

Chapter 17.1: The Reaction Process includes 8 full step-by-step solutions. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1. This expansive textbook survival guide covers the following chapters and their solutions. Modern Chemistry: Student Edition 2012 was written by Patricia and is associated to the ISBN: 9780547586632. Since 8 problems in chapter 17.1: The Reaction Process have been answered, more than 13951 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Acylation

    The process of introducing an acyl group, RCO! or ArCO!, onto an organic molecule.

  • aromatic hydrocarbon.

    A hydrocarbon that contains one or more benzene rings. (24.1)

  • band theory.

    Delocalized electrons move freely through “bands” formed by overlapping molecular orbitals. (21.3)

  • Boat conformation

    A nonplanar conformation of a cyclohexane ring in which carbons 1 and 4 of the ring are bent toward each other

  • chain reaction

    A reaction (generally involving radicals) in which one chemical entity can ultimately cause a chemical transformation for thousands of molecules.

  • Confi gurational isomers

    Isomers that differ by the confi guration of substituents on an atom. Refers to the arrangement of atoms about a stereocenter

  • critical mass

    The amount of fissionable material necessary to maintain a nuclear chain reaction. (Section 21.7)

  • Deshielding

    The term used to express the concept of less shielding in NMR

  • dihedral angle

    The angle by which two groups are separated in a Newman projection.

  • dihydroxylation

    A reaction characterized by the addition of two hydroxyl groups (OH) across an alkene.

  • E2

    A bimolecular eliminationreaction.eclipsed conformation (Sect. 4.7): A conformationin which groups are eclipsing each other in aNewman projection.

  • green chemistry

    Chemistry that promotes the design and application of chemical products and processes that are compatible with human health and that preserve the environment. (Section 18.5)

  • hydroperoxide

    A compound with the structure R!O!O!H.

  • Levorotatory

    Refers to a substance that rotates the plane of polarized light to the left.

  • Organic synthesis

    A series of reactions by which a set of organic starting materials is converted to a more complicated structure.

  • Pericyclic reaction

    A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons

  • phospholipid

    A form of lipid molecule that contains charged phosphate groups. (Section 24.9)

  • Polysaccharide

    A carbohydrate containing a large number of monosaccharide units, each joined to the next by one or more glycosidic bonds.

  • strong activators

    Groups that strongly activate an aromatic ring toward electrophilic aromatic substitution, thereby significantly enhancing the rate of the reaction.

  • Tertiary structure of proteins

    The three-dimensional arrangement in space of all atoms in a single polypeptide chain.

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