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Solutions for Chapter 16.7SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 16.7SE

Solutions for Chapter 16.7SE
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Since 2 problems in chapter 16.7SE have been answered, more than 66267 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 16.7SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxy substituent

    An OR group.

  • amino acids.

    A compound that contains at least one amino group and at least one carboxyl group. (25.3)

  • Basicity

    An equilibrium property measured by the position of equilibrium in an acid-base reaction, as, for example, the acid-base reaction between ammonia and water.

  • Boat conformation

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

  • Chlorofl uorocarbons (CFCs, Freons)

    Compounds with one or two carbons, chlorine, and fl uorine, formerly used as refrigerants

  • condensation reaction.

    A reaction in which two smaller molecules combine to form a larger molecule. Water is invariably one of the products of such a reaction. (24.4)

  • 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.

  • conductor.

    Substance capable of conducting electric current. (21.3)

  • conjugate base

    A substance formed by the loss of a proton from a Brønsted–Lowry acid. (Section 16.2)

  • cycloalkane

    An alkane whose structure contains a ring.

  • disulfide bridge

    The group that is formed when two cysteine residues of a polypeptide or protein are joined together.

  • E (Section 5.2C)

    From the German, entgegen, opposite. Specifi es that groups of higher priority on the carbons of a double bond are on opposite sides

  • Formal charge

    The charge on an atom in a polyatomic ion or molecule

  • 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)

  • miscible

    Two liquids that can be mixed with each other in any proportion.

  • Pro-S-hydrogen

    Replacing this hydrogen by deuterium gives a chiral center with an S confi guration

  • proton transfer

    One of the four arrow-pushing patterns for ionic reactions.

  • Schiff base

    An alternative name for an imine

  • stereoisomers

    Compounds that have the same constitution but differ in the 3D arrangement of atoms.

  • Transition state

    The highest energy point on a reaction coordinate diagram. The chemical structure at this point is commonly called an activated complex.

Textbook Survival Guides

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