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Solutions for Chapter 23.12: use and occurrence of amines

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 23.12: use and occurrence of amines

Solutions for Chapter 23.12
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This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Chapter 23.12: use and occurrence of amines includes 1 full step-by-step solutions. 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 23.12: use and occurrence of amines have been answered, more than 39407 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alloy.

    A solid solution composed of two or more metals, or of a metal or metals with one or more nonmetals. (21.2)

  • amorphous

    A region of a polymer in which nearby chains are not linearly extended and are not parallel to one another.

  • aryl amine

    An amine in which the nitrogen atom is connected directly to an aromatic ring.

  • basic oxide (basic anhydride)

    An oxide that either reacts with water to form a base or reacts with an acid to form a salt and water. (Section 22.5)

  • bond angles

    The angles made by the lines joining the nuclei of the atoms in a molecule. (Section 9.1)

  • chlorohydrin

    A compound containing a Cl group and a hydroxyl group (OH) on adjacent carbon atoms.

  • covalent-network solids

    Solids in which the units that make up the three-dimensional network are joined by covalent bonds. (Section 12.1)

  • crystalline solid.

    A solid that possesses rigid and long-range order; its atoms, molecules, or ions occupy specific positions. (11.4)

  • disulfide

    A compound with the structure R!S!S!R.

  • 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

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • Hydroperoxide

    A compound containing an !OOH group.

  • Isomers

    Different compounds with the same molecular formula.

  • matter waves

    The term used to describe the wave characteristics of a moving particle. (Section 6.4)

  • Mutarotation

    The change in specifi c rotation that occurs when an a or b hemiacetal form of a carbohydrate in aqueous solution is converted to an equilibrium mixture of the two forms.

  • percent yield

    The ratio of the actual (experimental) yield of a product to its theoretical (calculated) yield, multiplied by 100. (Section 3.7)

  • petroleum

    A naturally occurring combustible liquid composed of hundreds of hydrocarbons and other organic compounds. (Section 5.8)

  • proton

    A positively charged subatomic particle found in the nucleus of an atom. (Section 2.3)

  • simple lipid

    A lipid that does not undergo hydrolysis in aqueous acid or base to produce smaller fragments.

  • stereospecific

    A reaction in which the configuration of the product is dependent on the configuration of the starting material.

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