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Solutions for Chapter 10.5: Water

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 10.5: Water

Since 7 problems in chapter 10.5: Water have been answered, more than 14132 students have viewed full step-by-step solutions from this chapter. Chapter 10.5: Water includes 7 full step-by-step solutions. 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. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1.

Key Chemistry Terms and definitions covered in this textbook
  • amine

    A compound that has the general formula R3N, where R may be H or a hydrocarbon group. (Section 16.7)

  • Anomeric carbon

    The hemiacetal or acetal carbon of the cyclic form of a carbohydrate

  • Arene

    A term used to classify benzene and its derivatives.

  • Aryl group (Ar -)

    A group derived from an arene by removal of an H.

  • chlorofluorocarbons (CFCs)

    Compound containing only carbon, chlorine, and fluorine.

  • electrocyclic reaction

    A pericyclic process in which a conjugated polyene undergoes cyclization. In the process, one p bond is converted into a s bond, while the remaining p bonds all change their location. The newly formed s bond joins the ends of the original p system,thereby creating a ring.

  • excited state

    A state that is achieved when a compound absorbs energy.

  • heat capacity

    The quantity of heat required to raise the temperature of a sample of matter by 1 °C (or 1 K). (Section 5.5)

  • hydrate

    A compound containing two hydroxyl groups (OH) connected to the same carbon atom.

  • Hydroboration-oxidation

    A method for converting an alkene to an alcohol. The alkene is treated with borane (BH3) to give a trialkylborane, which is then oxidized with alkaline hydrogen peroxide to give an alcohol

  • hydrophobic

    A nonpolar group that does not have favorable interactions with water.

  • J value

    When signal splitting occurs in 1H NMR spectroscopy, the distance (in hertz) between the individual peaks of a signal.

  • Lewis structures

    A drawing style inwhich the electrons take center stage.linear polymer (Sect. 27.6): A polymer thathas only a minimal amount of branching or nobranching at all.

  • mean free path

    The average distance traveled by a gas molecule between collisions. (Section 10.8)

  • Optical purity

    The specifi c rotation of a mixture of enantiomers divided by the specifi c rotation of the enantiomerically pure substance (expressed as a percent). Optical purity is numerically equal to enantiomeric excess, but experimentally determined.

  • primary structure

    For proteins, the sequence of amino acid residues.

  • solution

    A mixture of substances that has a uniform composition; a homogeneous mixture. (Section 1.2)

  • sulfide

    A compound that is similar in structure to an ether, but the oxygen atom has been replaced with a sulfur atom. Also called a thioether.

  • vicinal

    A term used to describe two identical groups attached to adjacent carbon atoms.

  • Williamson ether synthesis

    A general method for the synthesis of dialkyl ethers by an SN2 reaction between a haloalkane and an alkoxide ion.

Textbook Survival Guides

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