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Solutions for Chapter 11.1: Gases and Pressure

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 11.1: Gases and Pressure

This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1. Modern Chemistry: Student Edition 2012 was written by and is associated to the ISBN: 9780547586632. Chapter 11.1: Gases and Pressure includes 8 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 8 problems in chapter 11.1: Gases and Pressure have been answered, more than 49753 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • addition reaction

    A reaction in which a reagent adds to the two carbon atoms of a carbon–carbon multiple bond. (Section 24.3)

  • Aufbau principle

    Orbitals fi ll in order of increasing energy, from lowest to highest.

  • Baeyer-Villiger oxidation

    A reaction in which a ketone is treated with a peroxy acid and is converted into an ester via the insertion of an oxygen atom.

  • calcination

    The heating of an ore to bring about its decomposition and the elimination of a volatile product. For example, a carbonate ore might be calcined to drive off CO2. (Section 23.2)

  • charcoal

    A form of carbon produced when wood is heated strongly in a deficiency of air. (Section 22.9)

  • column chromatography

    A technique by which compounds are separated from each other based on a difference in the way they interact with the medium (the adsorbent) through which they are passed.

  • 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.

  • cubic close packing

    A crystal structure where the atoms are packed together as close as possible, and the close-packed layers of atoms adopt a three-layer repeating pattern that leads to a face-centered cubic unit cell. (Section 12.3)

  • Deshielding

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

  • downfield

    The left side of an NMR spectrum.

  • Micelle

    A spherical arrangement of organic molecules in water solution clustered so that their hydrophobic parts are buried inside the sphere and their hydrophilic parts are on the surface of the sphere and in contact with water

  • molecular weight

    The mass of the collection of atoms represented by the chemical formula for a molecule. (Section 3.3)

  • Nucleophilicity

    A kinetic property measured by the rate at which a nucleophile causes nucleophilic substitution on a reference compound under a standardized set of experimental conditions.

  • phosphatidic acid

    A phosphoric monoester, which is the simplest kind of phosphoglyceride.

  • reaction mechanism

    A detailed picture, or model, of how the reaction occurs; that is, the order in which bonds are broken and formed and the changes in relative positions of the atoms as the reaction proceeds. (Section 14.6)

  • regiochemistry

    A term describing a consideration that must be taken into account for a reaction in which two or more constitutional isomers can be formed.

  • termination

    In radical reactions, a step in which two radicals are joined to give a compound with no unshared electrons.

  • torsional angle

    The angle between two groups in a Newman projection, also called the dihedral angle.

  • Transition state

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

  • Williamson ether synthesis

    A method for preparing an ether from an alkoxide ion and an alkyl halide (via an SN2 process).

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