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Solutions for Chapter 11: Chemical Bonding II: Additional Aspects

General Chemistry: Principles and Modern Applications | 10th Edition | ISBN: 9780132064521 | Authors: Ralph Petrucci

Full solutions for General Chemistry: Principles and Modern Applications | 10th Edition

ISBN: 9780132064521

General Chemistry: Principles and Modern Applications | 10th Edition | ISBN: 9780132064521 | Authors: Ralph Petrucci

Solutions for Chapter 11: Chemical Bonding II: Additional Aspects

Solutions for Chapter 11
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Textbook: General Chemistry: Principles and Modern Applications
Edition: 10
Author: Ralph Petrucci
ISBN: 9780132064521

Summary of Chapter 11: Chemical Bonding II: Additional Aspects

Since 108 problems in chapter 11: Chemical Bonding II: Additional Aspects have been answered, more than 193456 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: General Chemistry: Principles and Modern Applications, edition: 10. Chapter 11: Chemical Bonding II: Additional Aspects includes 108 full step-by-step solutions. General Chemistry: Principles and Modern Applications was written by and is associated to the ISBN: 9780132064521.

Key Chemistry Terms and definitions covered in this textbook
  • alkyl amines

    A format for naming amines containing simple alkyl groups.

  • coordinate covalent bond.

    A bond in which the pair of electrons is supplied by one of the two bonded atoms; also called a dative bond. (9.9)

  • cumulated diene

    A compound containing two adjacent p bonds.

  • Cyanohydrin

    A molecule containing an !OH group and a !CN group bonded to the same carbon.

  • Henry’s law

    A law stating that the concentration of a gas in a solution, Sg, is proportional to the pressure of gas over the solution: Sg = kPg. (Section 13.3)

  • hydrate

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

  • monomers

    Molecules with low molecular weights, which can be joined together (polymerized) to form a polymer. (Section 12.8)

  • nanomaterial

    A solid whose dimensions range from 1 to 100 nm and whose properties differ from those of a bulk material with the same composition. (Section 12.1)

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • parent ion

    In mass spectrometry,the ion that is generated when the compound is ionized.

  • Phasing

    The sign of the wave function at particular coordinates in space, either plus or minus. Phasing is often represented by colors, such as red or blue

  • photoionization

    The removal of an electron from an atom or molecule by absorption of light. (Section 18.2)

  • polynucleotide

    A polymer constructed from nucleotides linked together.

  • Primary structure of nucleic acids

    The sequence of bases along the pentose-phosphodiester backbone of a DNA or RNA molecule read from the 5’ end to the 3’ end

  • Tesla (T)

    The SI unit for magnetic fi eld strength.

  • thermodynamic control

    A reaction for which the ratio of products is determined solely by the distribution of energy among the products.

  • Thermodynamic control

    Experimental conditions that permit the establishment of equilibrium between two or more products of a reaction. The composition of the product mixture is determined by the relative stabilities of the products.

  • Thermoset plastic

    A polymer that can be molded when it is fi rst prepared, but once cooled, hardens irreversibly and cannot be remelted.

  • Valence-shell electron-pair repulsion (VSEPR)

    A method for predicting bond angles based on the idea that electron pairs repel each other and keep as far apart as possible.

  • Zwitterion

    An internal salt of an amino acid; the carboxylate is negatively charged, and the ammonium group is positively charged