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Solutions for Chapter 6: ELECTRONIC STRUCTURE OF ATOMS

Chemistry: The Central Science | 11th Edition | ISBN: 9780136006176 | Authors: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward

Full solutions for Chemistry: The Central Science | 11th Edition

ISBN: 9780136006176

Chemistry: The Central Science | 11th Edition | ISBN: 9780136006176 | Authors: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward

Solutions for Chapter 6: ELECTRONIC STRUCTURE OF ATOMS

Solutions for Chapter 6
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Textbook: Chemistry: The Central Science
Edition: 11
Author: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward
ISBN: 9780136006176

This expansive textbook survival guide covers the following chapters and their solutions. Chapter 6: ELECTRONIC STRUCTURE OF ATOMS includes 95 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780136006176. Since 95 problems in chapter 6: ELECTRONIC STRUCTURE OF ATOMS have been answered, more than 12387 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: 11.

Key Chemistry Terms and definitions covered in this textbook
  • acceptor impurities.

    Impurities that can accept electrons from semiconductors. (21.3)

  • acetal

    A functional group characterized by two alkoxy (OR) groups connected to the same carbon atom.Acetals can be used as protecting groups for aldehydes or ketones.

  • activate

    For a substituted aromatic ring, the effect of an electron-donating substituent that increases the rate of electrophilic aromatic substitution.

  • Chain-growth polymerization

    A polymerization that involves sequential addition reactions, either to unsaturated monomers or to monomers possessing other reactive functional groups.

  • Cumulated

    A cumulated diene is one in which two double bonds share an sp-hybridized carbon

  • Cycloaddition reaction

    A reaction in which two reactants add together in a single step to form a cyclic product. The best known of these is the Diels-Alder reaction

  • Edman degradation

    A method for analyzing the sequence of amino acids in apeptide by removing one amino acid residue at a time and identifying each residue as it is removed.

  • electron domain

    In the VSEPR model, a region about a central atom in which an electron pair is concentrated. (Section 9.2)

  • Fatty acid

    A long, unbranched-chain carboxylic acid, most commonly of 12 to 20 carbons, derived from the hydrolysis of animal fats, vegetable oils, or the phospholipids of biological membranes.

  • fingerprint region

    The region of an IR spectrum that contains signals resulting from the vibrational excitation of most single bonds (stretching and bending).

  • Henderson-Hasselbalch equation

    An equation that is often employed to calculate the pH of buffered solutions: pH = pKa + log 3conjugated base4 3acid4

  • kinetic energy

    The energy that an object possesses by virtue of its motion. (Section 5.1)

  • Low-density lipoprotein (LDL)

    Plasma particles, density 1.02–1.06 g/mL, consisting of approximately 26% proteins, 50% cholesterol, 21% phospholipids, and 4% triglycerides.

  • mineral

    A solid, inorganic substance occurring in nature, such as calcium carbonate, which occurs as calcite. (Section 23.1)

  • Peptide bond

    The special name given to the amide bond formed between the a-amino group of one amino acid and the a-carboxyl group of another amino acid

  • Polysaccharide

    A carbohydrate containing a large number of monosaccharide units, each joined to the next by one or more glycosidic bonds.

  • Potential energy

    The energy that can be released if given an opportunity

  • resonance hybrid

    A term used to describe the character of a chemical entity (molecule, ion, or radical) exhibiting more than one significant resonance structure.

  • Schiff base

    An alternative name for an imine

  • Unimolecular reaction

    A reaction in which only one species is involved in the rate-determining step

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