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Solutions for Chapter 6.1: Introduction toChemical Bonding

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 6.1: Introduction toChemical Bonding

Since 6 problems in chapter 6.1: Introduction toChemical Bonding have been answered, more than 51843 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: Modern Chemistry: Student Edition 2012, edition: 1. Modern Chemistry: Student Edition 2012 was written by and is associated to the ISBN: 9780547586632. Chapter 6.1: Introduction toChemical Bonding includes 6 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • a-Carbon

    A carbon atom adjacent to a carbonyl group

  • aldose

    A carbohydrate that contains an aldehyde group.

  • azo dyes

    A class of colored compounds that are formed via azo coupling.

  • b-Pleated sheet

    A type of polypeptide secondary structure in which sections of polypeptide chains are aligned parallel or antiparallel to one another.

  • bonding pair

    In a Lewis structure a pair of electrons that is shared by two atoms. (Section 9.2)

  • covalent compounds.

    Compounds containing only covalent bonds. (9.4)

  • Deshielding

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

  • diamagnetism

    A type of magnetism that causes a substance with no unpaired electrons to be weakly repelled from a magnetic field. (Section 9.8)

  • E1cb mechanism

    An eliminationreaction in which the leaving group only leavesafter deprotonation occurs. This process occurs atthe end of an aldol condensation.

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • Hydrogenolysis

    Cleavage of a single bond by H2, most commonly accomplished by treating a compound with H2 in the presence of a transition metal catalyst.

  • Le Châtelier’s principle

    A principle stating that when we disturb a system at chemical equilibrium, the relative concentrations of reactants and

  • molecular hydrides

    Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)

  • Nucleophilic aromatic substitution

    A reaction in which a nucleophile, most commonly a halogen, on an aromatic ring is replaced by another nucleophile.

  • 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.

  • oxime

    A compound with the structure R2CRN!OH.

  • ozonolysis

    A reaction in which the CRC bond of an alkene is cleaved to form two CRO bonds.

  • 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

  • reducing agent

    A compound that reduces another compound and in the process is itself oxidized. Sodium borohydride and lithium aluminum hydride are reducing agents.

  • weak activators

    Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.

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