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Solutions for Chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers

Solutions for Chapter 2.15
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Organic Chemistry, was written by and is associated to the ISBN: 9780073402741. Chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 2.15: Applying the IUPAC Rules: The Names of the C6H14 Isomers have been answered, more than 34026 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Acylation

    The process of introducing an acyl group, RCO! or ArCO!, onto an organic molecule.

  • anomeric carbon

    The C1 position of the cyclic hemiacetal of an aldose or the C2 position of the cyclic hemiacetal of a ketose.

  • Aramid

    A polyaromatic amide; a polymer in which the monomer units are an aromatic diamine and an aromatic dicarboxylic acid

  • asymmetric stretching

    In IR spectroscopy, when two bonds are stretching out of phase with each other.

  • atom.

    The basic unit of an element that can enter into chemical combination. (2.2)

  • bond enthalpy.

    The enthalpy change required to break a bond in a mole of gaseous molecules. (9.10)

  • Carboxylic acid

    A compound containing a carboxyl, !COOH, group.

  • Condensation polymerization

    A polymerization in which chain growth occurs in a stepwise manner between difunctional monomers. Also called step-growth polymerization.

  • coordination-sphere isomers

    Structural isomers of coordination compounds in which the ligands within the coordination sphere differ. (Section 23.4)

  • decomposition reaction

    A chemical reaction in which a single compound reacts to give two or more products. (Section 3.2)

  • E2

    A bimolecular b-elimination reaction.

  • Hückel’s rule

    The requirement for an odd number of p electron pairs in order for a compound to be aromatic.

  • ionization energy

    The energy required to remove an electron from a gaseous atom when the atom is in its ground state. (Section 7.4)

  • molal freezing-point-depression constant (Kf)

    A constant characteristic of a particular solvent that gives the decrease in freezing point as a function of solution molality: ?Tf = -Kf m. (Section 13.5)

  • Protic solvent

    A solvent that is a hydrogen-bond donor. Common protic solvents are water, low-molecular-weight alcohols, and low-molecular weight carboxylic acids.

  • Quaternary structure

    The arrangement of polypeptide monomers into a noncovalently bonded aggregate.

  • Racemic mixture

    A mixture of equal amounts of two enantiomers.

  • radioactive

    Possessing radioactivity, the spontaneous disintegration of an unstable atomic nucleus with accompanying emission of radiation. (Section 2.2; Chapter 21: Introduction)

  • Telechelic polymer

    A polymer in which its growing chains are terminated by formation of new functional groups at both ends of its chains. These new functional groups are introduced by adding reagents, such as CO2 or ethylene oxide, to the growing chains.

  • Trans

    A prefi x meaning across from.

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