Solutions for Chapter 7.2: HOW TO NAME A COMPOUND THAT HAS MORE THAN ONE FUNCTIONAL GROUP

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 8th Edition

ISBN: 9780134042282

Organic Chemistry | 8th Edition | ISBN: 9780134042282 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 7.2: HOW TO NAME A COMPOUND THAT HAS MORE THAN ONE FUNCTIONAL GROUP

Solutions for Chapter 7.2
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Organic Chemistry was written by and is associated to the ISBN: 9780134042282. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 8. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 7.2: HOW TO NAME A COMPOUND THAT HAS MORE THAN ONE FUNCTIONAL GROUP have been answered, more than 15211 students have viewed full step-by-step solutions from this chapter. Chapter 7.2: HOW TO NAME A COMPOUND THAT HAS MORE THAN ONE FUNCTIONAL GROUP includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • absorption spectrum

    In IR spectroscopy as well as UV-VIS spectroscopy, a plot that measures the percent transmittance or absorption as a function of frequency.

  • alpha (a) rays.

    Helium ions with a positive charge of 12. (2.2)

  • boiling-point elevation (DTb).

    The boiling point of the solution (Tb) minus the boiling point of the pure solvent (T° b). (12.6)

  • Confi guration

    Refers to the arrangement of atoms about a stereocenter

  • dash

    In bond-line structures, agroup going behind the page.

  • Deactivating group

    Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.

  • dipole

    A molecule with one end having a partial negative charge and the other end having a partial positive charge; a polar molecule. (Section 8.4)

  • endergonic

    Any process with a positive DG.

  • Frost circle

    A graphic method for determining the relative energies of p MOs for planar, fully conjugated, monocyclic compounds.

  • homogeneous catalysts

    A catalyst that dissolves in the reaction medium.

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • Melt transition (Tm)

    The temperature at which crystalline regions of a polymer melt.

  • Merrifield synthesis

    A method for building a peptide from protected building blocks.

  • molecular orbital (MO)

    An allowed state for an electron in a molecule. According to molecular-orbital theory, a molecular orbital is entirely analogous to an atomic orbital, which is an allowed state for an electron in an atom. Most bonding molecular orbitals can be classified as s or p, depending on the disposition of electron density with respect to the internuclear axis. (Section 9.7)

  • periplanar

    A conformation in which a hydrogen atom and a leaving group are approximately coplanar.

  • Planck constant (h)

    The constant that relates the energy and frequency of a photon, E = hn. Its value is 6.626 * 10-34 J@s. (Section 6.2)

  • positron

    A particle with the same mass as an electron but with a positive charge, 0 +1e, or b+. (Section 21.1)

  • Robinson annulation

    The combination of a Michael addition followed by an aldol condensation to form a ring.

  • Sigma (s) molecular orbital

    A molecular orbital in which electron density is concentrated between two nuclei, along the axis joining them, and is cylindrically symmetrical

  • sodium cyanoborohydride

    A selective reducing agent (NaBH3CN) that can be used for reductive amination.

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