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Solutions for Chapter 9.5SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 9.5SE

Solutions for Chapter 9.5SE
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This expansive textbook survival guide covers the following chapters and their solutions. Chapter 9.5SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 9.5SE have been answered, more than 245785 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • amino acids.

    A compound that contains at least one amino group and at least one carboxyl group. (25.3)

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • Chain termination

    A step in a chain reaction that involves destruction of reactive intermediates

  • Chain-transfer reaction

    The transfer of reactivity of an endgroup from one chain to another during a polymerization

  • Conjugate base

    The species formed when an acid transfers a proton to a base

  • coordination compound

    A compound containing a metal ion bonded to a group of surrounding molecules or ions that act as ligands. (Section 23.2)

  • Diaxial interactions

    Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring

  • Double helix

    A type of secondary structure of DNA molecules in which two anti parallel polynucleotide strands are coiled in a right-handed manner about the same axis

  • electron impact ionization (EI)

    In mass spectrometry, an ionization technique that involves bombarding a compoundwith high-energy electrons.

  • Enantiomeric excess (ee)

    The difference between the percentage of two enantiomers in a mixture

  • gauche conformation

    A conformation that exhibits a gauche interaction.

  • isoprene

    2-Methyl-1,3-butadiene.

  • l-Monosaccharide

    A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.

  • mass number

    The sum of the number of protons and neutrons in the nucleus of a particular atom. (Section 2.3)

  • Molecular orbital (MO) theory

    A theory of chemical bonding in which electrons in molecules occupy molecular orbitals that extend over the entire molecule and are formed by the combination of the atomic orbitals that make up the molecule

  • Part per million (ppm)

    Units used on NMR spectra to record chemical shift relative to the TMS standard.

  • Polarizability

    A measure of the ease of distortion of the distribution of electron density about an atom or group in response to interaction with other molecules or ions. Fluorine which has a high electronegativity and holds its electrons tightly, has a very low polarizability. Iodine, which has a lower electronegativity and holds its electrons less tightly, has a very high polarizability.

  • secondary alkyl halide

    An organohalide in which the alpha (a) position is connected to exactly two alkyl groups.

  • Tertiary structure of nucleic acids

    The threedimensional arrangement of all atoms of a nucleic acid, commonly referred to as supercoiling

  • Vicinal coupling

    a !CH"CH2 group

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