Solutions for Chapter 1.12SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

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

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 1.12SE

Solutions for Chapter 1.12SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 1.12SE have been answered, more than 147639 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 1.12SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • amine

    A compound that has the general formula R3N, where R may be H or a hydrocarbon group. (Section 16.7)

  • anti conformation

    A conformation in which the dihedral angle between two groups is 180°.

  • Aromatic amine

    An amine in which nitrogen is bonded to one or more aryl groups.

  • asymmetric stretching

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

  • Carbanion

    An ion in which carbon has an unshared pair of electrons and bears a negative charge.

  • carbon black

    A microcrystalline form of carbon. (Section 22.9)

  • Carboxyl group (Section 1.3D)

    A !COOH group.

  • Diastereotopic groups

    Atoms or groups on an atom that are bonded to an atom that is bonded to two nonidentical groups, one of which contains a chiral center. When one of the atoms or groups is replaced by another group, a new chiral center is created and a set of diastereomers results. The hydrogens of the CH2 group of 2-butanol, for example, are diastereotopic. Diastereotopic groups have different chemical shifts under all conditions

  • Enolate anion

    An anion derived by loss of a hydrogen from a carbon alpha to a carbonyl group; the anion of an enol.

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • gauche conformation

    A conformation that exhibits a gauche interaction.

  • 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.

  • Ka

    A measure of the strength of an acid: Ka = Keq 3H2O4 = 3H3O+ 4 3A- 4 3HA4

  • lipid bilayer

    The main fabricof cell membranes, assembled primarily fromphosphoglycerides.

  • Molar absorptivity (e)

    The absorbance of a 1 M solution of a compound.

  • Orbital

    A region of space that can hold two electrons

  • proteins

    Polypeptide chains comprised of more than 40 or 50 amino acids.

  • Rate determining step

    The step in a multistep reaction sequence that crosses the highest energy barrier.

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • Wohl degradation

    A process that involves the removal of a carbon atom from an aldose. The aldehyde group is first converted to a cyanohydrin, followed by loss of HCN in the presence of a base.

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