Solutions for Chapter 4.3SE: 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 4.3SE

Solutions for Chapter 4.3SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 4.3SE have been answered, more than 123339 students have viewed full step-by-step solutions from this chapter. Chapter 4.3SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Annulene

    A cyclic hydrocarbon with a continuous alternation of single and double bonds.

  • Aromatic amine

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

  • Atropisomers

    Enantiomers that lack a chiral center and differ because of hindered rotation.

  • Center of symmetry

    A point so situated that identical components of an object are located on opposite sides and equidistant from that point along any axis passing through it.

  • chemical changes

    Processes in which one or more substances are converted into other substances; also called chemical reactions. (Section 1.3)

  • chemistry.

    The study of matter and the changes it undergoes. (1.1)

  • Excited state

    A state of a system at higher energy than the ground state.

  • Fischer esterification

    A process in which a carboxylic acid is converted into an ester when treated with an alcohol in the presence of an acid catalyst.

  • folding

    The process by which a protein adopts its biologically active shape. (Section 24.7)

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • Homotopic groups

    Atoms or groups on an atom that give an achiral molecule when one of the groups is replaced by another group. The hydrogens of the CH2 group of propane, for example, are homotopic. Replacing either one of them with deuterium gives 2-deuteropropane, which is achiral. Homotopic groups have identical chemical shifts under all conditions

  • Lewis acid

    Any molecule or ion that can form a new covalent bond by accepting a pair of electrons.

  • Nucleic acid

    A biopolymer containing three types of monomer units: heterocyclic aromatic amine bases derived from purine and pyrimidine, the monosaccharides d-ribose or 2-deoxy-d-ribose, and phosphoric acid

  • parts per million (ppm)

    The concentration of a solution in grams of solute per 106 (million) grams of solution; equals milligrams of solute per liter of solution for aqueous solutions. (Section 13.4)

  • Pauli exclusion principle

    A rule stating that no two electrons in an atom may have the same four quantum numbers (n, l, ml, and ms). As a reflection of this principle, there can be no more than two electrons in any one atomic orbital. (Section 6.7)

  • peptidases

    A variety of enzymes that selectively hydrolyze specific peptide bonds.

  • spectrum

    The distribution among various wavelengths of the radiant energy emitted or absorbed by an object. (Section 6.3)

  • steric number

    The total of (single bonds + lone pairs) for an atom in a compound.

  • unsaturated

    A compound containingone or more p bonds.

  • Wave function

    A solution to a set of equations that defi nes the energy of an electron in an atom and the region of space it may occupy.

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