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Solutions for Chapter 11.2SE: 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 11.2SE

Solutions for Chapter 11.2SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 11.2SE 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. Since 2 problems in chapter 11.2SE have been answered, more than 68281 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxy substituent

    An OR group.

  • Bond length

    The distance between atoms in a covalent bond in picometers (pm; 1 pm 5 10212 m) or Å (1Å 5 10210 m).

  • bonding molecular orbital

    A molecular orbital in which the electron density is concentrated in the internuclear region. The energy of a bonding molecular orbital is lower than the energy of the separate atomic orbitals from which it forms. (Section 9.7)

  • chemical reactions

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

  • coordination number.

    In a crystal lattice it is defined as the number of atoms (or ions) surrounding an atom (or ion) (11.4). In coordination compounds it is defined as the number of donor atoms surrounding the central metal atom in a complex. (23.3)

  • Cyanohydrin

    A molecule containing an !OH group and a !CN group bonded to the same carbon.

  • cycloalkane

    An alkane whose structure contains a ring.

  • decarboxylation

    A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.

  • Dihedral angle

    The angle created by two intersecting planes.

  • Electrophoresis

    The process of separating compounds on the basis of their electric charge

  • Enantiomeric excess (ee)

    The difference between the percentage of two enantiomers in a mixture

  • Gauche conformation

    A conformation about a single bond of an alkane in which two groups on adjacent carbons lie at a dihedral angle of 60°

  • Histone

    A protein, particularly rich in the basic amino acids lysine and arginine, that is found associated with DNA molecules

  • Isotactic polymer

    A polymer with identical confi gurations (either all R or all S) at all chiral centers along its chain, as, for example, isotactic polypropylene

  • 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)

  • node

    In atomic and molecular orbitals, a location where the value of y is zero.

  • Racemic mixture

    A mixture of equal amounts of two enantiomers.

  • Secondary structure of nucleic acids

    The ordered arrangement of nucleic acid strands

  • third order

    A reaction that has a rate equation in which the sum of all exponents is three

  • Upfield

    A signal of an NMR spectrum that is shifted toward the right (smaller chemical shift) on the chart paper.

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