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Solutions for Chapter 7.10SE: 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 7.10SE

Solutions for Chapter 7.10SE
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This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Chapter 7.10SE includes 2 full step-by-step solutions. Since 2 problems in chapter 7.10SE have been answered, more than 64676 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417.

Key Chemistry Terms and definitions covered in this textbook
  • alkyl amines

    A format for naming amines containing simple alkyl groups.

  • Anion

    An atom or group of atoms bearing a negative charge.

  • Bond dipole moment

    A measure of the polarity of a covalent bond. The product of the charge on either atom of a polar bond times the distance between the atoms

  • 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)

  • carbide

    A binary compound of carbon with a metal or metalloid. (Section 22.9)

  • disulfide

    A compound with the structure R!S!S!R.

  • E2

    A bimolecular eliminationreaction.eclipsed conformation (Sect. 4.7): A conformationin which groups are eclipsing each other in aNewman projection.

  • effusion

    The escape of a gas through an orifice or hole. (Section 10.8)

  • electrolyte

    A solute that produces ions in solution; an electrolytic solution conducts an electric current. (Section 4.1)

  • electrophilic aromatic substitution

    A substitution reaction in which an aromatic proton is replaced by an electrophile and the aromatic moiety is preserved.

  • energy of activation

    In an energy diagram, the height of the energy barrier (the hump) between the reactants and the products.

  • exchange (metathesis) reaction

    A reaction between compounds that when written as a molecular equation appears to involve the exchange of ions between the two reactants. (Section 4.2)

  • 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°

  • homolitic bond cleavage

    Bond breaking that results in the formation of unchanged species called radicals.

  • indicator

    A substance added to a solution that changes color when the added solute has reacted with all the solute present in solution. The most common type of indicator is an acid–base indicator whose color changes as a function of pH. (Section 4.6)

  • miscible liquids

    Liquids that mix in all proportions. (Section 13.3)

  • peroxides

    Compounds with the general structure R!O!O!R.

  • Stereocenter

    An atom, most commonly carbon, about which exchange of two groups produces a stereoisomer. Chiral centers are one type of stereocenter

  • sulfone

    A compound that contains a sulfur atom that has double bonds with two oxygen atoms and is flanked on both sides by R groups.

  • Zaitsev’s rule

    A rule stating that the major product of a b-elimination reaction is the most stable alkene; that is, it is the alkene with the greatest number of substituents on the carboncarbon double bond

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