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Solutions for Chapter 12: Chemistry: The Central Science 12th Edition

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Full solutions for Chemistry: The Central Science | 12th Edition

ISBN: 9780321696724

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Solutions for Chapter 12

Solutions for Chapter 12
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Textbook: Chemistry: The Central Science
Edition: 12
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward
ISBN: 9780321696724

This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 12. 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: 9780321696724. Since 121 problems in chapter 12 have been answered, more than 201553 students have viewed full step-by-step solutions from this chapter. Chapter 12 includes 121 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Allylic substitution

    Any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon.

  • bond order.

    The difference between the numbers of electrons in bonding molecular orbitals and antibonding molecular orbitals, divided by two. (10.7)

  • catalyst

    A compound that can speed up the rate of a reaction without itself being consumed by the reaction.

  • cephalins

    Phosphoglycerides that contain ethanolamine.

  • chain reaction

    A series of reactions in which one reaction initiates the next. (Section 21.7)

  • concentration

    The quantity of solute present in a given quantity of solvent or solution. (Section 4.5)

  • coordinate covalent bond.

    A bond in which the pair of electrons is supplied by one of the two bonded atoms; also called a dative bond. (9.9)

  • denaturation

    A process during which a protein unfolds under conditions of mild heating.

  • exothermic process

    A process in which a system releases heat to its surroundings. (Section 5.2)

  • functional group

    An atom or group of atoms that imparts characteristic chemical properties to an organic compound. (Section 24.1)

  • Halohydrin

    A compound containing a halogen atom and a hydroxyl group on adjacent carbons; those containing Br and OH are bromohydrins, and those containing Cl and OH are chlorohydrins.

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • Histone

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

  • Lewis acid

    A compound capable offunctioning as an electron pair acceptor.

  • Mercaptan

    A common name for a thiol; that is, any compound that contains an -SH (sulfhydryl) group

  • miscible

    Two liquids that can be mixed with each other in any proportion.

  • molecular equation

    A chemical equation in which the formula for each substance is written without regard for whether it is an electrolyte or a nonelectrolyte. (Section 4.2)

  • positron

    A particle with the same mass as an electron but with a positive charge, 0 +1e, or b+. (Section 21.1)

  • quantum

    The smallest increment of radiant energy that may be absorbed or emitted; the magnitude of radiant energy is hn. (Section 6.2)

  • racemic mixture

    A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)

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